The generation of fibrinopeptide A in clinical blood samples: evidence for thrombin activity.
Open Access
- 1 November 1976
- journal article
- research article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 58 (5) , 1136-1144
- https://doi.org/10.1172/jci108566
Abstract
Plasma fibrinopeptide A (FPA) concentrations were measured in clinical blood samples incubated in the collecting syringe for different time periods before addition to heparin and Trasylol, and the rate of in vitro generation of FPA was calculated as the mean increment in FPA concentration per minute over the linear portion of the generation curve. 36 normal individuals had a mean plasma FPA level of 0.64 +/- 0.56 pmol/ml and an FPA generation rate of less than 0.5 pmol/ml per min. Clinical samples with elevated plasma FPA levels manifested slow (less than 1 pmol/ml per min) (28 patients) or rapid FPA generation (greater than 1 pmol/ml per min) (33 patients). Slow FPA generation was found in 10/10 patients with venous thrombosis, in 4/4 with aortic aneurysm, and in several patients with acquired hypofibrinogenemia. In one such patient, addition of fibrinogen resulted in rapid FPA generation whereas thrombin addition was without effect. Rapid FPA generation was generally linear, was usually associated with slower fibrinopeptide B generation and was inhibited by parenteral or in vitro heparin. It is thought to reflect increased thrombin activity and was seen in patients with pulmonary embolism, active systemic lupus erythematosus, renal transplant rejection, and after infusion of prothrombin concentrates. The initial rate of FPA cleavage by thrombin at fibrinogen concentrations from 0.05 to 4 mg/ml showed little change between 2 and 4 mg/ml with a Km of 2.99 muM. At a fibrinogen concentration of 2.5 mg/ml the FPA cleavage rate was 49.2 +/- 1.6 nmol/ml per min per U of thrombin. Exogenous thrombin added to normal blood generated 21.7 nmol/ml per U of thrombin FPA in the first minute with a nonlinear pattern reflecting inactivation of thrombin and the presence of alternative substrates. Hence, the thrombin concentration in the blood cannot be calculated from the FPA generation rate. The FPA generation rates in clinical samples with rapid generation (1-28 pmol/ml per min) could be produced by 2 X 10(-5) to 5.6 X 10(-4) thrombin U/ml acting on purified fibrinogen at physiological conditions of pH, ionic strength, and temperature.This publication has 24 references indexed in Scilit:
- Fibrinopeptide A in plasma of normal subjects and patients with disseminated intravascular coagulation and systemic lupus erythematosus.Journal of Clinical Investigation, 1976
- Radioimmunoassay of fibrinopeptide A - clinical applicationsThrombosis Research, 1976
- Radioimmunoassay of human fibrinopeptide B and kinetics of fibrinopeptide cleavage by different enzymes.Journal of Clinical Investigation, 1975
- An alternative pathway for fibrinolysis. I. The cleavage of fibrinogen by leukocyte proteases at physiologic pH.Journal of Clinical Investigation, 1975
- Plasma and serum antithrombin - III: Differentiation by crossed immunoelectrophoresisThrombosis Research, 1975
- Fibrinopeptide a immunoreactivity in human plasmaThrombosis Research, 1974
- Measurement of Fibrinopeptide A in Human BloodJournal of Clinical Investigation, 1974
- Degradation of Human Fibrinogen by Plasma α2-Macroglobulin-Enzyme ComplexesJournal of Clinical Investigation, 1973
- Activated Coagulation Factors: In-Vivo and in-Vitro StudiesBritish Journal of Haematology, 1969
- Human fibrinopeptides isolation, characterization and structureBiochimica et Biophysica Acta (BBA) - General Subjects, 1966