Effects of chromium supplementation on glycogen synthesis after high-intensity exercise

Med Sci Sports Exerc. 2006 Dec;38(12):2102-9. doi: 10.1249/01.mss.0000235353.09061.54.

Abstract

Purpose: Chromium enhances insulin signaling and insulin-mediated glucose uptake in cultured cells. We investigated the effect of chromium on glycogen synthesis and insulin signaling in humans.

Methods: Sixteen overweight men (BMI = 31.1 +/- 3.0 kg.m) were randomly assigned to supplement with 600 microg.d chromium as picolinate (Cr; N = 8) or a placebo (Pl; N = 8). After 4 wk of supplementation, subjects performed a supramaximal bout of cycling exercise to deplete muscle glycogen, which was followed by high-glycemic carbohydrate feedings for the next 24 h. Muscle biopsies were obtained at rest, immediately after exercise, and 2 and 24 h after exercise.

Results: Elevations in glucose and insulin during recovery were not different, but the lactate response was significantly higher in Cr. There was a significant depletion in glycogen immediately after exercise, an increase at 2 h, and a further increase above rest at 24 h (P < 0.05). The rate of glycogen synthesis during the 2 h after exercise was not different between groups (Cr: 25.8 +/- 8.0 and Pl: 17.1 +/- 4.7 mmol.kg.h). Glycogen synthase activity was significantly increased immediately after exercise in both groups. Muscle phosphatidylinositol 3-kinase (PI 3-kinase) activity decreased immediately after exercise and increased at 2 h (P < 0.05), with a trend for a lower PI 3-kinase response in Cr (P = 0.08).

Conclusions: Chromium supplementation did not augment glycogen synthesis during recovery from high-intensity exercise and high-carbohydrate feeding, although there was a trend for lower PI 3-kinase activity.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Biopsy, Needle
  • Diet, Carbohydrate-Restricted
  • Dietary Supplements*
  • Double-Blind Method
  • Exercise Test*
  • Glycogen / biosynthesis*
  • Humans
  • Iron Chelating Agents / pharmacology*
  • Lactic Acid / blood
  • Male
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • Overweight
  • Phosphatidylinositol 3-Kinases / metabolism
  • Physical Endurance*
  • Picolinic Acids / pharmacology*
  • Time Factors

Substances

  • Iron Chelating Agents
  • Picolinic Acids
  • Lactic Acid
  • Glycogen
  • Phosphatidylinositol 3-Kinases
  • picolinic acid