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三磷酸腺苷柠檬酸裂解酶(ACLY)在脂质代谢和动脉粥样硬化中的作用:最新综述。

ATP-citrate lyase (ACLY) in lipid metabolism and atherosclerosis: An updated review.

机构信息

The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230001, PR China.

Aab Cardiovascular Research Institute, Department of Medicine, University of Rochester, School of Medicine and Dentistry, Rochester, NY 14642, USA.

出版信息

Prog Lipid Res. 2020 Jan;77:101006. doi: 10.1016/j.plipres.2019.101006. Epub 2019 Sep 6.

Abstract

ATP citrate lyase (ACLY) is an important enzyme linking carbohydrate to lipid metabolism by generating acetyl-CoA from citrate for fatty acid and cholesterol biosynthesis. Mendelian randomization of large human cohorts has validated ACLY as a promising target for low-density-lipoprotein-cholesterol (LDL-C) lowering and cardiovascular protection. Among current ACLY inhibitors, Bempedoic acid (ETC-1002) is a first-in-class, prodrug-based direct competitive inhibitor of ACLY which regulates lipid metabolism by upregulating hepatic LDL receptor (LDLr) expression and activity. ACLY deficiency in hepatocytes protects from hepatic steatosis and dyslipidemia. In addition, pharmacological inhibition of ACLY by bempedoic acid, prevents dyslipidemia and attenuates atherosclerosis in hypercholesterolemic ApoE mice, LDLr mice, and LDLr miniature pigs. Convincing data from clinical trials have revealed that bempedoic acid significantly lowers LDL-C as monotherapy, combination therapy, and add-on with statin therapy in statin-intolerant patients. More recently, a phase 3 CLEAR Harmony clinical trial ("Safety and Efficacy of Bempedoic Acid to Reduce LDL Cholesterol") has shown that bempedoic acid reduces the level of LDL-C in hypercholesterolemic patients receiving guideline-recommended statin therapy with a good safety profile. Hereby, we provide a updated review of the expression, regulation, genetics, functions of ACLY in lipid metabolism and atherosclerosis, and highlight the therapeutic potential of ACLY inhibitors (such as bempedoic acid, SB-204990, and other naturally-occuring inhibitors) to treat atherosclerotic cardiovascular diseases. It must be pointed out that long-term large-scale clinical trials in high-risk patients, are warranted to validate whether ACLY represent a promising therapeutic target for pharmaceutic intervention of dyslipidemia and atherosclerosis; and assess the safety and efficacy profile of ACLY inhibitors in improving cardiovascular outcome of patients.

摘要

三磷酸腺苷柠檬酸裂解酶 (ACLY) 是一种重要的酶,通过将柠檬酸转化为乙酰辅酶 A,为脂肪酸和胆固醇的生物合成提供乙酰辅酶 A,从而将碳水化合物与脂质代谢联系起来。大规模人类队列的孟德尔随机化研究已经验证了 ACLY 是降低低密度脂蛋白胆固醇 (LDL-C) 和保护心血管的有前途的靶点。在现有的 ACLY 抑制剂中,贝美前列素 (ETC-1002) 是一种首创的、基于前药的 ACLY 直接竞争性抑制剂,通过上调肝 LDL 受体 (LDLr) 的表达和活性来调节脂质代谢。肝细胞中的 ACLY 缺乏可防止肝脂肪变性和血脂异常。此外,贝美前列素通过抑制 ACLY 可防止高脂血症 ApoE 小鼠、LDLr 小鼠和 LDLr 小型猪的血脂异常和动脉粥样硬化。临床试验的令人信服的数据表明,贝美前列素作为单药治疗、联合治疗和与他汀类药物联合治疗,在他汀类药物不耐受的患者中可显著降低 LDL-C。最近,一项 3 期 CLEAR Harmony 临床试验(“贝美前列素降低 LDL 胆固醇的安全性和疗效”)表明,贝美前列素降低了接受指南推荐的他汀类药物治疗的高胆固醇血症患者的 LDL-C 水平,且安全性良好。在此,我们提供了 ACLY 在脂质代谢和动脉粥样硬化中的表达、调节、遗传、功能的最新综述,并强调了 ACLY 抑制剂(如贝美前列素、SB-204990 和其他天然抑制剂)治疗动脉粥样硬化性心血管疾病的治疗潜力。必须指出,在高危患者中进行长期大规模临床试验,以验证 ACLY 是否代表治疗血脂异常和动脉粥样硬化的药物干预的有前途的治疗靶点,并评估 ACLY 抑制剂改善患者心血管结局的安全性和疗效特征。

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