Source:http://linkedlifedata.com/resource/pubmed/id/12963154
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2-3
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pubmed:dateCreated |
2003-9-9
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pubmed:abstractText |
The exposure of gastric mucosa to ethanol produces pathological changes such as inflammatory process, hemorrhagic erosions, even acute ulcers. The gastric mucosal lesions accompanied by a significant decrease of gastric blood flow and increase of reactive oxygen species (ROS) implicate a role of xanthine oxidase in ethanol-induced gastric hemorrhagic erosions. DA-9601, a novel antipeptic formulation of extracts of Artemisia asiatica Nakai, was studied for its inhibitory effect on gastric xanthine oxidase activity and type conversion of the enzyme that has a profound role in free radical generation. Intubation of absolute ethanol (4 g/kg) significantly induced gastrohemorrhagic lesions and lipid peroxidation in the rat stomach. Oral administration of DA-9601 at 40 mg/kg body weight significantly reduced ethanol-induced gastric mucosal hemorrhagic lesions and lipid peroxidation, which was proportional to the inhibitory effect of DA-9601 on alcohol-induced xanthine oxidase-type conversion and enzyme activity. The results suggest that alcohol-induced gastric mucosal damage may be, in part, due to the increased activity of xanthine oxidase and type conversion rate of the enzyme and that the preventive effect of DA-9601 on gastrohemorrhagic lesions would result from its inhibitory action against xanthine oxidase and oxidative stress in alcohol-treated rats.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Ulcer Agents,
http://linkedlifedata.com/resource/pubmed/chemical/DA 9601,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Ethanol,
http://linkedlifedata.com/resource/pubmed/chemical/Plant Extracts,
http://linkedlifedata.com/resource/pubmed/chemical/Xanthine Oxidase
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0378-8741
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
88
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
269-73
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:12963154-Administration, Oral,
pubmed-meshheading:12963154-Animals,
pubmed-meshheading:12963154-Anti-Ulcer Agents,
pubmed-meshheading:12963154-Artemisia,
pubmed-meshheading:12963154-Enzyme Inhibitors,
pubmed-meshheading:12963154-Ethanol,
pubmed-meshheading:12963154-Gastrointestinal Hemorrhage,
pubmed-meshheading:12963154-Lipid Peroxidation,
pubmed-meshheading:12963154-Male,
pubmed-meshheading:12963154-Plant Extracts,
pubmed-meshheading:12963154-Rats,
pubmed-meshheading:12963154-Rats, Sprague-Dawley,
pubmed-meshheading:12963154-Stomach,
pubmed-meshheading:12963154-Xanthine Oxidase
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pubmed:year |
2003
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pubmed:articleTitle |
Inhibitory effects of DA-9601 on ethanol-induced gastrohemorrhagic lesions and gastric xanthine oxidase activity in rats.
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pubmed:affiliation |
College of Pharmacy, Yeungnam University, Gyongsan 712-749, South Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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