Antioxidant and Anti-Inflammatory Activities of Berberine in the Treatment of Diabetes Mellitus

被引:227
作者
Li, Zheng [1 ,2 ]
Geng, Ya-Na [1 ,2 ]
Jiang, Jian-Dong [2 ,3 ]
Kong, Wei-Jia [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Inst Med Biotechnol, Dept Pharmacol, Beijing 100050, Peoples R China
[2] Peking Union Med Coll, Beijing 100050, Peoples R China
[3] Chinese Acad Med Sci, Inst Mat Med, State Key Lab Bioact Nat Prod & Funct, Beijing 100050, Peoples R China
关键词
ACTIVATED PROTEIN-KINASE; ENDOPLASMIC-RETICULUM STRESS; NITRIC-OXIDE SYNTHASE; FATTY LIVER-DISEASE; FACTOR B EXPRESSION; OXIDATIVE STRESS; INSULIN-RESISTANCE; UNCOUPLING PROTEIN-2; UP-REGULATION; NADPH OXIDASE;
D O I
10.1155/2014/289264
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Oxidative stress and inflammation are proved to be critical for the pathogenesis of diabetes mellitus. Berberine (BBR) is a natural compound isolated from plants such as Coptis chinensis and Hydrastis canadensis and with multiple pharmacological activities. Recent studies showed that BBR had antioxidant and anti-inflammatory activities, which contributed in part to its efficacy against diabetes mellitus. In this review, we summarized the antioxidant and anti-inflammatory activities of BBR as well as their molecular basis. The antioxidant and anti-inflammatory activities of BBR were noted with changes in oxidative stress markers, antioxidant enzymes, and proinflammatory cytokines after BBR administration in diabetic animals. BBR inhibited oxidative stress and inflammation in a variety of tissues including liver, adipose tissue, kidney and pancreas. Mechanisms of the antioxidant and anti-inflammatory activities of BBR were complex, which involved multiple cellular kinases and signaling pathways, such as AMP-activated protein kinase (AMPK), mitogen-activated protein kinases (MAPKs), nuclear factor erythroid-2-related factor-2 (Nrf2) pathway, and nuclear factor-kappa B (NF-kappa B) pathway. Detailed mechanisms and pathways for the antioxidant and anti-inflammatory activities of BBR still need further investigation. Clarification of these issues could help to understand the pharmacology of BBR in the treatment of diabetes mellitus and promote the development of antidiabetic natural products.
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页数:12
相关论文
共 128 条
[1]   Mitochondrial energy metabolism and redox responses to hypertriglyceridemia [J].
Alberici, Luciane C. ;
Vercesi, Anibal E. ;
Oliveira, Helena C. F. .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 2011, 43 (01) :19-23
[2]   TNFα-induced and berberine-antagonized tight junction barrier impairment via tyrosine kinase, Akt and NFκB signaling [J].
Amasheh, Maren ;
Fromm, Anja ;
Krug, Susanne M. ;
Amasheh, Salah ;
Andres, Susanne ;
Zeitz, Martin ;
Fromm, Michael ;
Schulzke, Joerg-Dieter .
JOURNAL OF CELL SCIENCE, 2010, 123 (23) :4145-4155
[3]   Disruption of the uncoupling protein-2 gene in mice reveals a role in immunity and reactive oxygen species production [J].
Arsenijevic, D ;
Onuma, H ;
Pecqueur, C ;
Raimbault, S ;
Manning, BS ;
Miroux, B ;
Couplan, E ;
Alves-Guerra, MC ;
Goubern, M ;
Surwit, R ;
Bouillaud, F ;
Richard, D ;
Collins, S ;
Ricquier, D .
NATURE GENETICS, 2000, 26 (04) :435-439
[4]   Berberine protects 6-hydroxydopamine-induced human dopaminergic neuronal cell death through the induction of heme oxygenase-1 [J].
Bae, Jinbum ;
Lee, Danbi ;
Kim, Yun Kyu ;
Gil, Minchan ;
Lee, Joo-Yong ;
Lee, Kyung Jin .
MOLECULES AND CELLS, 2013, 35 (02) :151-157
[5]   Protection of cholinergic and antioxidant system contributes to the effect of berberine ameliorating memory dysfunction in rat model of streptozotocin-induced diabetes [J].
Bhutada, Pravinkumar ;
Mundhada, Yogita ;
Bansod, Kuldeep ;
Tawari, Santosh ;
Patil, Shaktipal ;
Dixit, Pankaj ;
Umathe, Sudhir ;
Mundhada, Dharmendra .
BEHAVIOURAL BRAIN RESEARCH, 2011, 220 (01) :30-41
[6]   Glucose and reactive oxygen species [J].
Bonnefont-Rousselot, D .
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2002, 5 (05) :561-568
[7]   Glutathione antioxidant system as a marker of oxidative stress in chronic renal failure [J].
CeballosPicot, I ;
WitkoSarsat, V ;
MeradBoudia, M ;
Nguyen, AT ;
Thevenin, M ;
Jaudon, MC ;
Zingraff, J ;
Verger, C ;
Jungers, P ;
DescampsLatscha, B .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 21 (06) :845-853
[8]  
Chatuphonprasert W., 2013, Pharmaceutical biology
[9]   Berberine inhibits the expression of TNFα, MCP-1, and IL-6 in AcLDL-stimulated macrophages through PPARγ pathway [J].
Chen, F. L. ;
Yang, Z. H. ;
Liu, Y. ;
Li, L. X. ;
Living, W. C. ;
Wang, X. C. ;
Zhou, W. B. ;
Yang, Y. H. ;
Hu, Ren-Ming .
ENDOCRINE, 2008, 33 (03) :331-337
[10]  
CHEN Q-M, 1986, Yaoxue Xuebao, V21, P401