Source:http://linkedlifedata.com/resource/pubmed/id/17712721
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2007-8-22
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pubmed:abstractText |
Alterations in glucose sensing are well-known in both humans and animal models of non-insulin-dependent diabetes mellitus. However, the circadian- and age-dependent expression of glucose-sensing genes has not previously been investigated in vivo. In the present paper, we show a progressive loss of beta-cell GLUT2-mRNA and, by immunocytochemistry, a gain of soluble, cytoplasmic GLUT2-protein in Goto-Kakizaki rat islets. We report that GLUT2-mRNA shows significant diurnal variation, which is stronger in metabolically healthy rats. We also demonstrate the significant diurnal variation of glucokinase-mRNA, with higher levels in the pancreas of 6-week-old Goto-Kakizaki rats than in Wistar rats. This leads to a maximum glucose phosphorylation capacity in-phase with food intake, enhanced glucose-stimulated insulin secretion, and prevents postprandial hyperglycemia. Perfusion experiments showed a reduction in glucose-stimulated insulin secretion in Goto-Kakizaki rat islets with an impaired first phase. Hyperglycemia and hypoinsulinemia in newborn and up to 3-week-old Goto-Kakizaki rats are thus probably due to reduced pancreatic beta-cell content, reduced beta-cell insulin content and impaired glucose sensing. The de-compensation of the metabolic situation in 42-week-old Goto-Kakizaki rats is likely to be caused by beta-cell destruction accompanied by negligible accumulation of GLUT2 in the cell membrane and further reduction of glucokinase expression.
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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/Glucokinase,
http://linkedlifedata.com/resource/pubmed/chemical/Glucose,
http://linkedlifedata.com/resource/pubmed/chemical/Glucose Transporter Type 2,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin,
http://linkedlifedata.com/resource/pubmed/chemical/Slc2a2 protein, rat
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0018-5043
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
39
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
567-74
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:17712721-Age Factors,
pubmed-meshheading:17712721-Animals,
pubmed-meshheading:17712721-Blood Glucose,
pubmed-meshheading:17712721-Body Weight,
pubmed-meshheading:17712721-Circadian Rhythm,
pubmed-meshheading:17712721-Diabetes Mellitus, Experimental,
pubmed-meshheading:17712721-Gene Expression Regulation,
pubmed-meshheading:17712721-Glucokinase,
pubmed-meshheading:17712721-Glucose,
pubmed-meshheading:17712721-Glucose Transporter Type 2,
pubmed-meshheading:17712721-Insulin,
pubmed-meshheading:17712721-Insulin-Secreting Cells,
pubmed-meshheading:17712721-Male,
pubmed-meshheading:17712721-Rats,
pubmed-meshheading:17712721-Rats, Wistar
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pubmed:year |
2007
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pubmed:articleTitle |
Circadian and age-dependent expression patterns of GLUT2 and glucokinase in the pancreatic beta-cell of diabetic and nondiabetic rats.
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pubmed:affiliation |
Institute of Anatomy and Cell Biology, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany.
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pubmed:publicationType |
Journal Article,
Comparative Study
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