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dc.contributor.authorTosh, Darran Nicholasen
dc.contributor.authorFu, Qien
dc.contributor.authorCallaway, Christopher W.en
dc.contributor.authorMcNight, Robert A.en
dc.contributor.authorMcMillen, Isabella Carolineen
dc.contributor.authorRoss, Michael G.en
dc.contributor.authorLane, Robert H.en
dc.contributor.authorDesai, Minaen
dc.date.issued2010en
dc.identifier.citationAmerican Journal of Physiology - Gastrointestinal and Liver Physiology, 2010; 299(5):G1023-G1029en
dc.identifier.issn0193-1857en
dc.identifier.urihttp://hdl.handle.net/2440/64038-
dc.description.abstractMaternal food restriction (FR) during pregnancy results in intrauterine growth-restricted (IUGR) offspring that show rapid catch-up growth and develop metabolic syndrome and adult obesity. However, continued nutrient restriction during nursing delays catch-up growth and prevents development of obesity. Epigenetic regulation of IGF1, which modulates growth and is synthesized and secreted by the liver, may play a role in the development of these morbidities. Control (AdLib) pregnant rats received ad libitum food through gestation and lactation, and FR dams were exposed to 50% food restriction from days 10 to 21. FR pups were nursed by either ad libitum-fed control dams (FR/AdLib) or FR dams (FR/FR). All pups were weaned to ad libitum feed. Maternal FR resulted in IUGR newborns with significantly lower liver weight and, with the use of chromatin immunoprecipitation, decreased dimethylation at H3K4 in the IGF1 region was observed. Obese adult FR/AdLib males had decreased dimethylation and increased trimethylation of H3K4 in the IGF1 region. This corresponded to an increase in mRNA expression of IGF1-A (134 ± 5%), IGF1-B (165 ± 6%), IGF1 exon 1 (149 ± 6%), and IGF1 exon 2 (146 ± 7%) in the FR/AdLib compared with the AdLib/AdLib control group. In contrast, nonobese FR/FR had significantly higher IGF1-B mRNA levels (147 ± 19%) than controls with no difference in IGF1-A, exon 1 or exon 2. Modulation of the rate of IUGR newborn catch-up growth may thus protect against IGF1 epigenetic modifications and, consequently, obesity and associated metabolic abnormalities.en
dc.description.statementofresponsibilityDarran N. Tosh, Qi Fu, Christopher W. Callaway, Robert A. McKnight, Isabella C. McMillen, Michael G. Ross, Robert H. Lane and Mina Desaien
dc.language.isoenen
dc.publisherAmer Physiological Socen
dc.rightsCopyright © 2010 the American Physiological Societyen
dc.subjectintrauterine growth restriction; insulin-like growth factor 1; histone methylationen
dc.titleEpigenetics of programmed obesity: alteration in IUGR rat hepatic IGF1 mRNA expression and histone structure in rapid vs. delayed postnatal catch-up growthen
dc.typeJournal articleen
dc.contributor.schoolSchool of Molecular and Biomedical Science : Physiologyen
dc.identifier.rmid0020101402en
dc.identifier.doi10.1152/ajpgi.00052.2010en
Appears in Collections:Physiology publications

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