Back to Search
Start Over
Structural and hemostatic activities of a sulfated galactofucan from the brown alga Spatoglossum schroederi. An ideal antithrombotic agent?
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2005 Dec 16; Vol. 280 (50), pp. 41278-88. Date of Electronic Publication: 2005 Sep 20. - Publication Year :
- 2005
-
Abstract
- The brown alga Spatoglossum schroederi contains three fractions of sulfated polysaccharides. One of them was purified by acetone fractionation, ion exchange, and molecular sieving chromatography. It has a molecular size of 21.5 kDa and contains fucose, xylose, galactose, and sulfate in a molar ratio of 1.0:0.5:2.0:2.0 and contains trace amounts of glucuronic acid. Chemical analyses, methylation studies, and NMR spectroscopy showed that the polysaccharide has a unique structure, composed of a central core formed mainly by 4-linked beta-galactose units, partially sulfated at the 3-O position. Approximately 25% of these units contain branches of oligosaccharides (mostly tetrasaccharides) composed of 3-sulfated, 4-linked alpha-fucose and one or two nonsulfated, 4-linked beta-xylose units at the reducing and nonreducing end, respectively. This sulfated galactofucan showed no anticoagulant activity on several "in vitro" assays. Nevertheless, it had a potent antithrombotic activity on an animal model of experimental venous thrombosis. This effect is time-dependent, reaching the maximum 8 h after its administration compared with the more transient action of heparin. The effect was not observed with the desulfated molecule. Furthermore, the sulfated galactofucan was 2-fold more potent than heparin in stimulating the synthesis of an antithrombotic heparan sulfate by endothelial cells. Again, this action was also abolished by desulfation of the polysaccharide. Because this sulfated galactofucan has no anticoagulant activity but strongly stimulates the synthesis of heparan sulfate by endothelial cells, we suggested that this last effect may be related to the "in vivo" antithrombotic activity of this polysaccharide. In this case the highly sulfated heparan sulfate produced by the endothelial cells is in fact the antithrombotic agent. Our results suggested that this sulfated galactofucan may have a potential application as an antithrombotic drug.
- Subjects :
- Acetone chemistry
Acetone pharmacology
Animals
Anticoagulants chemistry
Anticoagulants pharmacology
Carbohydrate Sequence
Cattle
Chromatography
Chromatography, Ion Exchange
Culture Media, Conditioned pharmacology
Dose-Response Relationship, Drug
Electrophoresis, Agar Gel
Endothelial Cells cytology
Endothelial Cells metabolism
Factor Xa chemistry
Fibrinolytic Agents chemistry
Furans chemistry
Galactose chemistry
Glucuronic Acid chemistry
Heparin chemistry
Heparitin Sulfate chemistry
Humans
Magnetic Resonance Spectroscopy
Methylation
Molecular Sequence Data
Oligosaccharides chemistry
Polysaccharides chemistry
Rats
Sulfur chemistry
Sulfuric Acid Esters chemistry
Thymidine chemistry
Time Factors
Xylose chemistry
Fibrinolytic Agents pharmacology
Fucose chemistry
Hemostasis
Phaeophyceae metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 280
- Issue :
- 50
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 16174777
- Full Text :
- https://doi.org/10.1074/jbc.M501124200