Hydrodynamic delivery of mIL10 gene protects mice from high-fat diet-induced obesity and glucose intolerance

Mol Ther. 2013 Oct;21(10):1852-61. doi: 10.1038/mt.2013.125. Epub 2013 Jun 18.

Abstract

High-fat diet (HFD) induced obesity is associated with low-grade inflammation, insulin resistance (IR), and glucose intolerance. The objective of this study is to assess the effect of interleukin 10 (IL10), an anti-inflammatory cytokine, on blocking HFD-induced obesity and obesity-associated metabolic disorders by hydrodynamic delivery of IL10-containing plasmid. Animals fed a regular chow or HFD received two injections (one on day 1 and the other on day 31) of plasmids containing green fluorescence protein (GFP) or mouse IL10 (mIL10) gene. Blood concentration of mIL10 reached ~200 ng/ml on day 7 in animals receiving mIL10 plasmid DNA. The transfection efficiency of liver cells was the same in animals fed a regular chow or HFD. No difference was seen in animals on regular chow when injected with plasmids containing either gfp or mIL10 gene. Overexpression of mIL10 prevented weight gain of animals on HFD. Intraperitoneal glucose tolerance test (IPGTT) and insulin tolerance tests (ITT) showed that mIL10 maintained insulin sensitivity and prevented glucose intolerance. The mechanistic study reveals that mIL10 suppressed macrophage infiltration and reduced the development of crown-like structures in adipose tissue (AT). Collectively, these results suggest that maintaining a higher level of IL10 through gene transfer could be an effective strategy in preventing diet-induced obesity.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adipose Tissue
  • Animals
  • Diet, High-Fat / adverse effects*
  • Drug Evaluation, Preclinical
  • Genetic Vectors
  • Glucose Intolerance* / genetics
  • Glucose Intolerance* / metabolism
  • Glucose Tolerance Test
  • Hydrodynamics
  • Interleukin-10 / genetics*
  • Interleukin-10 / physiology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Models, Animal
  • Obesity / prevention & control*
  • Plasmids
  • Transfection
  • Weight Gain

Substances

  • IL10 protein, mouse
  • Interleukin-10