Abstract
The brown seaweed Spatoglossum schröederi (Dictyotaceae) contains three main fucans (fucans A, B and C) with different mobility in electrophoresis. The fucan with highest mobility (fucan C) was precipitated with 2.0 volumes of acetone, purified using a combination of ion exchange chromatography and electrophoresis. It showed an MW of 24 kDa determined by HPLC and Sephadex G-75 chromatography and migrates as a single band in three distinct electrophoretic systems. This fucan contains fucose, xylose, galactose and sulfate in a molar ratio 1 : 0.6 : 2:2.3. The fucan has neither anticoagulant (from 10 to 100 μg) nor hemorrhagic activities (100 μg/mL). In addition, fucan C is neither cytotoxic nor cytostatic. However, fucan C (100 μg/mL) stimulated the synthesis of an antithrombotic heparan sulfate from endothelial cells of rabbit aorta. The results suggest that fucan C might be used as an antithrombotic therapeutic compound.
References
1
Berteau O, Mulloy B.
Sulfated fucans, fresh perspectives: structures, functions and biological properties of sulfated fucans and overview of enzymes activity toward this class of polysaccharides.
Glycobiology.
2003;
13
29R-40R
2
Albuquerque I RL, Queiroz K CS, Alves L G, Santos E A, Leite E L, Rocha H AO.
Heterofucans from Dictyota menstrualis have anticoagulant activity.
Braz J Med Biol Res.
2004;
37
167-171
3
Mourão P AS.
Use of sulfated fucans as anticoagulant and antithrombotic agents: future perspectives.
Curr Pharm Des.
2004;
10
967-81
4
Boisson-Vidal C, Haroun F, Ellouali M, Blondin C, Fischer A M, Agostini A. et al .
et alBiological activities of polysaccharides from marine algae.
Drugs Fut.
1995;
20
1237-49
5
Rocha H AO, Franco C RC, Trindade E S, Carvalho L CM, Veiga S S, Leite E L. et al .
A fucan from the brown seaweed S. schröederi inhibits Chinese hamster ovary cell adhesion to several extracelular matrix proteins.
Braz J Med Biol Res.
2001;
34
621-6
6
Leite E L, Medeiros M GL, Rocha H AO, Farias G GM, Silva L F, Chavante S F. et al .
Structure and pharmacological activities of sulfated xylofucoglucuronan from the alga S. schröederi
.
Plant Sci.
1998;
132
215-28
7
Patankar M S, Oehninger S, Barnett T, Williams R L, Clark G F.
A revised structure for fucoidan may explain some of its biological activities.
J Biol Chem.
1993;
268
21 770-6
8
Kloareg B, Quatrano R S.
Cell walls of marine algae: structure and function.
Oceanogr Mar Biol Ann Rev.
1988;
26
259-315
9
Duarte M ER, Cardoso M AD, Cerezo A S, Noseda M.
Structural studies on fucoidan from brown seaweed Sargassum stenophyllum
.
Carbohyd Res.
2001;
333
281-93
10
Trindade E S, Oliver C, Jamur M C, Franco C RC, Gouveia T C, Dietrich C P. et al .
Biotinylated heparin stimulates production heparan sulfate without binding the cell surface.
Mol Biol Cell.
1999;
10
459-9
11
Nader H B, Lopes C C, Rocha H AO, Santos E A, Dietrich C P.
Heparins and heparinoids: Occurrence, structure and mechanism of antithrombotic and hemorrhagic activities.
Curr Pharm Des.
2004;
10
951-66
12
Dubois M, Gilles K A, Hamilton J K, Rebers P A, Smith F.
Colorimetric method for determination of sugars and related substances.
Anal Chem.
1956;
28
250-6
13
Kircher H W.
Gas-liquid partition chromatography of methylated sugars.
Anal Chem.
1960;
32
1103-6
14
Spector J.
Refinement of the Coomassie blue method of protein quantification. A simple and linear spectrophotometric assay of 0.5 to 50 μg of protein.
Anal Biochem.
1978;
86
142-3
15
Dietrich C P, Shinjo S K, Moraes F A, Castro R AB, Mendes A, Gouvea T C. et al .
Structural features and bleeding activity of commercial low molecular weight heparins: Neutralization by ATP and protamine.
Seminars in Thromb and Hemos.
1999;
25 (Suppl 3)
43-50
Hugo Alexande de Oliveira Rocha
Universidade Federal do Rio Grande do Norte
Centro de Biociências
Departamento de Bioquímica
Laboratório de Biotecnologia de Polímeros Naturais
Av. Salgado Filho S/N
Natal - RN 59097-570
Brazil
Phone: +55-84-211-9208
Fax: +55-84-211-9208
Email: hugo-alexandre@uol.com.br