Raspberry ketone protects against isoproterenol-induced myocardial infarction in rats

被引:63
作者
Khan, Vasim [1 ]
Sharma, Sumit [1 ]
Bhandari, Uma [1 ]
Ali, Syed Mansoor [2 ]
Haque, Syed Ehtaishamul [1 ]
机构
[1] Jamia Hamdard, SPER, Dept Pharmacol, New Delhi 110062, India
[2] Jamia Milia Islamia, Dept Biotechnol, New Delhi 110025, India
关键词
Inflammation; Isoproterenol; Myocardial infarction; Nitric oxide; Oxidative stress; Raspberry ketone; Rubus idaeus; PROLIFERATOR-ACTIVATED RECEPTORS; OXIDATIVE STRESS; HEART; ACID; ISCHEMIA; EXTRACT; INJURY; ATHEROSCLEROSIS; PEROXIDATION; MECHANISMS;
D O I
10.1016/j.lfs.2017.12.013
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aim: The cardioprotective role of raspberry ketone (RK) against isoproterenol (ISO)-induced myocardial infarction (MI) in rats was assessed. Materials and methods: Rats were randomly divided into Group I - Vehicle control; Group II - Toxic control ISO (85 mg/kg, s.c.); Group III, IV and V - RK (50, 100 and 200 mg/kg, respectively) with ISO; Group VI-RK (200 mg/kg) alone; Group VII - Propranolol (10 mg/kg) with ISO; and Group VIII -Propranolol (10 mg/kg) alone. After twenty-four hours of the last dose, animals were sacrificed and creatine kinase-MB, lactate dehydrogenase, total cholesterol, triglycerides, high-density-lipoprotein, low-density-lipoprotein, very-low-densitylipoprotein, malondialdehyde, reduced glutathione, superoxide dismutase, catalase, Na+, K+-ATPase, nitric oxide, histopathological and immunohistochemical analysis (tumor necrosis factor-a and inducible nitric oxide synthase) were performed. Key findings: Treatment with ISO significantly deviated the biochemical parameters from the normal levels, which were considerably restored by RK at 100 and 200 mg/kg doses. 50 mg/kg dose, however, did not demonstrate any significant cardioprotective action. The histopathological and immunohistochemical analysis further substantiated these findings.
引用
收藏
页码:205 / 212
页数:8
相关论文
共 59 条
[1]   Nitric oxide mechanism in the protective effect of naringin against post-stroke depression (PSD) in mice [J].
Aggarwal, Aditi ;
Gaur, Vaibhav ;
Kumar, Anil .
LIFE SCIENCES, 2010, 86 (25-26) :928-935
[2]   Role of the peroxisome proliferator-activated receptors (PPAR)-α, β/δ and γ triad in regulation of reactive oxygen species signaling in brain [J].
Aleshin, Stepan ;
Reiser, Georg .
BIOLOGICAL CHEMISTRY, 2013, 394 (12) :1553-1570
[3]  
Aman Upaganlawar Aman Upaganlawar, 2011, Journal of Pharmacology and Toxicology, V6, P1
[4]  
[Anonymous], HDB METHODS OXYGEN R
[5]   Targeted Complement Inhibitors Protect against Posttransplant Cardiac Ischemia and Reperfusion Injury and Reveal an Important Role for the Alternative Pathway of Complement Activation [J].
Atkinson, Carl ;
He, Songqing ;
Morris, Keeley ;
Qiao, Fei ;
Casey, Sarah ;
Goddard, Martin ;
Tomlinson, Stephen .
JOURNAL OF IMMUNOLOGY, 2010, 185 (11) :7007-7013
[7]   Apolipoprotein CIII and atherosclerosis - Beyond effects on lipid metabolism [J].
Bobik, Alex .
CIRCULATION, 2008, 118 (07) :702-704
[8]  
Bonting S. L., 1970, MEMBRANE ION TRANSPO, V1, P254
[9]   Merits of Non-Invasive Rat Models of Left Ventricular Heart Failure [J].
Carll, Alex P. ;
Willis, Monte S. ;
Lust, Robert M. ;
Costa, Daniel L. ;
Farraj, Aimen K. .
CARDIOVASCULAR TOXICOLOGY, 2011, 11 (02) :91-112
[10]   Peroxisome proliferator-activated receptors (PPARs) and their agonists for hypertension and heart failure: Are the reagents beneficial or harmful? [J].
Chen, Rui ;
Liang, Fengxia ;
Moriya, Junji ;
Yamakawa, Jun-ichi ;
Takahashi, Takashi ;
Shen, Lin ;
Kanda, Tsugiyasu .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2008, 130 (02) :131-139