ijms-logo

Journal Browser

Journal Browser

Molecular Advances in Psychiatric Therapies

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Neurobiology".

Deadline for manuscript submissions: closed (15 February 2024) | Viewed by 2773

Special Issue Editors


E-Mail Website
Guest Editor
Maj Institute of Pharmacology, Polish Academy of Sciences, Krakow, Poland
Interests: pharmacokinetics; pharmacology; biochemistry
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
Maj Institute of Pharmacology, Polish Academy of Sciences, 31-343 Kraków, Poland
Interests: psychopharmacology; brain metabolism; cytochrome P450; drug metabolism
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues, 

Psychiatric disorders (depression, schizophrenia, anxiety) are major public health concerns which influence individuals’ quality of life and cause an economic burden. Despite the availability of a wide range of psychotropics, remission rates are very low. The mechanisms underlying the causes of these disorders are complex and include social, psychological, and biological aspects. Antidepressants based on the regulation of monoaminergic systems and antipsychotics targeting dopamine D2 and serotonin 5-HT2A receptors are still the treatments used as the first line of defence. However, new targets involving glutamatergic, cannabinoid, and trace amine receptors are being tested for the treatment of depression and schizophrenia. Serotonergic psychedelics modulating brain networks and promoting neurogenesis and neuroplasticity are being investigated as a potential option for the treatment of depression and anxiety, including post-traumatic stress disorder. Currently available antipsychotics are effective for ameliorating positive symptoms but are not completely satisfying in terms of improving negative and cognitive symptoms. Targeting specific acetylcholine or serotonin receptor subtypes could ameliorate numerous symptoms of schizophrenia. Moreover, new technologies are imminent. Non-invasive brain stimulation seems promising in the treatment of antipsychotic-resistant schizophrenia, while deep brain stimulation has been extensively studied as a therapeutic option for treatment-resistant depression. Novel therapeutic strategies and developing pharmacogenomics and nanotechnology approaches for enhanced drug delivery should lead to more effective personalized therapies of psychiatric diseases.

Prof. Dr. Władysława Anna Daniel
Dr. Anna Haduch
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. International Journal of Molecular Sciences is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. There is an Article Processing Charge (APC) for publication in this open access journal. For details about the APC please see here. Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Published Papers (2 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Research

Jump to: Review

14 pages, 1755 KiB  
Article
The Novel Atypical Antipsychotic Lurasidone Affects Cytochrome P450 Expression in the Liver and Peripheral Blood Lymphocytes
by Przemysław J. Danek and Władysława A. Daniel
Int. J. Mol. Sci. 2023, 24(23), 16796; https://doi.org/10.3390/ijms242316796 - 27 Nov 2023
Viewed by 837
Abstract
Lurasidone is a novel atypical antipsychotic drug acting on dopaminergic, serotonergic and noradrenergic receptors; it is applied for the long-term treatment of schizophrenia and depression in patients with bipolar disorders. We aimed at performing a comparative study on the influence of chronic treatment [...] Read more.
Lurasidone is a novel atypical antipsychotic drug acting on dopaminergic, serotonergic and noradrenergic receptors; it is applied for the long-term treatment of schizophrenia and depression in patients with bipolar disorders. We aimed at performing a comparative study on the influence of chronic treatment with lurasidone on the expression of cytochrome P450 enzymes in the liver and in peripheral blood lymphocytes, and to evaluate the relationship between changes in the expression of CYP enzymes in the two experimental models. The obtained results show a fairly similar expression pattern of the main CYP enzymes in the rat livers and lymphocytes, and they indicate that in the liver, lurasidone exerts an inhibitory effect on the activity, protein and mRNA levels of CYP2B1/2 (not CYP2B2 mRNA), CYP2C11 and CYP2E1, while in the case of CYP3A1 and CYP3A2, it causes enzyme induction. At the same time, lurasidone decreases the expression of CYP2B, CYP2C11 (CYP2C11 protein only) and CYP2E1 but increases that of CYP3A2 (not CYP3A1) in lymphocyte cells. In conclusion, chronic treatment with lurasidone simultaneously and in the same way influences the expression and activity of CYP2B, CYP2C11, CYP2E1 and CYP3A2 in the liver and peripheral blood lymphocytes of rats. Thus, the lymphocyte cytochrome P450 profile may be utilized as an indicator of the hepatic cytochrome P450 profile in further clinical studies with lurasidone, and lymphocytes may serve as easily available surrogates for examining the impact of new drugs and chronic in vivo treatments on CYP enzyme expression, as well as to estimate drug–drug interactions and toxicity risk. Full article
(This article belongs to the Special Issue Molecular Advances in Psychiatric Therapies)
Show Figures

Figure 1

Review

Jump to: Research

21 pages, 1240 KiB  
Review
Molecular and Medical Aspects of Psychedelics
by Adam Wojtas and Krystyna Gołembiowska
Int. J. Mol. Sci. 2024, 25(1), 241; https://doi.org/10.3390/ijms25010241 - 23 Dec 2023
Cited by 1 | Viewed by 1540
Abstract
Psychedelics belong to the oldest psychoactive drugs. They arouse recent interest due to their therapeutic applications in the treatment of major depressive disorder, substance use disorder, end-of-life anxiety,= and anxiety symptoms, and obsessive–compulsive disorder. In this review, the current state of preclinical research [...] Read more.
Psychedelics belong to the oldest psychoactive drugs. They arouse recent interest due to their therapeutic applications in the treatment of major depressive disorder, substance use disorder, end-of-life anxiety,= and anxiety symptoms, and obsessive–compulsive disorder. In this review, the current state of preclinical research on the mechanism of action, neurotoxicity, and behavioral impact of psychedelics is summarized. The effect of selective 5-HT2A receptor agonists, 25I- and 25B-NBOMe, after acute and repeated administration is characterized and compared with the effects of a less selective drug, psilocybin. The data show a significant effect of NBOMes on glutamatergic, dopaminergic, serotonergic, and cholinergic neurotransmission in the frontal cortex, striatum, and nucleus accumbens. The increases in extracellular levels of neurotransmitters were not dose-dependent, which most likely resulted from the stimulation of the 5-HT2A receptor and subsequent activation of the 5-HT2C receptors. This effect was also observed in the wet dog shake test and locomotor activity. Chronic administration of NBOMes elicited rapid development of tolerance, genotoxicity, and activation of microglia. Acute treatment with psilocybin affected monoaminergic and aminoacidic neurotransmitters in the frontal cortex, nucleus accumbens, and hippocampus but not in the amygdala. Psilocybin exhibited anxiolytic properties resulting from intensification of GABAergic neurotransmission. The data indicate that NBOMes as selective 5-HT2A agonists exert a significant effect on neurotransmission and behavior of rats while also inducing oxidative DNA damage. In contrast to NBOMes, the effects induced by psilocybin suggest a broader therapeutic index of this drug. Full article
(This article belongs to the Special Issue Molecular Advances in Psychiatric Therapies)
Show Figures

Figure 1

Back to TopTop