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依折麦布:作用机制、药代动力学及近期临床试验的最新进展

Ezetimibe: an update on the mechanism of action, pharmacokinetics and recent clinical trials.

作者信息

Sweeney Mary Ellen, Johnson Rebecca R

机构信息

Emory University School of Medicine, Division of Endocrinology, Metabolism and Lipids, Atlanta VA Medical Center-111, 1670 Clairmont Rd, Atlanta, GA 30033, USA.

出版信息

Expert Opin Drug Metab Toxicol. 2007 Jun;3(3):441-50. doi: 10.1517/17425255.3.3.441.

Abstract

Elevated serum cholesterol is a known risk factor for the development of coronary artery disease. Circulating cholesterol is a product of both cholesterol absorption from the gut and cellular cholesterol production. Ezetimibe is a novel cholesterol-lowering drug that acts at the brush border of the small intestine. Recent studies have further identified the molecular target as the Niemann-Pick C1-like transporter. Ezetimibe blocks the absorption of dietary and biliary cholesterol and plant sterols resulting in intracellular cholesterol depletion. Clinical studies have demonstrated beneficial improvements in the lipid profile with ezetimibe as monotherapy, but dramatic effects are seen when ezetimibe is combined with other lipid-lowering drugs, particularly 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (statins). Combination studies of ezetimibe with statins, bile acid sequestrants, fenofibrate and niacin all demonstrate significant total and low density lipoprotein cholesterol lowering. An excellent safety and tolerability profile combined with once-daily dosing make this attractive adjunct therapy for the treatment of hypercholesterolemia.

摘要

血清胆固醇升高是已知的冠状动脉疾病发病风险因素。循环胆固醇是肠道胆固醇吸收和细胞胆固醇生成的产物。依折麦布是一种新型降胆固醇药物,作用于小肠刷状缘。最近的研究进一步确定其分子靶点为尼曼-匹克C1样转运蛋白。依折麦布可阻断膳食和胆汁胆固醇以及植物甾醇的吸收,导致细胞内胆固醇耗竭。临床研究表明,依折麦布单药治疗可使血脂谱得到有益改善,但当依折麦布与其他降血脂药物,特别是3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂(他汀类药物)联合使用时,效果显著。依折麦布与他汀类药物、胆汁酸螯合剂、非诺贝特和烟酸的联合研究均表明,总胆固醇和低密度脂蛋白胆固醇显著降低。出色的安全性和耐受性,加上每日一次给药,使其成为治疗高胆固醇血症颇具吸引力的辅助疗法。

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