Effect of Dextran on Factor VIII (Antihemophilic Factor) and Platelet Function
- 1 February 1979
- journal article
- Published by Wolters Kluwer Health in Annals of Surgery
- Vol. 189 (2) , 243-247
- https://doi.org/10.1097/00000658-197902000-00017
Abstract
Three different properties of factor VIII (antihemophilic globulin) were studied after infusion of 500 ml of six per cent Dextran 70 to healthy volunteers. This dose caused no change in the factor VIII coagulant activity while there was a significant but temporary decrease of factor VIII related antigen. The Ristocetin induced platelet aggregation analysed with native as well as with formalin-fixed platelets, also decreased significantly. The maximal decrease was found a few hours after the infusion. The decrease was seen only if Dextran was infused in vivo and not if Dextran was added to blood in vitro. The dysfunction of factor VIII caused by Dextran resembles that found in one variant of von Willebrand's disease. This finding probably explains the platelet function inhibiting properties of Dextran, and may be of significance for its antithrombotic effects.Keywords
This publication has 20 references indexed in Scilit:
- A method for measuring plasma ristocetin cofactor activity—normal distribution and stability during storageThrombosis Research, 1978
- EFFECTS OF PORCINE PLASMIN ON COAGULATION AND FIBRINOLYTIC SYSTEMS IN HUMANS1978
- Platelet Physiology and Abnormalities of Platelet FunctionNew England Journal of Medicine, 1975
- Studies of the human factor VIII/von Willebrand's factor protein. II. Identification and characterization of the von Willebrand protein.1975
- Von Willebrand’s Disease with Normal Factor VIII Activity in a HomozygotePathophysiology of Haemostasis and Thrombosis, 1974
- Quantitative Assay of a Plasma Factor Deficient in von Willebrand's Disease that is Necessary for Platelet Aggregation. RELATIONSHIP TO FACTOR VIII PROCOAGULANT ACTIVITY AND ANTIGEN CONTENTJournal of Clinical Investigation, 1973
- Isolation and Characterization of Human Factor VIII (Antihemophilic Factor)Journal of Biological Chemistry, 1973
- Genetic Variants of von Willebrand's DiseaseBMJ, 1972
- EFFECTS OF DEXTRAN INFUSION ON THE ADHESIVENESS OF HUMAN BLOOD-PLATELETSThe Lancet, 1966
- Determination of Fibrinogen and Fibrinogenolytic ActivityThrombosis and Haemostasis, 1962