Low anticoagulant activity of high sulphated heparan sulphates

Two high sulphated heparin-like polysaccharides (L1, MW 16,000 and L2, MW 11,700) were isolated from rat liver tissues, after DEAE-cellulose chromatography. Heparan sulphates from heart and lung tissues were isolated for comparison and fractionated according to their molecular weight. The anticoagul...

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Autores principales: Kovensky, J., Sassetti, B., Fernandez Cirelli, A., Kordich, L.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_03406245_v63_n3_p488_Kovensky
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spelling todo:paper_03406245_v63_n3_p488_Kovensky2023-10-03T15:25:46Z Low anticoagulant activity of high sulphated heparan sulphates Kovensky, J. Sassetti, B. Fernandez Cirelli, A. Kordich, L. anticoagulant agent heparan sulfate heparin proteoglycan article gel chromatography human priority journal rat Animal Anticoagulants Glycosaminoglycans Heparan Sulfate Proteoglycan Heparitin Sulfate Liver Proteochondroitin Sulfates Rats Support, Non-U.S. Gov't Two high sulphated heparin-like polysaccharides (L1, MW 16,000 and L2, MW 11,700) were isolated from rat liver tissues, after DEAE-cellulose chromatography. Heparan sulphates from heart and lung tissues were isolated for comparison and fractionated according to their molecular weight. The anticoagulant activities in vitro were studied using clotting antifactor Xa, antifactor IIa, and APTT assay methods, falling in a narrow range (5-44 IU/mg) although the wide variability in molecular weight and sulphate content. The heparan sulphate nature of fractions L1 and L2 (sulphate/disaccharide ratio 2.05 and 2.48, respectively) has been verified by: a) low iduronic/glucuronic acid ratio; b) nitrous acid degradataion followed by gel chromatography; c) heparinase treatment followed by gel chromatography; d) electrophoretic behaviour. Native proteoglycans have been isolated and the glycosidic chains compared with L1 and L2. Their anticoagulant activities in vitro and the fact that antiXa clotting activity was not neutralized by protamine sulphate are in accordance with the results of structural studies. Fil:Kovensky, J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Sassetti, B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Fernandez Cirelli, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Kordich, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03406245_v63_n3_p488_Kovensky
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic anticoagulant agent
heparan sulfate
heparin
proteoglycan
article
gel chromatography
human
priority journal
rat
Animal
Anticoagulants
Glycosaminoglycans
Heparan Sulfate Proteoglycan
Heparitin Sulfate
Liver
Proteochondroitin Sulfates
Rats
Support, Non-U.S. Gov't
spellingShingle anticoagulant agent
heparan sulfate
heparin
proteoglycan
article
gel chromatography
human
priority journal
rat
Animal
Anticoagulants
Glycosaminoglycans
Heparan Sulfate Proteoglycan
Heparitin Sulfate
Liver
Proteochondroitin Sulfates
Rats
Support, Non-U.S. Gov't
Kovensky, J.
Sassetti, B.
Fernandez Cirelli, A.
Kordich, L.
Low anticoagulant activity of high sulphated heparan sulphates
topic_facet anticoagulant agent
heparan sulfate
heparin
proteoglycan
article
gel chromatography
human
priority journal
rat
Animal
Anticoagulants
Glycosaminoglycans
Heparan Sulfate Proteoglycan
Heparitin Sulfate
Liver
Proteochondroitin Sulfates
Rats
Support, Non-U.S. Gov't
description Two high sulphated heparin-like polysaccharides (L1, MW 16,000 and L2, MW 11,700) were isolated from rat liver tissues, after DEAE-cellulose chromatography. Heparan sulphates from heart and lung tissues were isolated for comparison and fractionated according to their molecular weight. The anticoagulant activities in vitro were studied using clotting antifactor Xa, antifactor IIa, and APTT assay methods, falling in a narrow range (5-44 IU/mg) although the wide variability in molecular weight and sulphate content. The heparan sulphate nature of fractions L1 and L2 (sulphate/disaccharide ratio 2.05 and 2.48, respectively) has been verified by: a) low iduronic/glucuronic acid ratio; b) nitrous acid degradataion followed by gel chromatography; c) heparinase treatment followed by gel chromatography; d) electrophoretic behaviour. Native proteoglycans have been isolated and the glycosidic chains compared with L1 and L2. Their anticoagulant activities in vitro and the fact that antiXa clotting activity was not neutralized by protamine sulphate are in accordance with the results of structural studies.
format JOUR
author Kovensky, J.
Sassetti, B.
Fernandez Cirelli, A.
Kordich, L.
author_facet Kovensky, J.
Sassetti, B.
Fernandez Cirelli, A.
Kordich, L.
author_sort Kovensky, J.
title Low anticoagulant activity of high sulphated heparan sulphates
title_short Low anticoagulant activity of high sulphated heparan sulphates
title_full Low anticoagulant activity of high sulphated heparan sulphates
title_fullStr Low anticoagulant activity of high sulphated heparan sulphates
title_full_unstemmed Low anticoagulant activity of high sulphated heparan sulphates
title_sort low anticoagulant activity of high sulphated heparan sulphates
url http://hdl.handle.net/20.500.12110/paper_03406245_v63_n3_p488_Kovensky
work_keys_str_mv AT kovenskyj lowanticoagulantactivityofhighsulphatedheparansulphates
AT sassettib lowanticoagulantactivityofhighsulphatedheparansulphates
AT fernandezcirellia lowanticoagulantactivityofhighsulphatedheparansulphates
AT kordichl lowanticoagulantactivityofhighsulphatedheparansulphates
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