The activation of factor VII in citrated plasma by charged long-chain saturated fatty acids at the interface of large triglyceride-rich lipoproteins

Blood Coagul Fibrinolysis. 1993 Dec;4(6):943-51.

Abstract

The prolonged incubation of dilute plasma on ice in the presence of added sulphatide vesicles or the long-chain saturated fatty acids (FA) stearic acid (C18:0) or behenic acid (C22:0) induced a concentration-dependent increase in factor VII coagulant activity (VIIc). The addition of FA at various ratios to human serum albumin showed the micellar non-bound pool to be responsible for this effect, FA bound to the high-affinity or low-affinity binding sites of albumin having no influence on VIIc. Plasma VIIc also increased following addition of behenate-enriched lipoprotein particles produced by incubation of the d < 1.006 g/ml lipoprotein fraction with this FA, or addition of lipoprotein remnants produced by pre-incubation of the d < 1.006 g/ml fraction with lipoprotein lipase. Long-chain saturated fatty acids in the interface of lipoprotein remnants, produced by the interaction of triglyceride-rich lipoprotein particles with lipoprotein lipase, appear to provide a surface that activates the contact system of coagulation and subsequently factor VII.

MeSH terms

  • Anticoagulants
  • Citrates
  • Citric Acid
  • Factor VII / metabolism*
  • Fatty Acids / chemistry
  • Fatty Acids / pharmacology*
  • Female
  • Humans
  • Hydrogen-Ion Concentration
  • Lipoprotein Lipase / pharmacology
  • Lipoproteins / chemistry*
  • Lipoproteins, VLDL / chemistry
  • Lipoproteins, VLDL / pharmacology
  • Liposomes
  • Plasma
  • Pregnancy
  • Serum Albumin
  • Sulfoglycosphingolipids
  • Triglycerides / analysis*

Substances

  • Anticoagulants
  • Citrates
  • Fatty Acids
  • Lipoproteins
  • Lipoproteins, VLDL
  • Liposomes
  • Serum Albumin
  • Sulfoglycosphingolipids
  • Triglycerides
  • Citric Acid
  • Factor VII
  • Lipoprotein Lipase
  • behenic acid