AJP Legacy Watch the video to learn how APS reaches out to developing nations.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol 209: 415-424, 1965;
0002-9513/65 $5.00
This Article
Right arrow Full Text (PDF)
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hirsh, J.
Right arrow Articles by Sherry, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hirsh, J.
Right arrow Articles by Sherry, S.

Effect of fibrin and fibrinogen proteolysis products on clot physical properties

Jack Hirsh 1, Anthony P. Fletcher 1, and Sol Sherry 1

1 Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri

Clot formation in the presence of plasmin-stable proteolysis products of fibrinogen and fibrin was studied by thromboelastography and by a modified light-scattering method. Thromboelastography demonstrated that both types of proteolysis products lengthened the "r" and "k" values and decreased "ma" values; these findings were interpreted as demonstrating delayed fibrin formation and reduced clot tensile strength. Light-scattering measurements demonstrated that both sets of products inhibited fibrin polymerization rates. Neither qualitative nor quantitative differences were detected between the actions of fibrin or fibrinogen proteolysis products, and the degree of alteration in functional clotting parameters and in clot tensile strength was proportional to proteolysis product concentration. Platelet function tests, including clot retraction tests, microscopic and turbidometric measurement of thrombin, and ADP-induced platelet aggregation, were uninfluenced by plasmin-stable proteolysis products. Most conventional plasma fibrinogen assays yielded artifactually low values when the plasma contained proteolysis products, but the accuracy of a modified Ratnoff and Menzie procedure was unaffected in these circumstances. A rapid immunological assay (Fi test) also proved satisfactory.

Key Words: defective fibrin polymerization • fibrin proteolysis • clot tensile strength • thromboelastography • delayed polymerization • platelet aggregation • coagulation defect

Submitted on January 18, 1965







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 1965 by the American Physiological Society.