Rebec G V, Lee E H
Pharmacol Biochem Behav. 1983 Aug;19(2):219-23. doi: 10.1016/0091-3057(83)90042-4.
Rats were pretreated twice daily for 5 consecutive days with saline or 2.5 mg/kg d-amphetamine. Approximately 12 hr after the last injection, neuronal activity was recorded bilaterally from the central amygdaloid nucleus (CAN) and the animals were challenged every 2 min with 0.2 mg/kg d-amphetamine or with increasing incremental doses of apomorphine. In saline controls, all CAN neurons were inhibited by the 5th amphetamine injection and two-thirds were suppressed by 0.64 mg/kg apomorphine. In amphetamine-pretreated animals, on the other hand, the majority of CAN neurons failed to respond even by the 10th amphetamine injection and less than one-third were inhibited by apomorphine even at a dose of 2.56 mg/kg. These results indicate that tolerance develops to the inhibitory effects of d-amphetamine in the CAN and that this effect is mediated, at least in part, by a decrease in the sensitivity of postsynaptic dopamine receptors.
大鼠连续5天每天接受两次生理盐水或2.5毫克/千克右旋苯丙胺预处理。在最后一次注射后约12小时,从双侧杏仁核中央核(CAN)记录神经元活动,并且每2分钟用0.2毫克/千克右旋苯丙胺或递增剂量的阿扑吗啡对动物进行刺激。在生理盐水对照组中,所有CAN神经元在第5次苯丙胺注射时受到抑制,三分之二的神经元在0.64毫克/千克阿扑吗啡作用下受到抑制。另一方面,在经过苯丙胺预处理的动物中,即使到第10次苯丙胺注射时,大多数CAN神经元仍无反应,即使在2.56毫克/千克的剂量下,也只有不到三分之一的神经元被阿扑吗啡抑制。这些结果表明,对右旋苯丙胺在CAN中的抑制作用会产生耐受性,并且这种作用至少部分是由突触后多巴胺受体敏感性降低介导的。