Chronic hyper-leptinemia induces insulin signaling disruption in adipocytes: Implications of NOS2

Free Radic Biol Med. 2017 Nov:112:93-108. doi: 10.1016/j.freeradbiomed.2017.07.016. Epub 2017 Jul 22.

Abstract

Leptin, following its discovery, has developed a formidable interest in the scientific community to delineate its contribution towards overall metabolic homeostasis. Contradictory reports have been published on leptin administration effects on whole body insulin sensitivity. Following late reports, we surveyed human serum leptin levels along with other metabolic parameters including BMI and HOMA-IR. We found a positive correlation between leptin levels and insulin resistance parameters. Considering the presence of the long form of leptin receptor on adipocytes, we explored the effects of chronic physiological hyper-leptinemic exposure on adipocyte insulin sensitivity. Chronic leptin (50ng/ml) treatment in 3T3-L1 adipocytes decreased insulin-induced phosphorylation of nodal insulin signaling proteins along with reduced glucose uptake. Metabolic flux studies indicated mitochondrial dysfunction and reduced oxygen consumption rate. Leptin treatment also increased both cellular and mitochondrial superoxide levels concomitant to increased expression of nitric oxide synthase-2 (NOS2). Further, pharmacological depletion of NOS2 reversed leptin mediated effects on insulin signaling. In-vivo implantation of leptin osmotic pumps in C57BL/6 mice also decreased insulin responsiveness. Interestingly, these effects were lacking in NOS2 knockout strain. In conclusion, our studies put forward a potential link between leptin and adipocyte insulin responsiveness in an NOS2 dependent manner.

Keywords: Adipocyte; Insulin resistance; Leptin; NOS2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adolescent
  • Adult
  • Animals
  • Female
  • Gene Expression
  • Glucose / metabolism
  • Humans
  • Infusion Pumps, Implantable
  • Insulin / metabolism
  • Insulin / pharmacology
  • Insulin Resistance*
  • Leptin / genetics
  • Leptin / metabolism
  • Leptin / pharmacology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Middle Aged
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Mitochondria / pathology
  • Nitric Oxide Synthase Type II / deficiency
  • Nitric Oxide Synthase Type II / genetics*
  • Oxygen Consumption / drug effects
  • Phosphorylation / drug effects
  • Signal Transduction*

Substances

  • Insulin
  • Leptin
  • NOS2 protein, human
  • Nitric Oxide Synthase Type II
  • Glucose