Greenwell Thomas N, Walker Brendan M, Cottone Pietro, Zorrilla Eric P, Koob George F
Committee on the Neurobiology of Addictive Disorders, The Scripps Research Institute, 10550 North Torrey Pines Road, SP30-2400, La Jolla, CA 92037, United States.
Pharmacol Biochem Behav. 2009 Jan;91(3):295-302. doi: 10.1016/j.pbb.2008.07.012. Epub 2008 Jul 23.
Previous studies have reported that noradrenergic antagonists alleviate some of the symptoms of opiate withdrawal and dependence. Clinical studies also have shown that modification of the noradrenergic system may help protect patients from relapse. The present study tested the hypothesis that a dysregulated noradrenergic system has motivational significance in heroin self-administration of dependent rats. Prazosin, an alpha1-adrenergic antagonist (0.5, 1.0, 1.5 and 2.0 mg/kg, i.p.), was administered to adult male Wistar rats with a history of limited (1 h/day; short access) or extended (12 h/day; long access) access to intravenous heroin self-administration. Prazosin dose-dependently reduced heroin self-administration in long-access rats but not short-access rats, with 2 mg/kg of systemic prazosin significantly decreasing 1 h and 2 h heroin intake. Prazosin also reversed some changes in meal pattern associated with extended heroin access, including the taking of smaller and briefer meals (at 3 h), while also increasing total food intake and slowing the eating rate within meals (both 3 h and 12 h). Thus, prazosin appears to stimulate food intake in extended access rats by restoring meals to the normal size and duration. The data suggest that the alpha1 adrenergic system may contribute to mechanisms that promote dependence in rats with extended access.
先前的研究报告称,去甲肾上腺素能拮抗剂可缓解阿片类药物戒断和依赖的一些症状。临床研究还表明,调节去甲肾上腺素能系统可能有助于防止患者复发。本研究检验了一个假设,即失调的去甲肾上腺素能系统在依赖大鼠的海洛因自我给药中具有动机意义。将α1肾上腺素能拮抗剂哌唑嗪(0.5、1.0、1.5和2.0毫克/千克,腹腔注射)给予有过有限(每天1小时;短给药时间)或延长(每天12小时;长给药时间)静脉注射海洛因自我给药史的成年雄性Wistar大鼠。哌唑嗪剂量依赖性地减少了长给药时间大鼠的海洛因自我给药,但对短给药时间大鼠无效,2毫克/千克的全身哌唑嗪显著降低了1小时和2小时的海洛因摄入量。哌唑嗪还逆转了与延长海洛因给药时间相关的进食模式的一些变化,包括进食量更小、时间更短(3小时时),同时还增加了总食物摄入量并减缓了进食期间的进食速度(3小时和12小时时)。因此,哌唑嗪似乎通过将进食量恢复到正常大小和持续时间来刺激长给药时间大鼠的食物摄入。数据表明,α1肾上腺素能系统可能参与了促进长给药时间大鼠产生依赖的机制。