5-HT Receptors and the Development of New Antidepressants

Serotonin modulates several physiological and cognitive pathways throughout the human body that affect emotions, memory, sleep, and thermal regulation. The complex nature of the serotonergic system and interactions with other neurochemical systems indicate that the development of depression may be mediated by various pathomechanisms, the common denominator of which is undoubtedly the disturbed transmission in central 5-HT synapses. Therefore, the deliberate pharmacological modulation of serotonergic transmission in the brain seems to be one of the most appropriate strategies for the search for new antidepressants. As discussed in this review, the serotonergic system offers great potential for the development of new antidepressant therapies based on the combination of SERT inhibition with different pharmacological activity towards the 5-HT system. The aim of this article is to summarize the search for new antidepressants in recent years, focusing primarily on the possibility of benefiting from interactions with various 5-HT receptors in the pharmacotherapy of depression.


Introduction
Depression is a mental illness that affects over 250 million people worldwide [1]. Emotional (depressed mood, irritability, anhedonia), somatic (sleep, appetite, libido), and functional disorders (suicidal thoughts, slowed speech and movement, learning, memory and attention deficits) [2] make this disease the main cause of disabilities in the general population [3,4].
An important step in the treatment of depressive disorders is the introduction of SSRIs (serotonin reuptake inhibitors), which are currently first-line antidepressants (e.g., fluoxetine, sertraline, escitalopram). Their mechanism of action is based on the serotonergic system, and the molecular target is the serotonin transporter protein (SERT). The effectiveness of these therapeutics, unfortunately, leaves much to be desired; 60-70% of patients do not experience a remission of symptoms, and 30-40% do not respond to the treatment at all [5]. A serious drawback of selective serotonin reuptake inhibitors is their latency period, i.e., a delay in the therapeutic response by 2-6 weeks. Common side effects for SSRIs are sexual dysfunction, anxiety, and food intolerances.
Apart from SSRIs, other selective monoamine reuptake inhibitors are also used in pharmacotherapy. Reboxetine, a selective norepinephrine reuptake inhibitor, appears to be less effective than the SSRIs. These observations may, however, result from its relatively low tolerance [6]. Bupropion, on the other hand, is a norepinephrine and dopamine reuptake inhibitor and, therefore, has a more activating profile than SSRI drugs. Two drugs, venlafaxine and duloxetine, are classified as dual serotonin-norepinephrine reuptake inhibitors (SNRIs). However, the efficacy of the norepinephrine reuptake blocking at clinical doses of duloxetine is unclear [7]. Clinical guidelines often recommend the use of SNRIs in patients who do not respond to SSRIs [8][9][10].
There is a need for the further exploration of the neurochemical causes of depression. Recent studies report the influence of many various types of neurosignaling on There is a need for the further exploration of the neurochemical causes of depression. Recent studies report the influence of many various types of neurosignaling on the mechanism of depression [11][12][13][14]. The search for new generations of antidepressants using the triple reuptake inhibition mechanism (SSRI/SNRI/SDARI), or the combination of serotonin reuptake inhibition with affinities for various 5-hydroxytryptamine (5-HT) receptor subtypes, broadens the knowledge in this field [15][16][17].
A significant part of recent studies proves that serotonergic dysfunction, especially related to the postsynaptic 5-HT1A receptor, plays an important role in the pathomechanism of Major Depressive Disorder (MDD) [18][19][20][21][22][23][24]. Clinical trials show that the combination of SSRIs with both partial agonism and antagonism of the 5-HT1A receptor may result in an improvement in the speed and efficacy of the antidepressant effect [23,25,26]. This can be confirmed by the drugs recently introduced into the pharmacotherapy of depression-vilazodone and vortioxetine ( Figure 1). Vilazodone exhibits partial agonist activity at the 5-HT1A receptor, while vortioxetine binds to several 5-HT receptor subtypes (5-HT1A, 5-HT1B, 5-HT1D, 5-HT3, and 5-HT7). For example, the degree of sexual dysfunction associated with the use of vilazodone has been found to be relatively low [27]. Vortioxetine, on the other hand, positively influences cognitive impairment related to depression [10,28]. The targeted pharmacological modulation of serotonergic transmission in the brain continues to be a leading strategy in the search for new antidepressants. The careful selection of molecular targets for the proper use of the mechanisms of serotonergic modulation, which influences other neurotransmission systems, seems to be the most effective strategy for supplementing the activity of "serotonin-enhancing" drugs in the near future. A better understanding of the receptors and receptor signaling responsible for the effects of serotonin on neurogenesis can also help in the development of new and more effective drugs. The aim of this article is to summarize the search for new antidepressants in recent years, focusing primarily on the possibility of benefiting from interactions with various 5-HT receptors in the pharmacotherapy of depression.

The Serotonergic System and Depression
Serotonin, or 5-hydroxytryptamine (5-HT), is a monoamine neurotransmitter found throughout the human body [19,29]. Serotonin is synthesized in the midbrain in a small population of raphe nucleus neurons where tryptophan hydroxylase is expressed [30]. However, serotonin synthesis is not limited to the central nervous system (CNS), as tryptophan hydroxylase is also found in enterochromaffin cells in the gastrointestinal tract [31]. In fact, it should be noted that most of the serotonin in the human body is produced by this cell type [32]. Serotonin binds to more than 14 receptor proteins, most of which are G-protein coupled receptors [30,33]. This molecule mediates the transmission of several physiological and cognitive systems throughout the body that affect emotions, memory, sleep, and thermal regulation [34].
Serotonin is synthesized in the body from an essential amino acid-L-tryptophan. Ingested with food, L-tryptophan is converted into serotonin through a series of reactions. The targeted pharmacological modulation of serotonergic transmission in the brain continues to be a leading strategy in the search for new antidepressants. The careful selection of molecular targets for the proper use of the mechanisms of serotonergic modulation, which influences other neurotransmission systems, seems to be the most effective strategy for supplementing the activity of "serotonin-enhancing" drugs in the near future. A better understanding of the receptors and receptor signaling responsible for the effects of serotonin on neurogenesis can also help in the development of new and more effective drugs. The aim of this article is to summarize the search for new antidepressants in recent years, focusing primarily on the possibility of benefiting from interactions with various 5-HT receptors in the pharmacotherapy of depression.

The Serotonergic System and Depression
Serotonin, or 5-hydroxytryptamine (5-HT), is a monoamine neurotransmitter found throughout the human body [19,29]. Serotonin is synthesized in the midbrain in a small population of raphe nucleus neurons where tryptophan hydroxylase is expressed [30]. However, serotonin synthesis is not limited to the central nervous system (CNS), as tryptophan hydroxylase is also found in enterochromaffin cells in the gastrointestinal tract [31]. In fact, it should be noted that most of the serotonin in the human body is produced by this cell type [32]. Serotonin binds to more than 14 receptor proteins, most of which are G-protein coupled receptors [30,33]. This molecule mediates the transmission of several physiological and cognitive systems throughout the body that affect emotions, memory, sleep, and thermal regulation [34].
Serotonin is synthesized in the body from an essential amino acid-L-tryptophan. Ingested with food, L-tryptophan is converted into serotonin through a series of reactions. The first step, which simultaneously limits the rate of serotonin synthesis, is the hydroxylation of L-tryptophan to 5-hydroxy-L-tryptophan (5-HTP) by tryptophan hydroxylase (TPH) using oxygen and tetrahydropteridine as co-factors. There are two isoforms of TPH that can participate in this reaction: TPH1, expressed predominantly peripherally; and TPH2, expressed only in the brain. L-aromatic amino acid decarboxylase (AADC) then converts 5-HTP to serotonin [19,31].
The crossing of the blood-brain barrier (BBB) by serotonin is impossible due to its acid dissociation [35]; therefore, the amount of serotonin present in the CNS depends on the amount of centrally present L-tryptophan. The L-tryptophan present in the systemic circulation is actively transported by the BBB to the CNS using a carrier protein, where it is then converted into serotonin. Serotonin synthesized in the central nervous system is stored in secretory vesicles, where it remains until neuronal depolarization triggers its release into the synaptic cleft, allowing postsynaptic binding. Once released into the synapse, the serotonin molecules are eventually taken up by the serotonin transporter (5-HTT), which is located on the presynaptic axonal membrane. After the above-mentioned reuptake occurs, serotonin molecules are metabolized by monoamine oxidase (MAO) to 5-hydroxyindole acetic acid (5-HIAA) [29]. There are two isoforms of MAO (MAO-A and MAO-B), and both break down serotonin into neurons through oxidative deamination. The serotonin metabolite (5-HIAA) is actively transported from the CNS to the periphery and then excreted in the urine [19].
Already by the 1950s, it was noted that several mental illnesses showed abnormalities in the serotonergic system. The relationship between the serotonergic system and depression has been confirmed in clinical trials. They showed that an acute, transient relapse of depressive symptoms can be produced in subjects in remission using p-chlorophenylalanine (an irreversible inhibitor of serotonin synthesis). L-tryptophan depletion, causing a temporary reduction in central serotonin levels, had similar consequences. These findings have shown that the clinical efficacy of antidepressants depends on the presynaptic serotonergic function. Other studies have demonstrated a reduced concentration of the major metabolite of serotonin (5-HIAA) in the cerebrospinal fluid of untreated depressed patients and a reduced concentration of 5-HT and its major metabolite (5-HIAA) in the postmortem brain tissue of depressed and/or suicidal patients [20].
The serotonergic neurons of the mammalian brain constitute the most extensive and complex neurochemical network in the CNS after the glutamatergic system, which is the brain's primary transmission network. It has been estimated that the human brain contains approximately 250,000 5-HT neurons. For comparison, the total number of all neurons is around 10 11 [36]. While serotonergic neurons originate mainly in the brainstem dorsal and median raphe nuclei, they arborise over large areas such that they innervate almost every area of the brain with high densities of axonal varicosities. Some serotonergic projections create classical chemical synapses, but many release 5-HT in a paracrine manner (sometimes referred to as "volumetric transmission"). In addition, serotonin neurons exhibit slow (~1 Hz) and regular tonic activity that ceases during the rapid eye movement sleep phase (REM-off neurons). This activity is parallel to the noradrenergic neurons of the locus coeruleus [34]. Under normal conditions, the activity of serotonergic neurons is tightly controlled by a number of mechanisms, including: (i.) glutamatergic inputs from the forebrain (mainly the prefrontal cortex) [37], (ii.) the tonic noradrenergic input from the pontine nuclei [38], (iii.) inhibitory GABAergic signals from local interneurons [39], and (iv.) dopamine signals from the dopaminergic nuclei of the midbrain [40]. Moreover, the serotonin system is, in a way, self-regulating. The key control mechanism of 5-HT neurons is negative feedback through the 5-HT 1A autoreceptors [20]. This mechanism is currently being studied in great detail in the context of the treatment of CNS diseases.
The aforementioned anatomical and electrophysiological picture shows that changes in the activity of serotonergic neurons affect a large population of target neurons in the forebrain. The complex nature of the serotonergic system and interactions with other neurochemical systems indicate that the development of MDD may be mediated by various pathomechanisms. Currently suggested mechanisms include: (i.) low neuronal production of serotonin or of postsynaptic receptors, (ii.) decreased excitatory inputs or excessive

The 5-HT 1A Receptors
The 5-HT 1A receptors are located primarily in the following populations: (i.) presynaptic neurons of the raphe nuclei of the midbrain and (ii.) postsynaptic neurons, mainly in the hippocampus, septum, amygdala, and corticolimbic regions [42]. Autoreceptors are located within the bodies and dendrites of serotonin neurons. Their activation inhibits neuronal discharges and reduces the release of serotonin [43]. Thus, 5-HT 1A autoreceptors play an important role in the self-regulation of the serotonergic system; they partially inhibit the activity of adenylate cyclase [44] and activate G protein-dependent rectifying potassium channels (GIRK) with the use of the βγ subunit of G protein [45]. This causes membrane hyperpolarization, a reduction in neuronal excitability, and the inhibition of potentialdependent calcium channels, reducing the influx of calcium ions. The consequence is a reduction in the neural discharge rate. Given the significant influence of these neuronal discharges on the overall activity of the entire serotonergic system, it can be concluded that the reduction in the firing rate evoked by serotonin and other 5-HT 1A agonists immediately translates into an overall reduction in 5-HT release in most areas of the brain, particularly in regions innervated by the dorsal raphe [20].
The activation of 5-HT 1A autoreceptors by endogenous serotonin, therefore, plays an essential role in the physiological control of the activity of the 5-HT ascending neurons. The 5-HT neurons during waking periods show a slow and regular rate of discharge [36]. Under conditions of excessive excitatory input (e.g., stress), there is an increased release of serotonin in the vicinity of neuronal bodies. It activates 5-HT 1A autoreceptors, which allow low and regular neuronal activity to be maintained [40]. Thus, 5-HT 1A autoreceptors act as negative feedback physiological "safety valves" to maintain homeostasis.
The expression of 5-HT 1A heteroreceptors, in turn, takes place in populations of non-serotonin receptors, mainly in the limbic system within: (i.) bodies and dendrites of glutamatergic neurons [43] or (ii.) axons of GABA-ergic [46], and (iii.) cholinergic neurons [47]. These receptors are involved in regulating the release of various neurotransmitters: acetylcholine in the medial septum [48], glutamate in the prefrontal cortex [49], and dopamine in the ventral tegmental area [50]. In most regions of the brain, the inhibition of adenylate cyclase occurs due to the activation of the Gαi protein. The GIRK channels in the hippocampus are activated by the βγ subunits of the Gαo isoform [51]. The 5-HT 1A receptors in the cortex and hypothalamus bind to both the Gαi and Gαo subunits, while their preferential binding to the Gαi3 protein occurs within the raphe nucleus.
The differences in the properties of 5-HT 1A auto-and hetero-receptors are manifested in their different functional selectivity [52]: 5-HT 1A heteroreceptors stimulate [53], while 5-HT 1A autoreceptors inhibit ERK1/2 transmission [54]. The 5-HT 1A -biased agonism appears to result in the preferential activation of a specific signaling pathway without affecting or even blocking other pathways associated with this receptor subtype [55]. It has also been shown that there is an agonist-dependent modulation of G-protein coupling and a transduction of 5-HT 1A receptors in rat dorsal raphe nucleus. Moreover, 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT, a full 5-HT 1A receptor agonist) compared with buspirone (a partial 5-HT 1A receptor agonist) fails to modify forskolin-stimulated cAMP accumulation [56].
In general, 5-HT 1A receptor-deficient mice show a shorter immobility time in the forced swim test than wild-type control animals [57]. The lack of functional 5-HT 1A autoreceptors may, therefore, favor a less-depressed phenotype. The whole-life suppression of 5-HT 1A heteroreceptor expression in adolescence results in a broad depression-like phenotype. In addition, the group showed physiological and cellular changes within medial prefrontal cortex-dorsal raphe proper circuitry: (i.) increased basal serotonin levels in the medial prefrontal cortex, which is hyporeactive to stress and (ii.) decreased basal serotonin levels and firing rates in a dorsal raphe hyperactivated by the same stressor [57].
Animal studies show that both the stimulation and blockade of 5-HT 1A receptors can cause or accelerate the antidepressant effect [17]. It is difficult not to associate this with the above-described functional differences of 5-HT 1A auto-and hetero-receptors and the phenomenon of the biased 5-HT 1A agonism. Many studies have demonstrated the antidepressant effect of 8-OH-DPAT reversed by 5-HT 1A receptor antagonists [58]. Moreover, 5-HT 1A receptor-deficient mice showed no increase in adult neurogenesis in the hippocampus after chronic treatment with fluoxetine (SSRI) and not with imipramine (TCA) [59]. The preferential activation of postsynaptic 5-HT 1A receptors by F15599 (Figure 2), a biased 5-HT 1A agonist, resulted in an antidepressant-like effect [60]. Similar activity was shown by F13714, a non-selective agonist of 5-HT 1A receptors, but it induced a deeper "serotonin syndrome", hypothermia, and corticosterone release in rats. Elevated corticosterone levels accompany chronic stress in animals, leading to depression [61]. Moreover, the activation of 5-HT 1A receptors in the prefrontal cortex (PFC) by F15599 produces strong antidepressant-like effects in the forced swim test (FST) in rats, with a distinctive bimodal dose-response pattern. These data suggest that F15599 may target specific 5-HT 1A receptor subpopulations in the PFC, possibly located on the GABAergic and/or glutaminergic neurons [62]. 5-HT1A autoreceptors inhibit ERK1/2 transmission [54]. The 5-HT1A-biased agonism appears to result in the preferential activation of a specific signaling pathway without affecting or even blocking other pathways associated with this receptor subtype [55]. It has also been shown that there is an agonist-dependent modulation of G-protein coupling and a transduction of 5-HT1A receptors in rat dorsal raphe nucleus. Moreover, 8-hydroxy-2-(din-propylamino)tetralin (8-OH-DPAT, a full 5-HT1A receptor agonist) compared with buspirone (a partial 5-HT1A receptor agonist) fails to modify forskolin-stimulated cAMP accumulation [56].
In general, 5-HT1A receptor-deficient mice show a shorter immobility time in the forced swim test than wild-type control animals [57]. The lack of functional 5-HT1A autoreceptors may, therefore, favor a less-depressed phenotype. The whole-life suppression of 5-HT1A heteroreceptor expression in adolescence results in a broad depression-like phenotype. In addition, the group showed physiological and cellular changes within medial prefrontal cortex-dorsal raphe proper circuitry: (i.) increased basal serotonin levels in the medial prefrontal cortex, which is hyporeactive to stress and (ii.) decreased basal serotonin levels and firing rates in a dorsal raphe hyperactivated by the same stressor [57].
Animal studies show that both the stimulation and blockade of 5-HT1A receptors can cause or accelerate the antidepressant effect [17]. It is difficult not to associate this with the above-described functional differences of 5-HT1A auto-and hetero-receptors and the phenomenon of the biased 5-HT1A agonism. Many studies have demonstrated the antidepressant effect of 8-OH-DPAT reversed by 5-HT1A receptor antagonists [58]. Moreover, 5-HT1A receptor-deficient mice showed no increase in adult neurogenesis in the hippocampus after chronic treatment with fluoxetine (SSRI) and not with imipramine (TCA) [59]. The preferential activation of postsynaptic 5-HT1A receptors by F15599 (Figure 2), a biased 5-HT1A agonist, resulted in an antidepressant-like effect [60]. Similar activity was shown by F13714, a non-selective agonist of 5-HT1A receptors, but it induced a deeper "serotonin syndrome", hypothermia, and corticosterone release in rats. Elevated corticosterone levels accompany chronic stress in animals, leading to depression [61]. Moreover, the activation of 5-HT1A receptors in the prefrontal cortex (PFC) by F15599 produces strong antidepressant-like effects in the forced swim test (FST) in rats, with a distinctive bimodal doseresponse pattern. These data suggest that F15599 may target specific 5-HT1A receptor subpopulations in the PFC, possibly located on the GABAergic and/or glutaminergic neurons [62]. The previously described physiological function of 5-HT1A autoreceptors and their regulation of depressive behavior seem to be unfavorable in the context of the mechanism of action of antidepressants [20,63]. The negative feedback pathway through 5-HT1A autoreceptors may decrease the efficacy of the SSRI as the dose increases, thus creating a second, anomalous part of the dose-response curve. This effect may also be responsible for the so-called therapeutic window for such antidepressants [64]. The prolonged use of SSRIs translates into significantly higher levels of extracellular 5-HT than after a single administration [65]. The negative feedback loop is believed to be the cause of the slow and delayed clinical efficacy of antidepressant drugs [66]. Administration of antidepressants The previously described physiological function of 5-HT 1A autoreceptors and their regulation of depressive behavior seem to be unfavorable in the context of the mechanism of action of antidepressants [20,63]. The negative feedback pathway through 5-HT 1A autoreceptors may decrease the efficacy of the SSRI as the dose increases, thus creating a second, anomalous part of the dose-response curve. This effect may also be responsible for the so-called therapeutic window for such antidepressants [64]. The prolonged use of SSRIs translates into significantly higher levels of extracellular 5-HT than after a single administration [65]. The negative feedback loop is believed to be the cause of the slow and delayed clinical efficacy of antidepressant drugs [66]. Administration of antidepressants (tricyclic drugs, monoamine oxidase inhibitors, and SSRIs) significantly increases the level of extracellular 5-HT in the midbrain raphe [67]. This leads to: (i.) the activation of 5-HT 1A receptors, (ii.) the reduction in 5-HT cell firing [68], and (iii.) the terminal release of 5-HT [69]. The inhibition of SSRIs in the negative feedback pathway clearly decreases with the duration of treatment. This is most likely due to the serotonin-induced desensitization of raphe 5-HT 1A autoreceptors discussed earlier [70]. Thus, the desensitization of 5-HT 1A autoreceptors may accelerate the onset and/or enhance the antidepressant effect [71]. Mice with higher levels of 5-HT 1A autoreceptors showed a blunted physiological response to acute stress, increased behavioral despair, and no behavioral response to fluoxetine [72]. Moreover, mice with lower autoreceptor levels showed a strong behavioral response to fluoxetine after both chronic and subchronic administration [72]. Thus, lowering the level of 5-HT 1A autoreceptors prior to antidepressant treatment may accelerate and increase the effectiveness of antidepressant therapy. Combining SSRI treatment with the 5-HT 1A receptor antagonist pindolol significantly reduces the latency of the antidepressant response and improves the clinical response in previously untreated MDD patients (Table 1) [20,21,73]. The above data indicate that the stimulation of postsynaptic 5-HT 1A receptors or the blockade of presynaptic 5-HT 1A receptors results in antidepressant-like activity. (-)-pindolol may also stimulate somatodendritic 5-HT 1A receptors. Then, its accelerating antidepressant effect might stem from the accelerated adaptive changes like autoreceptor desensitization in response to both serotonin and pindolol. This mechanism can also be achieved by initiating the treatment with high-dose SSRI when a patient is suicidal. The antidepressant action of pindolol may also be related to its agonistic activity at the β 1 -adrenoreceptor as this drug possesses the strongest intrinsic sympathicomimetic activity among other β-blockers [74]. Table 1. Clinical effects of augmentation of SERT inhibition with different activities towards 5-HT receptors.

SSRI + pindolol SERT inhibition + 5-HT 1A agonism
Reduced latency of the antidepressant response and improved the clinical response in previously untreated MDD patients [21] SSRI + buspirone SERT inhibition + 5-HT 1A partial agonism Symptom remission in patients unsuccessfully treated with SSRIs [75] SSRI + mirtazapine SERT inhibition + 5-HT 2A antagonism Augmentation of the clinical response to SSRIs in treatment-resistant patients [76] Vilazodone SERT inhibition + 5-HT 1A partial agonism In contrast to prototypical SSRIs, vilazodone has not been associated with treatment-emergent sexual difficulties or dysfunction [27] Vortioxetine SERT, 5-HT 3 and 5-HT 7 receptors inhibition, 5-HT 1A agonism Potential rapid onset of action [77] According to the neurotrophic hypothesis of depression, decreased neurotrophic support causes neuronal atrophy, which in turn reduces hippocampal neurogenesis and leads to depression. Clinical data support this theory: postmortem analysis has shown reduced volumes of the hippocampus and prefrontal cortex in depressed patients [78,79]. Persons diagnosed with MDD showed decreased levels of BDNF (brain-derived neurotrophic factor) and NGF (nerve growth factor) in the hippocampus. A deficit of these neurotrophins may promote neuronal loss [80,81]. This phenomenon was confirmed by in vivo studies [82][83][84][85], which showed that antidepressants reversed these changes [86]. Chronic treatment with 8-OH-DPAT, in turn reduced the feeding delay in the noveltysuppressed feeding test and increased adult hippocampal neurogenesis in wild-type mice, but showed no effect in the 5-HT 1A receptor knockout group [59]. Thus, 5-HT 1A receptors mediate the action of 8-OH-DPAT, from which it can be concluded that the postsynaptic 5-HT 1A receptors mediate the antidepressant-like action of 8-OH-DPAT [87]. The specific deletion of the 5-HT 1A heteroreceptors from mature granular cells in the dentate gyrus of the hippocampus has also been found to abolish the effects of SSRIs in various behavioral tests [88]. It also attenuated the effects of SSRIs on adult neurogenesis and the expression of hippocampal neurotrophic factors: BDNF and VEGF (vascular endothelial growth factor). Whole-life 5-HT 1A heteroreceptor-knockout (but not autoreceptor-knockout) mice showed decreased mobility in the forced swim test [89]. Such a depression-like phenotype was not observed when the suppression of heteroreceptors was initiated in adulthood. Therefore, serotonergic signaling in the forebrain during development may stably influence the circuits underlying the behavioral response to the FST [89].
The STAR*D clinical trial shows that in patients unsuccessfully treated with SSRIs, the augmentation with buspirone resulted in symptom remission [75]. Buspirone (a partial agonist of the 5-HT 1A receptor) enhances the desensitization of 5-HT 1A autoreceptors, increasing the effectiveness of the SSRI treatment. Recently, a single transcription factor, Freud-1, has been found to be crucial for the expression of the 5-HT 1A autoreceptor [90]. Mice with a conditional knockout of Freud-1 in serotonin neurons were shown to have elevated levels of 5-HT 1A autoreceptors and exhibited the enhanced anxiety and depressive behavior in adulthood that was refractory to chronic SSRI treatment [90]. Interestingly, the double knockout of the Freud-1/5-HT 1A gene did not produce such effects. In this case, the depressive-like behavior was even reduced [90]. The study suggests that targeting specific transcription factors may increase the response to antidepressant treatment. These reports indicated the need to search for compounds targeting only the population of 5-HT 1A autoor heteroreceptors.
The results of postmortem and neuroimaging studies suggest an increased density of 5-HT 1A autoreceptors in patients with MDD compared to the control group [91][92][93]. Genetic studies have shown that individuals with an increased density or activity of 5-HT 1A autoreceptors are more prone to mood disorders and respond poorly to antidepressant treatment [94,95]. However, the number and density of postsynaptic 5-HT 1A receptors have been shown to be unaltered or reduced in depressed patients, and this alteration is not sensitive to antidepressant treatment [96]. Long-term antidepressant therapy causes the tonic activation of 5-HT 1A receptors in the dorsal hippocampus [97], and activation of 5-HT 1A receptors in the dentate gyrus increases hippocampal neurogenesis [98]. In light of the cited reports, the use of 5-HT 1A agonists as antidepressants seems natural [99]. Some agents possessing such activity (e.g., buspirone and gepirone) show antidepressant efficacy in placebo-controlled trials, but their potency is lower than that of SSRIs. Most 5-HT 1A agonists (especially azapirones, Figure 3) show the preferential activation of presynaptic 5-HT 1A receptors. Moreover, these agents tend to have a reduced efficacy at postsynaptic 5-HT 1A receptors. Thus, endogenous serotonin competes in the postsynaptic sites with an exogenous substance (with lower agonism), which causes a paradoxical reduction in the tone at the postsynaptic 5-HT 1A receptors. Higher doses of 5-HT 1A agonists (such as those used in experimental animals) are likely to result in the greater activation of postsynaptic 5-HT 1A receptors, which may explain the positive results of efficacy studies in animal models. Conversely, the administration of the selective 5-HT 1A receptor antagonist DU125530 with fluoxetine did not accelerate or increase the efficacy of fluoxetine in a double-blind, randomized, placebo-controlled clinical trial. DU125530 had similar binding to pre-and post-synaptic 5-HT 1A receptors [100], and the blockade of postsynaptic 5-HT 1A receptors likely offset the benefits of enhancing presynaptic serotonergic function [101]. This may show the importance of the activation of postsynaptic 5-HT 1A receptors in the mechanism of antidepressant action. ol. Sci. 2021, 22, 9015 8 of 32 Observations on the 5-HT1A receptor population contributed to a fruitful search for potential multimodal antidepressants that incorporate 5-HT1A receptor activity into their mechanism of action [102]. Recently developed compounds seem to overcome the aforementioned therapeutic problems of azapirones and other first-generation 5-HT1A agonists. Two new antidepressants, vilazodone [27,103] and vortioxetine [104,105], inhibit 5-HT reuptake and show the partial agonism at 5-HT1A receptors.
The 5-HT1A receptor ligands also possess their own potentially therapeutic activity. The 5-HT1A partial agonists show antianxiety [106,107], antidepressant [108], antiaggressive [109], anticraving [110], and anticataleptic properties [111]: • Animal studies show that both the stimulation and blockade of 5-HT1A receptors can cause or accelerate the antidepressant effect. It is difficult not to associate this with the functional differences of 5-HT1A auto-and hetero-receptors and the phenomenon of a biased 5-HT1A agonism; • A single transcription factor, Freud-1, has been found to be crucial for the expression of the 5-HT1A autoreceptor. Targeting it may increase the response to antidepressant treatment; • Observations on the 5-HT1A receptor population contributed to a fruitful search for potential multimodal antidepressants (vilazodone and vortioxetine) that incorporate 5-HT1A receptor activity into their mechanism of action.

The 5-HT1B Receptors
The 5-HT1B receptors, like 5-HT1A receptors, are located pre-and post-synaptically and are also negatively coupled to adenylate cyclase. Their highest densities are in the striatum, pallidum, nucleus accumbens, substantia nigra, and ventral tegmental area. Lower levels of 5-HT1B receptors are found in the hippocampus, amygdala, and cingulate cortex [112].
Unlike somatodendritic 5-HT1A autoreceptors, 5-HT1B autoreceptors are located on serotonergic axons, where they regulate the synthesis and release of 5-HT locally. The 5-HT1B postsynaptic receptors are located mainly in the centers of motor control (such as the basal ganglia), where they control the synaptic transmission of other neurotransmitters [112]. Studies have shown that 5-HT1B receptors play a role in depression, anxiety, migraines, locomotor activity, aggressive behavior, and the potentiation of the action of other drugs [112][113][114].
Animal studies show that the involvement of 5-HT1B receptors in the pathophysiology of depression is partly related to their responsiveness to environmental stress as well as their exposure to antidepressants [115]. The 5-HT1B heteroreceptors are involved in hippocampal neurogenesis, which may explain their importance for the antidepressant-like effect [116]. Mice lacking 5-HT1B autoreceptors showed an increased mobility in the FST as well as an increased preference for lower-sucrose concentrations in the sucrose preference test compared to the control group. After SSRI administration, elevated levels of serotonin in the hippocampus were observed [117]. Moreover, two common genetic polymorphisms of 5-HT1B receptors, G861C [118] and C129T [119], were associated with MDD and affective disorders. The 5-HT1B receptor gene knockout mice showed increased aggression [120]. Observations on the 5-HT 1A receptor population contributed to a fruitful search for potential multimodal antidepressants that incorporate 5-HT 1A receptor activity into their mechanism of action [102]. Recently developed compounds seem to overcome the aforementioned therapeutic problems of azapirones and other first-generation 5-HT 1A agonists. Two new antidepressants, vilazodone [27,103] and vortioxetine [104,105], inhibit 5-HT reuptake and show the partial agonism at 5-HT 1A receptors.
The 5-HT 1A receptor ligands also possess their own potentially therapeutic activity. The 5-HT 1A partial agonists show antianxiety [106,107], antidepressant [108], antiaggressive [109], anticraving [110], and anticataleptic properties [111]: • Animal studies show that both the stimulation and blockade of 5-HT 1A receptors can cause or accelerate the antidepressant effect. It is difficult not to associate this with the functional differences of 5-HT 1A auto-and hetero-receptors and the phenomenon of a biased 5-HT 1A agonism; • A single transcription factor, Freud-1, has been found to be crucial for the expression of the 5-HT 1A autoreceptor. Targeting it may increase the response to antidepressant treatment; • Observations on the 5-HT 1A receptor population contributed to a fruitful search for potential multimodal antidepressants (vilazodone and vortioxetine) that incorporate 5-HT 1A receptor activity into their mechanism of action.

The 5-HT 1B Receptors
The 5-HT 1B receptors, like 5-HT 1A receptors, are located pre-and post-synaptically and are also negatively coupled to adenylate cyclase. Their highest densities are in the striatum, pallidum, nucleus accumbens, substantia nigra, and ventral tegmental area. Lower levels of 5-HT 1B receptors are found in the hippocampus, amygdala, and cingulate cortex [112].
Unlike somatodendritic 5-HT 1A autoreceptors, 5-HT 1B autoreceptors are located on serotonergic axons, where they regulate the synthesis and release of 5-HT locally. The 5-HT 1B postsynaptic receptors are located mainly in the centers of motor control (such as the basal ganglia), where they control the synaptic transmission of other neurotransmitters [112]. Studies have shown that 5-HT 1B receptors play a role in depression, anxiety, migraines, locomotor activity, aggressive behavior, and the potentiation of the action of other drugs [112][113][114].
Animal studies show that the involvement of 5-HT 1B receptors in the pathophysiology of depression is partly related to their responsiveness to environmental stress as well as their exposure to antidepressants [115]. The 5-HT 1B heteroreceptors are involved in hippocampal neurogenesis, which may explain their importance for the antidepressant-like effect [116]. Mice lacking 5-HT 1B autoreceptors showed an increased mobility in the FST as well as an increased preference for lower-sucrose concentrations in the sucrose preference test compared to the control group. After SSRI administration, elevated levels of serotonin in the hippocampus were observed [117]. Moreover, two common genetic polymorphisms of 5-HT 1B receptors, G861C [118] and C129T [119], were associated with MDD and affective disorders. The 5-HT 1B receptor gene knockout mice showed increased aggression [120].
The p11 protein, which colocalizes with 5-HT 1B and 5-HT 4 receptors [121], plays a key role in modulating the function of the 5-HT 1B receptor. Its dysregulation has been reported in preclinical models of depression and in postmortem samples from MDD patients [122]. The p11 protein improves 5-HT 1B receptor function in various regions of the brain and contributes to an antidepressant-like effect in animal behavioral tests [123]. P11 knockout mice showed depression-like behavior and demonstrated a reduced responsiveness to 5-HT 1B receptor agonists and tricyclic antidepressants [123].
Studies in the learned helplessness model showed that 5-HT 1B receptors were upregulated in various regions of the brain following stress exposure. A reduced 5-HT 1B autoreceptor function and, thus, increased serotonin release, has also been demonstrated after chronic antidepressant treatment [124]. Moreover, chronic treatment with SSRIs induced a negative regulation and/or desensitization of 5-HT 1B autoreceptors [125] and facilitated the effect of SSRIs in serotonin neurotransmission [126]. Compounds exhibiting 5-HT 1B antagonism, administered alone or with antidepressants, have been shown to be effective in preclinical models of depression [127]. The pretreatment with 5-HT 1B receptor antagonists [128] or the genetic inactivation of the 5-HT 1B receptor [129] increased the SSRI-induced effect in mice. Therefore, the blockade of 5-HT 1B autoreceptors may promote the antidepressant effect. It has been suggested that the 5-HT 1B receptor antagonists themselves may be attributed to an antidepressant-like effect. SB-616234-A, a 5-HT 1B receptor antagonist, decreased immobility in a forced swim test in mice ( Figure 4) [130]. The selective 5-HT 1B receptor inverse agonist, SB236057A, increased, in turn, the extracellular concentration of serotonin in the dentate gyrus of a guinea pig. This effect was comparable to that of 14 days of paroxetine therapy [131]. The acute blockade of the 5-HT 1B receptor might cause a rapid antidepressant effect [131]. It appears that the agonist activation of 5-HT 1B heteroreceptors may also induce antidepressant-like effects [132]. CP94253, a selective 5-HT 1B receptor agonist, showed an antidepressant-like activity in a forced swimming test in mice [133]. Anpirtoline, as a selective 5-HT 1B receptor agonist, also reduced immobility in control mice but had no effect in 5-HT 1B knockout mice [132]. The effect of this compound in the FST was, therefore, due to the activation of the 5-HT 1B receptor. The above studies suggest that 5-HT 1B receptors play a role in antidepressant-like activity. Ther stimulation of postsynaptic receptors and the inhibition of presynaptic 5-HT 1B receptors may be beneficial in the treatment of depression [134]. The p11 protein, which colocalizes with 5-HT1B and 5-HT4 receptors [121], plays a key role in modulating the function of the 5-HT1B receptor. Its dysregulation has been reported in preclinical models of depression and in postmortem samples from MDD patients [122]. The p11 protein improves 5-HT1B receptor function in various regions of the brain and contributes to an antidepressant-like effect in animal behavioral tests [123]. P11 knockout mice showed depression-like behavior and demonstrated a reduced responsiveness to 5-HT1B receptor agonists and tricyclic antidepressants [123].
Studies in the learned helplessness model showed that 5-HT1B receptors were upregulated in various regions of the brain following stress exposure. A reduced 5-HT1B autoreceptor function and, thus, increased serotonin release, has also been demonstrated after chronic antidepressant treatment [124]. Moreover, chronic treatment with SSRIs induced a negative regulation and/or desensitization of 5-HT1B autoreceptors [125] and facilitated the effect of SSRIs in serotonin neurotransmission [126]. Compounds exhibiting 5-HT1B antagonism, administered alone or with antidepressants, have been shown to be effective in preclinical models of depression [127]. The pretreatment with 5-HT1B receptor antagonists [128] or the genetic inactivation of the 5-HT1B receptor [129] increased the SSRI-induced effect in mice. Therefore, the blockade of 5-HT1B autoreceptors may promote the antidepressant effect. It has been suggested that the 5-HT1B receptor antagonists themselves may be attributed to an antidepressant-like effect. SB-616234-A, a 5-HT1B receptor antagonist, decreased immobility in a forced swim test in mice ( Figure 4) [130]. The selective 5-HT1B receptor inverse agonist, SB236057A, increased, in turn, the extracellular concentration of serotonin in the dentate gyrus of a guinea pig. This effect was comparable to that of 14 days of paroxetine therapy [131]. The acute blockade of the 5-HT1B receptor might cause a rapid antidepressant effect [131]. It appears that the agonist activation of 5-HT1B heteroreceptors may also induce antidepressant-like effects [132]. CP94253, a selective 5-HT1B receptor agonist, showed an antidepressant-like activity in a forced swimming test in mice [133]. Anpirtoline, as a selective 5-HT1B receptor agonist, also reduced immobility in control mice but had no effect in 5-HT1B knockout mice [132]. The effect of this compound in the FST was, therefore, due to the activation of the 5-HT1B receptor. The above studies suggest that 5-HT1B receptors play a role in antidepressant-like activity. Ther stimulation of postsynaptic receptors and the inhibition of presynaptic 5-HT1B receptors may be beneficial in the treatment of depression [134]. As with 5-HT1A receptors, acute SSRI therapy activates terminally localized 5-HT1B receptors, thus reducing 5-HT synthesis and release. The long-term administration of SSRIs desensitizes terminal 5-HT1B autoreceptors [135], suggesting that the plasticity of the autoregulatory function of both 5-HT1A and 5-HT1B receptors may be important with respect to the therapeutic profile of SSRIs. Again, as with 5-HT1A receptor antagonists, the administration of 5-HT1B receptor antagonists increases the neurochemical and behavioral effects of SSRIs [128,136]. Interestingly, the co-administration of the selective 5-HT1A antagonist WAY-100635 and the 5-HT1B receptor antagonist SB-224289 has an additive effect, enhancing the neurochemical effects of fluoxetine. This has led to the suggestion that the As with 5-HT 1A receptors, acute SSRI therapy activates terminally localized 5-HT 1B receptors, thus reducing 5-HT synthesis and release. The long-term administration of SSRIs desensitizes terminal 5-HT 1B autoreceptors [135], suggesting that the plasticity of the autoregulatory function of both 5-HT 1A and 5-HT 1B receptors may be important with respect to the therapeutic profile of SSRIs. Again, as with 5-HT 1A receptor antagonists, the administration of 5-HT 1B receptor antagonists increases the neurochemical and behavioral effects of SSRIs [128,136]. Interestingly, the co-administration of the selective 5-HT 1A antagonist WAY-100635 and the 5-HT 1B receptor antagonist SB-224289 has an additive effect, enhancing the neurochemical effects of fluoxetine. This has led to the suggestion that the combination of the 5-HT 1A and 5-HT 1B receptor antagonism may increase CNS serotonin levels and, therefore, potentially be an effective treatment strategy for depression [20]: • Animal studies show that the involvement of 5-HT 1B receptors in the pathophysiology of depression is partly related to their responsiveness to environmental stress as well as an exposure to antidepressants; • The p11 protein improves 5-HT 1B receptor function in various regions of the brain and contributes to an antidepressant-like effect in animal behavioral tests; • The 5-HT 1B heteroreceptors are involved in hippocampal neurogenesis, which may explain their importance for the antidepressant-like effect. The stimulation of postsynaptic receptors and the inhibition of presynaptic 5-HT 1B receptors may be beneficial in the treatment of depression.

The 5-HT 1D , 5-HT 1E , and 5-HT 1F Receptors
The clinical significance of the remaining 5-HT 1 receptors (5-HT 1D , 5-HT 1E , 5-HT 1F ) is less clear. There is limited preclinical evidence linking some of the receptors with depressive states. The sensitivity of postsynaptic 5-HT 1D receptors in patients after treatment with SSRIs has been found to be impaired [137]. On the other hand, a postmortem study of untreated suicidal victims with a confirmed history of depression showed a much higher density of 5-HT 1D receptors in the globus pallidus [138]. The observed high expression of the 5-HT 1E receptor in the frontal cortex and hippocampus may indicate the relationship between 5-HT 1E receptors and cognitive functions and memory [20,139].

The 5-HT 2A Receptors
The 5-HT 2A receptors, like the others of the 5-HT 2 family, are preferentially coupled to the G protein of the Gq/11 type, so their activation increases the cellular level of inositol phosphate and, consequently, the cytosolic concentration of calcium ions. The 5-HT 2A receptors are distributed postsynaptically and presynaptically throughout the brain at serotonergic terminals, with the greatest concentration in the neocortex [140][141][142]. Recent anatomical and functional studies suggest that 5-HT 2A receptors are also present presynaptically as heteroreceptors, where they may enhance glutamatergic neurotransmission and participate in memory processes [143]. It has also been demonstrated that the 5-HT 2A receptors of the cerebral cortex are located on GABAergic interneurons as well as glutamatergic projection neurons in the brains of humans and rodents [42,144].
Many antidepressants and antipsychotic drugs possess a relatively high binding to 5-HT 2A receptors [145]. Although there is no direct correlation between the affinity of these drugs for 5-HT 2A receptors and clinically effective doses, there is ample evidence that the 5-HT 2A receptor plays a role in the pathomechanism of depression [20,146]. Some antidepressants mediate their action partly via the antagonism of 5-HT 2A receptors [147]. In addition, chronic treatment with antidepressants, such as tricyclic antidepressants, monoamine oxidase inhibitors, mianserin, mirtazapine, or sertraline, decreased the number of 5-HT 2A receptors in rodents [148]. Chronic electroconvulsive shock treatment resulted in the upregulation of cortical 5-HT 2A receptors in rodents [149].
Several clinical trials have shown that atypical antipsychotics [150] and the antidepressant mirtazapine with an affinity for α 2 -adrenoceptors and 5-HT 2A receptors [151] augment the clinical response to SSRIs in treatment-resistant patients [76]. A common feature of these substances is their ability, at clinical doses, to block responses to signals mediated by 5-HT 2A receptors [152]. Such downregulation could, inter alia, explain why the side effects of SSRIs diminish after 2 or 3 weeks. The high co-expression of 5-HT 1A and 5-HT 2A receptors in the neocortex [153] may indicate that the blockade of 5-HT 2A receptors enhances 5-HT 1A receptor-mediated neurotransmission in the cortical and limbic regions, an activity associated with antidepressant efficacy. The chronic administration of 5-HT 2A receptor antagonists has been shown to result in a paradoxically negative regulation of 5-HT 2A receptors [154,155], which may be beneficial in the treatment of depression. Moreover, preclinical studies indicate that 5-HT 2A antagonists have anxiolytic properties, as demonstrated by ritanserin, a 5-HT 2A antagonist with anxiolytic effects in humans [156].
Another issue is the relationship between the 5-HT 2A receptor and the noradrenergic system in relation to depression [157]. Studies have shown that the activation of 5-HT 2A receptors as a result of treatment with SSRIs causes an increase in serotonin levels in GABA neurons. This inhibits the neuronal activity of norepinephrine through the prolonged release of GABA [158][159][160]. In turn, citalopram, in addition to reducing norepinephrine firing, also has the effect of lowering basal and evoked extracellular norepinephrine levels in the amygdala [161]. This may underlie SSRI ineffectiveness in resistant depression. The co-administration of an SSRI and a 5-HT 2A receptor antagonist trazodone (as well as atypical antipsychotics, such as quetiapine, risperidone, olanzapine, and aripiprazole) reversed this inhibitory effect in noradrenergic neurons in rats and might be beneficial in the treatment of resistant depression [160,[162][163][164]. Increasing evidence shows that 5-HT 2A receptor antagonists display antidepressant effects. EMD 281014 ( Figure 5), a 5-HT 2A receptor antagonist, showed significant activity in the FST in congenital learned helpless rats [165]. A similar effect was shown by another 5-HT 2A receptor antagonist, FG5893, which significantly shortened the immobility time in the FST [166]. The selective 5-HT 2A receptor antagonist, M100907, enhanced the antidepressant-like behavioral effects of fluoxetine [167], suggesting that a selective 5-HT 2A receptor blockade may complement the behavioral effects of serotonin transporter inhibition. In contrast, recent studies in rats have shown that the functional disturbance of the 5-HT 2A receptor in the medial prefrontal cortex may contribute to postpartum mental disorders, including depression and psychosis [168]. In addition, prefrontal 5-HT 2A receptors may both have beneficial and negative effects on cognition, which might explain the aggravation of cognitive deficits after the onset of SSRI treatment in depressed patients, as well as the limited efficacy of second-generation antipsychotics that act as 5-HT 2A receptor antagonists against the strongly debilitating cognitive symptoms of schizophrenia and other psychiatric disorders [169]. A deficiency in 5-HT 2A receptors has also been shown to alter the metabolic and transcriptional, but not behavioral, consequences of chronic unpredictable stress in mice [170]. Moreover, preclinical studies indicate that 5-HT2A antagonists have anxiolytic properties, as demonstrated by ritanserin, a 5-HT2A antagonist with anxiolytic effects in humans [156]. Another issue is the relationship between the 5-HT2A receptor and the noradrenergic system in relation to depression [157]. Studies have shown that the activation of 5-HT2A receptors as a result of treatment with SSRIs causes an increase in serotonin levels in GABA neurons. This inhibits the neuronal activity of norepinephrine through the prolonged release of GABA [158][159][160]. In turn, citalopram, in addition to reducing norepinephrine firing, also has the effect of lowering basal and evoked extracellular norepinephrine levels in the amygdala [161]. This may underlie SSRI ineffectiveness in resistant depression. The co-administration of an SSRI and a 5-HT2A receptor antagonist trazodone (as well as atypical antipsychotics, such as quetiapine, risperidone, olanzapine, and aripiprazole) reversed this inhibitory effect in noradrenergic neurons in rats and might be beneficial in the treatment of resistant depression [160,[162][163][164]. Increasing evidence shows that 5-HT2A receptor antagonists display antidepressant effects. EMD 281014 (Figure 5), a 5-HT2A receptor antagonist, showed significant activity in the FST in congenital learned helpless rats [165]. A similar effect was shown by another 5-HT2A receptor antagonist, FG5893, which significantly shortened the immobility time in the FST [166]. The selective 5-HT2A receptor antagonist, M100907, enhanced the antidepressant-like behavioral effects of fluoxetine [167], suggesting that a selective 5-HT2A receptor blockade may complement the behavioral effects of serotonin transporter inhibition. In contrast, recent studies in rats have shown that the functional disturbance of the 5-HT2A receptor in the medial prefrontal cortex may contribute to postpartum mental disorders, including depression and psychosis [168]. In addition, prefrontal 5-HT2A receptors may both have beneficial and negative effects on cognition, which might explain the aggravation of cognitive deficits after the onset of SSRI treatment in depressed patients, as well as the limited efficacy of second-generation antipsychotics that act as 5-HT2A receptor antagonists against the strongly debilitating cognitive symptoms of schizophrenia and other psychiatric disorders [169]. A deficiency in 5-HT2A receptors has also been shown to alter the metabolic and transcriptional, but not behavioral, consequences of chronic unpredictable stress in mice [170]. The 5-HT2A blockade or SSRI-induced downregulation of 5-HT2A may lead to emotional blunting in patients. It is, therefore, very likely that 5-HT2A receptors may have different functions depending on the region of the brain:

The 5-HT 2B Receptors
The 5-HT 2B receptor is expressed mainly in peripheral tissues, especially in the liver, kidneys, and heart, and its distribution in the brain is low [171]. In the central nervous system, the 5-HT 2B receptor is present in septal nuclei, the dorsal hypothalamus, and the medial amygdala at levels similar to those found in the stomach [171]. The 5-HT 2B receptor, mRNA, is found in the dorsal raphe nucleus, suggesting a potential autoreceptor role [172]. The 5-HT 2B receptors are coupled to the Gq protein, which activates PLC (phospholipase C)/PKC (protein kinase C) and increases the concentration of calcium ions in the cytosol.
The knowledge about the function of the 5-HT 2B receptor in the CNS is limited; however, there are reports of the antidepressant properties of selective 5-HT 2B receptor agonists [173]. The presence of 5-HT 2B receptors in the dorsal raphe and their stimulatory role in 5-HT release has been demonstrated [173]. The pharmacological or genetic inactivation of the 5-HT 2B receptor abolished the effects of chronic treatment with SSRIs, and the stimulation of 5-HT 2B receptors induced an SSRI-like response in behavioral and neurogenic tests. In turn, the genetic inactivation of 5-HT 2B receptors in serotonergic neurons eliminated the neurogenic effects of fluoxetine [173]. It has recently been confirmed that 5-HT 2B receptors directly and positively regulated the activity of serotonin neurons [174]. In addition, the stimulation of the 5-HT 2B receptor via fluoxetine in astrocyte cell cultures resulted in the phosphorylation of extracellular signal-regulated kinases and the transactivation of the EGF (epidermal growth factor) receptor [175]. A reduced level of astroglial (but not neuronal) 5-HT 2B receptors in a mouse model of Parkinson's disease was also reported, which paralleled the development of the depression-like phenotype [176]. The stimulation of astroglial 5-HT 2B receptors may, therefore, be beneficial in treating depressive disorders [177].
Considering the role of peripherally located 5-HT 2B receptors, potential new antidepressants acting on 5-HT 2B receptors may adversely affect the function of the respiratory and circulatory systems [17,20]:

The 5-HT 2C Receptors
The 5-HT 2C receptors are mainly located in the choroid plexuses, cerebral cortex, hippocampus, substantia nigra, and cerebellum. They bind preferentially with Gq/11 and increase the concentrations of inositol phosphates and cytosolic Ca 2+ . Like 5-HT 2A receptors, they are involved in the regulation of mood, motor behavior, and appetite [178].
Several classes of antidepressants have an affinity for 5-HT 2C receptors. Although these receptors are usually somatodendritic, in some regions they are also present on axon terminals [179]. The location of 5-HT 2C receptors in relation to serotonergic and GABAergic neurons in the anterior raphe nuclei demonstrates complex systemic relationships in the brain. It has been shown that 5-HT 2C receptors are preferentially located on GABAergic interneurons (and not on serotonergic neurons). This suggests that the stimulation of GABAergic interneurons by 5-HT 2C receptors plays an important role in the suppression of serotonergic cell firing in the dorsal raphe and surrounding areas [180]. The immunoreactivity of the 5-HT 2C receptor has also been described in GABAergic cells in the PFC [181] and in the dopaminergic and GABAergic neurons of the mesolimbic pathway [182].
A potent 5-HT 2C receptor antagonist, S32006 (Figure 6), showed antidepressant activity in rodent behavioral tests and increased dopamine and norepinephrine levels in the frontal cortex [183]. This compound reduced immobility in the FST in mice, suppressed anhedonia in a chronic mild stress model, and increased cell proliferation and BDNF expression in the dentate gyri of rats [183]. In contrast, the inverse agonist of the 5-HT 2C receptor, S32212, showed an antidepressant effect in the FST in rats after both acute and chronic treatment [184].
On the other hand, some studies report that 5-HT2C agonists have been shown to be active in animal models of depression, suggesting an antidepressant-like effect [185,186]. WAY-163909, a selective 5-HT2C receptor agonist, elicited a rapid antidepressant effect in a rat FST that was blocked by the 5-HT2C/2B receptor antagonist, SB206553 [186]. Moreover, after chronic treatment, WAY163909 reduced the hyperactivity associated with olfactory bulbectomy in rats [186,187]. It is possible that the mediated antidepressant effects of these compounds were due to the stimulation of 5-HT2C receptors and the resulting activation of postsynaptic serotonin receptors [188]. Other selective 5-HT2C receptor agonists have also been effective in animal models of depression and obsessive-compulsive disorder [189]. Preclinical data show that the antagonism of 5-HT2C receptors increases the neurochemical and behavioral effects of SSRIs. Examples include: the increase in the effect of SSRIs on extracellular 5-HT concentrations in the hippocampus and cortex [190,191], or a significant increase in the effect of SSRIs in behavioral models of depression by selective and non-selective 5-HT2C antagonists [190].
Additionally, 5-HT2C receptors have been shown to be involved in the anti-immobility effect of antidepressants in the FST, increasing the serotonin level in the synapse [192]. Few studies suggest that 5-HT2C receptor antagonists alone may also exhibit antidepressant-like properties. The inactivation of 5-HT2C receptors has been shown to potentiate SSRI-induced serotonin release in rodents [190]. However, 5-HT2C receptor antagonists administered separately had no effect on serotonin levels [191].
An altered editing of the mRNA-encoding 5-HT2C receptors has been reported in the PFC of depressed suicide victims [193]. The desensitization of these receptors has been observed in patients after chronic treatment with SSRIs [194].
The 5-HT2C receptors are also involved in the tonic modulation of dopaminergic activity [195]. The role of the dopaminergic system in schizophrenia, along with the antagonism of atypical antipsychotics towards the 5-HT2C receptors, has aroused interest in this receptor for the treatment of schizophrenia [196]. Conversely, the ineffectiveness of SSRIs in some patients may be due to the serotonin-related inhibition of the neuronal activity of dopamine in the ventral capping region via 5-HT2C receptors [157]. Escitalopram has been shown to reduce the stimulation of dopamine neurons by activating 5-HT2C receptors located on GABA neurons. Some studies indicate that the co-administration of SSRIs with 5-HT2C receptor antagonists (including atypical antipsychotics, such as aripiprazole) may eliminate the inhibitory effects on dopaminergic neurons in rat brains and restore the effect of the SSRI [163]. The aforementioned 5-HT2C receptor antagonist S32006, with a potential antidepressant-and anxiolytic-like effect, increased dopamine levels in the frontal cortex of rats and enhanced dopaminergic neuron firing [183]. The modulation of dopaminergic activity may, therefore, be beneficial in the development of antidepressants due to the above-mentioned activity of 5-HT2C receptor ligands. Recent studies demonstrate the contradictory effect of 5-HT2C receptors on the effects of SSRIs on motor function and affective behavior, highlighting the potential benefits of 5-HT2C receptor antagonists both On the other hand, some studies report that 5-HT 2C agonists have been shown to be active in animal models of depression, suggesting an antidepressant-like effect [185,186]. WAY-163909, a selective 5-HT 2C receptor agonist, elicited a rapid antidepressant effect in a rat FST that was blocked by the 5-HT 2C / 2B receptor antagonist, SB206553 [186]. Moreover, after chronic treatment, WAY163909 reduced the hyperactivity associated with olfactory bulbectomy in rats [186,187]. It is possible that the mediated antidepressant effects of these compounds were due to the stimulation of 5-HT 2C receptors and the resulting activation of postsynaptic serotonin receptors [188]. Other selective 5-HT 2C receptor agonists have also been effective in animal models of depression and obsessive-compulsive disorder [189].
Preclinical data show that the antagonism of 5-HT 2C receptors increases the neurochemical and behavioral effects of SSRIs. Examples include: the increase in the effect of SSRIs on extracellular 5-HT concentrations in the hippocampus and cortex [190,191], or a significant increase in the effect of SSRIs in behavioral models of depression by selective and non-selective 5-HT 2C antagonists [190].
Additionally, 5-HT 2C receptors have been shown to be involved in the anti-immobility effect of antidepressants in the FST, increasing the serotonin level in the synapse [192]. Few studies suggest that 5-HT 2C receptor antagonists alone may also exhibit antidepressantlike properties. The inactivation of 5-HT 2C receptors has been shown to potentiate SSRIinduced serotonin release in rodents [190]. However, 5-HT 2C receptor antagonists administered separately had no effect on serotonin levels [191].
An altered editing of the mRNA-encoding 5-HT 2C receptors has been reported in the PFC of depressed suicide victims [193]. The desensitization of these receptors has been observed in patients after chronic treatment with SSRIs [194].
The 5-HT 2C receptors are also involved in the tonic modulation of dopaminergic activity [195]. The role of the dopaminergic system in schizophrenia, along with the antagonism of atypical antipsychotics towards the 5-HT 2C receptors, has aroused interest in this receptor for the treatment of schizophrenia [196]. Conversely, the ineffectiveness of SSRIs in some patients may be due to the serotonin-related inhibition of the neuronal activity of dopamine in the ventral capping region via 5-HT 2C receptors [157]. Escitalopram has been shown to reduce the stimulation of dopamine neurons by activating 5-HT 2C receptors located on GABA neurons. Some studies indicate that the co-administration of SSRIs with 5-HT 2C receptor antagonists (including atypical antipsychotics, such as aripiprazole) may eliminate the inhibitory effects on dopaminergic neurons in rat brains and restore the effect of the SSRI [163]. The aforementioned 5-HT 2C receptor antagonist S32006, with a potential antidepressant-and anxiolytic-like effect, increased dopamine levels in the frontal cortex of rats and enhanced dopaminergic neuron firing [183]. The modulation of dopaminergic activity may, therefore, be beneficial in the development of antidepressants due to the above-mentioned activity of 5-HT 2C receptor ligands. Recent studies demonstrate the contradictory effect of 5-HT 2C receptors on the effects of SSRIs on motor function and affective behavior, highlighting the potential benefits of 5-HT 2C receptor antagonists both for reducing SSRI motor side effects and enhancing the therapeutic antidepressant and anxiolytic effects [197].
Both 5-HT 2C receptor agonists and antagonists exhibit antidepressant-like activity, and there is still a need to further define the role of this receptor subtype in depression: • Several classes of antidepressants have an affinity for 5-HT 2C receptors. Alterations in their functional status have been observed in depressive and anxiety states; • Both 5-HT 2C agonists and antagonists have been shown to be active in animal models of depression. Preclinical data show that the antagonism of 5-HT 2C receptors increases the neurochemical and behavioral effects of SSRIs; • There is still a need to further define the role of 5-HT 2C receptor subtype in depression.

The 5-HT 3 Receptors
The activation of the 5-HT 3 receptor leads to a rapid opening of the transmembrane channel, resulting in an increase in the conductivity of Na + /K + ions and an immediate influx of extracellular Ca 2+ ions. This, in turn, triggers the release of neurotransmitters and/or peptides. The 5-HT 3 receptors are found throughout the brain and CNS and the highest density of 5-HT 3 receptors was found in the spinal cord and brainstem. The 5-HT 3 receptors present in the dorsal vagal complex are involved in the control of the emetic mechanism [142]. Many 5-HT 3 receptor antagonists have been developed as antiemetics for use in cancer chemotherapy. In the 1990s, lithoxetine, an antidepressant combining serotonin reuptake and 5-HT 3 receptor antagonism, was developed to prevent SSRI-induced gastrointestinal side effects [198]. In the forebrain, on the other hand, 5-HT 3 receptors were present mainly in structures of the limbic system, such as the hippocampus, amygdala, and entorhinal cortex [199].
The 5-HT 3 receptors are involved in the control of dopamine and acetylcholine release. They also control the functioning of the GABAergic system. Activity towards other neurotransmission systems is the main mechanism of action for 5-HT 3 receptor ligands. The 5-HT 3 receptors are expressed on different types of GABAergic interneurons in the forebrain [200,201]. The physiological stimulation of serotonergic neurons stimulates cortical (and possibly hippocampal) GABAergic neurons. This likely results in the inhibition of neighboring excitatory neurons by GABA A and GABA B receptors [201].
Preclinical studies suggest that the 5-HT 3 receptor plays a role in mental disorders [17]. The 5-HT 3 antagonists show antidepressant-like activity in various animal models [202]. The systemic administration of tropisetron (a 5-HT 3 receptor antagonist) prevented restraint stress-induced dopamine release in the nucleus accumbens and prefrontal cortex in rats. This suggested that 5-HT 3 receptors mediated the stress-dependent activation of dopaminergic neurotransmission [203]. Tropisetron additionally exerted an antidepressantlike effect in FST in rats. This effect was abolished after a pretreatment with mCPGB (1-(m-chlorophenyl)-biguanide), a potent 5-HT 3 receptor agonist (Figure 7) [204]. for reducing SSRI motor side effects and enhancing the therapeutic antidepressant and anxiolytic effects [197]. Both 5-HT2C receptor agonists and antagonists exhibit antidepressant-like activity, and there is still a need to further define the role of this receptor subtype in depression: • Several classes of antidepressants have an affinity for 5-HT2C receptors. Alterations in their functional status have been observed in depressive and anxiety states; • Both 5-HT2C agonists and antagonists have been shown to be active in animal models of depression. Preclinical data show that the antagonism of 5-HT2C receptors increases the neurochemical and behavioral effects of SSRIs; • There is still a need to further define the role of 5-HT2C receptor subtype in depression.

The 5-HT3 Receptors
The activation of the 5-HT3 receptor leads to a rapid opening of the transmembrane channel, resulting in an increase in the conductivity of Na + /K + ions and an immediate influx of extracellular Ca 2+ ions. This, in turn, triggers the release of neurotransmitters and/or peptides. The 5-HT3 receptors are found throughout the brain and CNS and the highest density of 5-HT3 receptors was found in the spinal cord and brainstem. The 5-HT3 receptors present in the dorsal vagal complex are involved in the control of the emetic mechanism [142]. Many 5-HT3 receptor antagonists have been developed as antiemetics for use in cancer chemotherapy. In the 1990s, lithoxetine, an antidepressant combining serotonin reuptake and 5-HT3 receptor antagonism, was developed to prevent SSRI-induced gastrointestinal side effects [198]. In the forebrain, on the other hand, 5-HT3 receptors were present mainly in structures of the limbic system, such as the hippocampus, amygdala, and entorhinal cortex [199].
The 5-HT3 receptors are involved in the control of dopamine and acetylcholine release. They also control the functioning of the GABAergic system. Activity towards other neurotransmission systems is the main mechanism of action for 5-HT3 receptor ligands. The 5-HT3 receptors are expressed on different types of GABAergic interneurons in the forebrain [200,201]. The physiological stimulation of serotonergic neurons stimulates cortical (and possibly hippocampal) GABAergic neurons. This likely results in the inhibition of neighboring excitatory neurons by GABAA and GABAB receptors [201].
The agonism of the 5-HT 3 receptor reduces the antidepressant effect in the FST in rats [219], while the antagonism of the 5-HT 3 receptor reduces the immobility time in the FST [220]. Ondansetron, a 5-HT 3 receptor antagonist, confirms these observations; it exhibits antidepressant properties in the TST (tail suspension test) and FST, also enhancing the effect of fluoxetine [220]. In a model of chronic unpredictable stress in mice, the administration of ondansetron reversed depressive behavior affecting the hypothalamicpituitary-adrenal axis [221]. Moreover, in mice with streptozotocin-induced diabetes, the drug displayed antidepressant and anxiolytic properties, possibly through the antagonism of the 5-HT 3 receptor [222]. Behavioral studies with ondansetron (and tropisetron) also suggested an interaction of 5-HT 3 and NMDA receptors, as well as an involvement of the nitric oxide-cyclic guanosine monophosphate pathway inhibition in the observed antidepressant-like effects [223,224]. Studies on genetically modified animals confirm the role of 5-HT 3 receptors in the antidepressant effect. The 5-HT 3 receptor knockout mice were reported to display an antidepressant-like phenotype [225].
In vitro electrophysiology studies showed that low-dose citalopram treatment desensitized the 5-HT 1A receptor only in the dorsal raphe nucleus of 5-HT 3 knockout mice, while high dose treatment caused similar 5-HT 1A autoreceptor desensitization in 5-HT 3 knockout and wild types [225]. Hence, lower doses of citalopram may be effective when 5-HT 3 receptors are deactivated. It has also been shown that the blockade of the 5-HT 3 receptor by ondansetron enhances the effect of citalopram on extracellular serotonin levels in the rat forebrain [102]. The use of combined SSRIs and 5HT 3 receptor antagonists is proposed as an improvement strategy to be tested in the treatment of depressive disorders [226]. The neurochemical, electrophysiological, and behavioral consequences of the repeated administration of this drug combination will need to be assessed.
The properties of 5-HT 3 receptor antagonists have also been used to alleviate substance abuse, which is often associated with most psychiatric disorders, including MDD [227]. The 5-HT 3 receptor antagonists have been reported to be effective in reducing ethanol and morphine intake [228]. It is worth noting that various antipsychotics are non-competitive 5-HT 3 receptor antagonists, and this may contribute to their efficacy [229]. There is likely to be an association between 5-HT 3 receptors and anxiety behavior [230]. The 5-HT 3 antagonists reverse helpless behavior in rats [231] and abolish the emotion-potentiated startle effect in humans [232]: • Activity towards other neurotransmission systems is the main mechanism of action for 5-HT 3 receptor ligands; • Rodent experiments show that the antidepressant-like effect should be attributed to postsynaptic rather than presynaptic 5-HT 3 antagonism, since the presynaptic and somatodendritic 5-HT 3 receptor blockade reduces serotonin levels; • Some antidepressants with different mechanisms of action exhibit functional 5-HT 3 receptor antagonism. The vortioxetine antagonism at the 5-HT 3 receptor may underlie its faster onset of action.

The 5-HT 4 Receptors
The 5-HT 4 receptors in the CNS are mainly located in the putamen, caudate nucleus, hippocampus, nucleus accumbens, globus pallidus, and substantia nigra. To a lesser extent, these receptors are present in the neocortex, raphe and pontine nuclei, and thalamus [233].
Studies using positron emission tomography show a slightly more limited regional distribution of 5-HT 4 receptors in the human brain, showing a high density of this receptor in the caudate-putamen and much lower densities in the frontal cortex and hippocampus [234]. The 5-HT 4 receptors are coupled to the Gs protein, which activates adenylate cyclase/PKC and increases the intracellular level of cAMP. Regarding peripheral tissues, these receptors play an important role in the heart, gastrointestinal tract, adrenal glands, and urinary bladder [235].
There are reports linking the 5-HT 4 receptor with depressive disorders [236]. Preclinical models of depression, such as the olfactory bulbectomized and glucocorticoid heterozygous receptor mice, show that the expression of 5-HT 4 receptors increased in the ventral hippocampus or striatum, respectively [237], while in the Flinders-sensitive line rat model of depression, the downregulation of 5-HT 4 receptors was observed in the ventral and dorsal hippocampus [238].
The 5-HT 4 receptor subtype is involved in the modulation of synaptic plasticity [239], which is influenced by antidepressants [240]. The signaling of the 5-HT 4 receptor may modulate the function of the dentate gyrus of the hippocampus by increasing the neurogenesis and expression of neurotrophic factors, which may contribute to the antidepressant effects of drugs that enhance serotonergic transmission [241]. The 5-HT 4 receptor interacts with the p11 protein, which determines the antidepressant activity mediated by 5-HT 1B and 5-HT 4 receptors [242].
In addition, 5-HT 4 knockout mice show an enhanced response of serotonergic neurons to citalopram [243]. Thus, 5-HT 4 receptors are possibly involved in the activation of 5-HT neurons during SERT inhibition. As observed for 5-HT 1A and 5-HT 2A receptors [37,40], 5-HT 4 receptors in the PFC control the firing rate of midbrain serotonergic neurons via descending inputs [244]. In addition, 5-HT 4 receptors mediate synaptic transmission between the dentate gyrus and the CA3 field of the hippocampus. Fluoxetine was observed to normalize the mossy fiber pathway by activating 5-HT 4 receptors [245]. Chronic treatment with fluoxetine and venlafaxine (but not reboxetine) decreased the 5-HT 4 receptor density in rat brain [246]. Although the 5-HT 4 receptor antagonist, SB 204070A, showed no independent effect and did not reduce the immobility time in the FST in naive rats [247], another receptor antagonist, GR 125487, blocked fluoxetine activity in a mouse corticosteroneinduced depression model [248]. Therefore, this study suggests that the activation of 5-HT 4 receptors mediates the antidepressant-like effects of fluoxetine. It has been shown that a knockout of the 5-HT 4 receptor can induce some adaptive changes in mice, leading to depression and anxiety-like behavior. Moreover, 5-HT 4 receptor knockout mice do not respond to fluoxetine in the olfactory bulbectomized model of depression and anxiety [249]. On the other hand, some studies suggest that the behavioral effects of fluoxetine in the corticosterone-induced model of depression and anxiety do not appear to be dependent on 5-HT 4 receptors [250].
Preclinical studies show that the administration of the 5-HT 4 agonists, RS67333 and prucalopride (Figure 8), reduces the immobility time in the FST, thus demonstrating the potential of the 5-HT 4 receptor as a molecular target of a potential new generation of antidepressants [251]. The agonism of the 5-HT 4 receptor may also play a role in the cognitive deficits associated with MDD. The use of RS67333 in chronic neuroendocrine animal models of depression/anxiety resulted in the restoration of induced learning and memory disorders [252]. Moreover, the studies show that administration of RS67333 and prucalopride causes 5-HT 1A autoreceptor desensitization, increased the tonus on hippocampal postsynaptic 5-HT 1A receptors, and increased CREB phosphorylation and neurogenesis in the hippocampus [251]. These parameters, which characterize the functioning of the brain, are used in antidepressant therapies. Importantly, these effects are noticeable after 3 days of treatment [251], while they are usually only seen after 2-3 weeks of treatment with SSRIs due to the latency phenomenon. The faster response to 5-HT 4 agonism has been suggested to be a result of the parallel rapid and sustained activation of 5-HT neuronal firing in the dorsal raphe nucleus [253]. Increased serotonergic neuronal firing may also underlie the apparently superior efficacy of 5-HT 4 agonists over SSRIs because the reuptake inhibitory effect depends on the basal rates of 5-HT cell firing. Since the 5-HT 4 receptor is not expressed in the raphe nuclei, the ability of 5-HT 4 receptors to stimulate the firing of 5-HT neurons appears to involve the activation of receptors located on neurons in the PFC [244]. The identity of the cells expressing 5-HT 4 receptors and their connections to the serotonergic neurons of the dorsal raphe nucleus are not yet well understood. It is possible that they project to other regions, contributing to the antidepressant effect of 5-HT 4 agonists [253].  [251], while they are usually only seen after 2-3 weeks of treatment with SSRIs due to the latency phenomenon. The faster response to 5-HT4 agonism has been suggested to be a result of the parallel rapid and sustained activation of 5-HT neuronal firing in the dorsal raphe nucleus [253]. Increased serotonergic neuronal firing may also underlie the apparently superior efficacy of 5-HT4 agonists over SSRIs because the reuptake inhibitory effect depends on the basal rates of 5-HT cell firing. Since the 5-HT4 receptor is not expressed in the raphe nuclei, the ability of 5-HT4 receptors to stimulate the firing of 5-HT neurons appears to involve the activation of receptors located on neurons in the PFC [244]. The identity of the cells expressing 5-HT4 receptors and their connections to the serotonergic neurons of the dorsal raphe nucleus are not yet well understood. It is possible that they project to other regions, contributing to the antidepressant effect of 5-HT4 agonists [253]. The activation of the 5-HT4 receptor may be a useful adjunct to antidepressant therapy, both to accelerate the onset of clinical antidepressant effects and to target cognitive symptoms that are not effectively treated with current therapies [254]:

•
There are reports linking the 5-HT4 receptor with depressive disorders. The 5-HT4 receptor interacts with the p11 protein, which determines the antidepressant activity mediated by 5-HT1B and 5-HT4 receptors; • 5-HT4 receptor signaling may modulate the function of the dentate gyrus of the hippocampus by increasing the neurogenesis and expression of neurotrophic factors, which may contribute to the antidepressant effects of drugs that enhance serotonergic transmission.

•
The activation of the 5-HT4 receptor may be a useful adjunct to antidepressant therapy, both to accelerate the onset of clinical antidepressant effects and to target cognitive symptoms that are not effectively treated with current therapies.

The 5-HT6 Receptors
The 5-HT6 receptors are the postsynaptic receptors most expressed in the striatum, nucleus accumbens, olfactory tubercle, and cortex. They are also moderately dense in the amygdala, hippocampus, hypothalamus, thalamus, and cerebellum [255].
This serotonin receptor subtype has been found to play a role in learning and memory [256] as well as in the central regulation of hunger and satiety behavior [257]. The 5-HT6 receptors may, therefore, serve as a novel molecular target for the improvement of cognitive functions [258]. Several of the tricyclic antidepressants (e.g., amitriptyline) and atypical antidepressants (e.g., mianserin) exhibit nanomolar 5-HT6 binding and antagonistic activity [259]. This fact, as well as the distribution of the 5-HT6 receptor in the limbic and cortical regions of the brain, may suggest that 5-HT6 receptors play an important role in the pathogenesis and/or treatment of depression [259]. The 5-HT6 antagonists (SB-399885, Figure 9) show antidepressant activity in the FST and in the TST in rodents (rats and mice) [260]. In addition, the combination of an ineffective dose of SB-399885 with ineffective doses of imipramine, desipramine, bupropion, or moclobemide has been shown to exert antidepressant effects in the rat FST [261]. This suggests that the inhibition of the The activation of the 5-HT 4 receptor may be a useful adjunct to antidepressant therapy, both to accelerate the onset of clinical antidepressant effects and to target cognitive symptoms that are not effectively treated with current therapies [254]:

•
There are reports linking the 5-HT 4 receptor with depressive disorders. The 5-HT 4 receptor interacts with the p11 protein, which determines the antidepressant activity mediated by 5-HT 1B and 5-HT 4 receptors; • 5-HT 4 receptor signaling may modulate the function of the dentate gyrus of the hippocampus by increasing the neurogenesis and expression of neurotrophic factors, which may contribute to the antidepressant effects of drugs that enhance serotonergic transmission.

•
The activation of the 5-HT 4 receptor may be a useful adjunct to antidepressant therapy, both to accelerate the onset of clinical antidepressant effects and to target cognitive symptoms that are not effectively treated with current therapies.

The 5-HT 6 Receptors
The 5-HT 6 receptors are the postsynaptic receptors most expressed in the striatum, nucleus accumbens, olfactory tubercle, and cortex. They are also moderately dense in the amygdala, hippocampus, hypothalamus, thalamus, and cerebellum [255].
This serotonin receptor subtype has been found to play a role in learning and memory [256] as well as in the central regulation of hunger and satiety behavior [257]. The 5-HT 6 receptors may, therefore, serve as a novel molecular target for the improvement of cognitive functions [258]. Several of the tricyclic antidepressants (e.g., amitriptyline) and atypical antidepressants (e.g., mianserin) exhibit nanomolar 5-HT 6 binding and antagonistic activity [259]. This fact, as well as the distribution of the 5-HT 6 receptor in the limbic and cortical regions of the brain, may suggest that 5-HT 6 receptors play an important role in the pathogenesis and/or treatment of depression [259]. The 5-HT 6 antagonists (SB-399885, Figure 9) show antidepressant activity in the FST and in the TST in rodents (rats and mice) [260]. In addition, the combination of an ineffective dose of SB-399885 with ineffective doses of imipramine, desipramine, bupropion, or moclobemide has been shown to exert antidepressant effects in the rat FST [261]. This suggests that the inhibition of the 5-HT 6 receptor potentiates the effects of clinically used antidepressants. This synergistic effect is interesting in the search for a multimodal antidepressant therapy with minimized side effects or a faster onset of action. Other preclinical studies show that 5-HT 6 agonism can be used in the treatment of depression. The reduction in the immobility of mice in the FST after the administration of WAY208466, a selective potent agonist of the 5-HT 6 receptor, has been demonstrated [262]. The 5-HT 6 receptor partial agonist, EMD386088, caused antidepressant-and anxiolytic-like effects after intrahippocampal administration [263]. This also occurred after acute and chronic treatment in rats [264], possibly because it directly stimulated the receptor. The stimulation of the 5-HT 6 receptor may initiate the biochemical and behavioral effects induced by SSRIs (fluoxetine) [122]. On the other hand, the 5-HT 6 receptor agonist LY-586713 increases the expression of BDNF (a marker of cellular antidepressant activity) in the hippocampus after just a single administration [265]. In comparison, SSRIs require multiple applications to produce the same effect [240]. Therefore, it is unclear what functional 5-HT 6 receptor ligand profile (antagonism or agonism) will be more beneficial in the treatment of depression. Moreover, the exact mechanism by which 5-HT 6 ligands induce antidepressant effects is unknown and may include effects on other neurotransmission systems [260,266]: Sci. 2021, 22, 9015 18 of 32 5-HT6 receptor potentiates the effects of clinically used antidepressants. This synergistic effect is interesting in the search for a multimodal antidepressant therapy with minimized side effects or a faster onset of action. Other preclinical studies show that 5-HT6 agonism can be used in the treatment of depression. The reduction in the immobility of mice in the FST after the administration of WAY208466, a selective potent agonist of the 5-HT6 receptor, has been demonstrated [262]. The 5-HT6 receptor partial agonist, EMD386088, caused antidepressant-and anxiolytic-like effects after intrahippocampal administration [263]. This also occurred after acute and chronic treatment in rats [264], possibly because it directly stimulated the receptor. The stimulation of the 5-HT6 receptor may initiate the biochemical and behavioral effects induced by SSRIs (fluoxetine) [122]. On the other hand, the 5-HT6 receptor agonist LY-586713 increases the expression of BDNF (a marker of cellular antidepressant activity) in the hippocampus after just a single administration [265]. In comparison, SSRIs require multiple applications to produce the same effect [240]. Therefore, it is unclear what functional 5-HT6 receptor ligand profile (antagonism or agonism) will be more beneficial in the treatment of depression. Moreover, the exact mechanism by which 5-HT6 ligands induce antidepressant effects is unknown and may include effects on other neurotransmission systems [260,266]: • The distribution of the 5-HT6 receptor in the limbic and cortical regions of the brain may suggest that 5-HT6 receptors play an important role in the pathogenesis and/or treatment of depression; • Several tricyclic and atypical antidepressants exhibit nanomolar 5-HT6 receptor binding. The inhibition of the 5-HT6 receptor potentiates the effects of clinically used antidepressants. This synergistic effect is interesting in the search for a multimodal antidepressant therapy with minimized side effects or a faster onset of action; • It is not exactly clear what functional 5-HT6 receptor ligand profile (antagonism or agonism) will be more beneficial in the treatment of depression. Moreover, the exact mechanism by which 5-HT6 ligands induce antidepressant effects is unknown and may include effects on other neurotransmission systems.

The 5-HT7 Receptors
The 5-HT7 receptor is highly expressed in the thalamus, hypothalamus, hippocampus, and cortex [267]. The results of immunolocation and autoradiography studies are generally consistent with the pattern of mRNA distribution [268,269], suggesting a dominant somatodendritic localization. The physiological role of 5-HT7 receptors is to regulate circadian rhythm, sleep, and mood [270].
As with the 5-HT6 receptors, several antidepressants [271] and antipsychotics [272] have been found to have a high affinity for the 5-HT7 receptor, leading to much further research into its antidepressant activity. One preclinical study in rats showed that several antidepressants, both tricyclic and SSRIs, induce c-fos expression in a manner consistent

•
The distribution of the 5-HT 6 receptor in the limbic and cortical regions of the brain may suggest that 5-HT 6 receptors play an important role in the pathogenesis and/or treatment of depression; • Several tricyclic and atypical antidepressants exhibit nanomolar 5-HT 6 receptor binding. The inhibition of the 5-HT 6 receptor potentiates the effects of clinically used antidepressants. This synergistic effect is interesting in the search for a multimodal antidepressant therapy with minimized side effects or a faster onset of action; • It is not exactly clear what functional 5-HT 6 receptor ligand profile (antagonism or agonism) will be more beneficial in the treatment of depression. Moreover, the exact mechanism by which 5-HT 6 ligands induce antidepressant effects is unknown and may include effects on other neurotransmission systems.

The 5-HT 7 Receptors
The 5-HT 7 receptor is highly expressed in the thalamus, hypothalamus, hippocampus, and cortex [267]. The results of immunolocation and autoradiography studies are generally consistent with the pattern of mRNA distribution [268,269], suggesting a dominant somatodendritic localization. The physiological role of 5-HT 7 receptors is to regulate circadian rhythm, sleep, and mood [270].
As with the 5-HT 6 receptors, several antidepressants [271] and antipsychotics [272] have been found to have a high affinity for the 5-HT 7 receptor, leading to much further research into its antidepressant activity. One preclinical study in rats showed that several antidepressants, both tricyclic and SSRIs, induce c-fos expression in a manner consistent with 5-HT 7 receptor activation within the suprachiasmatic nucleus, and that chronic treatment with antidepressant drugs downregulates 5-HT 7 receptor binding [271].
Preclinical studies also indicate the antidepressant and anxiolytic effects of the selective 5-HT 7 receptor antagonist, SB-269970, in rodents [273], as well as a synergistic interaction between subeffective doses of this agent and antidepressants, leading to a reduction in immobility in both the FST and the TST [274,275]. The intrahippocampal administra-tion of SB-269970 ( Figure 10) induced an antidepressant effect in the FST in rats [276]. The co-administration of citalopram and SB-269970 increased the activity of serotonin neurons in rats and improved the antidepressant effect in the TST [274]. SB-269970 enhanced the antidepressant effect of antidepressants (citalopram, imipramine, desipramine, and moclobemide) in the FST in mice [275]. It was also shown that the administration of SB-269970 for only one week caused the behavioral, electrophysiological, and neuroanatomical changes that usually occur after a long-term treatment with SSRIs. Therefore, 5-HT 7 receptor antagonists might represent a new class of antidepressants with a faster therapeutic effect. JNJ-18038683, another 5-HT 7 receptor antagonist, was also effective in mice TST [277]. Moreover, the compound potentiated serotonin transmission, REM suppression, and antidepressant-like behaviour induced by citalopram in rodents [277]. The above studies indicate that the participation of the 5-HT 7 receptor in the antidepressant-like action, and blockade of the 5-HT 7 receptor may not only induce but accelerate this action.
action between subeffective doses of this agent and antidepressants, leading to a reduction in immobility in both the FST and the TST [274,275]. The intrahippocampal administration of SB-269970 ( Figure 10) induced an antidepressant effect in the FST in rats [276]. The coadministration of citalopram and SB-269970 increased the activity of serotonin neurons in rats and improved the antidepressant effect in the TST [274]. SB-269970 enhanced the antidepressant effect of antidepressants (citalopram, imipramine, desipramine, and moclobemide) in the FST in mice [275]. It was also shown that the administration of SB-269970 for only one week caused the behavioral, electrophysiological, and neuroanatomical changes that usually occur after a long-term treatment with SSRIs. Therefore, 5-HT7 receptor antagonists might represent a new class of antidepressants with a faster therapeutic effect. JNJ-18038683, another 5-HT7 receptor antagonist, was also effective in mice TST [277]. Moreover, the compound potentiated serotonin transmission, REM suppression, and antidepressant-like behaviour induced by citalopram in rodents [277]. The above studies indicate that the participation of the 5-HT7 receptor in the antidepressant-like action, and blockade of the 5-HT7 receptor may not only induce but accelerate this action.
In addition, the genetic and pharmacological inactivation of 5-HT7 receptors partially reversed phencyclidine-induced deficits of pre-pulse inhibition, an animal model for antipsychotic activity [278]. Similarly, it should also be noted that the atypical antipsychotic aripiprazole, which has a high affinity for the 5-HT7 receptor, is sometimes used to enhance the effects of traditional antidepressants [279]. Similarly, there are reports that the antidepressant effect of amisulpride is mediated by its action on 5-HT7 receptors [280]. Vortioxetine is a high affinity inhibitor of the human 5-HT transporter, 5-HT3 and 5-HT7 receptors, and a 5-HT1A agonist [281]. Although the affinity of vortioxetine for the rat 5-HT7 receptor is lower compared to the human receptor [282], subacute administration (within 3 days) of an effective dose of vortioxetine rapidly lowers rat 5-HT7 receptor levels [283]. This preclinical evidence suggests that vortioxetine has a relatively low affinity for the 5-HT7 receptor compared to other 5-HT receptor subtypes but inhibits its action with a rapid 5-HT7 receptor downregulation as an inverse agonist, similar to other 5-HT7 receptor-inhibiting mood-stabilizing atypical antipsychotics: clozapine, lurasidone, and olanzapine [283,284]. In other words, the rapid-acting antidepressant and anxiolytic actions of 5-HT7 receptor antagonism are worth reassessing in the context of drug development after future clinical data have been accumulated. Overall, the 5-HT7 receptor is currently considered a promising target for the development of antidepressants [285]. Recent clinical studies have shown that both the intravenous and oral administration of vortioxetine resulted in a significant improvement in depression (Montgomery Åsberg Depression Rating Scale and Hospital Depression Scale) and anxiety (Hospital Anxiety Scale) after 3 days [77]: In addition, the genetic and pharmacological inactivation of 5-HT 7 receptors partially reversed phencyclidine-induced deficits of pre-pulse inhibition, an animal model for antipsychotic activity [278]. Similarly, it should also be noted that the atypical antipsychotic aripiprazole, which has a high affinity for the 5-HT 7 receptor, is sometimes used to enhance the effects of traditional antidepressants [279]. Similarly, there are reports that the antidepressant effect of amisulpride is mediated by its action on 5-HT 7 receptors [280].
Vortioxetine is a high affinity inhibitor of the human 5-HT transporter, 5-HT 3 and 5-HT 7 receptors, and a 5-HT 1A agonist [281]. Although the affinity of vortioxetine for the rat 5-HT 7 receptor is lower compared to the human receptor [282], subacute administration (within 3 days) of an effective dose of vortioxetine rapidly lowers rat 5-HT 7 receptor levels [283]. This preclinical evidence suggests that vortioxetine has a relatively low affinity for the 5-HT 7 receptor compared to other 5-HT receptor subtypes but inhibits its action with a rapid 5-HT 7 receptor downregulation as an inverse agonist, similar to other 5-HT 7 receptor-inhibiting mood-stabilizing atypical antipsychotics: clozapine, lurasidone, and olanzapine [283,284]. In other words, the rapid-acting antidepressant and anxiolytic actions of 5-HT 7 receptor antagonism are worth reassessing in the context of drug development after future clinical data have been accumulated. Overall, the 5-HT 7 receptor is currently considered a promising target for the development of antidepressants [285]. Recent clinical studies have shown that both the intravenous and oral administration of vortioxetine resulted in a significant improvement in depression (Montgomery Åsberg Depression Rating Scale and Hospital Depression Scale) and anxiety (Hospital Anxiety Scale) after 3 days [77]: • Several antidepressants have been found to have a high affinity for the 5-HT 7 receptor, leading to much further research into its antidepressant activity; • The antagonists of the 5-HT 7 receptor might represent a new class of antidepressants with a faster therapeutic effect. • Preclinical evidence suggests that vortioxetine has a relatively low affinity for the 5-HT 7 receptor compared to other 5-HT receptor subtypes but inhibits its action with a rapid 5-HT 7 receptor downregulation as an inverse agonist. Both the intravenous and oral administration of vortioxetine resulted in a significant improvement in depression and anxiety after 3 days.

Conclusions
The development of new antidepressants is based on monoamine systems. The targeted pharmacological modulation of serotonergic transmission in the brain continues to be a leading strategy in the search for new antidepressants. As can be seen from this review, the serotonergic system offers great potential for the development of new antidepressant therapies based on the combination of SERT inhibition with different pharmacological activities towards the 5-HT system. The careful selection of molecular targets for the proper use of the mechanisms of serotonergic autoregulation and selective/biased activation or the blockade of relevant receptors (e.g., stimulation of postsynaptic 5-HT 1A , postsynaptic 5-HT 1B , 5-HT 2B and 5-HT 4 receptors; or the blockade of presynaptic 5-HT 1A , presynaptic 5-HT 1B , 5-HT 2A , 5-HT 3 , and 5-HT 7 ), which also influences other neurotransmission systems, seems to be the most effective strategy for supplementing the activity of "serotonin-enhancing" drugs in the near future. A better understanding of receptors and the receptor signaling responsible for the effects of serotonin on neurogenesis could also help in the development of new and more effective drugs.