The contribution of skeletal muscle tumor necrosis factor-alpha to insulin resistance and hypertension in fructose-fed rats

J Hypertens. 2000 Nov;18(11):1605-10. doi: 10.1097/00004872-200018110-00011.

Abstract

Objective: The aim of this study was to determine the role of tumor necrosis factor-alpha (TNF-alpha) in skeletal muscle tissue in insulin resistance and hypertension and the effect of anti-hypertensive medicine on skeletal muscle TNF-alpha in fructose-induced insulin-resistant and hypertensive rats (fructose-fed rats: FFR).

Design and methods: Six-week-old male Sprague-Dawley rats were fed either normal rat chow or fructose-rich chow. For the last 2 weeks of a 6-week period of either diet, the rats were treated with a vehicle (control or FFR); temocapril, an angiotensin converting enzyme inhibitor (ACEI); or CS-866, an angiotensin II type 1 receptor blocker (ARB). The euglycemic hyperinsulinemic glucose clamp technique was performed to evaluate insulin sensitivity (M value). TNF-alpha levels in soleus and extensor digitorum longus (EDL) muscles and epididymal fat pads were measured. We also measured the TNF-alpha concentration in an incubated medium secreted from soleus muscle strips with or without angiotensin II.

Results: TNF-alpha levels were significantly higher in the soleus and EDL muscles, but not in the epididymal fat, in the FFRs compared with the control rats. Temocapril and CS-866 lowered systolic blood pressure, improved insulin resistance, and reduced TNF-alpha in both skeletal muscles. There were significant negative correlations between M values and TNF-alpha levels in both soleus and EDL muscles. Also, the soleus muscle strip incubation with 10(-7) mol/l angiotensin II increased TNF-alpha secreted into the incubation medium compared to the incubation without angiotensin II. These results suggest that skeletal muscle TNF-alpha is linked to insulin resistance and hypertension and that angiotensin II may be one of the factors that regulate skeletal muscle TNF-alpha.

MeSH terms

  • Adipose Tissue / metabolism
  • Angiotensin-Converting Enzyme Inhibitors / pharmacology
  • Animals
  • Blood Glucose
  • Blood Pressure / drug effects
  • Blood Pressure / physiology
  • Body Weight
  • Epididymis / metabolism
  • Fructose / pharmacology*
  • Glucose Clamp Technique
  • Heart Rate / drug effects
  • Heart Rate / physiology
  • Hypertension / metabolism*
  • Imidazoles / pharmacology
  • Insulin Resistance / physiology*
  • Male
  • Muscle, Skeletal / metabolism*
  • Olmesartan Medoxomil
  • Rats
  • Rats, Sprague-Dawley
  • Tetrazoles / pharmacology
  • Thiazepines / pharmacology
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Blood Glucose
  • Imidazoles
  • Tetrazoles
  • Thiazepines
  • Tumor Necrosis Factor-alpha
  • Fructose
  • Olmesartan Medoxomil
  • temocapril hydrochloride