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Circulating factors and insulin resistance. I. A novel myoinositol 1,2-cyclic phosphate phosphoglycan insulin antagonist from human plasma is elevated in noninsulin-dependent diabetes mellitus.

Abstract
A novel low mol wt inositol phosphoglycan inhibitor (M tau 1200-1500) of insulin action in rat adipocytes has been partially purified from normal human plasma. This inhibitor, termed fraction V after the first purification step and fraction V3 after the second, is different from other reported serum insulin antagonists. It contains myoinositol, galactosamine, and mannose in approximate molar ratios of 1:1:3.3. The myoinositol has a 1,2-cyclic phosphate substituent, which is essential for the inhibitory activity. Its inhibitory activity is significantly elevated (161%, P < 0.05 for fraction V; 278%, P < 0.05 for fraction V3) in plasma of humans with noninsulin-dependent diabetes mellitus as compared with plasma of nondiabetic controls. These findings represent the first report of a naturally occurring mammalian inositol 1,2-cyclic phosphate containing phosphoglycan related to insulin action.
AuthorsG T Galasko, Y Bao, S J Broomfield, N M Hooper, A J Turner, J Larner
JournalThe Journal of clinical endocrinology and metabolism (J Clin Endocrinol Metab) Vol. 80 Issue 8 Pg. 2419-29 (Aug 1995) ISSN: 0021-972X [Print] United States
PMID7629237 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Inositol Phosphates
  • Insulin
  • Insulin Antagonists
  • Lipids
  • Monosaccharides
  • Polysaccharides
  • inositol phosphate glycan
  • inositol cyclic phosphate
  • Inositol
Topics
  • Adipocytes (drug effects, metabolism)
  • Adult
  • Animals
  • Chromatography, Gel
  • Cohort Studies
  • Diabetes Mellitus, Type 2 (blood)
  • Female
  • Humans
  • Inositol (analysis)
  • Inositol Phosphates (analysis, blood, isolation & purification, pharmacology)
  • Insulin (pharmacology)
  • Insulin Antagonists (blood, isolation & purification, pharmacology)
  • Insulin Resistance
  • Lipids (biosynthesis)
  • Male
  • Middle Aged
  • Monosaccharides (analysis)
  • Polysaccharides (blood, isolation & purification, pharmacology)
  • Rats
  • Reference Values

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