Source:http://linkedlifedata.com/resource/pubmed/id/19375767
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007258,
umls-concept:C0017262,
umls-concept:C0021641,
umls-concept:C0033684,
umls-concept:C0034693,
umls-concept:C0038323,
umls-concept:C0040676,
umls-concept:C0041004,
umls-concept:C0087111,
umls-concept:C0185117,
umls-concept:C0205216,
umls-concept:C0205217,
umls-concept:C0220905,
umls-concept:C0332281,
umls-concept:C0392756,
umls-concept:C0442117,
umls-concept:C2911684
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pubmed:issue |
6
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pubmed:dateCreated |
2009-5-18
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pubmed:abstractText |
We previously reported that early insulin treatment reduced intramuscular triglyceride content in type 2 diabetes mellitus Sprague-Dawley rats; the underlying mechanisms are, however, not completely understood. Here we investigated the regulation of insulin on molecular expressions involved in lipid metabolism pathways in skeletal muscle of high-fat-diet and streptozotocin-induced diabetic Sprague-Dawley rats. Neutral protamine Hagedorn insulin and gliclazide were initiated at the third day after streptozotocin injection and lasted for 3 weeks. Compared with normal rats, untreated diabetic rats had a 30% and 61% increase in lipoprotein lipase protein expression and activity, which were decreased by insulin and gliclazide (P < .05). Fatty acid translocase protein was down-regulated by 45% in untreated diabetic rats, which was up-regulated by 31% and 26% with insulin and gliclazide, respectively (P < .05). Insulin failed to affect fatty acid transport protein 1 and fatty acid binding protein expressions. Carnitine palmitoyl transferase 1 had a 47% decrease in untreated diabetic rats, which was normalized by insulin (P < .05). Moreover, compared with normal rats, untreated diabetic rats had higher expressions of sterol regulatory element-binding protein 1c, tumor necrosis factor alpha, and Tyr(705) phosphorylation of signal transducer and activator of transcription 3 levels, which all were down-regulated after insulin treatment. These results suggested that early insulin reduced intramuscular triglyceride levels in diabetic rats potentially through amelioration of lipid dysfunction and inhibition of lipid synthesis.
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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/Carnitine O-Palmitoyltransferase,
http://linkedlifedata.com/resource/pubmed/chemical/Dietary Fats,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin,
http://linkedlifedata.com/resource/pubmed/chemical/Lipoprotein Lipase,
http://linkedlifedata.com/resource/pubmed/chemical/Sterol Regulatory Element Binding...,
http://linkedlifedata.com/resource/pubmed/chemical/Streptozocin,
http://linkedlifedata.com/resource/pubmed/chemical/Triglycerides
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1532-8600
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
58
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
779-86
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:19375767-Animals,
pubmed-meshheading:19375767-Carnitine O-Palmitoyltransferase,
pubmed-meshheading:19375767-Diabetes Mellitus, Experimental,
pubmed-meshheading:19375767-Dietary Fats,
pubmed-meshheading:19375767-Gene Expression Regulation,
pubmed-meshheading:19375767-Insulin,
pubmed-meshheading:19375767-Lipid Metabolism,
pubmed-meshheading:19375767-Lipoprotein Lipase,
pubmed-meshheading:19375767-Muscle, Skeletal,
pubmed-meshheading:19375767-Rats,
pubmed-meshheading:19375767-Rats, Sprague-Dawley,
pubmed-meshheading:19375767-Sterol Regulatory Element Binding Protein 1,
pubmed-meshheading:19375767-Streptozocin,
pubmed-meshheading:19375767-Triglycerides
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pubmed:year |
2009
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pubmed:articleTitle |
Increased carnitine palmitoyl transferase 1 expression and decreased sterol regulatory element-binding protein 1c expression are associated with reduced intramuscular triglyceride accumulation after insulin therapy in high-fat-diet and streptozotocin-induced diabetic rats.
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pubmed:affiliation |
Department of Endocrinology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, PR China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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