Impaired PI 3-kinase activation in adipocytes from early growth-restricted male rats
- PMID: 11171610
- DOI: 10.1152/ajpendo.2001.280.3.E534
Impaired PI 3-kinase activation in adipocytes from early growth-restricted male rats
Abstract
Epidemiological studies have established a relationship between early growth restriction and subsequent development of type 2 diabetes. Animal studies have shown that offspring of protein-restricted rats undergo a greater age-related loss of glucose tolerance than controls. The aim of this study was to investigate the possibility that this deterioration of glucose tolerance is associated with changes in adipocyte insulin action. Adipocytes from low-protein offspring had higher basal levels of glucose uptake than controls. Insulin stimulated glucose uptake into control adipocytes but had little effect on low-protein adipocytes. Both groups had similar levels of basal and isoproterenol-stimulated lipolysis. Insulin inhibited lipolysis in control adipocytes but had a reduced effect on low-protein adipocytes. These changes in insulin action were not related to altered expression of insulin receptors or insulin receptor tyrosine phosphorylation; however, they were associated with reduced phosphatidylinositol 3-kinase and protein kinase B activation. These results demonstrate that reduced glucose tolerance observed in late adult life after early growth restriction is associated with adipocyte insulin resistance.
Similar articles
-
Depot-specific effects of early growth retardation on adipocyte insulin action.Horm Metab Res. 2000 Feb;32(2):71-5. doi: 10.1055/s-2007-978592. Horm Metab Res. 2000. PMID: 10741689
-
Poor fetal nutrition causes long-term changes in expression of insulin signaling components in adipocytes.Am J Physiol. 1997 Jul;273(1 Pt 1):E46-51. doi: 10.1152/ajpendo.1997.273.1.E46. Am J Physiol. 1997. PMID: 9252478
-
Early growth restriction leads to down regulation of protein kinase C zeta and insulin resistance in skeletal muscle.J Endocrinol. 2003 May;177(2):235-41. doi: 10.1677/joe.0.1770235. J Endocrinol. 2003. PMID: 12740011
-
The long-term consequences of intra-uterine protein malnutrition for glucose metabolism.Proc Nutr Soc. 1999 Aug;58(3):615-9. doi: 10.1017/s0029665199000804. Proc Nutr Soc. 1999. PMID: 10604194 Review.
-
Insulin receptors and the molecular mechanism of insulin action.Diabetes Metab Rev. 1985;1(1-2):5-32. doi: 10.1002/dmr.5610010103. Diabetes Metab Rev. 1985. PMID: 3013542 Review. No abstract available.
Cited by
-
Maternal obesity programs mitochondrial and lipid metabolism gene expression in infant umbilical vein endothelial cells.Int J Obes (Lond). 2016 Nov;40(11):1627-1634. doi: 10.1038/ijo.2016.142. Epub 2016 Aug 17. Int J Obes (Lond). 2016. PMID: 27531045 Free PMC article.
-
The dangerous road of catch-up growth.J Physiol. 2003 Feb 15;547(Pt 1):5-10. doi: 10.1113/jphysiol.2002.024406. Epub 2002 Aug 2. J Physiol. 2003. PMID: 12562946 Free PMC article. Review.
-
Fetal stress and programming of hypoxic/ischemic-sensitive phenotype in the neonatal brain: mechanisms and possible interventions.Prog Neurobiol. 2012 Aug;98(2):145-65. doi: 10.1016/j.pneurobio.2012.05.010. Epub 2012 May 22. Prog Neurobiol. 2012. PMID: 22627492 Free PMC article. Review.
-
Low birthweight is associated with specific changes in muscle insulin-signalling protein expression.Diabetologia. 2005 Mar;48(3):547-52. doi: 10.1007/s00125-005-1669-7. Epub 2005 Feb 24. Diabetologia. 2005. PMID: 15729577
-
For debate: Fetal and early postnatal growth restriction lead to diabetes, the metabolic syndrome and renal failure.Diabetologia. 2003 Jul;46(7):1013-9. doi: 10.1007/s00125-003-1131-7. Epub 2003 Jun 21. Diabetologia. 2003. PMID: 12827239 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous