Effects of α-ketoglutarate on energy status in the intestinal mucosa of weaned piglets chronically challenged with lipopolysaccharide

Br J Nutr. 2011 Aug;106(3):357-63. doi: 10.1017/S0007114511000249. Epub 2011 Feb 23.

Abstract

The present study determined whether α-ketoglutarate (AKG) might affect the expression of AMP-activated protein kinase (AMPK) and energy status in the intestinal mucosa of piglets challenged with Escherichia coli lipopolysaccharide (LPS). A total of eighteen piglets (weaned at 21 d of age) were allocated to one of three treatments: (1) non-challenged (control); (2) LPS-challenged (LPS); (3) LPS+1 % AKG (LPS+AKG). Piglets in the control and LPS groups were fed a maize- and soyabean meal-based diet, and the LPS+AKG group was fed the basal diet supplemented with 1 % AKG. On days 10, 12, 14 and 16 of the trial, piglets in the LPS and LPS+AKG groups were challenged with LPS (80 μg/kg body weight), whereas piglets in the control group received the same volume of sterile saline. Pigs were euthanised 24 h after the last administration of LPS or saline to obtain intestinal mucosae for biochemical analysis. Compared with the control group, LPS administration decreased (P < 0·05) the oxidation of AKG, oleic acid, glutamine and glucose in enterocytes, decreased concentrations of ATP in the duodenal and jejunal mucosae and decreased adenylate energy charge (AMP:ATP ratio) in the jejunal and ileal mucosae. Additionally, LPS treatment reduced (P < 0·05) mucosal concentrations of phosphorylated AMPK in the jejunum and ileum as well as acetyl-CoA carboxylase in all segments of the small intestine. The adverse effects of LPS were reversed by AKG. Collectively, these results indicate that dietary supplementation with 1 % AKG beneficially modulates the AMPK signalling pathway to improve energy status in the small intestine of LPS-challenged piglets.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • AMP-Activated Protein Kinases / metabolism*
  • Acetyl-CoA Carboxylase / metabolism
  • Adenosine Monophosphate / metabolism
  • Adenosine Triphosphate / metabolism*
  • Animals
  • Dietary Supplements
  • Enterocytes / metabolism*
  • Escherichia coli
  • Female
  • Glucose / metabolism
  • Glutamine / metabolism
  • Intestinal Diseases / chemically induced
  • Intestinal Diseases / drug therapy
  • Intestinal Diseases / metabolism*
  • Intestinal Mucosa / metabolism*
  • Intestine, Small / metabolism*
  • Ketoglutaric Acids / pharmacology*
  • Ketoglutaric Acids / therapeutic use
  • Lipopolysaccharides
  • Oleic Acid / metabolism
  • Oxidation-Reduction
  • Phosphorylation
  • Signal Transduction / drug effects
  • Swine
  • Weaning

Substances

  • Ketoglutaric Acids
  • Lipopolysaccharides
  • Glutamine
  • Oleic Acid
  • Adenosine Monophosphate
  • Adenosine Triphosphate
  • AMP-Activated Protein Kinases
  • Acetyl-CoA Carboxylase
  • Glucose