Protective effects of L-carnitine on isoprenaline-induced heart and kidney dysfunctions: Modulation of inflammation and oxidative stress-related gene expression in rats

The aim of this study was to evaluate the effect of L-carnitine (L -CAR) treatment on isoprenaline (ISO) administered kidney and heart impairment in male Long Evans rats. Four groups of rats were engaged in this study such as control, ISO, control +L -CAR, and ISO +L -CAR, where n = 6 in each group. The rats were also provided with chow food and water ad libitum. At the end of the study, all rats were sacrificed, and blood and tissue samples were collected for bio-chemical analysis. Oxidative stress parameters and antioxidant enzyme activities were determined in plasma and tissues. Antioxidant and inflammatory genes expression were analyzed in the kidney cortex, and histopathological studies of kidney tissues were performed. This study showed that creatinine and uric acid in plasma were significantly increased in ISO -administered rats. L- carnitine treatment lowered the uric acid and creatinine level. ISO -administered rats showed increased lipid peroxidation and declined levels of antioxidant enzymes activities in kidneys and heart. L-carnitine treatment restored antioxidant enzymes activities and protect against oxidative stress in kidney and heart. This effect is correlated with the restoration of Nrf-2-HO-1 genes expression followed by increased SOD and catalase genes expression in the kidney. L-carnitine treatment also prevented the TNF-alpha, IL -6, and NF -KB expression in kidneys of ISO administered rats. Histopathology staining showed that L-carnitine treatment prevented kidney damage and collagen deposition in ISO administered rats. The result of this study exhibited that L-carnitine treatment reduced oxidative stress and increased antioxidant enzyme activities by enhancing antioxidant genes expression in ISO administered rats.