201. Extrusion process of Acanthopanax senticosus leaves enhances the gastroprotective effect of compound 48/80 on acute gastric mucosal lesion in rats
- Author
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Kang-Hyun Leem, Myung-Gyou Kim, and Hye Kyung Kim
- Subjects
Male ,0301 basic medicine ,Xanthine Oxidase ,Eleutherococcus ,Pharmacology ,medicine.disease_cause ,030226 pharmacology & pharmacy ,Gastric mucosal lesion ,Lipid peroxidation ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Malondialdehyde ,Compound 48/80 ,otorhinolaryngologic diseases ,Gastric mucosa ,Animals ,Humans ,p-Methoxy-N-methylphenethylamine ,Medicine ,Stomach Ulcer ,Rats, Wistar ,Medicine(all) ,Glutathione Peroxidase ,030102 biochemistry & molecular biology ,Traditional medicine ,Extrusion ,business.industry ,Drug Synergism ,General Medicine ,Mucus ,Rats ,Plant Leaves ,Famotidine ,Acanthopanax senticosus leaves ,medicine.anatomical_structure ,chemistry ,Gastric Mucosa ,Drug Therapy, Combination ,business ,Histamine ,Oxidative stress ,Drugs, Chinese Herbal ,medicine.drug - Abstract
Objective To investigate the gastroprotective effects of Acanthopanax senticosus leaves (ASLs) extrusion on acute gastric mucosal lesion in rats induced by compound 48 / 80 (C48 / 80). Methods Rats were divided into six groups: normal; C48/80-induced gastric lesion control; gastric lesion positive control (famotidine 4 mg/kg); gastric lesion administered with two levels of extruded ASLs (ASLE, 40 and 200 mg/kg); and gastric lesion treated with ASLs (ASL 200 mg/kg). Mucus secretion / damage was determined by immunohistological staining. Immunofluorescence and western blotting were performed to determine gastric mucosal Bax and Bcl-2 expression. Gastric mucosal oxidative-stress-related enzymes and malondialdehyde were determined. Results C48/80-induced mucus depletion and inflammation in the gastric mucosa were significantly attenuated by ASLs. The increased serum serotonin and histamine concentrations in C48/80-treated rats were also attenuated by ASLs. Gastric mucosal Bax protein expression was increased and Bcl-2 expression was decreased after C48/80 treatment, and ASLs ameliorated Bax and Bcl-2 expression. The extrusion process significantly augmented the effects of ASLs in a dose-dependent manner. ASLEs at 200 mg/kg normalized mucus damage / secretion, C48 / 80-induced increases of mucosal myeloperoxidase activity (index of inflammation), xanthine oxidase, and malondialdehyde content (index of lipid peroxidation). The effects of ASLs on Bax and Bcl-2 expression were also enhanced by extrusion. Furthermore, these effects of ASLEs at 200 mg/kg were similar to those of famotidine, a histamine H2-receptor antagonist commonly used to treat gastric ulcers. Conclusion ASLEs prevented acute gastric mucosal lesion progression induced by C48/80, possibly by inducing mucus production, and reduced inflammation and oxidative stress in gastric mucosa through an anti-apoptotic mechanism.
- Published
- 2016