nstantaneous and historical temperature effects on a-pinene
Cardioprotective effects of Commiphoramukul against
isoprenaline-induced cardiotoxicity:
A biochemical and
histopathological evaluation
Author Details
ShreeshOjha
Department of Pharmacology, All India Institute of
Medical Sciences, New Delhi - 110 029, India
JagritiBhatia
Department of Pharmacology, All India Institute of
Medical Sciences, New Delhi - 110 029, India
SachinArora
Department of Pharmacology, All India Institute of
Medical Sciences, New Delhi - 110 029, India
MahaveerGolechha
Department of Pharmacology, All India Institute of
Medical Sciences, New Delhi - 110 029, India
SantoshKumari
Division of Plant Physiology, Indian Agricultural
Research Institute, New Delhi - 110 012, India
DharamvirSinghArya
(Corresponding
author)
Department of Pharmacology, All India Institute
of Medical Sciences, New Delhi - 110 029, India
e-mail: dsarya16@hotmail.com
Publication Data
Paper received:
25 June 2010
Revised received:
02 November 2010
Accepted:
20 November
2010
Abstract
Commiphoramukulcommonly known as Guggul is one of the oldest and commonly consumed herb
for promoting heart and vascular health. Present study was undertaken to
evaluate cardioprotective potential of Commiphoramukul
against isoprenaline-induced myocardial necrosis in
rats. Wistar albino rats were divided
into three main groups: sham (saline only), isoprenaline
control (saline and isoprenaline) and Commiphoramukultreated
(Commiphoramukuland isoprenaline) groups. Commiphoramukulwas administered in three doses 100, 200
and 400 mg kg-1p.o. for 30 days. On 29th and 30th
day, the animals of isoprenaline control and Commiphoramukul
pretreatment groups were administered isoprenaline
(85 mg kg-1; s.c.), consecutively at an interval
of 24 hr. Isoprenaline administration produced a
significant (p<0.05) decrease in myocardial antioxidants; superoxidedismutase (SOD), catalase (CAT), glutathione peroxidase
(GSHPx), reduced glutathione (GSH), and myocyte injury marker enzymes creatine-
phosphokinase - MB (CK-MB) and lactate dehydrogenase (LDH) along with enhanced lipid peroxidation; malondialdehyde
(MDA) in heart. Commiphoramukul pretreatment reversed the isoprenaline-induced
oxidative changes in rat myocardium by significant (p<0.05) increase in
SOD, CAT, GSHPx, GSH and reduction of MDA. In
addition to improving myocardial antioxidant status, Commiphoramukulalso prevented the leakage of LDH and
CK-MB from heart. Further, histopathological examination showed the reduction
of necrosis, edema and inflammation following Commiphoramukul pretreatment. Based on present findings,
it is concluded that Commiphoramukul may be a potential preventive and therapeutic
agent against the oxidative stress associated ischemic heart disease owing to
antioxidant and antiperoxidative activity.
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