Chlorogenic Acids in Cardiovascular Disease: A Review of Dietary Consumption, Pharmacology, and Pharmacokinetics

被引:75
作者
Li, Lin [1 ]
Su, Congping [1 ]
Chen, Xiangyang [3 ]
Wang, Qing [1 ]
Jiao, Wenchao [1 ]
Luo, Hui [1 ]
Tang, Jiayang [1 ]
Wang, Wei [1 ]
Li, Sen [2 ]
Guo, Shuzhen [1 ]
机构
[1] Beijing Univ Chinese Med, Sch Tradit Chinese Med, Beijing 100029, Peoples R China
[2] Beijing Univ Chinese Med, Sch Life Sci, Beijing 100029, Peoples R China
[3] Beijing Univ Chinese Med, Sch Chinese Mat Med, Beijing 102488, Peoples R China
基金
中国国家自然科学基金;
关键词
chlorogenic acids; hypertension; atherosclerosis; heart failure; myocardial infarction; PROLIFERATOR-ACTIVATED RECEPTOR; COFFEE BEAN EXTRACT; HIGH-DENSITY-LIPOPROTEIN; FOAM CELL-FORMATION; OXIDATIVE STRESS; CAFFEIC ACID; IN-VITRO; CARDIAC-HYPERTROPHY; NITRIC-OXIDE; MYOCARDIAL-INFARCTION;
D O I
10.1021/acs.jafc.0c01554
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Chlorogenic acids (CGAs) have gained considerable attention as pervasive human dietary constituents with potential cardiovascular-preserving effects. The main sources include coffee, yerba mate, Eucommia ulmodies leaves, and Lonicerae Japonicae Flos. CGA consumption can reduce the risks of hypertension, atherosclerosis, heart failure, myocardial infarction, and other factors associated with cardiovascular risk, such as obesity and type 2 diabetes. This review recapitulates recent advances of CGAs in the cardiovascular-preserving effects, pharmacokinetics, sources, and safety. Emerging evidence indicates that CGAs exhibit circulatory guarding properties through the suppression of oxidative stress, leukocyte infiltration, platelet aggregation, platelet-leukocyte interactions, vascular remodeling, and apoptosis as well as the regulation of glucose and lipid metabolism and vasodilatory action in the cardiovascular system. CGAs exert these effects by acting on complex signaling networks, but the global mechanisms are still not clear. The oral bioavailability of CGA is poor, and there is a potential sensitization concern about CGA. The bioactive metabolites, systematic toxicity, and optimized structure are needed for further identification.
引用
收藏
页码:6464 / 6484
页数:21
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