
AbstractBackgroundThe present study was undertaken to evaluate the potential of the rhizomes of the Indian medicinal plant,Picrorhiza kurroain healing indomethacin-induced acute stomach ulceration in mice and examine its capacity to modulate oxidative stress and the levels of prostaglandin (PGE2) and EGF during the process.MethodsMale swiss albino mice, ulcerated with indomethacin (18 mg/kg, p. o., single dose) were treated up to 7 days with different doses of the methanol extract ofP. kurroarhizomes (designated as PK). The healing capacity of the most effective dose of PK (20 mg/kg, p. o. × 3 d) was compared with that of omeprazole (Omez) (3 mg/kg, p. o. × 3 d). The effects of the drug-treatment for one and three days on the biochemical parameters were assessed by comparing the results with that of untreated mice of the 1stand 3rdday of ulceration. The stomach tissues of the mice were used for the biochemical analysis.ResultsThe macroscopic indices revealed maximum ulceration on the 3rdday after indomethacin administration, which was effectively healed by PK. Under the optimized treatment regime, PK and Omez reduced the ulcer indices by 45.1% (P< 0.01), and 76.3% respectively (P< 0.001), compared to the untreated ulcerated mice.Compared to the ulcerated untreated mice, those treated with PK for 3 days showed decreased the levels of thiobarbituric acid reactive substances (TBARS) (32.7%,P< 0.05) and protein carbonyl (37.7%,P< 0.001), and increased mucin (42.2%,P< 0.01), mucosal PGE2(21.4%,P< 0.05), and expressions of COX-1 and 2 (26.9% and 18.5%,P< 0.05), EGF (149.0%,P< 0.001) and VEGF (56.9%,P< 0.01). Omez reduced the TBARS (29.4%,P< 0.05), and protein carbonyl (38.9%,P< 0.001), and increased mucin (38.3%,P< 0.01), without altering the other parameters significantly.ConclusionPK (20 mg/kg, p. o. × 3 days) could effectively heal indomethacin-induced stomach ulceration in mice by reducing oxidative stress, and promoting mucin secretion, prostaglandin synthesis and augmenting expressions of cyclooxygenase enzymes and growth factors.
Male, Indomethacin, Administration, Oral, Thiobarbituric Acid Reactive Substances, Dinoprostone, Other systems of medicine, Mice, Animals, Stomach Ulcer, Picrorhiza, Dose-Response Relationship, Drug, Epidermal Growth Factor, Plant Extracts, Stomach, Anti-Ulcer Agents, Oxidative Stress, Complementary and alternative medicine, Gastric Mucosa, RZ201-999, Rhizome, Research Article, Phytotherapy
Male, Indomethacin, Administration, Oral, Thiobarbituric Acid Reactive Substances, Dinoprostone, Other systems of medicine, Mice, Animals, Stomach Ulcer, Picrorhiza, Dose-Response Relationship, Drug, Epidermal Growth Factor, Plant Extracts, Stomach, Anti-Ulcer Agents, Oxidative Stress, Complementary and alternative medicine, Gastric Mucosa, RZ201-999, Rhizome, Research Article, Phytotherapy
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