Acute anorectic response to cannabinoid CB1 receptor antagonist/inverse agonist AM 251 in rats: indirect behavioural mediation

被引:26
作者
Tallett, Amy J. [1 ]
Blundell, John E. [1 ]
Rodgers, John R. [1 ]
机构
[1] Univ Leeds, Inst Psychol Sci, Behav Neurosci Lab, Leeds LS2 9JT, W Yorkshire, England
来源
BEHAVIOURAL PHARMACOLOGY | 2007年 / 18卷 / 07期
关键词
AM; 25; anorexia; behavioural specificity; cannabinoids; CB1; receptors; grooming; response competition; rat scratching; weight gain;
D O I
10.1097/FBP.0b013e3282eff0a9
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Despite a large and consistent literature on the suppressant effects of cannabinoid CB1 receptor antagonists/inverse agonists (e.g. rimonabant, AM 251) on food intake and weight gain in rodents, surprisingly little is known about the behavioural selectivity of such effects. In this study, ethological scoring was used to characterize the acute behavioural effects of the rimonabant analogue AM 251 (1.5 and 3.0 mg/kg, intraperitoneally) in nondeprived male rats during a 1-h test with palatable mash. Data were also collected on daily weight gain and on retest food intake 7 days after dosing. Results showed that the higher dose of AM 251 significantly inhibited mash consumption (32% decrease relative to vehicle control), reduced time spent feeding during the test and suppressed body weight gain over the 48-h period that followed acute dosing. No effects on mash consumption were observed when the animals were retested drug-free 1 week after drug treatment. Detailed video analysis of the test sessions showed that, over the dose range tested, AM 251 did not significantly interfere with the vast majority of noningestive behaviours. Both doses of the compound, however, significantly increased the incidence of and the time spent on scratching, whereas the higher dose additionally increased both the number and duration of grooming episodes. The latter effect in particular disrupted the normal structure of behaviour (behavioural satiety sequence) with atypically high levels of grooming displacing feeding during the middle part of the test session. Overall, the behavioural profile of AM 251 in a free-feeding context is very similar to (but approximately two-fold less potent than) that recently reported for the parent molecule, rimonabant. Together, these data strongly suggest that the acute anorectic response to CB1 receptor antagonists/inverse agonists; is indirectly mediated via major alterations to other components of the behavioural repertoire. Behavioural Pharmacology 18:591-600 (C) 2007 Wolters Kluwer Health I Lippincott Williams & Wilkins.
引用
收藏
页码:591 / 600
页数:10
相关论文
共 76 条
  • [1] Aceto MD, 1996, J PHARMACOL EXP THER, V278, P1290
  • [2] CHOLECYSTOKININ ELICITS COMPLETE BEHAVIORAL SEQUENCE OF SATIETY IN RATS
    ANTIN, J
    GIBBS, J
    HOLT, J
    YOUNG, RC
    SMITH, GP
    [J]. JOURNAL OF COMPARATIVE AND PHYSIOLOGICAL PSYCHOLOGY, 1975, 89 (07): : 784 - 790
  • [3] Selective inhibition of sucrose and ethanol intake by SR 141716, an antagonist of central cannabinoid (CB1) receptors
    Arnone, M
    Maruani, J
    Chaperon, F
    Thiebot, MH
    Poncelet, M
    Soubrie, P
    LeFur, G
    [J]. PSYCHOPHARMACOLOGY, 1997, 132 (01) : 104 - 106
  • [4] Anti-obesity drug development
    Bays, H
    Dujovne, C
    [J]. EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2002, 11 (09) : 1189 - 1204
  • [5] BEHAVIORAL STRUCTURE AND MECHANISMS OF ANOREXIA - CALIBRATION OF NATURAL AND ABNORMAL INHIBITION OF EATING
    BLUNDELL, JE
    ROGERS, PJ
    HILL, AJ
    [J]. BRAIN RESEARCH BULLETIN, 1985, 15 (04) : 371 - 376
  • [6] AM 251 produces sustained reductions in food intake and body weight that are resistant to tolerance and conditioned taste aversion
    Chambers, AP
    Koopmans, HS
    Pittman, QJ
    Sharkey, KA
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2006, 147 (01) : 109 - 116
  • [7] Chambers AP, 2004, PHYSIOL BEHAV, V82, P863, DOI 10.1016/S0031-9384(04)00302-6
  • [8] Synergistic effects of cannabinoid inverse agonist AM251 and opioid antagonist nalmefene on food intake in mice
    Chen, RZ
    Huang, RRC
    Shen, CP
    MacNeil, DJ
    Fong, TM
    [J]. BRAIN RESEARCH, 2004, 999 (02) : 227 - 230
  • [9] Pharmacotherapy of obesity: targets and perspectives
    Chiesi, M
    Huppertz, C
    Hofbauer, KG
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2001, 22 (05) : 247 - 254
  • [10] Anti-obesity drugs: a critical review of current therapies and future opportunities
    Clapham, JC
    Arch, JRS
    Tadayyon, M
    [J]. PHARMACOLOGY & THERAPEUTICS, 2001, 89 (01) : 81 - 121