Partial inhibition of adipose tissue lipolysis improves glucose metabolism and insulin sensitivity without alteration of fat mass

PLoS Biol. 2013;11(2):e1001485. doi: 10.1371/journal.pbio.1001485. Epub 2013 Feb 19.

Abstract

When energy is needed, white adipose tissue (WAT) provides fatty acids (FAs) for use in peripheral tissues via stimulation of fat cell lipolysis. FAs have been postulated to play a critical role in the development of obesity-induced insulin resistance, a major risk factor for diabetes and cardiovascular disease. However, whether and how chronic inhibition of fat mobilization from WAT modulates insulin sensitivity remains elusive. Hormone-sensitive lipase (HSL) participates in the breakdown of WAT triacylglycerol into FAs. HSL haploinsufficiency and treatment with a HSL inhibitor resulted in improvement of insulin tolerance without impact on body weight, fat mass, and WAT inflammation in high-fat-diet-fed mice. In vivo palmitate turnover analysis revealed that blunted lipolytic capacity is associated with diminution in FA uptake and storage in peripheral tissues of obese HSL haploinsufficient mice. The reduction in FA turnover was accompanied by an improvement of glucose metabolism with a shift in respiratory quotient, increase of glucose uptake in WAT and skeletal muscle, and enhancement of de novo lipogenesis and insulin signalling in liver. In human adipocytes, HSL gene silencing led to improved insulin-stimulated glucose uptake, resulting in increased de novo lipogenesis and activation of cognate gene expression. In clinical studies, WAT lipolytic rate was positively and negatively correlated with indexes of insulin resistance and WAT de novo lipogenesis gene expression, respectively. In obese individuals, chronic inhibition of lipolysis resulted in induction of WAT de novo lipogenesis gene expression. Thus, reduction in WAT lipolysis reshapes FA fluxes without increase of fat mass and improves glucose metabolism through cell-autonomous induction of fat cell de novo lipogenesis, which contributes to improved insulin sensitivity.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / drug effects
  • Adipose Tissue / metabolism*
  • Adipose Tissue, White / drug effects*
  • Adipose Tissue, White / metabolism
  • Adolescent
  • Adult
  • Aged
  • Animals
  • Glucose
  • Humans
  • Lipid Metabolism / drug effects*
  • Lipolysis / drug effects
  • Male
  • Mice
  • Middle Aged
  • Niacin / pharmacology
  • Sterol Esterase / metabolism
  • Young Adult

Substances

  • Niacin
  • Sterol Esterase
  • Glucose

Grants and funding

A.G. was supported by Inserm and Fondation pour la Recherche Médicale. Grants to D.L. from Agence Nationale de la Recherche (LIPOB and OBELIP projects), Région Midi-Pyrénées, GlaxoSmithKline, Inserm/DHOS, CHU de Toulouse, Fondation pour la Recherche Médicale, and the Commission of the European Communities (Projects HEPADIP, ADAPT and DIABAT). Grants to P.A. from the Swedish Research Council, the Swedish Diabetes Foundation, The Strategic Research Programme in Diabetes at Karolinska Institute, the Novo Nordisk Foundation, and the European Foundation for the Study of Diabetes/Lilly Programme. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.