Cardioprotective effect of tetrahydrocurcumin and rutin on lipid peroxides and antioxidants in experimentally induced myocardial infarction in rats

被引:37
作者
Ali, Md Sultan [1 ]
Mudagal, M. P. [1 ]
Goli, D. [1 ]
机构
[1] Acharya & BM Reddy Coll Pharm, Dept Pharmacol, Bangalore 560090, Karnataka, India
来源
PHARMAZIE | 2009年 / 64卷 / 02期
关键词
ISCHEMIA; CURCUMIN; MECHANISM;
D O I
10.1691/ph.2008.8628
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The present study was undertaken to evaluate the cardioprotective potential of tetrahydrocurcumin (THC) and rutin in an in vivo rat ischemia-reperfusion (I/R) model of myocardial infarction (MI). Male wistar rats were divided into six groups receiving saline (control MI/R group), vehicle control MI/R group, THC (5 mg kg(-1) and 10 mg kg(-1)) and rutin (5 mg kg(-1) and 10 mg kg(-1)) i.p. injection respectively. At the day of the experiment, each group was subjected to acute ischemia for 30 min by occlusion of the left anterior descending coronary artery (LAD). Thereafter reperfusion was allowed for 4 h. MI/R resulted in significant cardiac necrosis, elevation in lipid peroxidation, elevation in cardiac marker enzymes AST, ALT and decline in antioxidant status catalase, reduced glutathione in the normal control MI/R group and vehicle control MI/R group. Myocardial infarction produced after MI/R was significantly reduced in tetrahydrocurcumin and rutin of the myocardial antioxidant status, infarct size reduction compared to control and vehicle control MI/R group. Furthermore, MI/R induced lipid peroxidation was significantly reduced by tetrahydrocurcumin and rutin. Cardioprotection in the treatment group was probably a result from suppression of oxidative stress. Histopathological examination further confirmed the protective effect of tetrahydrocurcumin and rutin on the MI/R heart.
引用
收藏
页码:132 / 136
页数:5
相关论文
共 32 条
  • [1] CURCUMIN - A POTENT INHIBITOR OF LEUKOTRIENE-B4 FORMATION IN RAT PERITONEAL POLYMORPHONUCLEAR NEUTROPHILS (PMNL)
    AMMON, HPT
    ANAZODO, MI
    SAFAYHI, H
    DHAWAN, BN
    SRIMAL, RC
    [J]. PLANTA MEDICA, 1992, 58 (02) : 226 - 226
  • [2] CHANG WS, 1993, ANTICANCER RES, V13, P2165
  • [3] Chugh S N, 1999, J Assoc Physicians India, V47, P380
  • [4] DUKE JA, 1992, HDB PHYTOCHEMICAL CO, P75
  • [5] TISSUE SULFHYDRYL GROUPS
    ELLMAN, GL
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1959, 82 (01) : 70 - 77
  • [6] OCCURRENCE OF OXIDATIVE STRESS DURING MYOCARDIAL REPERFUSION
    FERRARI, R
    CECONI, C
    CURELLO, S
    CARGNONI, A
    DEGIULI, F
    VISIOLI, O
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 1992, 111 (1-2) : 61 - 69
  • [7] EARLY PHASE ACUTE MYOCARDIAL INFARCT SIZE QUANTIFICATION - VALIDATION OF THE TRIPHENYL TETRAZOLIUM CHLORIDE TISSUE ENZYME STAINING TECHNIQUE
    FISHBEIN, MC
    MEERBAUM, S
    RIT, J
    LANDO, U
    KANMATSUSE, K
    MERCIER, JC
    CORDAY, E
    GANZ, W
    [J]. AMERICAN HEART JOURNAL, 1981, 101 (05) : 593 - 600
  • [8] Halliwell Barry, 1993, American Journal of Clinical Nutrition, V57, p715S, DOI 10.1093/ajcn/57.5.715S
  • [9] ISOLATION AND STRUCTURE OF 2 PROSTAGLANDIN ENDOPEROXIDES THAT CAUSE PLATELET-AGGREGATION
    HAMBERG, M
    SVENSSON, J
    WAKABAYASHI, T
    SAMUELSSON, B
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (02) : 345 - 349
  • [10] JACOBSON MD, 1974, TRENDS BIOCH J, V243, P43