Abstract OBJECTIVE: To study the expression of insulin receptor substrate-1(IRS-1) and insulin receptor substrate-2 (IRS-2) in pancreas of rats with intrauterine growth retardation (IUGR). METHODS: An IUGR rat model was prepared by protein malnutrition during pregnancy. The pancreas samples of the IUGR pups were obtained at birth, and 3 weeks and 8 weeks of age. The expression of IRS-1 and IRS-2 mRNA were ascertained by RT-PCR. Western blot was used to measure the protein expression of IRS-1 and IRS-2. The rat pups born from the mother rats who received normal diet during pregnancy severed as the control group. RESULTS: The expression levels of IRS-2 mRNA and protein in pancreas of the IUGR group were significantly lower than those in the control group at all three time points (P<0.05). There were no significant differences in the expression levels of IRS-1 mRNA and protein in pancreas between the IUGR and the control groups. CONCLUSIONS: The IRS-2 expression levels in pancreas in IUGR rats decrease significantly at birth, and 3 weeks and 8 weeks of age. This might be one of the molecular mechanisms for the development of metabolic syndrome in later life in IUGR individuals.[Chin J Contemp Pediatr, 2010, 12 (12):972-975]
LI Yao,XIN Ying. Expression of insulin receptor substrates in pancreas of rats with intrauterine growth retardation[J]. 中国当代儿科杂志, 2010, 12(12): 972-975.
LI Yao,XIN Ying. Expression of insulin receptor substrates in pancreas of rats with intrauterine growth retardation[J]. CJCP, 2010, 12(12): 972-975.
[2]Arends NJ, Boonstra VH, Duivenvoorden HJ, Hofman PL, Cutfield WS, Hokken-Koelega ACS. Reduced insulin sensitivity and the presence of cardiovascular risk factors in short prepubertal children born small for gestational age(SGA)[J]. Clin Endocrinol(Oxf), 2005, 62(1): 44-50.
[4]Godfrey KM, Barker DJ. Fetal nutrition and adult disease[J]. Am J Clin Nutr, 2000, 71(5 Suppl): 1344s-1352s.
[5]Bazaes RA, Alegría A, Pittaluga E, Avila A, Iniguez G, Mericq V. Determinants of insulin sensitivity and secretion in very-low-birth-weight children[J]. J Clin Endocrinol Metab, 2004, 89(3): 1267-1272.
[6]Matharu K, Ozanne SE. The fetal origins of disease and associations with low birth weight[J]. NeoReviews, 2004, 5(12): 522-526.
[9]Lingohr MK, Briaud I, Dickson LM, McCuaig JF, Alárcon C, Wicksteed BL, et al. Specific regulation of IRS-2 expression by glucose in rat primary pancreatic islet beta-cells[J]. J Biol Chem, 2006, 281(23): 15884-15892.
[10]Park S, Hong SM, Sung SR. Exendin-4 and exercise promotes beta-cell function and mass through IRS2 induction in islets of diabetic rats[J]. Life Sci, 2008, 82(9-10): 503-511.