School of Basic Medical Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Key Laboratory of Birth Defects and Related Diseases of Women and Children of MOE, State Key Laboratory of Biotherapy, West China Second University Hospital, Sichuan University, Chengdu, China.
Clin Sci (Lond). 2020 Mar 27;134(6):657-676. doi: 10.1042/CS20200128.
Cardiovascular diseases (CVDs) are the leading cause of morbidity and mortality worldwide. Metabolic dysfunction is a fundamental core mechanism underlying CVDs. Previous studies generally focused on the roles of long-chain fatty acids (LCFAs) in CVDs. However, a growing body of study has implied that short-chain fatty acids (SCFAs: namely propionate, malonate, butyrate, 2-hydroxyisobutyrate (2-HIBA), β-hydroxybutyrate, crotonate, succinate, and glutarate) and their cognate acylations (propionylation, malonylation, butyrylation, 2-hydroxyisobutyrylation, β-hydroxybutyrylation, crotonylation, succinylation, and glutarylation) participate in CVDs. Here, we attempt to provide an overview landscape of the metabolic pattern of SCFAs in CVDs. Especially, we would focus on the SCFAs and newly identified acylations and their roles in CVDs, including atherosclerosis, hypertension, and heart failure.
心血管疾病 (CVDs) 是全球发病率和死亡率的主要原因。代谢功能障碍是 CVDs 的基本核心机制。先前的研究通常集中在长链脂肪酸 (LCFAs) 在 CVDs 中的作用。然而,越来越多的研究表明,短链脂肪酸 (SCFAs:即丙酸、丙二酸、丁酸、2-羟基异丁酸 (2-HIBA)、β-羟基丁酸、巴豆酸、琥珀酸和戊二酸) 及其同源酰化 (丙酰化、丙二酰化、丁酰化、2-羟基异丁酰化、β-羟基丁酰化、巴豆酰化、琥珀酰化和戊二酰化) 参与 CVDs。在这里,我们试图提供 CVDs 中 SCFAs 代谢模式的概述。特别是,我们将重点介绍 SCFAs 和新发现的酰化及其在 CVDs 中的作用,包括动脉粥样硬化、高血压和心力衰竭。