Periodontal disease decreases insulin sensitivity and insulin signaling

J Periodontol. 2012 Jul;83(7):864-70. doi: 10.1902/jop.2011.110349. Epub 2011 Nov 16.

Abstract

Background: The purpose of this study is to investigate whether local inflammatory events, such as periodontal disease, are able to increase tumor necrosis factor-alpha (TNF-α) plasmatic concentration and decrease insulin sensitivity and insulin signaling in non-diabetic rats.

Methods: Forty-eight male Wistar rats (2 months old) were divided into two groups, with either ligature-induced periodontal disease (LPD) or control conditions (CN). Experiments were performed in both groups 28 days after ligature placement. Plasmatic concentration of glycemia and TNF-α (n = 10) were analyzed by the glucose oxidase and enzyme-linked immunosorbent assay method, respectively. Insulin sensitivity (n = 7) was measured using the insulin tolerance test. Insulin signal transduction (n = 7) was measured by pp185 tyrosine phosphorylation status in insulin-sensitive tissues using the Western blotting method.

Results: The LPD group showed decreased insulin sensitivity (P <0.05), although no glycemic alterations were noted (P >0.05). TNF-α plasmatic concentration was higher in LPD rats compared to CN rats. In addition, a decrease in the pp185 tyrosine phosphorylation status was observed after insulin stimulus in both white adipose and skeletal muscle tissues of the LPD group compared with the CN group.

Conclusions: LPD is able to cause alterations to both insulin signaling and insulin sensitivity, probably because of the elevation of TNF-α plasmatic concentration. Thus, the present results emphasize the importance of the prevention of local inflammatory diseases, such as periodontitis, to prevent diabetes mellitus.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes, White / drug effects
  • Adipocytes, White / enzymology
  • Alveolar Bone Loss / diagnostic imaging
  • Alveolar Bone Loss / pathology
  • Alveolar Process / diagnostic imaging
  • Alveolar Process / pathology
  • Animals
  • Blood Glucose / analysis
  • Gingival Recession / pathology
  • Insulin / blood*
  • Insulin / pharmacology
  • Insulin Receptor Substrate Proteins / pharmacology
  • Insulin Resistance / physiology*
  • Male
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / enzymology
  • Periodontitis / blood*
  • Periodontitis / pathology
  • Phosphorylation
  • Radiography
  • Rats
  • Rats, Wistar
  • Receptor, Insulin / drug effects
  • Signal Transduction / physiology*
  • Tooth Cervix / diagnostic imaging
  • Tooth Cervix / pathology
  • Tumor Necrosis Factor-alpha / blood*

Substances

  • Blood Glucose
  • IRS1 protein, human
  • IRS2 protein, human
  • Insulin
  • Insulin Receptor Substrate Proteins
  • Tumor Necrosis Factor-alpha
  • Receptor, Insulin