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在离体豚鼠心脏中,硫磷酰胺对中性内肽酶的抑制作用不会改变冠状动脉对血管紧张素I、血管紧张素II和缓激肽的反应。

Inhibition of neutral endopeptidase by thiorphan does not modify coronary vascular responses to angiotensin I, angiotensin II and bradykinin in the isolated guinea pig heart.

作者信息

Kozlovski Valery I, Lomnicka Magdalena, Jakubowski Andrzej, Chlopicki Stefan

机构信息

Department of Experimental Pharmacology, Chair of Pharmacology, Jagiellonian University Medical College, Grzegórzecka 16, PL 31-531 Kraków, Poland.

出版信息

Pharmacol Rep. 2007 Jul-Aug;59(4):421-7.

Abstract

Both angiotensin-converting enzyme (ACE) and neutral endopeptidase (NEP) are involved in the regulation of renin-angiotensin and kallikrein-kinin systems. The aim of the present study was to assess the role of NEPand ACE in the regulation of vascular responses to angiotensin I (Ang I), angiotensin II (Ang II) and bradykinin (Bk) in the coronary circulation. For this purpose we used typical inhibitors of ACE and NEP, perindoprilate (1 microM) and thiorphan (1 micromM and 10 microM), respectively, and analyzed their effects on the coronary vasoconstrictor responses to Ang I and Ang II and coronary vasodilator responses to Bk in the isolated guinea pig heart. Perindoprilate abolished coronary vasoconstriction induced by Ang I and potentiated coronary vasodilation evoked by Bk. Thiorphan at a concentration of 1 muM slightly reduced response to Ang I without a significant effect on the responses to Ang II and Bk. However, thiorphan at a concentration of 10 muM abolished coronary vasoconstrictor response to Ang I and enhanced Bk-induced vasodilation. Importantly, in the presence of perindoprilate, addition of thiorphan (10 microM) did not modify further either responses to Ang I, Ang II or to Bk. In conclusion, vascular responses induced by Ang I, Ang II and Bk in the isolated guinea pig heart are regulated by ACE but not by NEP. Moreover, thiorphan is not a perfect tool to asses functional role of NEP as it displays ACE inhibitory activity.

摘要

血管紧张素转换酶(ACE)和中性内肽酶(NEP)均参与肾素-血管紧张素系统和激肽释放酶-激肽系统的调节。本研究旨在评估NEP和ACE在调节冠状动脉循环中血管对血管紧张素I(Ang I)、血管紧张素II(Ang II)和缓激肽(Bk)反应中的作用。为此,我们分别使用了ACE和NEP的典型抑制剂培哚普利拉(1 microM)和硫磷酰胺(1 microM和10 microM),并分析了它们对离体豚鼠心脏中冠状动脉对Ang I和Ang II的血管收缩反应以及对Bk的血管舒张反应的影响。培哚普利拉消除了Ang I诱导的冠状动脉收缩,并增强了Bk引起的冠状动脉舒张。浓度为1 microM的硫磷酰胺略微降低了对Ang I的反应,而对Ang II和Bk的反应无显著影响。然而,浓度为10 microM的硫磷酰胺消除了冠状动脉对Ang I的血管收缩反应,并增强了Bk诱导的血管舒张。重要的是,在存在培哚普利拉的情况下,添加硫磷酰胺(10 microM)对Ang I、Ang II或Bk的反应均未进一步改变。总之,离体豚鼠心脏中由Ang I、Ang II和Bk诱导的血管反应受ACE调节,而不受NEP调节。此外,硫磷酰胺不是评估NEP功能作用的理想工具,因为它具有ACE抑制活性。

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