Summary
1. A simple and reproducible technique for measuring the clottability of plasma fibrinogen
using iodinated fibrinogen is described, the coefficient of variance being less than
1 %.
2. In vivo experiments in rabbits and monkeys on one hand and in vitro studies with fibrinogens from various species on the other indicated that :
a) Aliquots of a fibrinogen preparation iodinated at the same mean substitution level
yield practically identical coagulabilities ;
b) Aliquots of one labelled preparation when injected into several healthy animals
or mixed with their plasmas give equal values for clottability;
c) In normal animals, the clottable proportion of the circulating protein-bound radioactivity
is at any time a function of the extra/intravascular distribution and of the catabolic
rate of fibrinogen relative to the corresponding values of the contaminating labelled
protein.
3. The significance of the behaviour of the non-clottable protein-bound radioactivities
during fibrinogen turnover experiments for the catabolic mechanism is discussed. It
is suggested that fibrinogen catabolism is probably an intracellular process.