Suppr超能文献

新型口服降糖药CS-045在体外可抑制人血浆低密度脂蛋白的脂质过氧化。

The new oral hypoglycemic agent, CS-045, inhibits the lipid peroxidation of human plasma low density lipoprotein in vitro.

作者信息

Nagasaka Y, Kaku K, Nakamura K, Kaneko T

机构信息

Department of Biochemistry, Yamaguchi University School of Medicine, Japan.

出版信息

Biochem Pharmacol. 1995 Sep 28;50(7):1109-11. doi: 10.1016/0006-2952(95)00235-r.

Abstract

Several lines of evidence have revealed that the oxidative modification of low-density lipoprotein (LDL) is probably associated with the genesis of the atherosclerotic region. CS-045 is a new (thiazolidine) class of oral hypoglycemic agent which has a hindered phenol in the side chain (an analogue of alpha-tocopherol). The present results indicate that CS-045 had a relatively high antioxidative potency in inhibiting the lipid peroxidation of human plasma LDL in vitro induced by 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH) compared with that of alpha-tocopherol. These findings suggest that CS-045 may be useful in preventing the progression of atherosclerosis in diabetic patients.

摘要

多项证据表明,低密度脂蛋白(LDL)的氧化修饰可能与动脉粥样硬化区域的形成有关。CS - 045是一种新型(噻唑烷类)口服降糖药,其侧链含有受阻酚(α - 生育酚的类似物)。目前的结果表明,与α - 生育酚相比,CS - 045在体外抑制2,2'-偶氮二(2 - 脒基丙烷)二盐酸盐(AAPH)诱导的人血浆LDL脂质过氧化方面具有相对较高的抗氧化能力。这些发现表明,CS - 045可能有助于预防糖尿病患者动脉粥样硬化的进展。

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