Activation of μ-opioid receptors improves insulin sensitivity in obese Zucker rats

• Published in: Life sciences (1973) 2007-03, Vol.80 (16), p.1508-1516
• Main Authors: Tzeng, Thing-Fong, Lo, Chia-Ying, Cheng, Juei-Tang, Liu, I-Min
• Format: Article
• Language: English
• Subjects: Analysis of Variance; Animals; Blood Glucose - metabolism; Immunoblotting; Immunoprecipitation; Insulin resistance; Insulin Resistance - physiology; Loperamide; Loperamide - pharmacology; Mice; Mice, Knockout; Naloxone; Obese Zucker rats; Rats; Rats, Zucker; Receptors, Opioid, mu - genetics; Receptors, Opioid, mu - metabolism; μ-Opioid receptors
• ISSN: 0024-3205; 1879-0631
• DOI: 10.1016/j.lfs.2007.01.016

In the current study we investigated the effect of μ-opioid receptor activation on insulin sensitivity. In obese Zucker rats, an intravenous injection of loperamide (18 μg/kg, three times daily for 3 days) decreased plasma glucose levels and the glucose–insulin index. Both effects of loperamide were subsequently inhibited by the administration of 10 μg/kg of naloxone or 10 μg/kg of naloxonazine, doses sufficient to block μ-opioid receptors. Other metabolic defects characteristic of obese Zucker rats, such as defects in insulin signaling, the decreased expression of insulin receptor substrate (IRS)-1, the p85 regulatory subunit of phosphatidylinositol 3-kinase (PI3 kinase), and the glucose transporter subtype 4 (GLUT 4), and the reduction of phosphorylation in IRS-1 or Akt serine, were also studied. These defects were all reversed by loperamide treatment in a dose which overcame μ-opioid receptor blockade. Moreover, loss of tolbutamide-induced plasma glucose lowering action (10 mg/kg) in wild-type mice given a fructose-rich diet was markedly delayed by repeated treatment with loperamide; however, this delay induced by loperamide did not occur in μ-opioid receptor knockout mice. These results indicate an important role of peripheral μ-opioid receptors in the loperamide-induced improvement of insulin sensitivity. Our results suggest that activation of peripheral μ-opioid receptors can ameliorate insulin resistance in animals, and provide a new target for therapy of insulin resistance.