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药物受体理论在缓激肽肌otropic效应分析中的应用。

Application of drug receptor theories to the analysis of the myotropic effects of bradykinin.

作者信息

Barabe J, Park W K, Regoli D

出版信息

Can J Physiol Pharmacol. 1975 Jun;53(3):345-53. doi: 10.1139/y75-050.

Abstract

Cat jejunum and terminal ileum, and rat stomach strip and rat uterus contract to bradykinin, while rat duodenum relaxes. Dose-response curves of classical hyperbolic shape are obtained in the first three preparations, but not in the others. The negative logs of the drug concentrations which give 50% of the maximal response. (pD2) Values were, respectively, 7.68 and 7.77 in the cat jejunum and terminal ileum, 6.78 in the rat stomach strip and 8.64 in the rat uterus in estrus. Theoretical dose-response curves, constructed by using experimental pD2 values in the equation of Clark, (General pharmacology. Verlag Van J. Springer, Berlin, 1937), are superimposed to experimental curves, obtained in the cat jejunum and terminal ileum, but not in the rat stomach strip. This comparison was not made in the rat uterus and duodenum. The myotropic effect of bradykinin appears to be a direct one in the cat jejunum, the terminal ileum and the rat stomach strip, because it is not affected by anticholinergics, antiadrenergics, antihistaminics and indomethacin. pD2 values and the slope of the dose-response curves of the rat uterus were reduced by indomethacin. The results indicate that cat jejunum and terminal ileum are sensitive and specific for bradykinin and appear to be the most reliable preparations for studies on the structure-activity relationships of this peptide.

摘要

猫的空肠和回肠末端,以及大鼠的胃条和大鼠子宫对缓激肽产生收缩反应,而大鼠十二指肠则松弛。在前三种标本中可得到经典双曲线形状的剂量-反应曲线,但在其他标本中则不然。产生最大反应50%的药物浓度的负对数(pD2)值,在猫的空肠和回肠末端分别为7.68和7.77,在大鼠胃条中为6.78,在发情期大鼠子宫中为8.64。利用Clark方程(《普通药理学》。Van J. Springer出版社,柏林,1937年)中的实验pD2值构建的理论剂量-反应曲线,与在猫的空肠和回肠末端得到的实验曲线叠加,但在大鼠胃条中未叠加。在大鼠子宫和十二指肠中未进行这种比较。缓激肽的肌otropic效应在猫的空肠、回肠末端和大鼠胃条中似乎是直接的,因为它不受抗胆碱能药、抗肾上腺素能药、抗组胺药和吲哚美辛的影响。吲哚美辛降低了大鼠子宫的pD2值和剂量-反应曲线的斜率。结果表明,猫的空肠和回肠末端对缓激肽敏感且具有特异性,似乎是研究该肽结构-活性关系最可靠的标本。

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