Resveratrol attenuates the inflammatory reaction induced by ischemia/reperfusion in the rat heart

被引:40
作者
Cong, Xiaoqiang [1 ,2 ]
Li, Ying [3 ]
Lu, Na [1 ]
Dai, Yajian [4 ]
Zhang, Huijie [4 ]
Zhao, Xin [1 ]
Liu, Ya [2 ]
机构
[1] Jilin Univ, Bethune Hosp 1, Dept Cardiol, Changchun 130021, Jilin, Peoples R China
[2] Jilin Univ, Sch Publ Hlth, Dept Nutr & Toxicol, Changchun 130021, Jilin, Peoples R China
[3] Peoples Hosp Jilin Prov, Dept Emergericy Internal Med, Changchun 130021, Jilin, Peoples R China
[4] Friendship Hosp Linjiang, Dept Internal Med, Linjiang 134600, Jilin, Peoples R China
关键词
resveratrol; ischemia/reperfusion injury; neutrophil; tumor necrosis factor-alpha; ISCHEMIA-REPERFUSION INJURY; NECROSIS-FACTOR-ALPHA; MYOCARDIAL-ISCHEMIA; NITRIC-OXIDE; SIRT1; PREVENTION; APOPTOSIS; CHEMOKINE; PROTECTS; SYNTHASE;
D O I
10.3892/mmr.2014.2090
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The role of resveratrol (Res) in inflammation induced by ischemia/reperfusion is not well understood. The aim of the present study was to investigate whether Res modulates neutrophil accumulation and tumor necrosis factor-alpha (TNF-alpha) induction in an ischemia/reperfusion-injured rat heart model. The rats were randomly exposed to sham surgery, myocardial ischemia/reperfusion (MI/R) alone, MI/R + Res, MI/R + Res + L-NG-nitroarginine methyl ester (L-NAME) and MI/R + Res + methylene blue (MB). The results demonstrated that compared with MI/R, Res reduced the myocardial infarct area, myocardial myeloperoxidase levels, serum creatinine kinase and lactate dehydrogenase levels, and serum and myocardial TNF-alpha production. All the effects of Res demonstrated were inhibited by L-NAME (a nitric oxide (NO) synthase inhibitor) and MB [a cyclic guanosine monophosphate (cGMP) inhibitor]. Thus, Res produces cardioprotective and anti-inflammatory effects. These effects may be associated with an increase in NO production, the inhibition of neutrophil accumulation, TNF-alpha induction and cGMP signaling pathways in myocardium subjected to MI/R.
引用
收藏
页码:2528 / 2532
页数:5
相关论文
共 34 条
[1]   Prevention of short-term ultraviolet B radiation-mediated damages by resveratrol in SKH-1 hairless mice [J].
Afaq, F ;
Adhami, VM ;
Ahmad, N .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2003, 186 (01) :28-37
[2]   Sirt1 regulates aging and resistance to oxidative stress in the heart [J].
Alcendor, Ralph R. ;
Gao, Shumin ;
Zhai, Peiyong ;
Zablocki, Daniela ;
Holle, Eric ;
Yu, Xianzhong ;
Tian, Bin ;
Wagner, Thomas ;
Vatner, Stephen F. ;
Sadoshima, Junichi .
CIRCULATION RESEARCH, 2007, 100 (10) :1512-1521
[3]  
Aluyen Julia Khristine, 2012, Journal of Dietary Supplements, V9, P45, DOI 10.3109/19390211.2011.650842
[4]   Resveratrol: A review of preclinical studies for human cancer prevention [J].
Athar, Mohammad ;
Back, Jung Ho ;
Tang, Xmwel ;
Kim, Kwang Ho ;
Kopelovich, Levy ;
Bickers, David R. ;
Kim, Arianna L. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2007, 224 (03) :274-283
[5]   Exercise training changes IL-10/TNF-α ratio in the skeletal muscle of post-MI rats [J].
Batista, M. L., Jr. ;
Rosa, J. C. ;
Lopes, R. D. ;
Lira, F. S. ;
Martins, E., Jr. ;
Yamashita, A. S. ;
Brum, P. C. ;
Lancha, A. H., Jr. ;
Lopes, A. C. ;
Seelaender, M. .
CYTOKINE, 2010, 49 (01) :102-108
[6]   Resveratrol is Not a Direct Activator of SIRT1 Enzyme Activity [J].
Beher, Dirk ;
Wu, John ;
Cumine, Suzanne ;
Kim, Ki Won ;
Lu, Shu-Chen ;
Atangan, Larissa ;
Wang, Minghan .
CHEMICAL BIOLOGY & DRUG DESIGN, 2009, 74 (06) :619-624
[7]   Methods for studying experimental myocardial ischemic and reperfusion injury [J].
Black, SC ;
Rodger, IW .
JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 1996, 35 (04) :179-190
[8]  
Chakrabarty SP, 2011, CURR MOL MED, V11, P709
[9]  
Chandrasekar B, 2001, CIRCULATION, V103, P2296
[10]   Resveratrol prevents doxorubicin cardiotoxicity through mitochondrial stabilization and the Sirt1 pathway [J].
Danz, Elizabeth D. Brookins ;
Skramsted, Jeremy ;
Henry, Nicholas ;
Bennett, James A. ;
Keller, Rebecca S. .
FREE RADICAL BIOLOGY AND MEDICINE, 2009, 46 (12) :1589-1597