L-Carnitine ameliorates immunological-induced hepatitis in rats

ABSTRACT

Immunological mediated hepatitis can be initiated by bacterial product; Lipopolysaccharide [LPS]. The later is increased during severe infection, bacterial overgrowth or translocation. LPS stimulates Kupffer cells. Activation of the kupffer cells contributes to the onset of liver injuries by producing and releasing cytotoxic agents, inflammatory cytokines and reactive oxygen species. In the present study, L-carnitine, a natural antioxidant and immunoprotective agent, is used to protect against LPS-induced hepatitis. Liver content of glutathione [GSH], malondialdehyde [MDA], nitric oxide [NO] and the DNA adduct S-hydroxydeoxyguanosine [8-HDG] are estimated. Serum activity of liver enzymes ALT, AST, and Gamma-GT, in addition to IL2 level are also estimated. Moreover, liver histopathological changes are determined. Results revealed that LPS [5mg/kg once i.p] significantly increased 8-HDG, MDA, NO and depleted GSH in the liver of the treated rats. It also, increased serum 1L2 and activity of all the estimated liver enzyme markers indicating massive hepatic cellular damage as also shown as a necrotic damage in liver histological sections. LCR administered [500 mg/kg] 3h before LPS protected against LPS-induced lethality by 100%. LCR also prevented the increase in liver content of 8-HDG, MDA and NO. It rescued the depleted GSH and prevented the necrotic damage in the liver tissue as shown by normalization of ALT, AST and Gamma-GT as well as IL2 and a remarkable improvement in liver histology. These data suggest that LCR could be used as an adjuvant therapy in severely infected and septic patients to counteract LPS-induced liver hepatitis