Basak Ajoy
Department of Pathology and Laboratory Medicine, Faculty of Medicine, University of Ottawa, 451 Smyth Road, Ottawa, ON K1H 8M5, Canada.
Biomolecules. 2025 Mar 22;15(4):468. doi: 10.3390/biom15040468.
The accumulation of high levels of cholesterol associated with low-density lipoprotein (LDL) in the bloodstream is the key risk factor for stroke and cardiovascular diseases. Therefore, reducing the concentration of LDL-cholesterol in the blood and maintaining it at an optimum level are vital especially for hypercholesterolemic individuals and cardiovascular patients. Thus, the study of cholesterol management and regulation in the physiological system has drawn significant attention from researchers across the globe. This led to the discovery of several cholesterol-lowering drugs which have been approved for administration either via oral or non-oral routes. Owing to the high comfort level, reduced or no pain, and fewer side effects with oral administration, more focus has been directed towards the development of oral-based cholesterol-lowering drugs. The other modes of administration such as intravenous or intramuscular injections are complex and sometimes painful and less tolerable. Therefore, there was a significant interest to develop oral drugs targeting PCSK9. In fact, some progress has been accomplished in recent years. This review provides an overview of the existing cholesterol-lowering drugs, and the progress made so far with oral-based PCSK9 drugs for lowering LDL-cholesterol. The review is presented in several sections highlighting the molecular targets, the individual drugs, and the modes of administration, with a focus on the oral route.
血液中与低密度脂蛋白(LDL)相关的高水平胆固醇积累是中风和心血管疾病的关键危险因素。因此,降低血液中低密度脂蛋白胆固醇的浓度并将其维持在最佳水平至关重要,尤其是对于高胆固醇血症患者和心血管疾病患者。因此,生理系统中胆固醇管理和调节的研究引起了全球研究人员的极大关注。这导致发现了几种已被批准通过口服或非口服途径给药的降胆固醇药物。由于口服给药具有高度的舒适度、减轻或无疼痛以及较少的副作用,更多的研究重点已转向开发口服降胆固醇药物。其他给药方式,如静脉注射或肌肉注射,操作复杂,有时会引起疼痛且耐受性较差。因此,开发针对前蛋白转化酶枯草溶菌素9(PCSK9)的口服药物引起了极大的兴趣。事实上,近年来已经取得了一些进展。本综述概述了现有的降胆固醇药物,以及迄今为止口服PCSK9药物在降低低密度脂蛋白胆固醇方面取得的进展。综述分为几个部分,重点介绍分子靶点、个别药物和给药方式,重点是口服途径。