Clay L H, Mazzio E A, Kolta M G, Soliman K F
College of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee 32307, USA.
Ann N Y Acad Sci. 1998 May 30;844:346-55.
Male Sprague-Dawley rats were administered 25 mg/kg, intraperitoneally (i.p.) cocaine-HCI twice daily for 14 consecutive days (total of 50 mg/kg), while control animals received an equivalent volume of 0.9% saline. After three days of withdrawal, the animals were sacrificed for dissection of striatal (STR) and nucleus accumbens (NA) brain regions. The treated group demonstrated a dose-dependent reduction for in vitro cocaine inhibition of [3H]dopamine (DA) uptake in the NA tissue verses controls. There were no significant differences amongst the treated and control groups for in vitro cocaine inhibition of [3H]DA in the STR. In vitro d-amphetamine (1, 5 and 10 microM)-stimulated DA release from STR tissue was not significantly different between the treated and the control groups. However, there was a significant decline in basal STR DA release and a significant enhancement of d-amphetamine (1 and 5 microM)-stimulated DA release in the NA for the treatment group versus controls. The results from the present study indicates sensitization to cocaine is primarily related to DA uptake and release in the NA.
雄性Sprague-Dawley大鼠连续14天每天两次腹腔注射25mg/kg盐酸可卡因(共50mg/kg),而对照组动物接受等量的0.9%生理盐水。戒断三天后,处死动物以解剖纹状体(STR)和伏隔核(NA)脑区。与对照组相比,治疗组NA组织中可卡因对[3H]多巴胺(DA)摄取的体外抑制呈剂量依赖性降低。治疗组和对照组在STR中可卡因对[3H]DA的体外抑制方面无显著差异。治疗组和对照组之间,体外d-苯丙胺(1、5和10μM)刺激的STR组织DA释放无显著差异。然而,与对照组相比,治疗组STR的基础DA释放显著下降,NA中d-苯丙胺(1和5μM)刺激的DA释放显著增强。本研究结果表明,对可卡因的敏感性主要与NA中的DA摄取和释放有关。