Suppr超能文献

α-萘黄酮通过诱导细胞外钙内流和内皮中一氧化氮的形成来诱导血管舒张。

Alpha-naphthoflavone induces vasorelaxation through the induction of extracellular calcium influx and NO formation in endothelium.

作者信息

Cheng Yu-Wen, Li Ching-Hao, Lee Chen-Chen, Kang Jaw-Jou

机构信息

School of Pharmacy, Taipei Medical University, 250 Wu Hsing Street, Taipei, Taiwan.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2003 Nov;368(5):377-85. doi: 10.1007/s00210-003-0820-6. Epub 2003 Oct 15.

Abstract

The effect of alpha-naphthoflavone (alpha-NF) on vascular function was studied in isolated ring segments of the rat thoracic aorta and in primary cultures of human umbilical vein endothelial cells (HUVECs). alpha-NF induced concentration-dependent relaxation of the phenylephrine-precontracted aorta endothelium-dependently and -independently at lower and higher concentrations, respectively. The cGMP, but not cAMP, content was increased significantly in alpha-NF-treated aorta. Pretreatment with N(omega)-nitro- l-arginine methyl ester (L-NAME) or methylene blue attenuated both alpha-NF induced vasorelaxation and the increase of cGMP content significantly. The increase of cGMP content induced by alpha-NF was also inhibited by chelating extracellular Ca(2+) with EGTA. These results suggest that the endothelium-dependent vasorelaxation induced by alpha-NF is mediated most probably through Ca(2+)-dependent activation of NO synthase and guanylyl cyclase. In HUVECs, alpha-NF induced concentration-dependent formation of NO and Ca(2+) influx. alpha-NF-induced NO formation was abolished by removal of extracellular Ca(2+) and by pretreatment with the Ca(2+) channel blockers SKF 96365 and Ni(2+), but not by the L-type Ca(2+) channel blocker verapamil. The Ca(2+) influx, as measured by (45)Ca(2+) uptake, induced by alpha-NF was also inhibited by SKF 96365 and Ni(2+). Our data imply that alpha-NF, at lower concentrations, induces endothelium-dependent vasorelaxation by promoting extracellular Ca(2+) influx in endothelium and the activation of the NO-cGMP pathway.

摘要

在大鼠胸主动脉离体环段和人脐静脉内皮细胞(HUVECs)原代培养物中研究了α-萘黄酮(α-NF)对血管功能的影响。α-NF分别在较低和较高浓度下,以浓度依赖性方式诱导苯肾上腺素预收缩的主动脉内皮依赖性和非内皮依赖性舒张。在α-NF处理的主动脉中,cGMP含量显著增加,而cAMP含量未增加。用N(ω)-硝基-L-精氨酸甲酯(L-NAME)或亚甲蓝预处理可显著减弱α-NF诱导的血管舒张和cGMP含量的增加。用EGTA螯合细胞外Ca(2+)也可抑制α-NF诱导的cGMP含量增加。这些结果表明,α-NF诱导的内皮依赖性血管舒张很可能是通过Ca(2+)依赖性激活一氧化氮合酶和鸟苷酸环化酶介导的。在HUVECs中,α-NF诱导浓度依赖性的一氧化氮形成和Ca(2+)内流。去除细胞外Ca(2+)以及用Ca(2+)通道阻滞剂SKF 96365和Ni(2+)预处理可消除α-NF诱导的一氧化氮形成,但L型Ca(2+)通道阻滞剂维拉帕米则不能。用(45)Ca(2+)摄取测量的α-NF诱导的Ca(2+)内流也受到SKF 96365和Ni(2+)的抑制。我们的数据表明,较低浓度的α-NF通过促进内皮细胞外Ca(2+)内流和激活NO-cGMP途径诱导内皮依赖性血管舒张。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验