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Updated: Aug 13, 2026

Ferric Chloride-induced Thrombosis Mouse Model on Carotid Artery and Mesentery Vessel
Published on: June 29, 2015
Choline inhibition of prothrombin activation
R D Leach1, S A DeWind, C W Slattery
1Department of Biochemistry, School of Medicine, Loma Linda University, California 92350.
A new spectrophotometric assay accurately measures thrombin generation kinetics. This method quantizes prothrombin activation, offering precise insights into blood coagulation processes.
Area of Science:
- Biochemistry
- Biophysical Chemistry
- Enzymology
Background:
- Prothrombin activation is central to blood coagulation.
- Accurate kinetic assays are crucial for studying coagulation factor interactions.
Purpose of the Study:
- To develop a computer-interfaced spectrophotometric kinetic assay for prothrombin activation.
- To characterize the kinetics of thrombin generation and inhibition.
Main Methods:
- Coupling thrombin production to a chromogenic substrate (S-2238) for spectrophotometric detection.
- Utilizing linear regression analysis of absorbance data to quantify thrombin production.
- Investigating the effects of factor Xa and choline on prothrombin activation kinetics.
Main Results:
- The assay demonstrated high linearity (R² > 0.99) for thrombin production.
- Factor Xa exhibited Michaelis-Menten kinetics with varying prothrombin concentrations.
- Choline acted as a mixed-type inhibitor, with apparent Ki and Ki' values determined in the presence and absence of factor Va.
Conclusions:
- The developed assay provides a reliable method for measuring thrombin generation.
- Choline's inhibitory effect on prothrombin activation is characterized, offering potential therapeutic targets.
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