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血管平滑肌细胞上的拉伸力通过超氧化物生成增强低密度脂蛋白的氧化。

Stretch force on vascular smooth muscle cells enhances oxidation of LDL via superoxide production.

作者信息

Inoue N, Kawashima S, Hirata K I, Rikitake Y, Takeshita S, Yamochi W, Akita H, Yokoyama M

机构信息

First Department of Internal Medicine, Kobe University School of Medicine, Kobe 650, Japan.

出版信息

Am J Physiol. 1998 Jun;274(6):H1928-32. doi: 10.1152/ajpheart.1998.274.6.H1928.

Abstract

Hemodynamic forces on vasculature profoundly influence atherogenesis. We examined the effect of stretch force on the oxidation of low-density lipoprotein (LDL) by rat aortic smooth muscle cells (RASM) and superoxide production. Stretch force was imposed on RASM cultured on deformable dishes by stretching the dishes. Incubation of native LDL with static RASM for 24 h resulted in LDL oxidation as indicated by increases in thiobarbituric acid-reacting substances from 9.5 +/- 2.3 to 24.5 +/- 2.3 nmol malondialdehyde/mg. Stretch force on RASM augmented cell-mediated LDL oxidation to 149.3 +/- 17.1% concomitantly with increase in superoxide production. LDL oxidation was inhibited by superoxide dismutase or depletion of the metal ion in the culture medium, indicating that it was a metal ion-dependent and superoxide-mediated process. The enhancement of LDL oxidation by stretch force was inhibited by diphenyliodonium, indicating the involvement of the NADH/NADPH oxidase system. Our findings suggest that the increased oxidant stress induced by stretch force is one of the potential mechanisms whereby hypertension facilitates atherosclerosis.

摘要

血管上的血流动力学力对动脉粥样硬化的发生发展有着深远影响。我们研究了拉伸力对大鼠主动脉平滑肌细胞(RASM)氧化低密度脂蛋白(LDL)及超氧化物生成的影响。通过拉伸培养在可变形培养皿上的RASM来施加拉伸力。天然LDL与静态RASM孵育24小时后导致LDL氧化,硫代巴比妥酸反应物质从9.5±2.3增加到24.5±2.3 nmol丙二醛/毫克即表明了这一点。对RASM施加拉伸力会使细胞介导的LDL氧化增加至149.3±17.1%,同时超氧化物生成增加。超氧化物歧化酶或培养基中金属离子的耗尽可抑制LDL氧化,表明这是一个金属离子依赖性和超氧化物介导的过程。拉伸力对LDL氧化的增强作用被二苯基碘鎓抑制,表明NADH/NADPH氧化酶系统参与其中。我们的研究结果表明,拉伸力诱导的氧化应激增加是高血压促进动脉粥样硬化的潜在机制之一。

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