Promising Anti-atherosclerotic Effect of Berberine: Evidence from In Vitro, In Vivo, and Clinical Studies

被引:37
作者
Fatahian, Alireza [1 ]
Haftcheshmeh, Saeed Mohammadian [2 ]
Azhdari, Sara [3 ]
Farshchi, Helaleh Kaboli [4 ]
Nikfar, Banafsheh [5 ]
Momtazi-Borojeni, Amir Abbas [6 ,7 ]
机构
[1] Mazandaran Univ Med Sci, Dept Cardiol, Cardiovasc Res Ctr, Sari, Iran
[2] Mashhad Univ Med Sci, Dept Med Immunol, Fac Med, Mashhad, Razavi Khorasan, Iran
[3] Bam Univ Med Sci, Sch Med, Dept Anat & Embryol, Bam, Iran
[4] Ferdowsi Univ Mashhad, Dept Hort, Fac Agr, Mashhad, Razavi Khorasan, Iran
[5] Iran Univ Med Sci, Pars Hosp, Pars Adv & Minimally Invas Med Manners Res Ctr, Tehran, Iran
[6] FDA, Halal Res Ctr IRI, Tehran, Iran
[7] Mashhad Univ Med Sci, Dept Med Biotechnol, Fac Med, Mashhad, Razavi Khorasan, Iran
来源
REVIEWS OF PHYSIOLOGY, BIOCHEMISTRY AND PHARMACOLOGY, VOL 178 | 2020年 / 178卷
关键词
AMP-activated protein kinase; Atherosclerosis; Berberine; Cholesterol; Endothelial cells; LDL-C; Macrophage dysfunction; Vascular smooth muscle cell; DENSITY-LIPOPROTEIN RECEPTOR; HIGH-FAT DIET; REVERSE CHOLESTEROL TRANSPORT; ACTIVATED PROTEIN-KINASE; SMOOTH-MUSCLE-CELLS; DOUBLE-BLIND; HIGH-RISK; TRANSCRIPTIONAL ACTIVATION; ENDOTHELIAL DYSFUNCTION; INSULIN SENSITIVITY;
D O I
10.1007/112_2020_42
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Elevated levels of plasma cholesterol, impaired vascular wall, and presence of inflammatory macrophages are important atherogenic risk factors contributing to atherosclerotic plaque formation and progression. The interventions modulating these risk factors have been found to protect against atherosclerosis development and to decrease atherosclerosis-related cardiovascular disorders. Nutritional approaches involving supplements followed by improving dietary habits and lifestyle have become growingly attractive and acceptable methods used to control atherosclerosis risk factors, mainly high levels of plasma cholesterol. There are a large number of studies that show berberine, a plant bioactive compound, could ameliorate atherosclerosis-related risk factors. In the present literature review, we put together this studies and provide integrated evidence that exhibits berberine has the potential atheroprotective effect through reducing increased levels of plasma cholesterol, particularly low-density lipoprotein (LDL) cholesterol (LDL-C) via LDL receptor (LDLR)-dependent and LDL receptor-independent mechanisms, inhibiting migration and inflammatory activity of macrophages, improving the functionality of endothelial cells via anti-oxidant activities, and suppressing proliferation of vascular smooth muscle cells. In conclusion, berberine can exert inhibitory effects on the atherosclerotic plaque development mainly through LDL-lowering activity and suppressing atherogenic functions of mentioned cells. As the second achievement of this review, among the signaling pathways through which berberine regulates intracellular processes, AMP-activated protein kinase (AMPK) has a central and critical role, showing that enhancing activity of AMPK pathway can be considered as a promising therapeutic approach for atherosclerosis treatment.
引用
收藏
页码:83 / 110
页数:28
相关论文
共 140 条
[71]  
Kruth HS, 2013, CURR PHARM DESIGN, V19, P5865
[72]   Anti-Atherogenic Effect of Berberine on LXRα-ABCA1-Dependent Cholesterol Efflux in Macrophages [J].
Lee, Tzong-Shyuan ;
Pan, Ching-Chian ;
Peng, Chien-Chung ;
Kou, Yu Ru ;
Chen, Chien-Yu ;
Ching, Li-Chieh ;
Tsai, Tsung-Huang ;
Chen, Shu-Fen ;
Lyu, Ping-Chiang ;
Shyue, Song-Kun .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2010, 111 (01) :104-110
[73]   Berberine-Improved Visceral White Adipose Tissue Insulin Resistance Associated with Altered Sterol Regulatory Element-Binding Proteins, Liver X Receptors, and Peroxisome Proliferator-Activated Receptors Transcriptional Programs in Diabetic Hamsters [J].
Li, Guo-Sheng ;
Liu, Xu-Han ;
Zhu, Hua ;
Huang, Lan ;
Liu, Ya-Li ;
Ma, Chun-Mei ;
Qin, Chuan .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2011, 34 (05) :644-654
[74]   Hepatocyte Nuclear Factor 1α Plays a Critical Role in PCSK9 Gene Transcription and Regulation by the Natural Hypocholesterolemic Compound Berberine [J].
Li, Hai ;
Dong, Bin ;
Park, Sahng Wook ;
Lee, Hyun-Sook ;
Chen, Wei ;
Liu, Jingwen .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (42) :28885-28895
[75]   Identification of mRNA binding proteins that regulate the stability of LDL receptor mRNA through AU-rich elements [J].
Li, Hai ;
Chen, Wei ;
Zhou, Yue ;
Abidi, Parveen ;
Sharpe, Orr ;
Robinson, William H. ;
Kraemer, Fredric B. ;
Liu, Jingwen .
JOURNAL OF LIPID RESEARCH, 2009, 50 (05) :820-831
[76]   Effect of Berberine on promoting the excretion of cholesterol in high-fat diet-induced hyperlipidemic hamsters [J].
Li, Xiao-Yang ;
Zhao, Zhen-Xiong ;
Huang, Min ;
Feng, Ru ;
He, Chi-Yu ;
Ma, Chao ;
Luo, Shi-Heng ;
Fu, Jie ;
Wen, Bao-Ying ;
Ren, Long ;
Shou, Jia-Wen ;
Guo, Fang ;
Chen, Yangchao ;
Gao, Xin ;
Wang, Yan ;
Jiang, Jian-Dong .
JOURNAL OF TRANSLATIONAL MEDICINE, 2015, 13
[77]   Berberine Analogues as a Novel Class of the Low-Density-Lipoprotein Receptor Up-Regulators: Synthesis, Structure-Activity Relationships, and Cholesterol-Lowering Efficacy [J].
Li, Ying-Hong ;
Yang, Peng ;
Kong, Wei-Jia ;
Wang, Yan-Xiang ;
Hu, Chang-Qin ;
Zuo, Zeng-Yan ;
Wang, Yue-Ming ;
Gao, Hong ;
Gao, Li-Mei ;
Feng, Yan-Chun ;
Du, Na-Na ;
Liu, Ying ;
Song, Dan-Qing ;
Jiang, Jian-Dong .
JOURNAL OF MEDICINAL CHEMISTRY, 2009, 52 (02) :492-501
[78]  
LI Z, 2014, EVID-BASED COMPL ALT, V2014, DOI DOI 10.1155/2014/289264
[79]   Berberine inhibits platelet-derived growth factor-induced growth and migration partly through an AMPK-dependent pathway in vascular smooth muscle cells [J].
Liang, Kae-Woei ;
Yin, Sui-Chu ;
Ting, Chih-Tai ;
Lin, Shing-Jong ;
Hsueh, Chi-Mei ;
Chen, Chiu-Yuan ;
Hsu, Shih-Lan .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2008, 590 (1-3) :343-354
[80]   Berberine suppresses MEK/ERK-dependent Egr-1 signaling pathway and inhibits vascular smooth muscle cell regrowth after in vitro mechanical injury [J].
Liang, KW ;
Ting, CT ;
Yin, SC ;
Chen, YT ;
Lin, SJ ;
Liao, JK ;
Hsu, SL .
BIOCHEMICAL PHARMACOLOGY, 2006, 71 (06) :806-817