Epidemiological studies have shown that infants exposed to an increased supply of nutrients before birth are at increased risk of type 2 diabetes in later life. We have investigated the hypothesis that fetal overnutrition results in reduced expression and phosphorylation of the cellular fuel sensor, AMP-activated kinase (AMPK) in liver and skeletal muscle before and after birth. From 115 days gestation, ewes were fed either at or ∼55% above maintenance energy requirements. Postmortem was performed on lamb fetuses at 139-141 days gestation (n = 14) and lambs at 30 days of postnatal age (n = 21), and liver and quadriceps muscle were collected at each time point. The expression of AMPKα1 and AMPKα2 mRNA was determined by quantitative RT-PCR (qRT-PCR). The abundance of AMPKα and phospho-AMPKα (P-AMPKα) was determined by Western blot analysis, and the proportion of the total AMPKα pool that was phosphorylated in each sample (%P-AMPKα) was determined. The ratio of AMPKα2 to AMPKα1 mRNA expression was lower in fetuses compared with lambs in both liver and muscle, independent of maternal nutrition. Hepatic %P-AMPKα was lower in both fetuses and lambs in the Overfed group and %P-AMPKα in the lamb liver was inversely related to plasma glucose concentrations in the first 24 h after birth (r = 0.73, P < 0.025). There was no effect of maternal overnutrition on total AMPKα or P-AMPKα abundance in liver or skeletal muscle. We have, therefore, demonstrated that AMPKα responds to signals of increased nutrient availability in the fetal liver. Suppression of hepatic AMPK phosphorylation may contribute to increased glucose production, and basal hyperglycemia, present in lambs of overfed ewes in early postnatal life.
|Journal||American Journal of Physiology - Regulatory Integrative and Comparative Physiology|
|Publication status||Published - 1 Dec 2008|
ASJC Scopus subject areas
- Physiology (medical)