Antianxiety profile of ondansetron, a selective 5-HT3 antagonist, in a novel animal model

被引:0
|
作者
Roychoudhury, M [1 ]
Kulkarni, SK [1 ]
机构
[1] PANJAB UNIV,UNIV INST PHARMACEUT SCI,DIV PHARMACOL,CHANDIGARH 160014,INDIA
来源
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY | 1997年 / 19卷 / 02期
关键词
ondansetron; anxiety; mirrored chamber; approach-conflict; mice;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The profile of action of ondansetron ondansetron was assessed in a novel animal model of anxiety. The mirrored chamber is a nonpunishing quantitative model of anxiety which measures approach-conflict behavior. Ondansetron in all the doses tested (0.01, 0.1 and 1 mg/kg i.p.) showed significant anxiolytic action as compared to naive mice, but it was less potent as compared to a well-known anxiolytic, diazepam (1 mg/kg). These results suggest that ondansetron has anxiolytic efficacy in nonconflict paradigms of anxiety, a response not mediated by the conventional neurotransmitter receptors, GABA-benzodiazepine as flumazenil (4 mg/kg), a benzodiazepine receptor antagonist, failed to reverse the behavioral parameters evoked by ondansetron.
引用
收藏
页码:107 / 111
页数:5
相关论文
共 50 条
  • [31] Effects of the 5-HT3 receptor antagonist ondansetron on the ketamine- and dizocilpine-induced place preferences in mice
    Suzuki, T
    Aoki, T
    Kato, H
    Yamazaki, M
    Misawa, M
    EUROPEAN JOURNAL OF PHARMACOLOGY, 1999, 385 (2-3) : 99 - 102
  • [32] NEUROANATOMICAL STRUCTURES INVOLVED IN THE ACTION OF THE 5-HT3 ANTAGONIST ONDANSETRON - A 2-DEOXYGLUCOSE AUTORADIOGRAPHIC STUDY IN THE RAT
    MITCHELL, EA
    PRATT, JA
    BRAIN RESEARCH, 1991, 538 (02) : 289 - 294
  • [33] Dose-related impairment of spatial learning by intrahippocampal scopolamine: Antagonism by ondansetron, a 5-HT3 receptor antagonist
    Carli, M
    Luschi, R
    Samanin, R
    BEHAVIOURAL BRAIN RESEARCH, 1997, 82 (02) : 185 - 194
  • [34] EFFECT OF THE 5-HT3 ANTAGONIST ONDANSETRON ON VOLUNTARY ETHANOL INTAKE IN RATS AND MICE MAINTAINED ON A LIMITED ACCESS PROCEDURE
    TOMKINS, DM
    LE, AD
    SELLERS, EM
    PSYCHOPHARMACOLOGY, 1995, 117 (04) : 479 - 485
  • [35] The 5-HT3 receptor antagonist, ondansetron, blocks the development and expression of ethanol-induced locomotor sensitization in mice
    Umathe, Sudhir N.
    Bhutada, Pravinkumar S.
    Raut, Vivek S.
    Jain, Nishant S.
    Mundhada, Yogita R.
    BEHAVIOURAL PHARMACOLOGY, 2009, 20 (01): : 78 - 83
  • [36] Combination of 5-HT3 Antagonist and Dexamethasone Is Superior to 5-HT3 Antagonist Alone for PONV Prophylaxis After Laparoscopic Surgeries: A Meta-analysis
    Som, Anirban
    Bhattacharjee, Sulagna
    Maitra, Souvik
    Arora, Mahesh K.
    Baidya, Dalim Kumar
    ANESTHESIA AND ANALGESIA, 2016, 123 (06) : 1418 - 1426
  • [37] ONDANSETRON - PHARMACOLOGY OF A SPECIFIC 5HT3-RECEPTOR ANTAGONIST
    DEEGAN, R
    AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1992, 304 (06) : 373 - 378
  • [38] Ondansetron, a highly selective 5-HT3 receptor antagonist, reduces L-DOPA-induced dyskinesia in the 6-OHDA-lesioned rat model of Parkinson's disease
    Kwan, Cynthia
    Frouni, Imane
    Bedard, Dominique
    Hamadjida, Adjia
    Huot, Philippe
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2020, 871
  • [39] THE 5-HT3 ANTAGONIST ONDANSETRON REDUCES GASTROINTESTINAL SIDE-EFFECTS INDUCED BY A SPECIFIC SEROTONIN REUPTAKE INHIBITOR IN MAN
    BAILEY, JE
    POTOKAR, J
    COUPLAND, N
    NUTT, DJ
    JOURNAL OF PSYCHOPHARMACOLOGY, 1995, 9 (02) : 137 - 141
  • [40] VAGOTOMY AND ONDANSETRON (5-HT3 ANTAGONIST) INHIBITED THE INCREASE OF SEROTONIN CONCENTRATION INDUCED BY CYTOTOXIC DRUGS IN THE AREA POSTREMA OF FERRETS
    ENDO, T
    MINAMI, M
    MONMA, Y
    YOSHIOKA, M
    SAITO, H
    PARVEZ, SH
    BIOGENIC AMINES, 1992, 9 (03) : 163 - 175