Increased platelet arachidonic acid metabolism in diabetes mellitus.

P V Halushka, R Mayfield, H J Wohltmann, R C Rogers, A K Goldberg, S A McCoy, C B Loadholt, J A Colwell
Author Information

Abstract

Platelets obtained from some diabetic patients show enhanced in vitro Platelet aggregation. This study sought to determine if platelet obtained from insulin-dependent diabetic subjects synthesize increased quantities of the labile aggregating substance, thromboxane A2 (TXA2), and if it may play a role in the enhanced Platelet aggregation. Arachidonic acid (1 mM)-stimulated TXA2 synthesis, as determined via radioimmunoassay of its stable metabolite TXB2, was significantly greater (P less than 0.01, N = 12) in platelet-rich plasma obtained from diabetics compared with matched controls. Arachidonic acid-stimulated TXB2 synthesis in the diabetic platelet-rich plasma was positively correlated with the ambient fasting plasma glucose (r = 0.61, P less than 0.02, N = 15). Platelet aggregation induced by Arachidonic acid (0.4-0.8 mM) was inhibited significantly less by 13-azaprostanoic acid (P less than 0.04, N = 14), a competitive antagonist of the actions of prostaglandin H2 or TXA2 on platelets, compared with matched controls. The results support the notion that platelets obtained from some insulin-dependent diabetic subjects manifest increased synthesis of TXA2, which may contribute to the enhanced Platelet aggregation.

Grants

  1. GM20387/NIGMS NIH HHS

MeSH Term

Arachidonic Acid
Arachidonic Acids
Blood Glucose
Blood Platelets
Diabetes Mellitus
Epinephrine
Humans
Kinetics
Platelet Aggregation
Prostanoic Acids
Thromboxane B2

Chemicals

Arachidonic Acids
Blood Glucose
Prostanoic Acids
Arachidonic Acid
Thromboxane B2
13-azaprostanoic acid
Epinephrine

Word Cloud

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