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The Inhibitory Effect of Shikonin on the Agonist-Induced Regulation of Vascular Contractility

机译:紫草素对激动剂诱导的血管收缩调节的抑制作用

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摘要

Shikonin, a natural flavonoid found in the roots of Lithospermum erythrorhizon, has been shown to possess many biological functions. The present study was undertaken to investigate the influence of shikonin on vascular smooth muscle contractility and to determine the mechanism involved. Denuded aortic rings from male rats were used and isometric contractions were recorded and combined with molecular experiments. Shikonin significantly relaxed fluoride-, thromboxane A(2)- or phorbol ester-induced vascular contraction suggesting as a possible anti-hypertensive on the agonist-induced vascular contraction regardless of endothelial nitric oxide synthesis. Furthermore, shikonin significantly inhibited fluoride-induced increases in pMYPT1 levels and phorbol ester-induced increases in pERK1/2 levels suggesting the mechanism involving the inhibition of Rho-kinase activity and the subsequent phosphorylation of MYPT1 and the inhibition of MEK activity and the subsequent phosphorylation of ERK1/2. This study provides evidence regarding the mechanism underlying the relaxation effect of shikonin on agonist-induced vascular contraction regardless of endothelial function.
机译:紫草素(Shikonin)是一种在紫草紫苏根中发现的天然黄酮,具有多种生物学功能。进行本研究以研究紫草素对血管平滑肌收缩力的影响并确定所涉及的机制。使用雄性大鼠的裸露的主动脉环,记录等距收缩并将其与分子实验结合。紫草素显着放宽了氟化物,血栓烷A(2)或佛波酯引起的血管收缩,提示可能对激动剂引起的血管收缩具有抗高血压作用,而与内皮一氧化氮的合成无关。此外,紫草素显着抑制了氟化物诱导的pMYPT1水平的增加和佛波酯诱导的pERK1 / 2水平的增加,表明该机制涉及抑制Rho激酶活性和随后的MYPT1磷酸化以及抑制MEK活性和随后的磷酸化。的ERK1 / 2。这项研究提供了有关紫草素对激动剂诱导的血管收缩的松弛作用的潜在机制的证据,而与内皮功能无关。

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