Therapeutic effects of glutamic acid in piglets challenged with deoxynivalenol.

PLoS One

Scientific Observing and Experimental Station of Animal Nutrition and Feed Science in South-Central China, Ministry of Agriculture, Hunan Provincial Engineering Research Center of Healthy Livestock Key Laboratory of Agro-Ecological Processes in Subtropical Region, Institute of Subtropical Agriculture, Chinese Academy of Scienses, Changsha, Hunan, China; Department of Animal Science, Texas A&M University, College Station, Texas, United State of America.

Published: November 2015

AI Article Synopsis

  • The study investigates how glutamic acid can protect piglets from digestive tract damage and oxidative stress caused by the mycotoxin deoxynivalenol (DON).
  • Twenty-eight piglets were divided into four diet groups to assess the effects of DON and glutamic acid on various physiological parameters and tissue health over a 37-day period.
  • Results indicated that while DON increased oxidative stress and harmed intestinal health, glutamic acid supplementation significantly mitigated these negative effects and improved key signaling pathways.

Article Abstract

The mycotoxin deoxynivalenol (DON), one of the most common food contaminants, primarily targets the gastrointestinal tract to affect animal and human health. This study was conducted to examine the protective function of glutamic acid on intestinal injury and oxidative stress caused by DON in piglets. Twenty-eight piglets were assigned randomly into 4 dietary treatments (7 pigs/treatment): 1) uncontaminated control diet (NC), 2) NC+DON at 4 mg/kg (DON), 3) NC+2% glutamic acid (GLU), and 4) NC+2% glutamic acid + DON at 4 mg/kg (DG). At day 15, 30 and 37, blood samples were collected to determine serum concentrations of CAT (catalase), T-AOC (total antioxidant capacity), H2O2 (hydrogen peroxide), NO (nitric oxide), MDA (maleic dialdehyde), DAO (diamine oxidase) and D-lactate. Intestinal morphology, and the activation of Akt/mTOR/4EBP1 signal pathway, as well as the concentrations of H2O2, MDA, and DAO in kidney, liver and small intestine, were analyzed at day 37. Results showed that DON significantly (P<0.05) induced oxidative stress in piglets, while this stress was remarkably reduced with glutamic acid supplementation according to the change of oxidative parameters in blood and tissues. Meanwhile, DON caused obvious intestinal injury from microscopic observations and permeability indicators, which was alleviated by glutamic acid supplementation. Moreover, the inhibition of DON on Akt/mTOR/4EBP1 signal pathway was reduced by glutamic acid supplementation. Collectively, these data suggest that glutamic acid may be a useful nutritional regulator for DON-induced damage manifested as oxidative stress, intestinal injury and signaling inhibition.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077692PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0100591PLOS

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