Nutrient-specific feeding and endocrine effects of jejunal infusions in obese animals

Am J Physiol Regul Integr Comp Physiol. 2014 Mar 15;306(6):R420-8. doi: 10.1152/ajpregu.00410.2013. Epub 2014 Jan 22.

Abstract

Intestinal nutrient infusions result in variable decreases in food intake and body weight based on the nutrient type and the specific intestinal infusion site. We previously found that intrajejunal infusions of a fatty acid and glucose, but not casein hydrolysate, decreases food intake and body weight in lean chow-fed laboratory rats. To test whether obese, high fat-fed animals would show similar decreases in food intake and body weight in response to intrajejunal infusions of the same nutrients, equal kilocalorie loads of these nutrients (11.4 kcal) or vehicle were infused into the jejunum of obese, high fat-fed male Sprague-Dawley rats over 7 h/day for 5 consecutive days. Food intake was continuously monitored, and body weight was measured daily. After the infusion on the final day, rats were killed and plasma was collected. Similar to lean chow-fed rats, intrajejunal infusions of linoleic acid (LA) and glucose (Glu), but not casein hydrolysate (Cas), suppressed food intake with no compensatory increase in food intake after the infusion period. In contrast to lean chow-fed rats, only the LA, and not the Glu or Cas, produced decreases in body weight in the obese high fat-fed rat. There also were no differences in plasma glucagon-like peptide-1 levels in any of the nutrient infusion groups compared with saline infusion. These results suggest that there is a differential response to the same nutrients in lean vs. obese animals.

Keywords: food intake; glucagon-like peptide-1; intestinal infusion; obese.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Body Weight / physiology
  • Caseins / pharmacokinetics
  • Eating / physiology*
  • Endocrine System / physiology*
  • Enteral Nutrition / methods*
  • Glucagon-Like Peptide 1 / blood
  • Glucose / pharmacokinetics
  • Jejunum / metabolism*
  • Linoleic Acid / pharmacokinetics
  • Male
  • Obesity / metabolism
  • Obesity / physiopathology*
  • Peptide YY / blood
  • Rats
  • Rats, Sprague-Dawley
  • Satiation / physiology

Substances

  • Caseins
  • Peptide YY
  • casein hydrolysate
  • Glucagon-Like Peptide 1
  • Linoleic Acid
  • Glucose