Abstract
Hepatitis is an inflammatory disease of the liver and is considered one of the leading causes of death worldwide. Due to its scavenging activity,
Punica granatum
may be used for the treatment and prevention of liver diseases. The current study investigated the protective mechanism underlying the effects of pomegranate against a rat model of carbon tetrachloride–induced liver injury. Intraperitoneal injection of CCl
4
resulted in liver inflammation, oxidative stress, and accumulation of lipid in hepatocytes. CCl
4
induced a downregulation of superoxide dismutase (SOD), glutathione (GSH), and melonaldehyde (MDA). Pomegranate protection was assessed in terms of biochemical parameters, histopathology, and immunohistochemistry. Promegranate administration decreased inflammation, elevated serum enzymes and ROS production, and countered the debilitating effects caused by CCl
4
. In addition, CCl
4
-induced histological changes were absent in the crude pomegranate extract group, which also enhanced the scavenging activity of reactive oxygen species by enhancing the antioxidant defense mechanism as confirmed by detecting MDA, SOD, and GSH expressions. The migration of CD68
+
macrophages was halted at the injured area of the central vein and the number of macrophages was reduced to the normal control by the crude extract compared to the positive control silymarin group. Likewise, protective effects of ethylacetate and the aqueous fraction of the crude extract were also observed. However, the butanol and
n
-hexane fractions displayed increased levels of ALT, AST, and ALP as compared to silymarin. About 25% damage to hepatocytes was observed in the butanol and
n
-hexane group by histopathological examination, which is a little better compared to the CCl
4
-treated group. The crude extract and its ethyl acetate and aqueous fractions may be accountable for the hepatoprotective potential of
Punica granatum
, which was further confirmed by
in vivo
experiments. Together, these findings confirm that pomegranate exerts hepatoprotective activity against CCl
4
-induced oxidative stress and liver damage.