Protective effect of L-carnitine against cisplatin-induced liver and kidney oxidant injury in rats

K Cayir, A Karadeniz, A Yildirim, Y Kalkan… - … European journal of …, 2009 - Springer
K Cayir, A Karadeniz, A Yildirim, Y Kalkan, A Karakoc, M Keles, SB Tekin
Central European journal of medicine, 2009Springer
The present study was designed to investigate the protective effects of L-carnitine (LC) on
changes in the levels of lipid peroxidation and endogenous antioxidants induced by
cisplatin (cis-diamminedichloroplatinum II, CDDP) in the liver and kidney tissues of rats.
Twenty-four Sprague Dawley rats were equally divided into four groups of six rats each:
control, cisplatin, L-carnitine, and L-carnitine plus cisplatin. The degree of protection
produced by L-carnitine was evaluated by determining the level of malondialdehyde (MDA) …
Abstract
The present study was designed to investigate the protective effects of L-carnitine (LC) on changes in the levels of lipid peroxidation and endogenous antioxidants induced by cisplatin (cis-diamminedichloroplatinum II, CDDP) in the liver and kidney tissues of rats. Twenty-four Sprague Dawley rats were equally divided into four groups of six rats each: control, cisplatin, L-carnitine, and L-carnitine plus cisplatin. The degree of protection produced by L-carnitine was evaluated by determining the level of malondialdehyde (MDA). The activity of glutathione (GSH), glutathione peroxidase (GSH-Px), glutathione S-transferase (GST), and superoxide dismutase (SOD) were estimated from liver and kidney homogenates, and the liver and kidney were histologically examined as well. L-carnitine elicited significant liver and kidney protective activity by decreasing the level of lipid peroxidation (MDA) and elevating the activity of GSH, GSHPx, GST, and SOD. Furthermore, these biochemical observations were supported by histological findings. In conclusion, the present study indicates a significant role for reactive oxygen species (ROS) and their relation to liver and kidney dysfunction, and points to the therapeutic potential of LC in CDDP-induced liver and kidney toxicity.
Springer
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