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Psychopharmacology

, Volume 147, Issue 4, pp 412–417 | Cite as

5-HT3- and 5-HT2C-antagonist properties of cyamemazine: significance for its clinical anxiolytic activity

  • M. Alvarez-Guerra
  • F. d’Alché-Birée
  • W. A. Wolf
  • F. Vargas
  • M. Dib
  • R. P. Garay
Original Investigation

Abstract 

Rationale: Cyamemazine is a neuroleptic compound which possesses anxiolytic properties in humans. On the other hand, 5-HT3- and 5-HT2C-receptors have been implicated in anxiety disorders and a previous binding study has shown that cyamemazine possesses high affinity for both serotonin receptor types. Objective: The present study was undertaken to establish whether cyamemazine antagonizes 5-HT3- and/or 5-HT2C-mediated responses, and whether it compares with reference compounds. Methods: Cyamemazine was tested for its ability to antagonize: (i) 5-HT3-dependent contraction of the isolated guinea-pig ileum and bradycardic responses in the rat and (ii) 5-HT2C-dependent phospholipase C (PLC) stimulation in rat brain membranes. Results: In isolated guinea-pig ileum, cyamemazine potently and competitively antagonized 5-HT-dependent contractions (pA2=7.52±0.08; n=5). In this test, cyamemazine was 5–7 times more potent (pIC50=6.75±0.13) than tropisetron (pIC50=6.02±0.04). In rats, cyamemazine i.v. antagonized 5-HT-dependent bradycardic responses with ID50%=3.2±1.5 mg/kg (n=4). Finally, in rat brain membranes cyamemazine antagonized 5-HT2C-dependent PLC stimulation with Ki=424 nM (mianserin exhibits a Ki=113 nM). Conclusions: Cyamemazine behaves as an antagonist at both 5-HT3- and 5-HT2C-receptors, which compares well with reference compounds. These 5-HT3- and 5-HT2C-antagonistic actions of cyamemazine can be involved, at least in part, in its beneficial therapeutic actions in anxiety disorders.

Key words Cyamemazine Anxiety Serotonin 5-HT3-receptor 5-HT2C-receptor 

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Copyright information

© Springer-Verlag Berlin Heidelberg 2000

Authors and Affiliations

  • M. Alvarez-Guerra
    • 1
  • F. d’Alché-Birée
    • 1
  • W. A. Wolf
    • 1
  • F. Vargas
    • 1
  • M. Dib
    • 1
  • R. P. Garay
    • 1
  1. 1.INSERM U400, Faculté de Médecine de Créteil & Rhône-Poulenc-Rorer, Montrouge, France e-mail: garay@im3.inserm.fr, Fax: +33-1-49-81-94-26FR

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