Roberts A J, Crabbe J C, Keith L D
Department of Medical Psychology, Oregon Health Sciences University, Portland 97201.
Brain Res. 1992 May 8;579(2):296-302. doi: 10.1016/0006-8993(92)90064-g.
There is a growing body of evidence suggesting that corticosteroids contribute to the increased neural excitability observed during ethanol withdrawal. In the present study, this was further investigated using mouse strains which differ in ethanol withdrawal severity. DBA/2 (DBA) mice were found to display more severe acute ethanol withdrawal seizures than C57BL/6 (C57) mice. Additionally, DBA mice showed a greater stress response than C57 mice, as measured by higher plasma concentrations of adrenocorticotropic hormone (ACTH) and corticosterone, to an acute dose of ethanol. Mimicking withdrawal plasma corticosterone levels by administering corticosterone to ethanol-naive mice resulted in increases in handling-induced convulsions in the range observed during withdrawal. There did not appear to be a strain difference in sensitivity to the excitatory effects of corticosterone. In summary, the greater stress response to ethanol by DBA mice may account, in part, for the more severe ethanol withdrawal syndrome of this strain.
越来越多的证据表明,皮质类固醇会导致在乙醇戒断期间观察到的神经兴奋性增加。在本研究中,使用乙醇戒断严重程度不同的小鼠品系对此进行了进一步研究。发现DBA/2(DBA)小鼠比C57BL/6(C57)小鼠表现出更严重的急性乙醇戒断性癫痫发作。此外,通过更高的促肾上腺皮质激素(ACTH)和皮质酮血浆浓度测量,DBA小鼠对急性剂量乙醇的应激反应比C57小鼠更大。通过向未接触过乙醇的小鼠施用皮质酮来模拟戒断时的血浆皮质酮水平,导致处理诱导的惊厥增加,其幅度在戒断期间观察到的范围内。对皮质酮的兴奋作用的敏感性似乎没有品系差异。总之,DBA小鼠对乙醇的更大应激反应可能部分解释了该品系更严重的乙醇戒断综合征。