Xing Lu, Zhou Xin, Li Ai-Hong, Li Hui-Jin, He Chun-Xia, Qin Wei, Zhao Dong, Li Peng-Quan, Zhu Li, Cao Hui-Ling
Shaanxi Key Laboratory of Ischemic Cardiovascular Disease, Institute of Basic and Translational Medicine, Xi'an Medical University, Xi'an, China.
Shaanxi Key Laboratory of Chinese Herb and Natural Drug Development, Medicine Research Institute, Shaanxi Pharmaceutical Holding Group Co., Ltd., Xi'an, China.
Front Mol Biosci. 2021 Nov 16;8:762673. doi: 10.3389/fmolb.2021.762673. eCollection 2021.
Cardiovascular diseases remain the leading cause of morbidity and mortality worldwide. Atherosclerosis is the main pathological basis of cardiovascular diseases and it is closely associated with hyperlipidemia, endothelial injury, macrophage-derived foam cells formation, proliferation and migration of vascular smooth muscle cells (VSMCs), platelet aggregation, and altered gut microbiota. Various symptomatic treatments, that are currently used to inhibit atherosclerosis, need to be administered in long term and their adverse effects cannot be ignored. Berberine (BBR) has beneficial effects on atherosclerosis through regulating multiple aspects of its progression. This review highlights the recent advances in understanding the anti-atherosclerosis mechanism of BBR. BBR alleviated atherosclerosis by attenuation of dyslipidemia, correction of endothelial dysfunction, inhibition of macrophage inflammation and foam cell formation, activation of macrophage autophagy, regulation of the proliferation and migration of VSMCs, attenuation of platelet aggregation, and modulation of gut microbiota. This review would provide a modern scientific perspective to further understanding the molecular mechanism of BBR attenuating atherosclerosis and supply new ideas for atherosclerosis management.
心血管疾病仍然是全球发病和死亡的主要原因。动脉粥样硬化是心血管疾病的主要病理基础,它与高脂血症、内皮损伤、巨噬细胞源性泡沫细胞形成、血管平滑肌细胞(VSMCs)的增殖和迁移、血小板聚集以及肠道微生物群改变密切相关。目前用于抑制动脉粥样硬化的各种对症治疗需要长期给药,其不良反应不容忽视。黄连素(BBR)通过调节动脉粥样硬化进展的多个方面对其具有有益作用。本综述重点介绍了近年来在理解BBR抗动脉粥样硬化机制方面的进展。BBR通过减轻血脂异常、纠正内皮功能障碍、抑制巨噬细胞炎症和泡沫细胞形成、激活巨噬细胞自噬、调节VSMCs的增殖和迁移、减轻血小板聚集以及调节肠道微生物群来减轻动脉粥样硬化。本综述将为进一步理解BBR减轻动脉粥样硬化的分子机制提供现代科学视角,并为动脉粥样硬化的管理提供新思路。