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大麻素受体拮抗剂SR141716A在食物强化操作性范式中的部分激动剂样特征。

Partial agonist-like profile of the cannabinoid receptor antagonist SR141716A in a food-reinforced operant paradigm.

作者信息

De Vry J, Jentzsch K R

机构信息

CNS Research, Bayer HealthCare, Wuppertal, Germany.

出版信息

Behav Pharmacol. 2004 Feb;15(1):13-20. doi: 10.1097/00008877-200402000-00002.

Abstract

Both cannabinoid CB1 receptor agonists, such as delta-tetrahydrocannabinol (delta-THC), CP 55,940 and WIN 55,212-2, and the antagonist/inverse agonist SR141716A, dose-dependently suppress operant behavior. The present study investigated to what extent combined i.p. application of SR141716A with these cannabinoids resulted in mutually antagonistic effects, in additive effects, or in no interactive effects on operant responding in rats trained in a fixed-ratio 10, food-reinforced 10-min procedure. Pretreatment with SR141716A either had no effect on (at 0.3-1mg/kg), or partially blocked (at 3 mg/kg), the inhibitory effects on responding induced by delta-THC (3-5 mg/kg) and CP 55,940 (0.03-0.2 mg/kg). Interestingly, while 3 mg/kg SR141716A induced moderate inhibitory effects on operant responding, its combination with either agonist resulted in the same level of inhibitory activity on responding as that obtained by SR141716A when tested alone. Pretreatment with a low dose of CP 55,940 (0.01 mg/kg) or WIN 55,212-2 (0.3 mg/kg) did not affect response inhibition induced by SR141716A. Combination of SR141716A (0.5 and 1mg/kg) with delta-THC (3 mg/kg) resulted in the same level of response inhibition, independently of whether SR141716A was given 5 min before or 15 min after delta-THC. Although alternative explanations are conceivable, the data may indicate that SR141716A is a partial agonist at those cannabinoid receptors mediating the response-rate suppressive effects of cannabinoids.

摘要

大麻素CB1受体激动剂,如δ-四氢大麻酚(δ-THC)、CP 55,940和WIN 55,212-2,以及拮抗剂/反向激动剂SR141716A,均呈剂量依赖性地抑制操作性行为。本研究调查了在以固定比例10、食物强化的10分钟程序训练的大鼠中,SR141716A与这些大麻素联合腹腔注射在多大程度上会对操作性反应产生相互拮抗作用、相加作用或无交互作用。用SR141716A预处理对δ-THC(3-5mg/kg)和CP 55,940(0.03-0.2mg/kg)诱导的反应抑制作用要么无影响(0.3-1mg/kg时),要么部分阻断(3mg/kg时)。有趣的是,虽然3mg/kg的SR141716A对操作性反应有中度抑制作用,但其与任何一种激动剂联合使用时,对反应的抑制活性水平与单独测试SR141716A时相同。用低剂量的CP 55,940(0.01mg/kg)或WIN 55,212-2(0.3mg/kg)预处理不影响SR141716A诱导的反应抑制。SR141716A(0.5和1mg/kg)与δ-THC(3mg/kg)联合使用时,无论SR141716A是在δ-THC之前5分钟还是之后15分钟给药,反应抑制水平相同。尽管可以设想其他解释,但这些数据可能表明,SR141716A在介导大麻素反应率抑制作用的那些大麻素受体上是一种部分激动剂。

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