Literature DB >> 1349746

Anxiolytic potential of 5-HT3 receptor antagonists.

B Costall1, R J Naylor.   

Abstract

The 5-HT3 receptor antagonists such as ondansetron have been shown to have anxiolytic-like activity in a wide range of preclinical tests: in the mouse black: white test, the rat social interaction test, the rat elevated X-maze and the marmoset human threat test. Ondansetron, like other 5-HT3 receptor antagonists appears to have important advantages over existing anxiolytic therapies. Thus, the 5-HT3 receptor antagonists are not sedative, they do not have addictive liabilities, there are no problems of withdrawing from chronic treatment and they can be used following benzodiazepine withdrawal. Such compounds even inhibit the behavioural syndrome associated with withdrawal from drugs of abuse, nicotine, alcohol, cocaine, opiates. The preclinical data, therefore, indicates the 5-HT3 receptor antagonists as novel anxiolytics of the future, and there is new clinical work in support of this suggestion.

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Year:  1992        PMID: 1349746     DOI: 10.1111/j.1600-0773.1992.tb00448.x

Source DB:  PubMed          Journal:  Pharmacol Toxicol        ISSN: 0901-9928


  14 in total

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Authors:  Lesley A Ricci; Thomas R Morrison; Richard H Melloni
Journal:  Horm Behav       Date:  2013-10-11       Impact factor: 3.587

2.  Improvement of hemichorea with ondansetron.

Authors:  O O Erdinç; G Ozdemir; S Uysal; D Gücüyener; S Torun
Journal:  Postgrad Med J       Date:  1997-02       Impact factor: 2.401

3.  Contribution of Hippocampal 5-HT3 Receptors in Hippocampal Autophagy and Extinction of Conditioned Fear Responses after a Single Prolonged Stress Exposure in Rats.

Authors:  Zhong-Min Wu; Li-Hua Yang; Rong Cui; Gui-Lian Ni; Feng-Tian Wu; Yong Liang
Journal:  Cell Mol Neurobiol       Date:  2016-06-21       Impact factor: 5.046

4.  Effects of quipazine and m-chlorophenylbiguanide (m-CPBG) on temporal differentiation: evidence for the involvement of 5-HT2A but not 5-HT3 receptors in interval timing behaviour.

Authors:  S Body; K Asgari; J F Rickard; Z Zhang; K C F Fone; C M Bradshaw; E Szabadi
Journal:  Psychopharmacology (Berl)       Date:  2005-10-14       Impact factor: 4.530

5.  Ondansetron, an antagonist of 5-HT3 receptors, antagonizes the anti-exploratory effect of caerulein, an agonist of CCK receptors, in the elevated plus-maze.

Authors:  E Vasar; E Peuranen; T Oöpik; J Harro; P T Männistö
Journal:  Psychopharmacology (Berl)       Date:  1993       Impact factor: 4.530

6.  Visceral perception in irritable bowel syndrome. Rectal and gastric responses to distension and serotonin type 3 antagonism.

Authors:  J Zighelboim; N J Talley; S F Phillips; W S Harmsen; A R Zinsmeister
Journal:  Dig Dis Sci       Date:  1995-04       Impact factor: 3.199

7.  Effects of dexfenfluramine and 5-HT3 receptor antagonists on stress-induced reinstatement of alcohol seeking in rats.

Authors:  Anh Dzung Lê; Douglas Funk; Stephen Harding; W Juzytsch; Paul J Fletcher; Yavin Shaham
Journal:  Psychopharmacology (Berl)       Date:  2006-03-07       Impact factor: 4.530

8.  Acute selective serotonin reuptake inhibitors increase conditioned fear expression: blockade with a 5-HT(2C) receptor antagonist.

Authors:  Nesha S Burghardt; David E A Bush; Bruce S McEwen; Joseph E LeDoux
Journal:  Biol Psychiatry       Date:  2007-05-23       Impact factor: 13.382

9.  Profile of action of 5-HT3 receptor antagonists, ondansetron and WAY 100289, in the elevated plus-maze test of anxiety of mice.

Authors:  R J Rodgers; J C Cole; J M Tredwell
Journal:  Psychopharmacology (Berl)       Date:  1995-02       Impact factor: 4.530

10.  Modulation of mood States as a major factor in relapse to substance use.

Authors:  Gal Yadid; Lior Redlus; Royi Barnea; Ravid Doron
Journal:  Front Mol Neurosci       Date:  2012-07-23       Impact factor: 5.639

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