Mechanisms Underlining Inflammatory Pain Sensitivity in Mice Selected for High and Low Stress-Induced Analgesia—The Role of Endocannabinoids and Microglia

In this work we strived to determine whether endocannabinoid system activity could account for the differences in acute inflammatory pain sensitivity in mouse lines selected for high (HA) and low (LA) swim-stress-induced analgesia (SSIA). Mice received intraplantar injections of 5% formalin and the intensity of nocifensive behaviours was scored. To assess the contribution of the endocannabinoid system, mice were intraperitoneally (i.p.) injected with rimonabant (0.3–3 mg/kg) prior to formalin. Minocycline (45 and 100 mg/kg, i.p.) was administered to investigate microglial activation. The possible involvement of the endogenous opioid system was investigated with naloxone (1 mg/kg, i.p.). Cannabinoid receptor types 1 and 2 (Cnr1, Cnr2) and opioid receptor subtype (Oprm1, Oprd1, Oprk1) mRNA levels were quantified by qPCR in the structures of the central nociceptive circuit. Levels of anandamide (AEA) and 2-arachidonoylglycerol (2-AG) were measured by liquid chromatography coupled with the mass spectrometry method (LC-MS/MS). In the interphase, higher pain thresholds in the HA mice correlated with increased spinal anandamide and 2-AG release and higher Cnr1 transcription. Downregulation of Oprd1 and Oprm1 mRNA was noted in HA and LA mice, respectively, however no differences in naloxone sensitivity were observed in either line. As opposed to the LA mice, inflammatory pain sensitivity in the HA mice in the tonic phase was attributed to enhanced microglial activation, as evidenced by enhanced Aif1 and Il-1β mRNA levels. To conclude, Cnr1 inhibitory signaling is one mechanism responsible for decreased pain sensitivity in HA mice in the interphase, while increased microglial activation corresponds to decreased pain thresholds in the tonic inflammatory phase.


Introduction
Numerous reports dedicated to studying the role of the endocannabinoid system in pain modulation have unequivocally determined that the enhancement of endocannabinoid tone produces an anti-inflammatory phenotype in animal models or pain insensitivity in human subjects [1][2][3][4][5]. Endocannabinoid modulation of the inflammatory response includes cannabinoid receptor 2 (CNR2)-mediated suppression of proinflammatory cytokines (e.g., IL-1β, IL-6, IL-8), suppression of dendritic cell activation and mast cell maturation as well as cannabinoid receptor 1 (CNR1)-dependent actions like mobilization of myeloid-derived suppressor cells (MDSCs) or inhibition of the contractile response [6]. Recent findings Int. J. Mol. Sci. 2022, 23, 11686 2 of 17 have demonstrated that agonists with dual CNR1 and CNR2 activities show promise with regard to quenching the neuroinflammatory and excitotoxic cascades in multiple sclerosis [7]. Moreover, the new trend in cannabinoid drug design also features bitopic molecules that target both the orthostatic and allosteric CNR2 sites for enhanced antiinflammatory activity and lower side effect liability [8]. Positive allosteric modulation of the CNR1 receptor was also proven effective in alleviating inflammatory pain [9].
Blocking endocannabinoid activity by directly targeting both subtypes of cannabinoid receptors (CNR1 and CNR2) with antagonists/inverse agonists or by hindering their breakdown via the inhibition of fatty acid amide hydrolase (FAAH) or monoacylglycerol lipase (MAGL) are common approaches for studying the importance of the endocannabinoid system in pain sensitivity. Genetically engineered cell-type specific knock-in or knock-down models or models with disrupted FAAH, MAGL or CNR receptor subtype function are also popular [10,11]. However, some reports point to the disadvantages of such pharmacologic or genetic manipulations, which include no sustained analgesic activity or paradoxical exacerbation of inflammatory or neuropathic pain [12][13][14].
Rodent models showing divergent endocannabinoid system activity as a result of stringent, multigenerational selection protocols show a more stable phenotype, thus the employment of such models opens new possibilities for unraveling the complex mechanisms that govern pain sensitivity. Two mouse lines selected for over 100 generations to express either depressed (HA-high analgesia line) or enhanced (LA-low analgesia line) pain sensitivity show divergent activity in the two important neurotransmitter systems engaged in pain perception. Namely, the HA line shows a greater contribution of the opioid and cannabinoid systems in the acute antinociceptive response to noxious or stressful stimuli and are also more sensitive to exogenous opioid and cannabinoids ligands [15][16][17][18].
Additionally, HA mice were also described to show a more profound inflammatory pain phenotype in comparison with their LA counterparts, possibly owing to the previously discovered congenital blood-brain barrier (BBB) disruption in this line [19,20]. Thus, the notion that HA mice might show enhanced microglial activation, particularly in response to inflammatory stimuli, seems plausible. Endocannabinoids are vital players in promoting microglial activation directed towards tissue remodeling to maintain central nervous system (CNS) homeostasis [21,22]. Similar observations were made for dynorphins and enkephalins acting via κ and δ opioid receptors, respectively [23,24]. Therefore, one can expect that upregulation of the endocannabinoid and endogenous opioid system in HA mice could represent a compensatory mechanism that counteracts the pro-inflammatory microglial activation.
There were previous attempts to confirm that the mechanistic underpinnings of increased susceptibility to inflammatory pain is linked to endogenous opioid system activity. It is a widely accepted belief that endogenous opioids exert anti-inflammatory activity mainly by suppressing the stress response pro-inflammatory cytokine positive feedback loop [25]. Endogenous opioids can also inhibit splenocyte proliferation and T-cell activation [26,27]. As shown before, downregulation of enkephalin expression correlates with the upregulation of pro-inflammatory markers in a number of inflammatory diseases like arthritis, Crohn's disease or dry eye disease [28][29][30]. Additionally, the phenomenon of downregulating IL-1 family cytokines is thought to constitute the basis for placebo-based analgesia, where an increase in endogenous opioid tone is key.
Surprisingly, the results obtained so far from HA and LA mice did not confirm any meaningful engagement of endogenous opioid peptides in inflammatory pain sensitivity as previously hypothesized [31]. Moreover, no attempts have been made so far to explain the role of endogenous opioids and cannabinoids in transient dorsal horn neuron hyperpolarization following irritant injection. Thus, in the study herein presented, we aimed at verifying the hypothesis that differences in tonic inflammatory pain sensitivity and the magnitude of transient neuron irresponsiveness after formalin injection between HA and LA mice emerged from the divergent endocannabinoid system tone and possibly from differences in congenital BBB function. We believe that increased endocannabinoid, rather than endogenous opioid system tone, serves as a mechanism compensating for microglialactivation-induced increased inflammatory pain sensitivity in HA mice. Additionally, we showed that endocannabinoids suppressed the transient inhibition of neuron excitability in response to formalin injection.

Sensitivity to Acute Inflammatory Pain in HA and LA Mice
As revealed by two-way ANOVA with line and phase as the independent factors, mice from the HA and LA lines differed in the intensity of nocifensive responses (measured as paw licking time) to formalin injection in the interphase and second phase of the formalin test [F(1,41) = 43.2; p ≤ 0.001] (Figure 1) rather than endogenous opioid system tone, serves as a mechanism c microglial-activation-induced increased inflammatory pain sensitivity ditionally, we showed that endocannabinoids suppressed the transi neuron excitability in response to formalin injection.

Sensitivity to Acute Inflammatory Pain in HA and LA Mice
As revealed by two-way ANOVA with line and phase as the ind mice from the HA and LA lines differed in the intensity of nocifensive ured as paw licking time) to formalin injection in the interphase and se formalin test [F(1,41) = 43.2; p ≤ 0.001] (Figure 1)  Intensity of acute inflammatory pain in HA and LA mice (n = 9-13) upon injection of 5% formalin (in PBS) into the dorsum of the hind foot. Paw measured in the interphase (INT, 5-20 min) and the second phase (2nd, 20-60 m sults were analysed with two-way and one-way ANOVA, followed by Bonfer for multiple comparisons. Statistical significance was depicted as follows: *** p within each phase).

Role of the Endogenous opioid System in Acute Inflammatory Pain Sensiti Mice
Two-way ANOVA with treatment and phase as the independen that the administration of naloxone (NLX) did not affect licking time in 0.09; p = 0.92] nor in the LA mice [F(1,29) = 0.21; p = 0.64] (Figure 2A,B) Figure 1. Intensity of acute inflammatory pain in HA and LA mice (n = 9-13) in the formalin test upon injection of 5% formalin (in PBS) into the dorsum of the hind foot. Paw licking time was measured in the interphase (INT, 5-20 min) and the second phase (2nd, 20-60 min) of the test. Results were analysed with two-way and one-way ANOVA, followed by Bonferroni's post-hoc test for multiple comparisons. Statistical significance was depicted as follows: *** p ≤ 0.001 (HA vs. LA within each phase).      Results were analysed with two-way ANOVA with treatment and phase as independent factors and with one-way ANOVA within each phase for each mouse line, followed by Bonferroni's post-hoc test. Statistical significance was depicted as follows: ** p ≤ 0.01; *** p ≤ 0.001 (vs. control within each phase and line).

Structure
1.01 ± 0.08; formalin: 2.08 ± 0.10; p ≤ 0.001). In the LA mice, Cnr2 expression increased from 1.07 ± 0.21 to 2.03 ± 0.43 in the periaqueductal gray matter and from 1.02 ± 0.11 to 1.49 ± 0.11 in the hypothalamus. Table 2. Cannabinoid receptor 2 (Cnr2) mRNA levels in HA and LA mice in the interphase of the formalin test. Mice were injected with 5% formalin (in PBS) into the dorsal aspect of the hind paw (n = 4-6). Samples were harvested 15 min post-formalin. Results were analysed within each line with two-way ANOVA followed by Bonferroni's post-hoc test. Statistical significance was depicted as follows: * p ≤ 0.05; *** p ≤ 0.001 (vs. control).

Opioid Receptor Expression in HA and LA Mice
No changes in opioid receptor expression following formalin injection were evidenced with two-way ANOVA with line and treatment (saline or formalin) as the independent factors in brain structures other than the periaqueductal gray matter. When Oprm1 expression was studied in the periaqueductal gray matter, two-way ANOVA revealed that formalin injection significantly decreased Oprm1 mRNA expression in the LA (1.01 ± 0.06 vs. 0.74 ± 0.16; p ≤ 0.05), but not in the HA mice [F(1,21) = 9.8; p ≤ 0.01] ( Table 3). Table 3. Mu opioid receptor 1 (Oprm1) mRNA levels in HA and LA mice in the interphase of the formalin test. Mice were injected with 5% formalin (in PBS) into the dorsal aspect of the hind paw (n = 4-6). Samples were harvested 15 min post-formalin. Results were analysed within each line with two-way ANOVA followed by Bonferroni's post-hoc test. Statistical significance was depicted as follows: * p ≤ 0.05 (vs. control).

Involvement of Microglial Activation in Inflammatory Pain Sensitivity
To assess the role of microglial activation as a potential mechanism responsible for the differences in inflammatory pain sensitivity between both lines, the HA and LA mice were injected with minocycline 30 min prior to formalin injection. As evidenced by twoway ANOVA with phase and treatment as the independent factors, minocycline significantly decreased paw licking time in both the HA [F(2,44) = 12.5; p ≤ 0.001] and LA mice [F(2,44) = 9.9; p ≤ 0.001] ( Figure 5). Only the 100 mg/kg dose of minocycline was effective. In the HA line, minocycline did not have any effect in the interphase, but dose-dependently reduced licking time in the second phase (255 ± 24 s vs. 72 ± 5 s, p ≤ 0.001), as evidenced by a positive phase x treatment interaction [F(2,42) = 13.4; p ≤ 0.001]. In the LA line, minocycline significantly reduced the intensity of paw licking both in the interphase (95 ± 14 s vs. 34 ± 9 s, p ≤ 0.05) and the second phase (90 ± 11.4 s vs. 56.3 ± 8.9 s, p ≤ 0.05). Thus, the effect of minocycline was not only phase-but also line-dependent as confirmed by a positive treatment x phase x line interaction [F(2,84) = 8.2; p ≤ 0.001].
Two-way ANOVA with line and treatment (saline or formalin) as the independent factors revealed that, in the interphase, formalin affected Aif1 mRNA levels in the amygdala [F(1,15) = 8.26; p ≤ 0.01] ( Table 6). Namely, relative Aif1 expression increased from 1.49 ± 0.79 to 4.69 ± 0.68 (p ≤ 0.05) in the HA mice, while its level was unchanged in the LA line. However, two-way ANOVA failed to detect any significant line x treatment interaction [F(1,15) = 2.70; p = 0.12] ( Table 6).
Two-way ANOVA with line and treatment (saline or formalin) as the independent factors evidenced no changes in Il-1β expression following formalin injection in any of the examined brain structures (Table 7). However, in the spinal cord, formalin elevated Il-1β mRNA levels in the HA mice as opposed to the LA mice, where Il-1β levels significantly decreased. This bidirectional pattern of Il-1β expression between the HA and LA mice was confirmed by a significant line x treatment interaction [F(1,16) = 8.18; p ≤ 0.05] and the main effect of line [F(1,16) = 9.24; p ≤ 0.01]. A downward trend for Il-1β expression was visible in the LA mice, but it did not reach significance. The expression of anti-inflammatory M2 microglial marker Il-10 was below the detection level.
fective. In the HA line, minocycline did not have any effect in the interphase, but dose-dependently reduced licking time in the second phase (255 ± 24 s vs. 72 ± 5 s, p ≤ 0.001), as evidenced by a positive phase x treatment interaction [F(2,42) = 13.4; p ≤ 0.001]. In the LA line, minocycline significantly reduced the intensity of paw licking both in the interphase (95 ± 14 s vs. 34 ± 9 s, p ≤ 0.05) and the second phase (90 ± 11.4 s vs. 56.3 ± 8.9 s, p ≤ 0.05). Thus, the effect of minocycline was not only phase-but also line-dependent as confirmed by a positive treatment x phase x line interaction [F(2,84) = 8.2; p ≤ 0.001].  (Table 6). Namely, relative Aif1 expression increased from 1.49 ± 0.79 to 4.69 ± 0.68 (p ≤ 0.05) in the HA mice, while its level was unchanged in the LA line. However, two-way ANOVA failed to detect any significant line x treatment interaction [F(1,15) = 2.70; p = 0.12] ( Table 6).  Table 6. Allograft inflammatory factor 1 (Aif1) mRNA levels in HA and LA mice in the interphase of the formalin test. Mice were injected with 5% formalin (in PBS) into the dorsal aspect of the hind paw (n = 4-6). Samples were harvested 15 min post-formalin. Results were analysed within each line with two-way ANOVA followed by Bonferroni's post-hoc test. Statistical significance was depicted as follows: * p ≤ 0.05 (vs. control).

Discussion
In the study herein presented, we explained, at least in part, the possible mechanisms underlying the divergent susceptibility to acute inflammatory pain in mice selected for high (HA) and low (LA) swim-stress-induced analgesia (SSIA). Our results were in accordance with an early study by Lutfy and colleagues [31] who were the first to demonstrate that HA mice were more sensitive to inflammatory pain than LA mice in the formalin test. We observed a similar pattern in the present study, where an intraplantar injection of formalin produced more profound nocifensive behaviours in the HA than the LA mice in the tonic phase (Figure 1). Differential levels of microglial activation could serve as one possible mechanism, as minocycline more profoundly suppressed formalin-induced paw licking in the HA than in the LA mice ( Figure 5). This theory was supported by higher mRNA levels of pro-inflammatory markers Aif1 and Il-1β in the HA mice as early as 15 min post-formalin, while their levels were either unchanged or decreased in the LA line (Tables 6 and 7). The Aif1 gene encodes the Iba-1 protein that regulates actin cross-linking, which is essential for morphological changes in spinal microglia during the early stages of activation and its expression correlates with hypersensitivity. As Aif1 expression is also present in ramified microglia, Il-1β, a hallmark neuroinflammatory marker, was additionally studied [32][33][34].
We further enhanced the original study by Lutfy [31] by additionally measuring pain thresholds in the interphase of the formalin test. The interphase is characterized by the cessation of excessive neuronal firing provoked by an irritant, such as formalin. Henry et al. argued that this phase is governed by a yet unknown spinally mediated active inhibition mechanism [35]. Our current investigation clearly showed that the HA mice presented significantly less nocifensive behaviours in the interphase than the LA mice ( Figure 1). Thus, we hypothesized that this active inhibitory mechanism could be attributed to the endocannabinoid system, as our previous studies indicated substantial differences in its activity between HA and LA mice [17,36]. The HA mice showed a significant increase in spinal and amygdalar Cnr1 transcripts (Table 1), while Cnr2 mRNA levels were elevated only in the amygdala (Table 2). Additionally, increased concentrations of anandamide (AEA) and 2-AG were detected in the spinal cord ( Figure 4). Moreover, rimonabant-a selective Cnr1 receptor antagonist-dose-dependently intensified pain behaviour in the interphase, but only in the HA line ( Figure 3).
Compelling evidence exists for a compensatory peripheral and central increase in AEA and 2-AG in many inflammatory states such as arthritis and osteoarthritis as well as in relapsing multiple sclerosis patients [37,38]. In addition, enhanced AEA signaling resulting from fatty-acid amide hydrolase (FAAH) loss of function was associated with pain insensitivity [3]. These findings imply a significant role of endocannabinoids in neuronal excitability and may account for the divergence in inflammatory pain sensitivity between the HA and LA mice seen in the interphase. Their effect is executed by either a direct action at the Cnr1 receptors and/or modulation of ion channel conductance. It has been recognized that endocannabinoids inhibit Ca 2+ influx in a Cnr1-dependent and independent manner [39] and also inhibit the tetrodotoxin (TTX)-sensitive Na + channels in cortical and hippocampal neurons [40,41]. Moreover, endocannabinoids activate inwardly rectifying K + channels and induce neuron hyperpolarization [42].
It is commonly acknowledged that spinal Cnr1 receptors are important modulators of nociceptive transmission as their intrathecal delivery produces antinociception in numerous models of pain [43][44][45]. Namely, their activation reduces dorsal horn C-and Aδ-fiber electrical activity both in anesthetized animals and in animals with peripheral inflammation [46,47]. Moreover, loss of spinal Cnr1 receptors produces hyperalgesia [48]. Endocannabinoid binding to Cnr1 receptors in the amygdala is important for the activation of the descending inhibitory pain pathway. Namely, they enhance glutamatergic neurotransmission by suppressing GABA-ergic inhibitory interneurons and increase the firing of periaqueductal gray matter (PAG) projection neurons. This allows stronger input from the rostral ventromedial medulla (RVM) "off" cells to the spinal cord dorsal horn and triggers analgesia. This mechanism is responsible for the effect of WIN 55212-2 microinjection into the amygdalar basolateral nucleus, where it suppresses formalin-induced pain behaviour in the first and tonic phases [49]. Moreover, overexpression of Cnr1 and Cnr2 receptors in the amygdala could possibly serve as an adaptive anxiolytic response to a stressful stimulus such as irritant injection. For instance, it was demonstrated that mice overexpressing Cnr2 receptors were more resistant to stressful stimuli and that Cnr1 receptors mediate the anxiolytic effects of drugs [50,51]. Additionally, stimulation of both Cnr receptor subtypes was implicated in the early, first line mechanism impairing fear memory consolidation and generalization to facilitate aversive memory extinction [52].
To our surprise, nocifensive behaviours seen in the tonic phase in the HA line were not dependent on Cnr1 receptor activation as even the highest dose of rimonabant failed to intensify inflammatory pain in this line. It is possible that increased levels of AEA and 2-AG paired with increased receptor availability in HA mice could alleviate the pronociceptive effect of Cnr1 blockage. Another hypothesis assumes that Cnr1 receptor blockage triggers the compensatory activation of Cnr2 receptor-mediated signaling in the amygdala and in the spinal cord. As shown before, even low-grade inflammation is sufficient to induce anandamide synthesis and enhance spinal Cnr2 receptor expression [53]. The sole role of the Cnr2 receptors in pain sensitivity was evidenced before in nerve injury models, where Cnr2 knockouts showed enhanced ipsilateral pain sensitivity and also developed mirror hyperalgesia [54,55]. Despite no differences in post-formalin spinal Cnr2 expression in HA mice, these mostly microglia-residing receptors, could still be a possible target for spinal 2-AG binding to produce antihyperalgesia in conditions of Cnr1 inhibition, especially when HA mice showed more pronounced microglial activation reflected by an increase in Aif1 and Il-1β transcripts in response to formalin than LA mice. Moreover, AEA release could be an attempt to reduce microglial polarization towards the inflammatory M1 phenotype, which is Cnr2-receptor-dependent [21]. Additionally, mice from the LA line show impaired G-protein Cnr2 receptor coupled function [17], hence a more prevalent involvement of Cnr1 receptor signaling in the tonic phase and compensatory upregulation of Cnr2 receptors in the PAG and hypothalamus.
The contribution of the endogenous opioid system to inflammatory pain sensitivity in HA and LA mice was also addressed. However, naloxone was ineffective in both lines and both phases (Figure 2), thus providing evidence of the endogenous opioid system not playing a major role in modulation of formalin-induced acute inflammatory pain. One possible explanation for the compromised contribution of the endogenous opioid system in formalin-induced pain sensitivity is the downregulation of Oprd1 expression in the PAG of HA mice ( Table 4). As we have previously shown, δ-opioid receptors significantly influenced nociceptive thresholds in HA mice. For instance, HA mice showed higher basal hypothalamic Oprd1 expression than their LA counterparts (Table 4). In addition, we have previously identified an A107V substitution in the Oprd1 gene that renders it less responsive to ligands [56]. An upregulation of the Oprk1 gene coding the κ-opioid receptor was also evidenced in the PAG of HA mice (Table 5). This phenomenon could be associated with the triggering of aversion circuits in response to a stressful stimulus such as formalin injection [57,58]. HA mice are more vulnerable to stress than LA mice, thus acute stress could induce Oprk1-mediated adaptive changes to trigger aversive and defensive behaviours. The ineffectiveness of naloxone in LA mice may be explained by the widely recognized opioid system hypoactivity and opioid ligand insensitivity in this line [36,59]. Additionally, as shown in the current study, formalin induced Oprm1 downregulation in the PAG in LA mice, which could also contribute to naloxone insensitivity (Table 3).

Animals
10-12-week-old male Swiss-Webster mice selected for 101 generations for high (HA) and low (LA) swim-stress-induced analgesia were used in behavioural studies. Mice were kept at the Institute of Genetics and Animal Biotechnology Polish Academy of Sciences animal facility under standard ambient temperature (22 ± 2 • C) and humidity (55 ± 10%) under a 12/12 h light/dark cycle (lights on at 7 a.m.). Mice were housed in groups of 3-4 in conventional shoebox cages with sawdust bedding and environmental enrichment. Animals had unlimited access to fresh tap water and pelleted food (Labofeed H, Kcynia, Poland). Experiments were carried out according to the 2010/63/UE directive and received ethical clearance from the I Local Ethics Committee for Animal Experimentation in Warsaw (permit no. WAW2/134/2021). Eight to thirteen animals were used per treatment group. One animal was used only once and a total of 210 animals were used in the study.

Formalin Test
For formalin injection, mice were put under isoflurane anesthesia (Forane, Baxter Deerfield, IL, USA) delivered by an MSS-3 vaporizer (periVet, Szczejkowice, Poland) as described earlier [60]. The flow of isoflurane (in oxygen) was set to 5% (induction) and 3.5% for maintenance. Next, 20 µL of 5% formalin (formaldehyde diluted with phosphate buffered saline) was injected into the dorsum of the right hindpaw with a Hamilton syringe. Due to animal welfare concerns, mice remained under anesthesia for 5 min until the most painful phase of the test (first phase) had resolved. Next, mice were placed in Plexiglas observation chambers mounted on a glass pane surface and the duration of paw licking was manually scored with a stopwatch. Paw licking time was measured in the 5-20 and 20-60 min timeframes representing the interphase and second (tonic) phase respectively in 5-min intervals. The experimenter performing the experiments was blinded to both the line of the animals tested as well as treatment. Twenty-two animals were used to determine formalin sensitivity between HA and LA mice.

Antagonist Administration
Rimonabant (a selective Cnr1 receptor antagonist) was dissolved in a mixture of DMSO/Tween80/saline (1:1:18 v/v). Naloxone (a nonselective opioid receptor antagonist) was dissolved in saline. Both compounds were delivered intraperitoneally (i.p.) at 100 µL/10 g body weight, 15 min before formalin injection. Control animals received vehicles for rimonabant (a mixture of 5% DMSO, 5% Tween80 and 90% saline) or naloxone (in saline). The solutions were prepared by a laboratory technician and coded to ensure that the experimenter was blind to the treatment. Animals were assigned to different drug treatments by means of a randomization calculator provided by GraphPad QuickCalcs online tool (GraphPad Software, San Diego, CA, USA). A total of 40 animals received naloxone treatment; 72 were treated with rimonabant, 48 with minocycline and 50 received vehicle.

Tissue Harvest
Mice were sacrificed by decapitation under isoflurane (FORANE, Baxter Deerfield, IL, USA) anaesthesia delivered with an MSS-3 vaporizer (periVet, Szczejkowice, Poland). Fifteen minutes following formalin injection, their brains were removed and placed on ice on a Petri dish. Next, the following structures were isolated using the Mouse Brain Matrix (AgnTho's, Lidingo, Sweden): periaqueductal gray matter, amygdala, hypothalamus and thalamus. The spinal cord was isolated by means of hydraulic extrusion. Briefly, the spinal column was cut at the level of cauda equine and an 18 G needle attached to a 5 mL syringe was inserted into the spinal canal. Hydraulic pressure was applied, and the spinal cord was flushed with ice-cold phosphate-buffered saline onto a clean Petri dish. Next, the lumbar enlargement was located and separated from the sacral and thoracic regions. All central nervous system (CNS) structures were placed on dry ice following dissection and stored at −80 • C. Fourteen animals each were used for qPCR and LC/MS/MS analyses.

Statistical Analysis
Data were processed with STATISTICA 13.3 software (TIBCO Software Inc., Palo Alto, CA, USA). Graphs were created with GraphPad Prism 5.04 software for Windows (GraphPad Software, San Diego, CA, USA). Behavioural and receptor expression data were analysed with two-way ANOVA with phase and treatment or line and phase as independent factors, followed by Bonferroni's post hoc-test and expressed as means ± SEM. One-way ANOVA was used for comparisons within each line for each phase separately. LC-MS/MS analysis of 2-AG and anandamide concentrations in the brain structures of HA and LA mice were processed with one-way ANOVA with Bonferroni's post hoc-test and expressed as means ± SEM. The statistician was blinded to the line of the animal data and treatment. Normality was assessed with the Shapiro-Wilk test.

Conclusions
In conclusion, this was the first study that underlines the possible mechanisms underpinning the differences in inflammatory pain sensitivity between HA and LA mice. The possible mechanism behind decreased pain behaviour in HA mice observed in the interphase encompasses enhanced Cnr1-dependent inhibitory signaling related to both enhanced spinal 2-AG and AEA release along with increased Cnr1 gene transcription. Conversely, the pronociceptive response of HA mice in the tonic phase was not modulated by Cnr1 receptor activation and was mediated by increased microglial activation. Endogenous opioid system activation exerted no evident modulatory function regarding inflammatory pain sensitivity.