International Journal of Molecular Sciences · 2017 · 41 citations · 28 references
Life SciencesBotanyPharmacologyBiochemical PharmacologyEthnobotanyPlant BiochemistryChemical Defense In PlantsGastrointestinal PharmacologyMedicinal PlantsOxidative Stress In InflammationPeptic Ulcer DiseaseStress BiochemistryAntioxidant PropertiesAntioxidant TreatmentGastric InjuryGastric Ulcer DiseaseGastroprotective AgentsGastroprotective TherapyNuclear Factor Kappa B InhibitionPlant Extract Antioxidants
hydro-alcoholic extract (AMHAE) against ethanol-induced gastric ulcer in a rat model. Different concentrations (50, 100, and 200 mg/kg) of AMHAE, or 30 mg/kg of omeprazole, significantly inhibited the gastric injury formation. The ethanol-induced ulcer group showed significant increases of malondialdehyde (MDA), myeloperoxidase (MPO), tumor necrosis factor (TNF)-α, nuclear factor-kappaB p65 (NF-κB p65), and monocyte chemoattractant protein (MCP)-1, and decreased activities of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-px), and interleukin (IL)-4. However, AMHAE (200 mg/kg) pretreatment significantly reversed the altered pathophysiological levels of these biomolecules to near normal stages. The gastroprotective activity of AMHAE was abolished by pretreatment with l-NAME, naloxone, capsazepine, and indomethacin, demonstrating the participation of nitric oxide (NO), opioids, TRPV (vanilloid receptor-related transient receptor potential), and prostaglandins in AMHAE-assisted gastroprotection against ethanol-induced gastric injuries. This gastroprotective effect of AMHAE might be due to the downregulation of TNF-α-based NF-κB, MCP-1 signaling and strong antioxidant properties.
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