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中性内肽酶抑制剂可增强P物质诱导的肠道平滑肌收缩。

Neutral endopeptidase inhibitors potentiate substance P-induced contraction in gut smooth muscle.

作者信息

Djokic T D, Sekizawa K, Borson D B, Nadel J A

机构信息

Cardiovascular Research Institute, University of California, San Francisco 94143.

出版信息

Am J Physiol. 1989 Jan;256(1 Pt 1):G39-43. doi: 10.1152/ajpgi.1989.256.1.G39.

Abstract

To determine the role of endogenous neutral endopeptidase (NEP), also called enkephalinase (EC 3.4.24.11), in regulating tachykinin-induced contraction of gut smooth muscle, we studied the effects of NEP inhibitors on the contractile responses to substance P (SP) in isolated longitudinal strips of ileum or duodenum in rats and ferrets. Leucine-thiorphan and phosphoramidon shifted the concentration-response curves of SP to lower concentrations in all tissues studied, but the sensitivity to SP was greater and the effect of leucine-thiorphan was less in the ferret, a finding that correlated with the observation that the ferret ileum contained substantially less NEP activity than rat ileum. Captopril, bestatin, MGTA, leupeptin, and physostigmine did not alter contractile responses to SP, suggesting that kininase II, aminopeptidases, carboxypeptidase N, serine proteinases, and acetylcholinesterase do not modulate the SP-induced effects. These studies suggest that, in the ileum and duodenum, NEP modulates the actions of SP and, furthermore, that the sensitivity of tissues may be determined, at least in part, by the amount of enzymatically active NEP present.

摘要

为了确定内源性中性内肽酶(NEP),也称为脑啡肽酶(EC 3.4.24.11)在调节速激肽诱导的肠道平滑肌收缩中的作用,我们研究了NEP抑制剂对大鼠和雪貂离体回肠或十二指肠纵行肌条对P物质(SP)收缩反应的影响。亮氨酸-硫代吗啡酮和磷酰胺素使所研究的所有组织中SP的浓度-反应曲线向较低浓度偏移,但雪貂对SP的敏感性更高,且亮氨酸-硫代吗啡酮的作用更小,这一发现与雪貂回肠中NEP活性明显低于大鼠回肠的观察结果相关。卡托普利、贝司他汀、MGTA、亮抑酶肽和毒扁豆碱并未改变对SP的收缩反应,表明激肽酶II、氨肽酶、羧肽酶N、丝氨酸蛋白酶和乙酰胆碱酯酶不调节SP诱导的效应。这些研究表明,在回肠和十二指肠中,NEP调节SP的作用,此外,组织的敏感性可能至少部分由存在的酶活性NEP的量决定。

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