Prasad B M, Ulibarri C, Sorg B A
Department of Veterinary and Comparative Anatomy, Pharmacology and Physiology, Washington State University, Pullman 99164-6520, USA.
Psychopharmacology (Berl). 1998 Mar;136(1):24-33. doi: 10.1007/s002130050535.
We have recently shown that adrenalectomy (ADX) in rats blocks the appearance of cocaine-induced sensitization when this behavioral response is tested at early withdrawal times (1-2 days), but not after later withdrawal from cocaine (12 days). To determine if a similar phenomenon occurred with stress-induced sensitization, male Sprague-Dawley rats were given a sham ADX, ADX surgery, or ADX plus s.c. implanted corticosterone (CORT) pellets (CORT 12.5% pellets or CORT 50% pellets). A fifth group was given ADX surgery, but CORT 50% pellets were implanted after repeated stress treatment. One week after surgery, each group was divided into two additional groups, naive and stress. Naive animals remained unhandled, while stress rats were given a variety of daily stressors administered twice per day for 6 consecutive days. One day after the last stress, rats were given a saline injection followed by a cocaine injection (15 mg/kg, i.p.) the next day, and locomotor activity was monitored (early withdrawal). Two weeks after the last stress, the locomotor responses to an additional saline and cocaine injection were monitored (late withdrawal). At early withdrawal, no significant sensitization occurred for horizontal activity, but cross-sensitization was demonstrated for vertical activity. At late withdrawal, sham controls showed a stress-induced elevation in horizontal activity, with only a trend toward increased vertical activity. Animals given ADX surgery or ADX and CORT 12.5% pellets did not demonstrate sensitization to repeated stress, while CORT 50% pellets in ADX rats restored the sensitized horizontal response to cocaine challenge at late withdrawal. In contrast, stress-pretreated rats which were given CORT 50% pellets during the 2-week withdrawal period after the stress showed a marked decrease in horizontal activity in response to cocaine challenge at late withdrawal. The results provide evidence for a necessary role for adrenal hormones in long term, but not short-term, stress-induced cross-sensitization. Together with our previous study on the role of CORT in cocaine-induced sensitization, the results indicate that CORT is not the common factor mediating the long-term sensitization to cocaine and stress.
我们最近发现,当在早期撤药时间(1 - 2天)测试这种行为反应时,大鼠肾上腺切除术(ADX)会阻断可卡因诱导的敏化现象的出现,但在后期撤药(12天)后则不会。为了确定应激诱导的敏化是否会出现类似现象,将雄性Sprague-Dawley大鼠进行假ADX手术、ADX手术或ADX加皮下植入皮质酮(CORT)丸剂(CORT 12.5%丸剂或CORT 50%丸剂)。第五组接受ADX手术,但在重复应激处理后植入CORT 50%丸剂。手术后一周,每组再分为另外两组,即未处理组和应激组。未处理的动物不进行处理,而应激组大鼠每天接受多种应激源,每天两次,连续6天。最后一次应激后一天,大鼠注射生理盐水,第二天注射可卡因(15 mg/kg,腹腔注射),并监测运动活动(早期撤药)。最后一次应激两周后,监测对额外生理盐水和可卡因注射的运动反应(后期撤药)。在早期撤药时,水平活动未出现明显的敏化,但垂直活动表现出交叉敏化。在后期撤药时,假手术对照组显示应激诱导的水平活动升高,垂直活动仅呈增加趋势。接受ADX手术或ADX加CORT 12.5%丸剂的动物对重复应激未表现出敏化,而ADX大鼠中的CORT 50%丸剂在后期撤药时恢复了对可卡因激发的敏化水平反应。相比之下,在应激后2周撤药期给予CORT 50%丸剂的应激预处理大鼠在后期撤药时对可卡因激发的水平活动明显降低。结果证明肾上腺激素在长期而非短期应激诱导的交叉敏化中起必要作用。连同我们之前关于CORT在可卡因诱导的敏化中的作用的研究,结果表明CORT不是介导对可卡因和应激的长期敏化的共同因素。