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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1994-8-2
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pubmed:abstractText |
Silymarin, a commercial crude drug used as a hepatoprotective, was found to inhibit 53% of beta-glucuronidase activity at a final concentration of 0.8 mg/ml. Of three compounds A, silybin and C, which were isolated from silymarin, A and silybin potently inhibited the enzyme activity, followed by C. beta-Glucuronidases of intestinal bacteria, HGU-1 and HGU-2, and E. coli HB101 were noncompetitively inhibited by silybin. beta-Glucuronidase of the feces of a healthy human and of a human with colon cancer were also inhibited by silybin, silymarin and saccharic acid 1,4-lactone at 0.03-0.15 mg/ml. Silymarin and silybin protected the increase in enzyme activity in the serum of the rats treated with CCl4.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0918-6158
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
17
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
443-5
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:8019514-Animals,
pubmed-meshheading:8019514-Bacteria,
pubmed-meshheading:8019514-Carbon Tetrachloride Poisoning,
pubmed-meshheading:8019514-Chromatography, Thin Layer,
pubmed-meshheading:8019514-Colonic Neoplasms,
pubmed-meshheading:8019514-Feces,
pubmed-meshheading:8019514-Glucuronidase,
pubmed-meshheading:8019514-Humans,
pubmed-meshheading:8019514-Intestines,
pubmed-meshheading:8019514-Liver,
pubmed-meshheading:8019514-Male,
pubmed-meshheading:8019514-Microsomes, Liver,
pubmed-meshheading:8019514-Rats,
pubmed-meshheading:8019514-Rats, Wistar,
pubmed-meshheading:8019514-Silymarin
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pubmed:year |
1994
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pubmed:articleTitle |
Silymarin and its components are inhibitors of beta-glucuronidase.
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pubmed:affiliation |
College of Pharmacy, Kyunghee University, Seoul, Korea.
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pubmed:publicationType |
Journal Article
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