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P物质可能存在多种受体。

The possible existence of multiple receptors for substance P.

作者信息

Lee C M, Iversen L L, Hanley M R, Sandberg B E

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1982 Mar;318(4):281-7. doi: 10.1007/BF00501166.

Abstract
  1. The possible existence of multiple receptors for substance P (SP) was investigated by examining the relative pharmacological potencies of SP and related peptides in contracting guinea pig ileum, in potentiating electrically evoked contractions of rat vas deferens preparations and in competing for 3H-SP receptor binding in rat brain membranes, and by comparing the extent of cross-tachyphylaxis of various analogues with SP in the guinea pig ileum. 2. Different rank orders of potencies were observed among SP, its C-terminal fragments, analogues and related tachykinins in the different test systems, and these could not be explained by differential access to the target organ receptors. 3. In contrast to SP and physalaemin, both eledoisin and a metabolically stable SP analogue, [pGlu5, MePhe8, Sar9]-SP5-11 exhibited differential recovery from SP tachyphylaxis in the guinea pig ileum, and part of their spasmogenic action in this preparation was atropine-sensitive. 4. The results suggest the possible existence of multiple SP receptors, and the specificity of those in the brain may be different from those in the gut. The structural and pharmacological basis for subdividing tachykinins into SP-physalaemin and eledoisin-kassinin families is also discussed.
摘要
  1. 通过检测P物质(SP)及其相关肽在豚鼠回肠收缩、增强大鼠输精管标本电诱发收缩以及竞争大鼠脑膜中3H-SP受体结合方面的相对药理效力,并比较各种类似物与SP在豚鼠回肠中的交叉快速耐受性程度,研究了SP多种受体存在的可能性。2. 在不同测试系统中,观察到SP及其C末端片段、类似物和相关速激肽之间存在不同的效力等级顺序,且这些不能通过对靶器官受体的不同作用来解释。3. 与SP和 Physalaemin不同,伊索克肽和一种代谢稳定的SP类似物[pGlu5, MePhe8, Sar9]-SP5-11在豚鼠回肠中对SP快速耐受性的恢复表现出差异,且它们在该制剂中的部分致痉作用对阿托品敏感。4. 结果表明可能存在多种SP受体,且脑中的受体特异性可能与肠道中的不同。还讨论了将速激肽分为SP-Physalaemin和伊索克肽-卡辛宁家族的结构和药理学基础。

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