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Gastroprotective potential of Dolichandrone falcata extract via modulation of oxidative stress, inflammation, and mucosal healing

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Background: Dolichandrone falcata, traditionally used for gastrointestinal disorders, has demonstrated antiulcer activity, but the underlying protective mechanisms remain unclear. This study evaluated the methanolic extract of D. falcata for gastroprotective, antioxidant, and anti-inflammatory activities using ethanol- and pylorus-ligation–induced ulcer models in rats. Methodology: Wistar rats were divided into control, standard, and treatment groups. Ulcers were induced by ethanol or pyloric ligation. The extract (100, 200, and 400 mg/kg) and omeprazole (20 mg/kg) were administered orally. Ulcer index, gastric parameters, oxidative stress markers [malondialdehyde (MDA), glutathione (GSH), superoxide dismutase (SOD), catalase (CAT)], and inflammatory cytokines [TNF-α, IL-6] were assessed, supported by histopathological examination. Results and Discussion: The extract produced a dose-dependent reduction in the ulcer index in both models, with 76.6% protection at 400 mg/kg, comparable to omeprazole (79.7%). Histology revealed marked restoration of the gastric mucosa with minimal necrosis. MDA levels decreased significantly, while GSH, SOD, and CAT levels were elevated toward normal. TNF-α and IL-6 were markedly suppressed, indicating a reduction in oxidative and inflammatory injury. Conclusion: D. falcata extract demonstrated potent gastroprotective effects through antioxidative, anti-inflammatory, and mucosal-healing mechanisms. This is the first biochemical and cytokine-based validation of its traditional use, suggesting strong potential for developing D. falcata as a plant-derived therapeutic for ulcer management.

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Comparative study of proton pump inhibitors on dexamethasone plus pylorus ligation induced ulcer model in rats.
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  • Indian Journal of Pharmaceutical Sciences
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The present study was designed to compare ulcer protective effect of proton pump inhibitors viz. omeprazole, rabeprazole and lansoprazole against dexamethasone plus pylorus ligation induced ulcer model. Dexamethasone (5 mg/kg) was used as an ulcerogen. Dexamethasone suspended in 1% CMC in water was given orally to all the rats 15 min after the pylorus ligation. Omeprazole (20 mg/kg), rabeprazole (20 mg/kg), and lansoprazole (20 mg/kg) were administered by oral route 30 min prior to ligation was used for ulcer protective studies, gastric secretion and mucosal studies. Effects of proton pump inhibitors were determined by the evaluation of various biochemical parameters such as ulcer index, free and total acidity, gastric pH, mucin, pepsin and total proteins. Oral administration of proton pump inhibitors showed significant reduction in gastric acid secretion and ulcer protective activity against dexamethasone plus pylorus ligation induced ulcer model. The % protection of omeprazole, rabeprazole and lansoprazole was 84.04, 89.36 and 79.78, respectively. Rabeprazole significantly inhibited the acid-pepsin secretion and increased the gastric mucin secretion. The observations made in the present study suggest that rabeprazole is the most effective gastric antisecretory and ulcer healing agent as compared to omeprazole and lansoprazole.

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Anti-ulcer Properties of Ziziphus jujuba Lam Leaves Extract in Rats
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  • M S Ganachari + 1 more

Objective: To evaluate the antiulcer activity of Ziziphus jujuba leaves extract (ZJE) at various doses using different experimentally induced gastric ulcer models in rats. Methods: Gastric ulcers were induced in rats by Pylorus ligation, 80% ethanol (1ml/rat) and aspirin (200mg/kg). In pylorus ligation induced ulcer model the parameters studied were gastric volume, free acidity, total acidity and ulcer index. Lesion index and gastric mucus content were determined in ethanol induced ulcer model and in aspirin induced ulcer model the ulcer index was determined. Results: In pylorus ligation model, ZJE pretreatment caused significant reduction in gastric volume, free acidity, total acidity and ulcer index as compared to control group. In ethanol-induced ulcers, ZJE was effective in reducing lesion index and increasing the gastric mucus content. It was also effective in decreasing ulcer index in aspirin-induced ulcers. All the results obtained with ZJE were dose dependent. Conclusions: The results suggest that ZJE possesses significant and dose dependent antiulcer activity. The antiulcer activity of ZJE can be attributed to its cytoprotective and antisecretory action.

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Protective Effect of Ginger oil on Aspirin and Pylorus Ligation-Induced Gastric Ulcer model in Rats
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The present investigation was performed in aspirin and pylorus ligation-induced ulcer model in Wistar rats, in which ability of ginger oil to provide gastric protection was studied at two different doses, 0.5 and 1 g/kg po. Gastric protection was evaluated by measuring the ulcer index, serum γ-GTP levels, total acidity of gastric juice and gastric wall mucus thickness. The results obtained in the present study indicated that ginger oil has a protective action against gastric ulcers induced by aspirin plus pylorus ligation in Wistar rats.

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Background: Gastric ulcer is one of the most prevalent gastrointestinal disorders, which affects approximately 5-10% of people during their life. In recent years, abundant work has been carried out on herbal medicine to clarify their potential efficacy in gastric ulcer prevention or management. The present study was carried out to evaluate the antiulcer activity of the methanolic root extract of Berberis lycium in albino rats. Method: The methanolic root extract of Berberis lycium was prepared by hot extraction method. Anti-ulcer activity was evaluated and method employed was pylorus ligation and ethanol induced in albino rats. Preliminary methanolic extract of Berberis lycium was subjected to the acute oral toxicity study according to the OECD guideline no. 425. Animals were divided into four groups of six animals each. The animals of Group I served as normal control (vehicle) which received distilled water. Group II and III received 250 mg/kg and 500 mg/kg of methanolic root extract, respectively. In pylorus ligation induced ulcer model, various parameters were studied viz. gastric volume, pH, total acidity, free acidity, and ulcer index. Ulcer index and percentage inhibition of ulceration was determined for ethanol induced ulcer model. Group IV received Ranitidine at 50 mg/kg was used as the standard drug. Pretreatment of methanol root extract of Berberis lycium showed significant (P˂0.05) decrease in the gastric volume, total acidity and free acidity. However, pH of the gastric juice was significantly increased only at higher dose 500 mg/kg. It showed also significant (P˂0.05) decrease in number of ulcers and ulcer score index in pylorus ligation and ethanol induced ulceration models. Results: The methanol root extract of Berberis lycium showed a significant reduction in the total acidity, free acidity and acid volume. The efficacy of plant extract at high dose was comparable with the standard drug Ranitidine. Conclusion: Our study results support the ethnomedical use of root of Berberis lycium. Keywords: Antiulcer activity, Berberis lycium, Pylorus ligation, Ranitidine, Ulcer Index.

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Anti-ulcerogenic activity of dentatin from clausena excavata Burm.f. against ethanol-induced gastric ulcer in rats: Possible role of mucus and anti-oxidant effect
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Anti-ulcerogenic activity of dentatin from clausena excavata Burm.f. against ethanol-induced gastric ulcer in rats: Possible role of mucus and anti-oxidant effect

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  • Research Article
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Leathery Murdah, Terminalia coriacea (Roxb.) Wight & Arn. from family Combretaceae is used in Ayurveda and Siddha traditional systems of medicine to heal ulcers. The present study was conducted to assess the gastroprotective effect and understand the fundamental mechanism of action of Leathery Murdah, Terminalia coriacea (Roxb.) Wight & Arn. Leaf Methanolic Extract. The test extract was screened for anti-ulcer activity by Aspirin induced ulcerogenesis in pyloric ligation and ethanol induced gastric ulcers at three doses - 125, 250, and 500 mg/kg, p.o. using Ranitidine 50 mg/kg and Misoprostol 100 μg/kg as standard drug in respective models. Seven parameters were carefully examined, that is, ulcer index, total protein, mucin, catalase, malondialdehyde, and superoxide dismutase levels and histopathology. High Performance Liquid Chromatographic - Ultra Violet profiling and Liquid Chromatography - Mass Spectral analysis of crude Terminalia coriacea leaves methanolic extract were carried out as a part of chemical characterization to identify bioactive compounds. All the test doses exhibited significant gastroprotective function, particularly the higher doses demonstrated improved action. The results revealed a significant increase in the levels of catalase, superoxide dismutase, and Mucin with reduction in ulcer index, the levels of total protein, and malondialdehyde. Histopathological observations also illustrated the gastroprotective effect of Terminalia coriacea leaves methanolic extract. Terminalia coriacea leaves methanolic extract exhibited strong anti-oxidant and anti-secretory activities mediated gastroprotection besides inducing the gastric mucosal production. The observed pharmacological response can be attributed to the flavonoidal compounds namely - Quercetin-3-O-rutinoside, Luteolin-7-O-glucoside, Myricetin hexoside, Quercetin-3-O-glucoside, Isorhamnetin-3-O-rhamnosylglucoside and Isorhamnetin-3-O-glucoside identified in the extract for the first time with High Performance Liquid Chromatographic - Ultra Violet and Liquid Chromatography - Mass Spectral analysis.

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MS/MS-based molecular networking for exploring the chemical diversity of Chiliadenus montanus (Vahl.) brullo and Chiliadenus candicans (Delile) brullo and their anti-ulcer potential via modulation of Nrf2/ICAM-1 in rats.
  • Oct 28, 2026
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  • Alaa M Shaheen + 7 more

MS/MS-based molecular networking for exploring the chemical diversity of Chiliadenus montanus (Vahl.) brullo and Chiliadenus candicans (Delile) brullo and their anti-ulcer potential via modulation of Nrf2/ICAM-1 in rats.

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