Increased Hepatic Insulin Sensitivity in Mice Lacking Inhibitory Leptin Receptor Signals

• Published in: Endocrinology (Philadelphia) 2011-06, Vol.152 (6), p.2237-2246
• Main Authors: Tom, Robby Zachariah, Sjögren, Rasmus J. O, Vieira, Elaine, Glund, Stephan, Iglesias-Gutiérrez, Eduardo, Garcia-Roves, Pablo M, Myers, Martin G, Björnholm, Marie
• Format: Article
• Language: English
• Subjects: Amino Acid Motifs; Animals; Biological and medical sciences; Clamps; Energy expenditure; Female; Females; Food intake; Fundamental and applied biological sciences. Psychology; Glucose; Glucose - metabolism; Glucose tolerance; Glucose transport; Homeostasis; Insulin; Insulin - metabolism; Insulina; Leptin; Leptin - metabolism; Leptina; Liver; Liver - metabolism; Liver diseases; Malalties del fetge; Male; Males; Medicin och hälsovetenskap; Mice; Mice (Laboratory animals); Mice, Knockout; Muscle, Skeletal - metabolism; Muscles; Mutation; Phosphorylation; Ratolins (Animals de laboratori); Receptors; Receptors, Leptin - chemistry; Receptors, Leptin - genetics; Receptors, Leptin - metabolism; Signal Transduction; Skeletal muscle; Tyrosine; Vertebrates: endocrinology
• ISSN: 0013-7227; 1945-7170; 1945-7170
• DOI: 10.1210/en.2010-0040

Signals emanating from leptin receptor Tyr985 control hepatic insulin sensitivity through increased insulin action on the suppression of hepatic glucose production. Leptin regulates food intake and energy expenditure by activating the long form of the leptin receptor (LepRb). Leptin also regulates glucose homeostasis by improving whole-body insulin sensitivity, but the mechanism remains undefined. Leptin action is mediated by phosphorylation of several tyrosine residues on LepRb. LepRb-Tyr985 plays an important role in the attenuation of LepRb signaling. We determined the contribution of LepRb-Tyr985-mediated signals to leptin action on insulin sensitivity using LepRb-Tyr985 mutant mice (l/l mice). Glucose tolerance and whole-body insulin-mediated glucose utilization were determined in wild-type (+/+) and l/l mice. Glucose tolerance was unaltered between female +/+ and l/l mice but enhanced in the male l/l mice. Serum insulin concentration was decreased at baseline and 15 min after a glucose injection in female l/l vs. +/+ mice (P < 0.05) but unaltered in the male l/l mice. However, basal and insulin-stimulated glucose transport in isolated soleus and extensor digitorum longus muscle was similar between +/+ and l/l mice, indicating skeletal muscle insulin sensitivity in vitro was not enhanced. Moreover, euglycemic-hyperinsulinemic clamps reveal hepatic, rather than peripheral, insulin sensitivity is enhanced in female l/l mice, whereas male l/l mice display both improved hepatic and peripheral insulin sensitivity. In conclusion, signals emanating from leptin receptor Tyr985 control hepatic insulin sensitivity in both female and male l/l mice. Lack of LepRb-Tyr985 signaling enhances whole-body insulin sensitivity partly through increased insulin action on the suppression of hepatic glucose production.