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Clin Ther ; 6(5): 636-42, 1984.
Article in English | MEDLINE | ID: mdl-6206948

ABSTRACT

Plasma levels of beta-thromboglobin (beta-TH) and of thromboxane B2 (TXB2) and 6-keto-prostaglandin F1-alpha, the stable metabolites of thromboxane A2 and prostacyclin, were determined by radioimmunoassay methods in eight patients with noninsulin-dependent diabetes before and after dietary treatment and after administration of the sulfonylurea drug glibenclamide. Blood examinations were performed when hyperglycemia was detected for the first time, four weeks after a dietary regimen was started, and four and eight weeks after glibenclamide treatment was begun. Drug treatment was instituted because, despite a suitable diet, patients' postprandial blood sugar was higher than 8 mmol/L (145 mg/dl). At the initial examination, elevated TXB2 and beta-TH levels indicating platelet hyperactivity and hyperglycemia were found. TXB2 and beta-TH levels decreased significantly after glibenclamide treatment was started, as did the blood glucose level. There was no change in 6-keto-PGF1-alpha. We interpret these results to indicate that diabetes is associated with hyperactivity of platelet aggregation and that control of blood glucose is important because a lower blood glucose level attenuates platelet hyperactivity. Whether the decrease in platelet hyperactivity is a direct result of the lowered blood sugar or reflects the influence of the drug treatment requires clarification.


Subject(s)
6-Ketoprostaglandin F1 alpha/blood , Beta-Globulins/analysis , Diabetes Mellitus, Type 2/blood , Glyburide/therapeutic use , Thromboxane B2/blood , Thromboxanes/blood , beta-Thromboglobulin/analysis , Adult , Blood Glucose/analysis , Blood Platelets/metabolism , Diabetes Mellitus, Type 2/diet therapy , Diabetes Mellitus, Type 2/drug therapy , Female , Humans , Male , Middle Aged , Platelet Aggregation , Radioimmunoassay
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