Cardioprotective potential of Korean Red Ginseng extract on isoproterenol-induced cardiac injury in rats.

J Ginseng Res

Department of Veterinary Physiology, College of Veterinary Medicine, Biosafety Research Institute, Chonbuk National University, Jeonju 561-756, Korea.

Published: July 2013

AI Article Synopsis

  • The study examines the protective effects of Korean Red Ginseng (KRG) on heart injury caused by isoproterenol (ISO) in rats, focusing on various heart function metrics, serum enzyme levels, and inflammation markers.
  • KRG pretreatment significantly improved analyses such as cardiac function and reduced harmful enzyme activity, countering the negative effects of ISO.
  • The findings indicate that KRG enhances antioxidant activity in heart tissue and could be a potential therapeutic agent against cardiac injuries.

Article Abstract

The present study was designed to investigate the cardioprotective effects of Korean Red Ginseng extract (KRG) on isoproterenol (ISO)-induced cardiac injury in rats, particularly in regards to electrocardiographic changes, hemodynamics, cardiac function, serum cardiac enzymes, components of the myocardial antioxidant defense system, as well as inflammatory markers and histopathological changes in heart tissue. ISO (150 mg/kg, subcutaneous, two doses administered at 24-hour intervals) treatment induced significant decreases in P waves and QRS complexes (p<0.01), as well as a significant increase in ST segments. Moreover, ISO-treated rats exhibited decreases in left-ventricular systolic pressure, maximal rate of developed left ventricular pressure (+dP/dtmax) and minimal rate of developed left ventricular pressure (-dP/dtmax), in addition to significant increases in lactate dehydrogenase, aspartate transaminase, alanine transaminase and creatine kinase activity. Heart rate, however, was not significantly altered. And the activities of superoxide dismutase, catalase and glutathione peroxidase were decreased, whereas the activity of malondialdehyde was increased in the ISO-treated group. ISO-treated group also showed increased caspase-3 level, release of inflammatory markers and neutrophil infiltration in heart tissue. KRG pretreatment (250 and 500 mg/kg, respectively) significantly ameliorated almost all of the parameters of heart failure and myocardial injury induced by ISO. The protective effect of KRG on ISO-induced cardiac injury was further confirmed by histopathological study. In this regard, ISO treatment induced fewer morphological changes in rats pretreated with 250 or 500 mg/kg of KRG. Compared with the control group, all indexes in rats administered KRG (500 mg/kg) alone were unaltered (p>0.05). Our results suggest that KRG significantly protects against cardiac injury and ISO-induced cardiac infarction by bolstering antioxidant action in myocardial tissue.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818953PMC
http://dx.doi.org/10.5142/jgr.2013.37.273DOI Listing

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