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KRG contains more than 30 kinds of saponin components and has been reported as having various biological properties, such as anti-fatigue action, immune restoration, and neurovegetative effect. The purpose of this study was to assess the effects of a KRG-containing drug (KRGCD) on gastric ulcer models in mice.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Stomach ulcers were induced by oral ingestion of hydrochloride (HCl)\/ethanol or indomethacin. Treatment with KRGCD (30, 100, and 300 mg\/kg, p.o.) occurred 1 hr before the ulcer induction. Effect of KRGCD on anti-oxidant activity and gastric mucosal blood flow with a laser Doppler flowmeter in mice stomach tissue was evaluated.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>KRGCD (100 and 300 mg\/kg, p.o.) significantly decreased ethanol- and indomethacin-induced gastric ulcer compared with the vehicle-treated (control) group. KRGCD (100 and 300 mg\/kg) also decreased the level of thiobarbituric acid reactive substance (TBARS) and increased gastric mucosal blood flow compared with the control group.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>These results suggest that the gastroprotective effects of KRGCD on mice ulcer models can be attributed to its ameliorating effect on oxidative damage and improving effect of gastric mucosal blood flow.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1186\/1472-6882-10-45","type":"journal-article","created":{"date-parts":[[2010,8,18]],"date-time":"2010-08-18T14:19:28Z","timestamp":1282141168000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":47,"title":["Protective effects of a gastrointestinal agent containing Korean red ginseng on gastric ulcer models in mice"],"prefix":"10.1186","volume":"10","author":[{"given":"Atsushi","family":"Oyagi","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kenjirou","family":"Ogawa","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mamoru","family":"Kakino","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hideaki","family":"Hara","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2010,8,18]]},"reference":[{"key":"322_CR1","doi-asserted-by":"publisher","first-page":"1685","DOI":"10.1016\/S0006-2952(99)00212-9","volume":"58","author":"AS Attele","year":"1999","unstructured":"Attele AS, Wu JA, Yuan CS: Ginseng pharmacology: multiple constituents and multiple actions. 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