Effect of Indigofera oblongifolia on the Hepatic Oxidative Status and Expression of Inflammatory and Apoptotic Genes during Blood-Stage Murine Malaria.
Mohamed Abdel Monam DkhilEsam M Al-ShaebiSaleh Al-QuraishyPublished in: Oxidative medicine and cellular longevity (2019)
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 Indigofera oblongifolia leaf extract (IE) on hepatic inflammation in mice with Plasmodium chabaudi-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 106 erythrocytes parasitized by P. chabaudi. 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-1β (IL-1β), IL-6, interferon-γ, and tumor necrosis factor-α). Therefore, IE exerts significant effects against malaria and protects the liver from injury caused by P. chabaudi via antioxidant and anti-inflammatory ways.
Keyphrases
- oxidative stress
- induced apoptosis
- anti inflammatory
- cell death
- plasmodium falciparum
- cell cycle arrest
- genome wide
- nitric oxide
- high fat diet induced
- immune response
- reactive oxygen species
- endoplasmic reticulum stress
- dna damage
- poor prognosis
- bioinformatics analysis
- genome wide identification
- rheumatoid arthritis
- diabetic rats
- ischemia reperfusion injury
- type diabetes
- toll like receptor
- skeletal muscle
- wild type
- diffuse large b cell lymphoma
- transcription factor
- adipose tissue
- combination therapy
- high resolution
- mass spectrometry
- binding protein
- cell proliferation
- pi k akt
- replacement therapy
- genome wide analysis
- hydrogen peroxide
- single molecule