Exercise training ameliorates glucosamine-induced insulin resistance in ovariectomized rats

Menopause. 2017 Jun;24(6):617-623. doi: 10.1097/GME.0000000000000811.

Abstract

Objective: Glucosamine (GlcN), which has been reported to induce insulin resistance (IR), is a popular nutritional supplement used to treat osteoarthritis in menopausal women. We previously demonstrated that GlcN treatment caused IR in ovariectomized rats by reducing the expression of glucose transport protein subtype 4 (GLUT-4) in skeletal muscle. In the present study, we hypothesized that endurance exercise training can reverse GlcN-induced IR.

Methods: Fifty female rats were randomly divided into five groups with 10 rats in each group: (1) sham-operated group; (2) sham-operated group with GlcN treatment for 14 days; (3) ovariectomy (OVX) group; (4) OVX with GlcN treatment; and (5) OVX with GlcN treatment followed by exercise training (running program) for 8 weeks.

Results: Fasting plasma glucose increased in the OVX + GlcN group, and fasting plasma insulin and the homeostasis model assessment-insulin resistance (HOMA-IR) were significantly higher only in this group. After the rats received exercise training for 8 weeks, no increase in the fasting plasma glucose, insulin, or HOMA-IR was observed. In an intraperitoneal glucose tolerance test, the plasma glucose, plasma insulin, HOMA-IR, and glucose-insulin index were significantly elevated only in the OVX with GlcN treatment group. However, the plasma glucose, plasma insulin, HOMA-IR, and glucose-insulin index decreased after exercise training for 8 weeks, implying that GlcN-induced IR in OVX rats could be reversed through exercise. A histological analysis revealed that exercise training can reduce islet hypertrophy and maintain GLUT-4 in skeletal muscle.

Conclusions: Exercise training can alleviate IR in OVX rats treated with GlcN. Islet hyperplasia was subsequently prevented. Preserving GLUT-4 expression may be one of the mechanisms by which exercise prevents IR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / analysis
  • Fasting
  • Female
  • Glucosamine / pharmacology*
  • Glucose Tolerance Test
  • Glucose Transporter Type 4 / analysis
  • Hypertrophy
  • Insulin / blood
  • Insulin Resistance / physiology*
  • Islets of Langerhans / drug effects
  • Islets of Langerhans / pathology
  • Muscle, Skeletal / chemistry
  • Muscle, Skeletal / drug effects
  • Ovariectomy*
  • Physical Conditioning, Animal / physiology*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Blood Glucose
  • Glucose Transporter Type 4
  • Insulin
  • Glucosamine