Malaria is a dangerous disease spread across several countries. Recent studies have focused on medicinal plants to discover alternative agents to the currently used drugs for malaria treatment. Here， we investigated the potential role of leaf extract (IE) on hepatic inflammation in mice with -infected erythrocytes. Female C57BL/6 mice were divided into three groups. The first group served as a control noninfected group， while the second and third groups were intraperitoneally injected with 10 erythrocytes parasitized by . Mice from the third group were treated daily with a dose of 100?mg/kg of IE for 7 days. IE significantly reduced the number of leukocytes and apoptotic cells. The numbers of CD68-positive cells decreased in the livers of mice from the treatment group. Moreover， IE raised the hepatic antioxidant levels (glutathione and catalase) and reduced the levels of hepatic oxidative stress markers (malondialdehyde， nitric oxide， and reactive oxygen species). IE regulated some functions of the genes related to immune responses， including apoptotic genes (B-cell lymphoma-2， Bax， and caspase-3) and cytokine genes (interleukin-1 (IL-1)， IL-6， interferon-， and tumor necrosis factor-). Therefore， IE exerts significant effects against malaria and protects the liver from injury caused by via antioxidant and anti-inflammatory ways.