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Mechanisms of Bioactivities of Fucoidan from the Brown Seaweed Fucus vesiculosus L. of the Barents Sea

The aim of this study was to elucidate some mechanisms of radical scavenging and the anti-inflammatory, anti-hyperglycemic, and anti-coagulant bioactivities of high molecular weight fucoidan from Fucus vesiculosus in several in vitro models. Fucoidan has displayed potent 1, 1-diphenyl-2-picryl hydra...

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Autores principales: Pozharitskaya, Olga N., Obluchinskaya, Ekaterina D., Shikov, Alexander N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281726/
https://www.ncbi.nlm.nih.gov/pubmed/32456047
http://dx.doi.org/10.3390/md18050275
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author Pozharitskaya, Olga N.
Obluchinskaya, Ekaterina D.
Shikov, Alexander N.
author_facet Pozharitskaya, Olga N.
Obluchinskaya, Ekaterina D.
Shikov, Alexander N.
author_sort Pozharitskaya, Olga N.
collection PubMed
description The aim of this study was to elucidate some mechanisms of radical scavenging and the anti-inflammatory, anti-hyperglycemic, and anti-coagulant bioactivities of high molecular weight fucoidan from Fucus vesiculosus in several in vitro models. Fucoidan has displayed potent 1, 1-diphenyl-2-picryl hydrazil radical scavenging and reduction power activities. It significantly inhibits the cyclooxygenase-2 (COX-2) enzyme (IC(50) 4.3 μg mL(−1)) with a greater selectivity index (lg(IC(80) COX-2/IC(80)COX-1), −1.55) than the synthetic non-steroidal anti-inflammatory drug indomethacin (lg(IC(80) COX-2/IC(80)COX-1), −0.09). A concentration-dependent inhibition of hyaluronidase enzyme with an IC(50) of 2.9 μg mL(−1) was observed. Fucoidan attenuated the lipopolysaccharide-induced expression of mitogen-activated protein kinase p38. Our findings suggest that the inhibition of dipeptidyl peptidase-IV (DPP-IV) (IC(50) 1.11 μg mL(−1)) is one of the possible mechanisms involved in the anti-hyperglycemic activity of fucoidan. At a concentration of 3.2 μg mL(−1), fucoidan prolongs the activated partial thromboplastin time and thrombin time by 1.5-fold and 2.5-fold compared with a control, respectively. A significant increase of prothrombin time was observed after the concentration of fucoidan was increased above 80 μg mL(−1). This evidenced that fucoidan may have an effect on intrinsic/common pathways and little effect on the extrinsic mechanism. This study sheds light on the multiple pathways of the bioactivities of fucoidan. As far as we know, the inhibition of hyaluronidase and DPP-IV by high molecular fucoidan was studied for the first time in this work. Our results and literature data suggest that molecular weight, sulfate content, fucose content, and polyphenols may contribute to these activities. It seems that high molecular weight fucoidan has promising therapeutic applications in different pharmacological settings. Anti-oxidant, anti-inflammatory and anti-coagulant drugs have been used for the management of complications of COVID19. Taken as a whole, fucoidan could be considered as a prospective candidate for the treatment of patients with COVID19; however, additional research in this field is required.
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spelling pubmed-72817262020-06-15 Mechanisms of Bioactivities of Fucoidan from the Brown Seaweed Fucus vesiculosus L. of the Barents Sea Pozharitskaya, Olga N. Obluchinskaya, Ekaterina D. Shikov, Alexander N. Mar Drugs Article The aim of this study was to elucidate some mechanisms of radical scavenging and the anti-inflammatory, anti-hyperglycemic, and anti-coagulant bioactivities of high molecular weight fucoidan from Fucus vesiculosus in several in vitro models. Fucoidan has displayed potent 1, 1-diphenyl-2-picryl hydrazil radical scavenging and reduction power activities. It significantly inhibits the cyclooxygenase-2 (COX-2) enzyme (IC(50) 4.3 μg mL(−1)) with a greater selectivity index (lg(IC(80) COX-2/IC(80)COX-1), −1.55) than the synthetic non-steroidal anti-inflammatory drug indomethacin (lg(IC(80) COX-2/IC(80)COX-1), −0.09). A concentration-dependent inhibition of hyaluronidase enzyme with an IC(50) of 2.9 μg mL(−1) was observed. Fucoidan attenuated the lipopolysaccharide-induced expression of mitogen-activated protein kinase p38. Our findings suggest that the inhibition of dipeptidyl peptidase-IV (DPP-IV) (IC(50) 1.11 μg mL(−1)) is one of the possible mechanisms involved in the anti-hyperglycemic activity of fucoidan. At a concentration of 3.2 μg mL(−1), fucoidan prolongs the activated partial thromboplastin time and thrombin time by 1.5-fold and 2.5-fold compared with a control, respectively. A significant increase of prothrombin time was observed after the concentration of fucoidan was increased above 80 μg mL(−1). This evidenced that fucoidan may have an effect on intrinsic/common pathways and little effect on the extrinsic mechanism. This study sheds light on the multiple pathways of the bioactivities of fucoidan. As far as we know, the inhibition of hyaluronidase and DPP-IV by high molecular fucoidan was studied for the first time in this work. Our results and literature data suggest that molecular weight, sulfate content, fucose content, and polyphenols may contribute to these activities. It seems that high molecular weight fucoidan has promising therapeutic applications in different pharmacological settings. Anti-oxidant, anti-inflammatory and anti-coagulant drugs have been used for the management of complications of COVID19. Taken as a whole, fucoidan could be considered as a prospective candidate for the treatment of patients with COVID19; however, additional research in this field is required. MDPI 2020-05-22 /pmc/articles/PMC7281726/ /pubmed/32456047 http://dx.doi.org/10.3390/md18050275 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pozharitskaya, Olga N.
Obluchinskaya, Ekaterina D.
Shikov, Alexander N.
Mechanisms of Bioactivities of Fucoidan from the Brown Seaweed Fucus vesiculosus L. of the Barents Sea
title Mechanisms of Bioactivities of Fucoidan from the Brown Seaweed Fucus vesiculosus L. of the Barents Sea
title_full Mechanisms of Bioactivities of Fucoidan from the Brown Seaweed Fucus vesiculosus L. of the Barents Sea
title_fullStr Mechanisms of Bioactivities of Fucoidan from the Brown Seaweed Fucus vesiculosus L. of the Barents Sea
title_full_unstemmed Mechanisms of Bioactivities of Fucoidan from the Brown Seaweed Fucus vesiculosus L. of the Barents Sea
title_short Mechanisms of Bioactivities of Fucoidan from the Brown Seaweed Fucus vesiculosus L. of the Barents Sea
title_sort mechanisms of bioactivities of fucoidan from the brown seaweed fucus vesiculosus l. of the barents sea
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281726/
https://www.ncbi.nlm.nih.gov/pubmed/32456047
http://dx.doi.org/10.3390/md18050275
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