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应激可防止大鼠大脑中慢性乙醇诱导的δ阿片受体超敏反应。

Stress prevents the chronic ethanol-induced delta opiod receptor supersensitivity in the rat brain.

作者信息

Przewłocka B, Lasoń W

机构信息

Department of Neuropeptides Research, Polish Academy of Sciences, Kraków, Poland.

出版信息

Pol J Pharmacol Pharm. 1990 Mar-Apr;42(2):137-42.

PMID:2177189
Abstract

The effects of ethanol administration on binding characteristics of the highly selective mu and delta opioid receptor agonists 8H-[D-Ala2-MePhe4-Gly5-ol]enkephalin (3H-DAGO) and 3H-[D-Pen2, D-Pen5] enkephalin (3H-DPDPE), respectively, were investigated in the rat brain. Chronic but not acute ethanol administration profoundly increased affinity of 3H-DPDPE without changing the number of delta receptors. Stress, applied before each ethanol administration, prevents the above changes. On the other hand, chronic treatment with ethanol did not affect the binding characteristics of 3H-DAGO. These results suggest particular sensitivity of the delta opioid receptor to chronic ethanol administration. Furthermore, a possible involvement of endogenous opioid peptide systems in the enhancement of delta opioid receptor sensitivity is postulated.

摘要

在大鼠脑中研究了乙醇给药对高选择性μ和δ阿片受体激动剂8H-[D-丙氨酸2-甲基苯丙氨酸4-甘氨酸5-醇]脑啡肽(3H-DAGO)和3H-[D-青霉胺2,D-青霉胺5]脑啡肽(3H-DPDPE)结合特性的影响。长期而非急性乙醇给药显著增加了3H-DPDPE的亲和力,而不改变δ受体的数量。在每次乙醇给药前施加应激可防止上述变化。另一方面,乙醇长期治疗不影响3H-DAGO的结合特性。这些结果表明δ阿片受体对长期乙醇给药具有特殊敏感性。此外,推测内源性阿片肽系统可能参与了δ阿片受体敏感性的增强。

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