Inhibition of atherosclerosis and myocardial lesions in the JCR:LA-cp rat by beta, beta'-tetramethylhexadecanedioic acid (MEDICA 16)

Arterioscler Thromb Vasc Biol. 1995 Jul;15(7):918-23. doi: 10.1161/01.atv.15.7.918.

Abstract

Atherosclerosis-prone, insulin-resistant JCR:LA-cp male rats were treated from 6 weeks to 39 weeks of age with beta,beta'-tetramethylhexadecanedioic acid (MEDICA 16). Body weights were reduced (13%, P < .001) at 36 weeks without any accompanying decrease in food consumption. The treatment did not cause any significant change in plasma glucose or fasting insulin concentrations. There was a significant decrease in the extreme hyperplasia of the islets of Langerhans (38%, P < .05). The marked VLDL hypertriglyceridemia was decreased by 70% (P < .001), with an accompanying significant reduction in cholesterol concentrations. The severity of raised atherosclerotic lesions on the aortic arch was very markedly reduced (P < .01) in treated rats. This was accompanied by a reduction (P < .01) in the incidence of ischemic myocardial lesions. We conclude that long-term (33 weeks) MEDICA 16 treatment of an animal model for the obesity/insulin-resistant/hyperlipidemic syndrome not only markedly improved lipid metabolism, but also inhibited the development of advanced cardiovascular disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aorta / pathology
  • Arteriosclerosis / pathology
  • Arteriosclerosis / prevention & control*
  • Body Weight
  • Cardiomyopathies / pathology
  • Cardiomyopathies / prevention & control*
  • Endothelium, Vascular / pathology
  • Lipids / blood
  • Macrophages / pathology
  • Male
  • Microscopy, Electron, Scanning
  • Palmitic Acids / therapeutic use*
  • Pancreas / pathology
  • Rats
  • Rats, Mutant Strains

Substances

  • Lipids
  • Palmitic Acids
  • MEDICA 16