Matrix metalloproteinase-9 is increased in obese subjects and decreases in response to pioglitazone

J Clin Endocrinol Metab. 2010 Jun;95(6):2993-3001. doi: 10.1210/jc.2009-2623. Epub 2010 Apr 14.

Abstract

Context: The study investigated the regulation of matrix metalloproteinases (MMP)-9 in obesity-associated insulin resistance in humans.

Objectives: The objectives of the investigation were to study MMP-9 regulation by insulin resistance and pioglitazone treatment in impaired glucose tolerant subjects using adipose tissue biopsies and study the mechanism of MMP-9 regulation by pioglitazone in adipocyte cultures.

Research design: 86 nondiabetic, weight-stable subjects between 21 and 66 yr of age were recruited in a university hospital research center setting. All subjects underwent a sc adipose tissue incisional biopsy from the lower abdominal wall and insulin sensitivity testing using a frequently sampled iv glucose tolerance test. Impaired glucose-tolerant subjects were randomized to receive metformin or pioglitazone for 10 wk. To study the mechanism of MMP-9 regulation in adipocytes, cells were treated with pioglitazone or protein kinase C alpha antisense oligomers, and MMP-9 levels were examined.

Results: There was a positive correlation between MMP-9 and body mass index (r = 0.40, P < 0.01) and negative correlation between MMP-9 and insulin sensitivity (r = -0.46, P < 0.001). The improvement in insulin sensitivity from pioglitazone resulted in a 52 +/- 0.2% reduction in MMP-9 mRNA. Fractionation of adipose tissue indicated that MMP-9 was mostly in the stromal vascular fraction. Pioglitazone also decreased MMP-9 in 3T3-F442A adipocytes and THP1 macrophages. Coculture of adipocytes with macrophages augmented MMP-9 expression in adipocytes and pioglitazone decreased MMP-9 in both adipocytes and macrophages.

Conclusion: These data indicate that MMP-9 is elevated in insulin resistance and is reduced by pioglitazone.

Publication types

  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adipocytes / drug effects
  • Adipocytes / enzymology
  • Adipose Tissue / enzymology
  • Adult
  • Aged
  • Blotting, Western
  • Body Mass Index
  • Cells, Cultured
  • Coculture Techniques
  • Female
  • Humans
  • Hypoglycemic Agents / therapeutic use*
  • Insulin Resistance
  • Male
  • Matrix Metalloproteinase 9 / biosynthesis
  • Matrix Metalloproteinase 9 / metabolism*
  • Matrix Metalloproteinase Inhibitors*
  • Middle Aged
  • Obesity / enzymology*
  • Oligonucleotides / metabolism
  • Pioglitazone
  • Protein Kinase C-alpha / metabolism
  • RNA / biosynthesis
  • RNA / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stromal Cells / drug effects
  • Stromal Cells / enzymology
  • Th1 Cells / drug effects
  • Th1 Cells / enzymology
  • Thiazolidinediones / therapeutic use*
  • Transfection
  • Young Adult

Substances

  • Hypoglycemic Agents
  • Matrix Metalloproteinase Inhibitors
  • Oligonucleotides
  • Thiazolidinediones
  • RNA
  • Protein Kinase C-alpha
  • Matrix Metalloproteinase 9
  • Pioglitazone