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Review
. 2023 Feb 7;13(2):309.
doi: 10.3390/biom13020309.

Progress in Investigational Agents Targeting Serotonin-6 Receptors for the Treatment of Brain Disorders

Affiliations
Review

Progress in Investigational Agents Targeting Serotonin-6 Receptors for the Treatment of Brain Disorders

Ramakrishna Nirogi et al. Biomolecules. .

Abstract

Serotonin (5-HT) plays an important role in the regulation of several basic functions of the central and peripheral nervous system. Among the 5-HT receptors, serotonin-6 (5-HT6) receptor has been an area of substantial research. 5-HT6 receptor is a G-protein-coupled receptor mediating its effects through diverse signaling pathways. Exceptional features of the receptors fueling drug discovery efforts include unique localization and specific distribution in the brain regions having a role in learning, memory, mood, and behavior, and the affinity of several clinically used psychotropic agents. Although non-clinical data suggest that both agonist and antagonist may have similar behavioral effects, most of the agents that entered clinical evaluation were antagonists. Schizophrenia was the initial target; more recently, cognitive deficits associated with Alzheimer's disease (AD) or other neurological disorders has been the target for clinically evaluated 5-HT6 receptor antagonists. Several 5-HT6 receptor antagonists (idalopirdine, intepirdine and latrepirdine) showed efficacy in alleviating cognitive deficits associated with AD in the proof-of-concept clinical studies; however, the outcomes of the subsequent phase 3 studies were largely disappointing. The observations from both non-clinical and clinical studies suggest that 5-HT6 receptor antagonists may have a role in the management of neuropsychiatric symptoms in dementia. Masupirdine, a selective 5-HT6 receptor antagonist, reduced agitation/aggression-like behaviors in animal models, and a post hoc analysis of a phase 2 trial suggested potential beneficial effects on agitation/aggression and psychosis in AD. This agent will be assessed in additional trials, and the outcome of the trials will inform the use of 5-HT6 receptor antagonists in the treatment of agitation in dementia of the Alzheimer's type.

Keywords: 5-HT6 receptor antagonist; Alzheimer’s disease; SAM-760; agitation; avisetron; cerlapirdine; clinical trials; dementia; idalopirdine; intepirdine; landipirdine; latrepirdine; masupirdine; neuropsychiatric symptoms; psychosis; schizophrenia.

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Conflict of interest statement

Cummings has provided consultation to AB Science, Acadia, Alkahest, AlphaCognition, ALZPathFinder, Annovis, AriBio, Artery, Avanir, Biogen, Biosplice, Cassava, Cerevel, Clinilabs, Cortexyme, Diadem, EIP Pharma, Eisai, GatehouseBio, GemVax, Genentech, Green Valley, Grifols, Janssen, Karuna, Lexeo, Lilly, Lundbeck, LSP, Merck, NervGen, Novo Nordisk, Oligomerix, Ono, Otsuka, PharmacotrophiX, PRODEO, Prothena, ReMYND, Renew, Resverlogix, Roche, Signant Health, Suven, Unlearn AI, Vaxxinity, VigilNeuro pharmaceutical, assessment, and investment companies. Ramakrishna Nirogi, Pradeep Jayarajan, Anil Shinde, Abdul Rasheed Mohammed, Venkata Ramalingayya Grandhi, Vijay Benade, Vinod Kumar Goyal, Renny Abraham, Venkat Jasti are fulltime employees of Suven Life Sciences Ltd.

Figures

Figure 1
Figure 1
PRISMA flow diagram.
Figure 2
Figure 2
Clinical candidates targeting 5-HT6 receptors.

References

    1. Erspamer V., Vialli M. Ricerche sul secreto delle cellule enterocromaffini. Boll. Soc. Med.-Chir. Pavia. 1937;51:357–363.
    1. Twarog B.M., Page I.H. Serotonin content of some mammalian tissues and urine and a method for its determination. Am. J. Physiol. 1953;175:157–161. doi: 10.1152/ajplegacy.1953.175.1.157. - DOI - PubMed
    1. Berger M., Gray J.A., Roth B.L. The expanded biology of serotonin. Annu. Rev. Med. 2009;60:355–366. doi: 10.1146/annurev.med.60.042307.110802. - DOI - PMC - PubMed
    1. Bockaert J., Roussignol G., Becamel C., Gavarini S., Joubert L., Dumuis A., Fagni L., Marin P. GPCR-interacting proteins (GIPs): Nature and functions. Biochem. Soc. Trans. 2004;32:851–855. doi: 10.1042/BST0320851. - DOI - PubMed
    1. Millan M.J., Marin P., Bockaert J., Mannoury la Cour C. signaling at G-protein-coupled serotonin receptors: Recent advances and future research directions. Trends. Pharmacol. Sci. 2008;29:454–464. doi: 10.1016/j.tips.2008.06.007. - DOI - PubMed

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