1. Leucine is essential for attenuating fetal growth restriction caused by a protein-restricted diet in rats.
- Author
-
Teodoro GF, Vianna D, Torres-Leal FL, Pantaleão LC, Matos-Neto EM, Donato J Jr, and Tirapegui J
- Subjects
- Animals, Animals, Newborn, Body Composition drug effects, Body Composition physiology, Body Weight drug effects, Body Weight physiology, Diet, Protein-Restricted adverse effects, Dietary Proteins blood, Female, Liver physiology, Male, Muscle, Skeletal physiology, Organ Size drug effects, Organ Size physiology, Pregnancy, Proteins genetics, Proteins metabolism, Rats, Rats, Wistar, Serum Albumin metabolism, Signal Transduction drug effects, Signal Transduction physiology, TOR Serine-Threonine Kinases metabolism, Weight Gain drug effects, Weight Gain physiology, Dietary Proteins pharmacology, Fetal Growth Retardation diet therapy, Fetal Growth Retardation prevention & control, Leucine pharmacology
- Abstract
Certain amino acids, such as leucine (Leu) are not only substrates for protein synthesis but also are important regulators of protein metabolism. Moreover, it is known that alterations in intrauterine growth favor the development of chronic diseases in adulthood. Therefore, we investigated the role of Leu in combination with other BCAA on effects that are induced by maternal protein restriction on fetal growth. Wistar rats were divided into 4 groups according to the diet provided during pregnancy: control (C; 20% casein); V+I [5% casein + 2% L-valine (Val) + 2% L-isoleucine (Ile)]; KYT [5% casein + 1.8% L-lysine (Lys) + 1.2% L-tyrosine (Tyr) + 1% L-threonine (Thr)]; and BCAA (5% casein + 1.8% L-Leu + 1.2% L-Val + 1% L-Ile). Maternal protein restriction reduced the growth and organ weight of the offspring of dams receiving the V+I and KYT diets compared with the C group. Supplementation with BCAA reversed this growth deficit, minimizing the difference or restoring the mass of organs and carcass fat, the liver and muscle protein, and the RNA concentrations compared with newborns in the C group (P < 0.05). These effects could be explained by the activation of the mTOR signaling pathway, because phosphorylation of 4E-BP1 in the liver of offspring of the BCAA group was greater than that in the C, V+I, and KYT groups. The present results identify a critical role for Leu in association with other BCAA in the activation of the mTOR signaling pathway for the control of altered intrauterine growth induced by a maternal low-protein diet.
- Published
- 2012
- Full Text
- View/download PDF