Jodogne C, Tirelli E
Laboratoire de Psychologie Expérimentale, Université de Liège au Sart Tilman, Belgium.
Behav Brain Res. 1990 Jan 1;36(1-2):33-40. doi: 10.1016/0166-4328(90)90157-a.
The present experiment assessed the extent to which environmental stimulation could influence tolerance to the sedative and catatonic effects of the GABAA agonist, 4,5,6,7-tetrahydroisoxozolo(5,4-c)pyridin-3-ol (THIP), through associative learning processes. A conditioning paradigm was used, with THIP as unconditioned stimulus and environmental cues as conditioned stimulus. One group of mice received 15 mg/kg THIP in the testing environment; the second group was exposed to THIP in the colony room, while a third group received only saline. On a tolerance testing session, all mice received 15 mg/kg THIP in the testing environment. Results show that mice previously given THIP in the testing environment display a greater tolerance than mice receiving the drug in the alternative environment. Subsequently, a placebo was given to all mice in the testing environment to assess the influence of environmental cues alone; mice previously given THIP in the testing environment exhibited an enhancement of motility. The results agree with an associative model of tolerance which predicts that environmental cues associated with drug exposure elicit a conditioned compensatory response that cancels the unconditioned effect of the drug.
本实验评估了环境刺激通过联想学习过程,能够在多大程度上影响对GABAA激动剂4,5,6,7-四氢异恶唑并(5,4-c)吡啶-3-醇(THIP)的镇静和紧张性木僵作用的耐受性。采用了一种条件反射范式,将THIP作为非条件刺激,环境线索作为条件刺激。一组小鼠在测试环境中接受15mg/kg的THIP;第二组在饲养室接触THIP,而第三组只接受生理盐水。在一次耐受性测试中,所有小鼠在测试环境中接受15mg/kg的THIP。结果表明,先前在测试环境中给予THIP的小鼠比在其他环境中接受药物的小鼠表现出更高的耐受性。随后,在测试环境中给所有小鼠给予安慰剂,以评估单独环境线索的影响;先前在测试环境中给予THIP的小鼠表现出运动能力增强。这些结果与耐受性的联想模型一致,该模型预测与药物暴露相关的环境线索会引发一种条件性补偿反应,从而抵消药物的非条件作用。