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离体肺动脉对C5a过敏毒素的反应。

Responses of isolated pulmonary arteries to the C5a anaphylatoxin.

作者信息

Crowell R E, Van Epps D E, Reed W P

机构信息

Department of Medicine, University of New Mexico School of Medicine, Albuquerque.

出版信息

Am J Physiol. 1990 Nov;259(5 Pt 2):H1325-9. doi: 10.1152/ajpheart.1990.259.5.H1325.

Abstract

The anaphylatoxin C5a possesses spasmogenic activity in smooth muscle tissues. In this study, we examined the effect of C5a on isolated rabbit pulmonary artery (PA) ring segments under a variety of experimental conditions. C5a (1-100 nM) caused transient constriction of PA at resting tension. C5a-induced PA constriction was not affected by the histamine H1-receptor antagonist pyrilamine (1 microM) but was significantly decreased by the cyclooxygenase inhibitor indomethacin (1 microM). Disruption of the endothelial layer of the vessel had no effect on C5a activity in resting PA. PA, which had been preconstricted with norepinephrine (5 microM), exhibited a different response to C5a than PA at resting tension, however. C5a (1-10 nM) induced a biphasic response in preconstricted PA, initially causing further constriction followed by a greater degree of relaxation resulting in an overall decrease in PA tension. All responses of preconstricted PA to C5a were completely eliminated by indomethacin and significantly depressed by endothelial disruption. These data indicate that C5a interacts directly with isolated rabbit PA, but the nature of the PA response to this peptide depends on several variables including the presence or absence of active PA tension and cyclooxygenase metabolites, and the presence of intact endothelium.

摘要

过敏毒素C5a在平滑肌组织中具有致痉挛活性。在本研究中,我们在多种实验条件下检测了C5a对离体兔肺动脉(PA)环段的作用。C5a(1 - 100 nM)在静息张力下引起PA短暂收缩。C5a诱导的PA收缩不受组胺H1受体拮抗剂吡苄明(1 μM)的影响,但被环氧化酶抑制剂吲哚美辛(1 μM)显著降低。血管内皮层的破坏对静息PA中的C5a活性没有影响。然而,用去甲肾上腺素(5 μM)预收缩的PA对C5a的反应与静息张力下的PA不同。C5a(1 - 10 nM)在预收缩的PA中诱导双相反应,最初引起进一步收缩,随后是更大程度的舒张,导致PA张力总体下降。吲哚美辛完全消除了预收缩的PA对C5a的所有反应,内皮破坏使其显著降低。这些数据表明C5a直接与离体兔PA相互作用,但PA对该肽的反应性质取决于几个变量,包括是否存在活性PA张力和环氧化酶代谢产物,以及完整内皮的存在。

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