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血管生成素样蛋白8(ANGPTL8)拮抗剂同时降低甘油三酯和提高血浆高密度脂蛋白胆固醇水平的潜力。

The Potential of ANGPTL8 Antagonism to Simultaneously Reduce Triglyceride and Increase HDL-Cholesterol Plasma Levels.

作者信息

Zhang Ren

机构信息

Center for Molecular Medicine and Genetics, School of Medicine, Wayne State University, Detroit, MI, United States.

出版信息

Front Cardiovasc Med. 2021 Nov 16;8:795370. doi: 10.3389/fcvm.2021.795370. eCollection 2021.

Abstract

Elevated triglyceride (TG) and reduced high-density lipoprotein-cholesterol (HDL-C) plasma levels are risk factors for atherosclerosis and cardiovascular disease. Therefore, a drug that simultaneously reduces TG and increases HDL-C plasma levels has the potential to prevent and treat these diseases. Angiopoietin-like 3 (ANGPTL3) regulates plasma TG and HDL-C levels by inhibiting lipoprotein lipase (LPL) and endothelial lipase (EL), respectively. ANGPTL3 inhibition of LPL requires complex formation with ANGPTL8, which is not required for its inhibition of EL. Therefore, the entire pool of plasma ANGPTL3 can be classified as ANGPTL8-associated ANGPTL3 and ANGPTL8-free ANGPTL3, where the former inhibits LPL and the latter inhibits EL. ANGPTL8 antibodies or inhibitors that block its interactions with ANGPTL3 can disrupt or preclude the ANGPTL3-8 complex formation, resulting in fewer ANGPTL3-8 complexes (reduced LPL inhibition), but more free ANGPTL3 (enhanced EL inhibition). Therefore, ANGPTL8 antagonism increases LPL activity while decreasing EL activity, thus leading to reduced plasma TG while simultaneously increasing HDL-C levels. In humans, carriers of ANGPTL8 truncating variants consistently have lower TG but higher HDL-C levels, supporting this hypothesis.

摘要

甘油三酯(TG)水平升高和高密度脂蛋白胆固醇(HDL-C)血浆水平降低是动脉粥样硬化和心血管疾病的危险因素。因此,一种能同时降低TG并提高HDL-C血浆水平的药物有预防和治疗这些疾病的潜力。血管生成素样3(ANGPTL3)分别通过抑制脂蛋白脂肪酶(LPL)和内皮脂肪酶(EL)来调节血浆TG和HDL-C水平。ANGPTL3对LPL的抑制需要与ANGPTL8形成复合物,而其对EL的抑制则不需要。因此,血浆中所有的ANGPTL3可分为与ANGPTL8相关的ANGPTL3和不含ANGPTL8的ANGPTL3,前者抑制LPL,后者抑制EL。阻断ANGPTL8与ANGPTL3相互作用的ANGPTL8抗体或抑制剂可破坏或阻止ANGPTL3-8复合物的形成,导致ANGPTL3-8复合物减少(LPL抑制减弱),但游离ANGPTL3增多(EL抑制增强)。因此,拮抗ANGPTL8可增加LPL活性,同时降低EL活性,从而降低血浆TG水平,同时提高HDL-C水平。在人类中,携带ANGPTL8截短变体的个体TG水平持续较低,但HDL-C水平较高,支持了这一假说。

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