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

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.
AuthorsJ C Russell, R M Amy, S E Graham, P J Dolphin, G O Wood, J Bar-Tana
JournalArteriosclerosis, thrombosis, and vascular biology (Arterioscler Thromb Vasc Biol) Vol. 15 Issue 7 Pg. 918-23 (Jul 1995) ISSN: 1079-5642 [Print] United States
PMID7600124 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Lipids
  • Palmitic Acids
  • MEDICA 16
Topics
  • Animals
  • Aorta (pathology)
  • Arteriosclerosis (pathology, prevention & control)
  • Body Weight
  • Cardiomyopathies (pathology, prevention & control)
  • Endothelium, Vascular (pathology)
  • Lipids (blood)
  • Macrophages (pathology)
  • Male
  • Microscopy, Electron, Scanning
  • Palmitic Acids (therapeutic use)
  • Pancreas (pathology)
  • Rats
  • Rats, Mutant Strains

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