Source:http://linkedlifedata.com/resource/pubmed/id/11753757
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2001-12-25
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pubmed:abstractText |
Excessive glucose production by the liver contributes significantly to diabetic hyperglycemia. The enzyme system glucose-6-phosphatase plays a key role in regulating hepatic glucose production and therefore its inhibition is a potential therapeutic target for the correction of hyperglycemia. It has previously been shown that sulfated steroids, such as estrone sulfate and dehydroepiandrosterone sulfate, inhibit the glucose-6-phosphatase system in vitro, principally through inhibition of endoplasmic reticulum glucose-6-phosphate transport. We report here that in the obese/diabetic ob/ob mouse model, orally administered estrone sulfate reduces the abnormally elevated hepatic glucose-6-phosphatase enzyme activity and enzyme protein levels that are characteristic in the ob/ob mouse, and that this reduction is associated with normalization of blood glucose levels. Other sulfated and non-sulfated steroids also reduced, to a lesser extent, glucose-6-phosphatase enzyme activity - with the exception of dehydroepiandrosterone sulfate, which had no apparent effect on this system in ob/ob mice. Estrone sulfate is therefore an effective antihyperglycemic agent in ob/ob mice, and the glucose-6-phosphatase system can be successfully targeted for the therapeutic management of hyperglycemia in this animal model of non-insulin-dependent diabetes mellitus.
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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/Blood Glucose,
http://linkedlifedata.com/resource/pubmed/chemical/Dehydroepiandrosterone Sulfate,
http://linkedlifedata.com/resource/pubmed/chemical/Estradiol,
http://linkedlifedata.com/resource/pubmed/chemical/Estrone,
http://linkedlifedata.com/resource/pubmed/chemical/Glucose-6-Phosphatase,
http://linkedlifedata.com/resource/pubmed/chemical/Hypoglycemic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/estradiol sulfate,
http://linkedlifedata.com/resource/pubmed/chemical/estrone sulfate
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0018-5043
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
33
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
721-6
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pubmed:dateRevised |
2009-2-19
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pubmed:meshHeading |
pubmed-meshheading:11753757-Aging,
pubmed-meshheading:11753757-Animals,
pubmed-meshheading:11753757-Blood Glucose,
pubmed-meshheading:11753757-Dehydroepiandrosterone Sulfate,
pubmed-meshheading:11753757-Diabetes Mellitus,
pubmed-meshheading:11753757-Estradiol,
pubmed-meshheading:11753757-Estrone,
pubmed-meshheading:11753757-Female,
pubmed-meshheading:11753757-Glucose-6-Phosphatase,
pubmed-meshheading:11753757-Hypoglycemic Agents,
pubmed-meshheading:11753757-Liver,
pubmed-meshheading:11753757-Male,
pubmed-meshheading:11753757-Mice,
pubmed-meshheading:11753757-Mice, Inbred C57BL,
pubmed-meshheading:11753757-Mice, Obese,
pubmed-meshheading:11753757-Microsomes, Liver,
pubmed-meshheading:11753757-Obesity
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pubmed:year |
2001
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pubmed:articleTitle |
The antihyperglycemic effect of estrone sulfate in genetically obese-diabetic (ob/ob) mice is associated with reduced hepatic glucose-6-phosphatase.
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pubmed:affiliation |
Department of Obstetrics & Gynecology, University of Dundee, Ninewells Hospital and Medical School, Dundee, Scotland, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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