Suppr超能文献

鸟嘌呤核苷酸对中枢神经系统神经肽受体的影响。

Effects of guanine nucleotides on CNS neuropeptide receptors.

作者信息

Moody T W, Taylor D P, Pert C B

机构信息

Section on Biochemistry and Pharmacology, National Institute of Mental Health, Bethesda, Maryland 20205.

出版信息

J Supramol Struct Cell Biochem. 1981;15(2):153-9. doi: 10.1002/jsscb.1981.380150206.

Abstract

The effect of nucleotides on central nervous system neuropeptide receptor binding was investigated. The guanine nucleotides, guanosine-5'-triphosphate and guanylyl-5'-imidodiphosphate, significantly inhibited the binding of radiolabeled vasoactive intestinal polypeptide but not that of [Tyr4]bombesin to rat brain membranes. Vasoactive intestinal polypeptide binding was inhibited by guanine nucleotides in a dose-dependent manner. Using a 20 microM dose, 60% of the specific vasoactive intestinal polypeptide binding was inhibited by guanylyl-5'-imido-diphosphate, which was more potent than guanosine-5'-triphosphate, whereas other nucleotides were not effective. This reduction in binding was a consequence of lower affinity of the receptor for vasoactive intestinal polypeptide, which in turn resulted from an increased rate of dissociation.

摘要

研究了核苷酸对中枢神经系统神经肽受体结合的影响。鸟嘌呤核苷酸,即鸟苷-5'-三磷酸和鸟苷-5'-亚氨基二磷酸,显著抑制放射性标记的血管活性肠肽与大鼠脑膜的结合,但不影响[酪氨酸4]蛙皮素的结合。鸟嘌呤核苷酸以剂量依赖的方式抑制血管活性肠肽的结合。使用20微摩尔的剂量时,鸟苷-5'-亚氨基二磷酸抑制了60%的特异性血管活性肠肽结合,其效力比鸟苷-5'-三磷酸更强,而其他核苷酸则无效。这种结合的减少是受体对血管活性肠肽亲和力降低的结果,而这又是解离速率增加所致。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验