治疗结果不佳的酗酒者解毒后多巴胺能传递恢复时间延长的证据。

A Heinz, B Lichtenberg-Kraag, S S Baum, K Graf, F Kruger, M Dettling, H Rommelspacher
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引用次数: 25

摘要

酒精成瘾的发病机制可能与多巴胺能神经传递功能障碍有关。因此,我们测量了45名酒精依赖患者解毒前后和10名健康对照者的外周多巴胺水平、中枢多巴胺受体(阿吗啡诱导的生长激素(GH)分泌)的敏感性以及g蛋白对腺苷酸环化酶活性(作为多巴胺d2受体偶联第二信使机制的指标)的抑制效果。适应戒断条件所需的时间在治疗效果好和治疗效果差的患者之间存在差异。在随后的戒酒者中,在戒酒的最初24小时内已经发现了酒精戒断的影响(生长激素反应的正常化,多巴胺水平的增加和g蛋白的抑制作用)。在接下来的7天戒断期间,评估变量没有观察到更显著的变化。在随后的复发中,没有发现急性乙醇戒断对相同措施的显著影响。然而,在戒断的第8天,观察到阿帕吗啡诱导的生长激素分泌增加(趋于正常化),多巴胺血浆水平增加,g蛋白抑制效果增加(高于正常水平)。这种多巴胺能信号转导的调节迟缓似乎反映了治疗无效的复发风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evidence for prolonged recovery of dopaminergic transmission after detoxification in alcoholics with poor treatment outcome.

It has been hypothesized that dysfunction of dopaminergic neurotransmission is involved in the pathogenesis of alcohol addiction. Therefore, peripheral dopamine levels, sensitivity of central dopamine receptors (apomorphine-induced Growth Hormone (GH) secretion), and the inhibitory efficacy of G-proteins on adenylyl cyclase activity (as an indicator for dopamine D2-receptor coupled second messenger mechanisms) were measured in 45 alcohol-dependent patients before and after detoxification and in 10 healthy controls. The time needed to adjust to abstinence conditions differed between patients with good and poor treatment outcome. In subsequent abstainers, effects of alcohol withdrawal were already found during the first 24 hours of abstinence (normalisation of GH response, increases in dopamine levels and the inhibitory efficacy of G-proteins). During the next 7 days of abstinence, no more significant changes were observed in the assessed variables. In subsequent relapsers, no significant effect of acute ethanol withdrawal on the same measures was found. However, at day 8 of abstinence, increases in apomorphine-induced GH secretion (towards normalisation), in dopamine plasma levels, and in the inhibitory efficacy of G-proteins (towards above-normal levels) were observed. This retarded adjustment of dopaminergic signal transduction seems to reflect the relapse risk of treatment nonresponders.

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