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一种碘化物质P类似物与大鼠垂体前叶分离细胞膜上的NK-1受体的结合。

Binding of a iodinated substance P analog to a NK-1 receptor on isolated cell membranes from rat anterior pituitary.

作者信息

Larsen P J, Mikkelsen J D, Saermark T

机构信息

Institute of Medical Anatomy B, University of Copenhagen, Denmark.

出版信息

Endocrinology. 1989 May;124(5):2548-57. doi: 10.1210/endo-124-5-2548.

Abstract

The characteristics of binding sites for substance-P (SP) on rat anterior pituitary membranes were studied, using 125I-labeled Bolton-Hunter SP as a ligand. The binding of [125I]Bolton-Hunter SP was saturable and reversible, and reached a plateau of maximal binding after approximately 12 min of incubation. Scatchard and Hill analyses of specific binding revealed a single class of noninteracting binding sites with a high affinity (Kd = 0.72 nM) and a moderate density (binding capacity = 32.16 fmol/mg protein). The biologically active tachykinins, which, in addition to SP, consist of physalaemin, eledoisin, kassinin, neurokinin-A, and neurokinin-B, could inhibit the binding in a concentration-dependent manner. Based on titration curves, the IC50 values of the tachykinins were measured, and the receptor was classified as a NK-1 receptor. These results demonstrate that a population of specific SP-binding sites is present in rat anterior pituitary and further support evidence that this peptide has an influence on pituitary function.

摘要

以125I标记的博尔顿-亨特P物质(SP)作为配体,研究了大鼠垂体前叶膜上SP结合位点的特征。[125I]博尔顿-亨特SP的结合具有饱和性和可逆性,孵育约12分钟后达到最大结合平台期。对特异性结合进行Scatchard和Hill分析,结果显示存在一类单一的非相互作用结合位点,其具有高亲和力(解离常数Kd = 0.72 nM)和中等密度(结合容量 = 32.16 fmol/mg蛋白质)。除SP外,具有生物活性的速激肽还包括蛙皮素、eledoisin、肛褶蛙肽、神经激肽A和神经激肽B,它们能以浓度依赖性方式抑制结合。根据滴定曲线测定了速激肽的半数抑制浓度(IC50)值,并将该受体归类为NK-1受体。这些结果表明,大鼠垂体前叶存在特异性SP结合位点群体,并进一步支持了该肽对垂体功能有影响的证据。

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