Broadbear J H, Winger G, Cicero T J, Woods J H
Department of Psychology, University of Michigan Medical School, Ann Arbor, Michigan.
J Pharmacol Exp Ther. 1999 Jul;290(1):393-402.
Earlier studies of cocaine's effects on the hypothalamic-pituitary-adrenal (HPA) axis used nonresponse-contingent designs in which the investigator determined dose, timing, and route of administration. It is important to evaluate whether "control" over cocaine delivery is a significant determinant of cocaine's HPA axis effect. This study measured cocaine's effects on plasma adrenocorticotropic hormone and cortisol, using nonresponse-contingent injections followed later by response-contingent cocaine delivery. In addition, the effects of cocaine history on the HPA response to a noncontingent injection of 1 mg/kg of cocaine were measured. HPA effects of corticotropin-releasing hormone (CRF) were also measured. Male and female rhesus monkeys, with surgically placed venous catheters, were tested in their home cages. Up to 13 injections of saline and cocaine (0.01-, 0.03-, 0.1-, and 0.3-mg/kg/injection) were administered at 10-min intervals (nonresponse-contingent condition) and on a fixed ratio 30, time out 10-min schedule of reinforcement. Overall, cocaine delivered response contingently produced larger, more dose-dependent HPA responses than did noncontingent delivery. The HPA response to a 1 mg/kg cocaine infusion in cocaine-naive monkeys was not predictive of the HPA effect of this dose subsequent to acquisition of cocaine self-administration. Overall, male monkeys had larger HPA responses to cocaine than did female monkeys. Finally, the HPA effects of CRF were significantly correlated with those of large cocaine doses delivered nonresponse contingently, but not with response-contingent administration.
早期关于可卡因对下丘脑 - 垂体 - 肾上腺(HPA)轴影响的研究采用了非反应性设计,即研究者决定给药剂量、时间和途径。评估对可卡因给药的“控制”是否是可卡因对HPA轴影响的重要决定因素很重要。本研究测量了可卡因对血浆促肾上腺皮质激素和皮质醇的影响,先进行非反应性注射,随后进行反应性可卡因给药。此外,还测量了可卡因使用史对HPA对1mg/kg可卡因非条件注射反应的影响。同时也测量了促肾上腺皮质激素释放激素(CRF)对HPA的影响。对有外科植入静脉导管的雄性和雌性恒河猴在其笼舍中进行测试。以10分钟的间隔(非反应性条件)以及固定比率30、10分钟超时强化时间表给予多达13次的生理盐水和可卡因(0.01 -、0.03 -、0.1 - 和0.3mg/kg/次注射)。总体而言,反应性给药的可卡因比非反应性给药产生更大、更具剂量依赖性的HPA反应。在未接触过可卡因的猴子中,对1mg/kg可卡因输注的HPA反应并不能预测在获得可卡因自我给药后该剂量的HPA效应。总体而言,雄性猴子对可卡因的HPA反应比雌性猴子更大。最后,CRF对HPA的影响与非反应性给予的大剂量可卡因的影响显著相关,但与反应性给药无关。