Waltman C, Levine M A, McCaul M E, Svikis D S, Wand G S
Endocrine Division, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Alcohol Clin Exp Res. 1993 Apr;17(2):315-20. doi: 10.1111/j.1530-0277.1993.tb00769.x.
Ethanol exposure alters signal transduction through the adenylyl cyclase (AC) system. To elucidate the basis for this effect, we investigated the AC system in peripheral lymphocytes from abstinent alcoholic men (n = 22), actively drinking alcoholic men (n = 41), and nonalcoholic control men (n = 16). Immunoblot analysis of lymphocyte membranes from abstinent alcoholics demonstrated a 3.0-fold increase in the level of Gi2 alpha protein (p < 0.05) compared with controls. However, levels of Gs alpha protein were similar in both groups. Abstinent alcoholics had a 2.9-fold increase in Gi2 alpha mRNA (p < 0.001) and a 2.7-fold increase in Gs alpha mRNA (p < 0.03) compared with lymphocytes from control subjects. Actively drinking alcoholics, in contrast, had unaltered Gs alpha protein, Gi2 alpha protein, and Gi2 alpha mRNA levels compared with control subjects, but did have a 1.8-fold increase (p < 0.01) in Gs alpha mRNA. Consistent with enhanced Gi2 alpha expression, lymphocyte membranes from abstinent alcoholics had decreased basal, prostaglandin E1-, guanosine 5'-0-(3-thiotriphosphate)-gamma S-, and forskolin-stimulated AC activity compared with both controls and actively drinking alcoholics (p < 0.05). We conclude that lymphocyte AC is reduced during abstinence from alcohol and enhanced expression of the inhibitory G-protein, Gi2 alpha, may account for this change.
乙醇暴露会改变通过腺苷酸环化酶(AC)系统的信号转导。为了阐明这种效应的基础,我们研究了戒酒男性(n = 22)、正在饮酒的男性(n = 41)和非酒精性对照男性(n = 16)外周淋巴细胞中的AC系统。与对照组相比,对戒酒者淋巴细胞膜进行免疫印迹分析显示,Gi2α蛋白水平增加了3.0倍(p < 0.05)。然而,两组中Gsα蛋白水平相似。与对照受试者的淋巴细胞相比,戒酒者的Gi2α mRNA增加了2.9倍(p < 0.001),Gsα mRNA增加了2.7倍(p < 0.03)。相比之下,正在饮酒的酗酒者与对照受试者相比,Gsα蛋白、Gi2α蛋白和Gi2α mRNA水平未改变,但Gsα mRNA确实增加了1.8倍(p < 0.01)。与增强的Gi2α表达一致,与对照组和正在饮酒的酗酒者相比,戒酒者的淋巴细胞膜基础、前列腺素E1、鸟苷5'-O-(3-硫代三磷酸)-γS和福斯高林刺激的AC活性降低(p < 0.05)。我们得出结论,戒酒期间淋巴细胞AC减少,抑制性G蛋白Gi2α的表达增强可能是这种变化的原因。