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载脂蛋白与动脉粥样硬化。载脂蛋白E和载脂蛋白(a)作为动脉粥样硬化过早发展的候选基因。

Apolipoproteins and atherosclerosis. Apolipoprotein E and apolipoprotein(a) as candidate genes of premature development of atherosclerosis.

作者信息

Horejsí B, Ceska R

机构信息

Third Medical Department, First Faculty of Medicine, Charles University and General Faculty Hospital, Prague, Czech Republic.

出版信息

Physiol Res. 2000;49 Suppl 1:S63-9.

Abstract

Apolipoprotein E (apoE) is a plasma lipoprotein which plays a basic role in the degradation of particles rich in cholesterol and triglycerides. It is able to bind to LDL receptors, but also to receptors for chylomicron remnants. There are three major apoE isoforms, E2, E3, and E4. Their role in lipoprotein metabolism is related to their affinity for receptors. Allele E3 is predominant and apoE3 affects metabolism of lipoproteins in a standard way. When compared to allele E3, allele E2 is associated with lower LDL levels, whereas allele E4 with higher LDL levels. This has an impact on the progression of atherosclerosis. Allele E2 exhibits a protective role, whereas allele E4 is associated with a high risk factor. Lipoprotein(a) [Lp(a)] is a plasma lipoprotein, consisting of apolipoprotein(a), linked by a covalent bond with the LDL particle. Increased Lp(a) levels are associated with an increased incidence of diseases based on atherosclerosis, namely the ischemic heart disease. Another effect of Lp(a) is its competition with plasminogen, resulting in a decrease of fibrinolysis and thrombogenic activity. ApoE and Lp(a) are independent risk factors for premature development of atherosclerosis and therefore can be considered as candidate genes of premature atherosclerosis.

摘要

载脂蛋白E(apoE)是一种血浆脂蛋白,在富含胆固醇和甘油三酯的颗粒降解中起基本作用。它能够与低密度脂蛋白(LDL)受体结合,也能与乳糜微粒残粒受体结合。有三种主要的apoE异构体,即E2、E3和E4。它们在脂蛋白代谢中的作用与其对受体的亲和力有关。等位基因E3占主导地位,apoE3以标准方式影响脂蛋白代谢。与等位基因E3相比,等位基因E2与较低的LDL水平相关,而等位基因E4与较高的LDL水平相关。这对动脉粥样硬化的进展有影响。等位基因E2具有保护作用,而等位基因E4与高风险因素相关。脂蛋白(a)[Lp(a)]是一种血浆脂蛋白,由载脂蛋白(a)组成,通过共价键与LDL颗粒相连。Lp(a)水平升高与基于动脉粥样硬化的疾病发病率增加有关,即缺血性心脏病。Lp(a)的另一个作用是它与纤溶酶原竞争,导致纤维蛋白溶解和血栓形成活性降低。ApoE和Lp(a)是动脉粥样硬化过早发生的独立危险因素,因此可被视为早发性动脉粥样硬化的候选基因。

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