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苦参根中的低密度脂蛋白(LDL)抗氧化类黄酮。

Low density lipoprotein (LDL)-antioxidant flavonoids from roots of Sophora flavescens.

作者信息

Jeong Tae-Sook, Ryu Young Bae, Kim Hoi Young, Curtis-Long Marcus John, An Sojin, Lee Jin Hwan, Lee Woo Song, Park Ki Hun

机构信息

National Research Laboratory of Lipid Metabolism & Atherosclerosis, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.

出版信息

Biol Pharm Bull. 2008 Nov;31(11):2097-102. doi: 10.1248/bpb.31.2097.

Abstract

Oxidation of low density lipoprotein (LDL) is strongly implicated as a key process in the onset of atherosclerosis. In this study, nine alkylated (C10-C5) flavonoids from Sophora flavescens were examined for their inhibitory effects on copper-induced LDL oxidation. Of the flavonoids tested, sophoraflavanone G (1), kurarinone (2), kurarinol (3), norkurarinol (4), and kuraridin (9) inhibited the generation of thiobarbituric acid reactive substances (TBARS) with IC50s of 7.9, 14.5, 22.0, 26.9, and 17.5 microM, respectively. The most potent inhibitor, compound 1, also demonstrated significant activities in complementary in vitro investigations, such as lag time (130 min at 5 microM), relative electrophoretic mobility (REM) of ox-LDL (80% inhibition at 20 microM), and fragmentation of apoB-100 (inhibition of 71% at 20 microM). Analysis of the structures of these compounds reveals that a resorcinol moiety in the B-ring is strongly correlated with protection of LDL-oxidation.

摘要

低密度脂蛋白(LDL)的氧化被强烈认为是动脉粥样硬化发病的关键过程。在本研究中,检测了来自苦参的9种烷基化(C10 - C5)黄酮类化合物对铜诱导的LDL氧化的抑制作用。在所测试的黄酮类化合物中,苦参黄酮G(1)、苦参酮(2)、苦参醇(3)、去甲苦参醇(4)和苦参定(9)抑制硫代巴比妥酸反应性物质(TBARS)的生成,IC50分别为7.9、14.5、22.0、26.9和17.5微摩尔。最有效的抑制剂化合物1在补充的体外研究中也表现出显著活性,如延迟时间(5微摩尔时为130分钟)、氧化型LDL的相对电泳迁移率(REM)(20微摩尔时抑制80%)和载脂蛋白B - 100的片段化(20微摩尔时抑制71%)。对这些化合物结构的分析表明,B环中的间苯二酚部分与LDL氧化的保护密切相关。

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