Protein-caloric food restriction affects insulin-like growth factor-1 in fetal Wistar rat
2005
Martín, M. Ángeles | Serradas, Patricia | Ramos, Sonia | Fernández-Millán, Elisa | Goya, Luis | Gangnerau, Marie-Noëlle | Lacorne, Matthieu | Pascual-Leone, Ana María | Escrivá, Fernando | Portha, Bernard | Álvarez, Carmen | Ministerio de Ciencia y Tecnología (España) | Consejo Superior de Investigaciones Científicas (España) | Centre National de la Recherche Scientifique (France)
We have previously shown that fetuses from protein-caloric undernourished pregnant rats (35% of control diet during the last week of pregnancy) at 21.5 d post coitum exhibit increased beta-cell mass. This alteration is correlated with increased insulinemia and total pancreatic insulin content, a pattern similar to that reported in infants of mild diabetic mothers. In this work, we investigated in undernourished fetuses: 1) whether availability of growth factors such as insulin, GH, and IGFs and their binding proteins (IGFBPs) could be implicated in this alteration, and 2) the beta-cell mitogenic response to IGFs in vitro. The results show that maternal undernutrition increases pancreatic IGF-I expression and islet IGF-I receptor content in undernourished fetuses, whereas hepatic IGF-I expression and serum IGF-I levels were decreased. No changes were observed in serum IGF-II, and its expression was diminished in undernourished pancreases and unchanged in the liver, compared with control fetuses. Serum levels and liver and pancreatic mRNA expression of IGFBP-1 were found to be normal in undernourished fetuses, whereas the serum concentration and abundance of IGFBP-2 mRNA in pancreas were increased. Finally, the beta-cell mitogenic response to IGFs in vitro was significantly increased in undernourished fetal islets, compared with controls. In conclusion, in undernourished fetuses the increased beta-cell mass can be related to the stimulation of replicative beta-cell response due to locally increased pancreatic IGF-I mRNA; this effect is perhaps potentiated or favored by the enhanced islet IGF-I receptor content and pancreatic IGFBP-2 gene expression.
Show more [+] Less [-]This work was supported by Grants BFI2001-2125 and BFI2002-00253 from Ministerio de Ciencia y Tecnología, Spain, and the France/Spain Program for Science (Cooperation Franco-Espagnole Centre National de la Recherche Scientifique/Consejo Superior Investigaciones Cientificas; projects 5249 and 7963).
Show more [+] Less [-]Peer Reviewed
Show more [+] Less [-]Bibliographic information
This bibliographic record has been provided by Instituto de Ciencia y Tecnología de Alimentos y Nutrición