Pharmacological enhancement of cannabinoid CB1 receptor activity elicits an antidepressant-like response in the rat forced swim test

被引:180
作者
Hill, MN [1 ]
Gorzalka, BB [1 ]
机构
[1] Univ British Columbia, Dept Psychol, Vancouver, BC V6T 1Z4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
cannabinoid; antidepressant; forced swim test; oleamide; rat;
D O I
10.1016/j.euroneuro.2005.03.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
These experiments aimed to assess whether enhanced activity at the cannabinoid CB1 receptor elicits antidepressant-Re effects. To examine this we administered 1 and 5 mg/kg doses of the endocannabinoid uptake inhibitor AM404; 5 and 25 Vg/kg doses of HU-210, a potent CB1 receptor agonist; 1, 2.5 and 5 mg/kg of oleamide, which elicits cannabinoidergic actions; 1 and 5 mg/kg doses of AM 251, a selective CB1 receptor antagonist, as well as 10 mg/kg desipramine (a positive antidepressant control) and measured the duration of immobility, during a 5-min test session of the rat Porsolt forced swim test. Results demonstrated that administration of desipramine reduced immobility duration by about 50% and that all of AM404, oleamide and HU-210 administration induced comparable decreases in immobility that were blocked by pretreatment with AM 251. Administration of the antagonist AM 251 alone had no effect on immobility at either dose. These data suggest that enhancement of CB1 receptor signaling results in antidepressant effects in the forced swim test similar to that seen following conventional antidepressant administration. (c) 2005 Elsevier B.V. and ECNP. All rights reserved.
引用
收藏
页码:593 / 599
页数:7
相关论文
共 50 条
[1]   GRADIENT OF ALARM SUBSTANCE IN THE FORCED SWIMMING TEST [J].
ABEL, EL .
PHYSIOLOGY & BEHAVIOR, 1991, 49 (02) :321-323
[2]   BEHAVIORAL AND PHYSIOLOGICAL-EFFECTS OF DIFFERENT WATER DEPTHS IN THE FORCED SWIM TEST [J].
ABEL, EL .
PHYSIOLOGY & BEHAVIOR, 1994, 56 (02) :411-414
[3]  
ABLON SL, 1974, AM J PSYCHIAT, V131, P448
[4]   In-vitro and in-vivo action of cannabinoids [J].
Akinshola, BE ;
Chakrabarti, A ;
Onaivi, ES .
NEUROCHEMICAL RESEARCH, 1999, 24 (10) :1233-1240
[5]   Selective inhibition of sucrose and ethanol intake by SR 141716, an antagonist of central cannabinoid (CB1) receptors [J].
Arnone, M ;
Maruani, J ;
Chaperon, F ;
Thiebot, MH ;
Poncelet, M ;
Soubrie, P ;
LeFur, G .
PSYCHOPHARMACOLOGY, 1997, 132 (01) :104-106
[6]  
BANERJEE SP, 1975, J PHARMACOL EXP THER, V194, P74
[7]   SR-141716A-induced stimulation of locomotor activity - A structure-activity relationship study [J].
Bass, CE ;
Griffin, G ;
Grier, M ;
Mahadevan, A ;
Razdan, RK ;
Martin, BR .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2002, 74 (01) :31-40
[8]   Functional role of high-affinity anandamide transport, as revealed by selective inhibition [J].
Beltramo, M ;
Stella, N ;
Calignano, A ;
Lin, SY ;
Makriyannis, A ;
Piomelli, D .
SCIENCE, 1997, 277 (5329) :1094-1097
[9]   Involvement of the opioid system in the anxiolytic-like effects induced by Δ9-tetrahydrocannabinol [J].
Berrendero, F ;
Maldonado, R .
PSYCHOPHARMACOLOGY, 2002, 163 (01) :111-117
[10]  
BORSINI F, 1988, PSYCHOPHARMACOLOGY, V94, P147