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Fotio, A.L., Olleros, M.L., Vesin, D., Tauzin, S., Bisig, R., Dimo, T., Nguelefack, T.B., Dongo, E., Kamtchouing, P. and Garcia, I. (2010) in Vitro Inhibition of LPS and Mycobacterium Bovis BCG-Induced Inflammatory Cytokines and in Vivo Protection from Gain/LPS-Mediated Liver Injury by the Medicinal Plant Sclerocarya birrea. International Journal of Immunopathology and Pharmacology, 23, 61-72.
https://doi.org/10.1177/039463201002300106

has been cited by the following article:

• TITLE: Protective Activity of Markhamia tomentosa (Benth.) K. Schum. (Bignoniaceae) Methanol Leaves Extract against D-Galactosamine/Lipopolysaccharide-Induced Acute Liver Injury in Mice

  AUTHORS: Roméo Joel Guemmogne Temdie, Agathe Lambou Fotio, Flaure Donfack Metchi, Edwige Chiogo Vouffo Ymele, Gilbert Thierry Nkoulou Tabi, Théophile Dimo

  KEYWORDS: Markhamia tomentosa, D-Galactosamine/Lipopolysaccharide, Oxidative Stress, Liver Injury

  JOURNAL NAME: Journal of Biosciences and Medicines, Vol.8 No.10, October 21, 2020

  ABSTRACT: Markhamia tomentosa (Benth.) K. Schum. (Mt) is a Cameroonian medicinal plant, traditionally used to treat painful and inflammatory illness. This study aimed to examine the effects of methanol leaves extract (MLE) of Mt in D-galactosamine (D-GaIN)/lipopolysaccharide (LPS)-induced liver injury. The MLE (100 and 200 mg/kg), Ascorbic acid (10 mg/kg) and distilled water were administered 12 h and 1 h before intraperitoneal injection of D-GaIN (10 mg/mouse)/LPS (0.1 μg/g). Animals were sacrificed 6 h after D-GalN/LPS challenge. Liver injury was assessed biochemically by determination of aspartate aminotransferase (ASAT), alanine aminotransferase (ALAT), alkaline phosphatase (ALP), superoxide dismutase (SOD) and catalase activities. Malondialdehyde (MDA), reduced glutathione (GSH), nitrites, total protein and bilirubin levels were explored. Histopathological examination of liver tissue was also performed. Liver enzymes (ALAT, ASAT, ALP) activity, nitrites, MDA and bilirubin levels were increased, while protein level, SOD and catalase activities were significantly reduced by D-GalN/LPS administration. MLE (100 or 200 mg/kg) protected mice against D-GalN/LPS-induced death. In addition, the plant extract significantly reduced ALAT and ALP activity, exhibiting 23.00% and 62.20% protection, respectively. SOD activity and total protein were significantly (p D-GaIN/LPS-induced liver injury. The obtained results showed that MLE of Mt may possess hepatoprotective effects. Protection afforded by MLE against D-GalN/LPS-induced fulminant liver injury may result from reduction of oxidative stress.