Literature DB >> 26739950

5-HT2C receptors in psychiatric disorders: A review.

A Chagraoui1, F Thibaut2, M Skiba3, C Thuillez4, M Bourin5.   

Abstract

5-HT2Rs have a different genomic organization from other 5-HT2Rs. 5HT2CR undergoes post-transcriptional pre-mRNA editing generating diversity among RNA transcripts. Selective post-transcriptional editing could be involved in the pathophysiology of psychiatric disorders through impairment in G-protein interactions. Moreover, it may influence the therapeutic response to agents such as atypical antipsychotic drugs. Additionally, 5-HT2CR exhibits alternative splicing. Central serotonergic and dopaminergic systems interact to modulate normal and abnormal behaviors. Thus, 5HT2CR plays a crucial role in psychiatric disorders. 5HT2CR could be a relevant pharmacological target in the treatment of neuropsychiatric disorders. The development of drugs that specifically target 5-HT2C receptors will allow for better understanding of their involvement in the pathophysiology of psychiatric disorders including schizophrenia, anxiety, and depression. Among therapeutic means currently available, most drugs used to treat highly morbid psychiatric diseases interact at least partly with 5-HT2CRs. Pharmacologically, 5HT2CRs, have the ability to generate differentially distinct response signal transduction pathways depending on the type of 5HT2CR agonist. Although this receptor property has been clearly demonstrated, in vitro, the eventual beneficial impact of this property opens new perspectives in the development of agonists that could activate signal transduction pathways leading to better therapeutic efficiency with fewer adverse effects.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  5HT2C signaling; Constitutive activity; Gene polymorphism; MRNA-editing; Psychiatric disorders

Mesh:

Substances:

Year:  2015        PMID: 26739950     DOI: 10.1016/j.pnpbp.2015.12.006

Source DB:  PubMed          Journal:  Prog Neuropsychopharmacol Biol Psychiatry        ISSN: 0278-5846            Impact factor:   5.067


  26 in total

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Journal:  World J Biol Psychiatry       Date:  2016-07-15       Impact factor: 4.132

4.  Increased temporal discounting after chronic stress in CHL1-deficient mice is reversed by 5-HT2C agonist Ro 60-0175.

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5.  Ketamine up-regulates a cluster of intronic miRNAs within the serotonin receptor 2C gene by inhibiting glycogen synthase kinase-3.

Authors:  Steven F Grieco; Dmitry Velmeshev; Marco Magistri; Hagit Eldar-Finkelman; Mohammad A Faghihi; Richard S Jope; Eleonore Beurel
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6.  Modulation of Monoaminergic Systems by Antidepressants in the Frontal Cortex of Rats After Chronic Mild Stress Exposure.

Authors:  David Martín-Hernández; Marta P Pereira; Hiram Tendilla-Beltrán; José L M Madrigal; Borja García-Bueno; Juan C Leza; Javier R Caso
Journal:  Mol Neurobiol       Date:  2019-05-03       Impact factor: 5.590

7.  5-HT2C receptor blockade reverses SSRI-associated basal ganglia dysfunction and potentiates therapeutic efficacy.

Authors:  Elena Y Demireva; Deepika Suri; Emanuela Morelli; Darshini Mahadevia; Nao Chuhma; Catia M Teixeira; Annette Ziolkowski; Marc Hersh; James Fifer; Sneha Bagchi; Alexei Chemiakine; Holly Moore; Jay A Gingrich; Peter Balsam; Stephen Rayport; Mark S Ansorge
Journal:  Mol Psychiatry       Date:  2018-08-17       Impact factor: 15.992

Review 8.  The serotonergic system and cognitive function.

Authors:  Dubravka Švob Štrac; Nela Pivac; Dorotea Mück-Šeler
Journal:  Transl Neurosci       Date:  2016-05-09       Impact factor: 1.757

Review 9.  The serotonin 5-HT2C receptor and the non-addictive nature of classic hallucinogens.

Authors:  Clinton E Canal; Kevin S Murnane
Journal:  J Psychopharmacol       Date:  2016-11-15       Impact factor: 4.153

Review 10.  Adenosine-to-inosine RNA editing in neurological development and disease.

Authors:  Yuxi Yang; Shunpei Okada; Masayuki Sakurai
Journal:  RNA Biol       Date:  2021-01-06       Impact factor: 4.652

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