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组胺及组胺拮抗剂对肠毛细血管通透性的影响。

Effects of histamine and histamine antagonists on intestinal capillary permeability.

作者信息

Mortillaro N A, Granger D N, Kvietys P R, Rutili G, Taylor A E

出版信息

Am J Physiol. 1981 May;240(5):G381-6. doi: 10.1152/ajpgi.1981.240.5.G381.

Abstract

Steady-state lymph flow, blood flow, and lymph and plasma total protein concentration were measured in an autoperfused cat ileum preparation during the continuous infusion of histamine at venous pressures of 0, 10, 20, and 30 mmHg. The capillary osmotic reflection coefficients for total proteins and each protein fraction were estimated. In addition, the ileum was pretreated with an H1-receptor antagonist (diphenhydramine) or with an H2-receptor antagonist (cimetidine). The results suggest that histamine selectively increases the ileal vascular permeability to plasma proteins of a molecular radius up to 96 A. The H1-receptor antagonist did not alter the histamine-induced permeability changes but did block the observed initial vasodilation. The H2-receptor antagonist significantly reduced the permeability changes associated with histamine while having only a slight effect on the initial vasodilation. It is concluded that the activation of H1-receptors is predominantly associated with the initial vasodilation, whereas the H2-receptors are predominantly associated with permeability.

摘要

在静脉压分别为0、10、20和30 mmHg的情况下,对自体灌注的猫回肠制剂持续输注组胺,测量其稳态淋巴流量、血流量以及淋巴和血浆总蛋白浓度。估算了总蛋白和各蛋白组分的毛细血管渗透反射系数。此外,回肠先用H1受体拮抗剂(苯海拉明)或H2受体拮抗剂(西咪替丁)进行预处理。结果表明,组胺选择性增加回肠对分子半径达96 Å的血浆蛋白的血管通透性。H1受体拮抗剂未改变组胺诱导的通透性变化,但确实阻断了观察到的初始血管舒张。H2受体拮抗剂显著降低了与组胺相关的通透性变化,而对初始血管舒张仅有轻微影响。得出的结论是,H1受体的激活主要与初始血管舒张有关,而H2受体主要与通透性有关。

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