Metabolic alterations associated with the antidiabetic effect of beta 3-adrenergic receptor agonists in obese mice

Am J Physiol. 1995 Apr;268(4 Pt 1):E678-84. doi: 10.1152/ajpendo.1995.268.4.E678.

Abstract

Treatment of obese (ob/ob) mice with the beta 3-adrenergic receptor (beta 3-AR) agonist BRL-35135 (1 mg.kg body wt-1.day-1 for 20 days) normalized plasma glucose levels and significantly decreased plasma insulin and nonesterified fatty acid levels. The time frame for the hypoglycemic effect, which reached a maximum after 10 days of treatment, paralleled an increase in brown adipose tissue DNA and protein content. The basal level of mRNA for the beta 3-AR and mitochondrial uncoupling protein was found to be markedly decreased in the ob/ob animals relative to the lean group. Chronic treatment of ob/ob mice for 20 days resulted in a twofold increase in beta 3-AR mRNA and a fivefold increase in uncoupling protein mRNA in brown adipose tissue relative to the placebo group. These findings indicate that chronic treatment of ob/ob animals with a beta 3-AR agonist results in proliferation of brown adipose tissue, with an upregulation of the beta 3-AR, which is associated with a decrease in plasma glucose, insulin, and nonesterified fatty acid levels.

MeSH terms

  • Adipose Tissue / drug effects
  • Adipose Tissue, Brown / drug effects
  • Adipose Tissue, Brown / pathology
  • Adrenergic beta-Agonists / pharmacology*
  • Animals
  • Carrier Proteins / genetics
  • Cell Division
  • Diabetes Mellitus / prevention & control*
  • Female
  • Glucose Transporter Type 4
  • Heart / drug effects
  • Ion Channels
  • Membrane Proteins / genetics
  • Mice
  • Mice, Obese
  • Mitochondrial Proteins
  • Monosaccharide Transport Proteins / genetics
  • Muscle Proteins*
  • Muscle, Skeletal / drug effects
  • RNA, Messenger / metabolism
  • Receptors, Adrenergic, beta / genetics
  • Time Factors
  • Uncoupling Protein 1

Substances

  • Adrenergic beta-Agonists
  • Carrier Proteins
  • Glucose Transporter Type 4
  • Ion Channels
  • Membrane Proteins
  • Mitochondrial Proteins
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • RNA, Messenger
  • Receptors, Adrenergic, beta
  • Slc2a4 protein, mouse
  • Uncoupling Protein 1