Diurnal changes in intestinal apolipoprotein A-IV and its relation to food intake and corticosterone in rats

Am J Physiol Gastrointest Liver Physiol. 2005 Jan;288(1):G48-53. doi: 10.1152/ajpgi.00064.2004. Epub 2004 Aug 26.

Abstract

To further investigate the role of intestinal aplipoprotein A-IV (apo A-IV) in the management of daily food intake, we examined the diurnal patterns in apo A-IV gene and protein expression in freely feeding (FF) and food-restricted (FR; food provided 4 h daily for 4 wk) rats that were killed at 3-h intervals throughout the 24-h diurnal cycle. In FF rats, the intestinal apo A-IV mRNA and protein levels showed a circadian rhythm concomitant with the feeding pattern. The daily pattern of fluctuation of apo A-IV, however, was altered in FR rats, which had a marked increase in intestinal apo A-IV levels during the 4-h feeding period of light phase. In both FF and FR rats, increased plasma corticosterone (Cort) levels temporally coincided with the increasing phase of intestinal apo A-IV mRNA and protein expression. Depletion of Cort by adrenalectomy abolished the diurnal rhythm by decreasing the apo A-IV expression during the dark period but did not change the feeding rhythm. Exposure of adrenalectomized rats to consistent Cort level (50-mg continuous release Cort pellet) resulted in fixed apo A-IV levels throughout the day. These results indicate that intestinal apo A-IV exhibits a diurnal rhythm, which can be regulated by endogenous Cort independently of the light-dark cue. The fact that intestinal apo A-IV levels were consistent with the food intake during the normal diurnal cycle as well as during the cycle of 4-h feeding each day suggests that intestinal apo A-IV is involved in the regulation of daily food intake.

Publication types

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

MeSH terms

  • Animals
  • Antioxidants / analysis*
  • Antioxidants / pharmacology*
  • Apolipoproteins A / analysis*
  • Apolipoproteins A / pharmacology*
  • Circadian Rhythm*
  • Corticosterone / pharmacology
  • Feeding Behavior / physiology*
  • Male
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Antioxidants
  • Apolipoproteins A
  • apolipoprotein A-IV
  • Corticosterone