Beneficial and deleterious effects of hydroxycitrate in rats fed a high-fructose diet

Nutrition. 2006 Sep;22(9):905-12. doi: 10.1016/j.nut.2006.05.015. Epub 2006 Jul 10.

Abstract

Objective: The present study assessed whether long-term supplementation of a high-fructose diet with hydroxycitrate (HCA), an inhibitor of de novo lipogenesis that is widely used as a non-prescription dietary aid, decreases food intake, visceral fat accumulation, hypertriglyceridemia, and hyperinsulinemia in rats.

Methods: We examined the effects of HCA (1.8% of diet) on food intake, body weight gain, visceral fat accumulation, hypertriglyceridemia, and hyperinsulinemia in rats during a 4-wk period of ad libitum access to a 50% fructose diet after a 3-wk period of food restriction in which they lost about 20% of their body weight.

Results: HCA decreased food intake and weight gain throughout the test and reduced visceral fat accumulation compared with control rats fed ad libitum (CON). Rats that were pair-fed (PF) to the HCA rats showed similar decreases in weight gain and visceral fat. HCA did not ameliorate the hypertriglyceridemia induced by high-fructose feeding. HCA improved insulin sensitivity on day 10 in comparison with CON rats, but by day 27 insulin levels were similarly higher and liver glycogen levels were similarly lower in HCA and CON rats in comparison with PF rats. Liver lipid content was elevated in HCA rats compared with CON and PF rats.

Conclusion: These findings indicate that, although HCA attenuates body weight gain and visceral fat accumulation by reducing food intake under these conditions, it has no lasting beneficial effects on hypertriglyceridemia and hyperinsulinemia and leads to the accumulation of liver lipids.

MeSH terms

  • Animals
  • Body Composition / drug effects
  • Body Composition / physiology
  • Citrates / administration & dosage*
  • Dietary Supplements
  • Drug Interactions
  • Energy Intake / drug effects*
  • Energy Intake / physiology
  • Fructose / administration & dosage*
  • Fructose / adverse effects
  • Hyperinsulinism / blood
  • Hyperinsulinism / drug therapy
  • Hypertriglyceridemia / blood
  • Hypertriglyceridemia / drug therapy
  • Intra-Abdominal Fat / drug effects*
  • Intra-Abdominal Fat / metabolism
  • Liver / drug effects
  • Liver / metabolism*
  • Male
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Weight Gain / drug effects*
  • Weight Gain / physiology

Substances

  • Citrates
  • Fructose
  • hydroxycitric acid