Hayase T, Abiru H, Yamamoto Y, Yamamoto K, Fukui Y
Department of Legal Medicine, Kyoto University Faculty of Medicine, Japan.
Pharmacol Biochem Behav. 1998 May;60(1):263-70. doi: 10.1016/s0091-3057(97)00590-x.
The present study examines alterations in the cytoplasmic immunoreactivity of brain beta-endorphin, an endogenous opioid peptide regarded as the mediator of both euphoria and antinociceptive systems, in relation to toxicities due to cocaine and combined cocaine-ethanol. Beta-endorphin-immunoreactive cells were visualized and counted in adjacent sections from male rat brains at the level of the arcuate nucleus. In this region, cytoplasmic beta-endorphin immunoreactivity is prevalent. An intraperitoneal injection of cocaine (75 or 15 mg/kg) was given 15 min after an intraperitoneal injection of 3 g/kg ethanol or vehicle. With a fatally toxic dose (75 mg/kg) of cocaine, the number of neurons exhibiting cytoplasmic beta-endorphin immunoreactivity (immunoreactive nerve cells) was significantly increased immediately after the drug administration. Ethanol further enhanced the effects of both 15 and 75 mg/kg of cocaine. When the immunoreactivity was visually estimated by computer imaging analysis, lightly stained, weakly immunoreactive cells with photographic light absorption values greater than 50% were enhanced in the cocaine-ethanol groups compared to the cocaine only groups. Fatal toxicities were only observed in the groups treated with the high cocaine doses (75 mg/kg), with or without ethanol. In these groups, the number of strongly immunoreactive cells had increased significantly compared to the other groups. In the group treated with the high cocaine dose (75 mg/kg) plus ethanol, an increased frequency of late deaths that occurred over 1 h after the drug administration was observed, together with a decreased severity of cocaine-induced seizures and an early enhancement of weakly immunoreactive cells. Unlike the strongly immunoreactive cells, the weakly immunoreactive cells appeared to be continuously enhanced, based on an experiment examining beta-endorphin immunoreactivity at 24 h after an injection of 50 mg/kg cocaine.
本研究检测了脑β-内啡肽的细胞质免疫反应性变化,β-内啡肽是一种内源性阿片肽,被认为是欣快感和抗痛觉系统的介质,研究其与可卡因及可卡因-乙醇联用所致毒性的关系。在雄性大鼠脑弓状核水平的相邻切片中,对β-内啡肽免疫反应性细胞进行可视化和计数。在该区域,细胞质β-内啡肽免疫反应性普遍存在。在腹腔注射3 g/kg乙醇或溶剂15分钟后,腹腔注射可卡因(75或15 mg/kg)。给予致死毒性剂量(75 mg/kg)的可卡因后,给药后立即显示细胞质β-内啡肽免疫反应性的神经元数量(免疫反应性神经细胞)显著增加。乙醇进一步增强了15和75 mg/kg可卡因的作用。当通过计算机成像分析对免疫反应性进行视觉评估时,与仅使用可卡因的组相比,可卡因-乙醇组中光吸收值大于50%的浅染、弱免疫反应性细胞增加。仅在给予高剂量可卡因(75 mg/kg)的组中观察到致死毒性,无论是否使用乙醇。在这些组中,与其他组相比,强免疫反应性细胞的数量显著增加。在给予高剂量可卡因(75 mg/kg)加乙醇的组中,观察到给药后1小时以上发生的晚期死亡频率增加,同时可卡因诱发的癫痫严重程度降低,弱免疫反应性细胞早期增加。与强免疫反应性细胞不同,根据一项在注射50 mg/kg可卡因后24小时检测β-内啡肽免疫反应性的实验,弱免疫反应性细胞似乎持续增加。