ABSTRACT
The increase of circulating tissue factor pathway inhibitor (TFPI) in plasma by heparins
is thought to contribute to their overall antithrombotic activity. In a clinical study
in healthy volunteers, we recently found that the specific potency of a heparin to
mobilize TFPI from the vessel wall increases with its molecular weight (MW). The released
TFPI originally is not associated with lipoproteins, but it is not known whether it
remains free circulating in plasma. A further question is whether the MW of heparin
influences not only the release of TFPI but also its potential association with lipoproteins.
In the present study, the release of free TFPI was compared with the release of total
TFPI after application of four heparins with different MWs. Only the TFPI released
by unfractionated heparin (UFH) circulated completely as free TFPI. With decreasing
heparin MW, the percentage of released free TFPI on released total TFPI decreased
to 57%. As a consequence, the longer the heparin chains are, the better they are at
preventing the binding of the released, originally free, TFPI to plasma lipoproteins.
Because only free TFPI is known to exhibit anticoagulant activity, the activity of
released TFPI is better the higher the MW of the applied heparin is. In conclusion,
in addition to the potency of heparin to mobilize TFPI, there is its influence on
the circulating form, and thus the anticoagulant activity of the released TFPI depends
on its MW.
KEYWORD
TFPI - heparin - molecular weight - free TFPI - lipoproteins