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Structural Characterization and Anticoagulant Activities of a Keratan Sulfate-like Polysaccharide from the Sea Cucumber Holothuria fuscopunctata.

Authors :
Chen, Ru
Wang, Weili
Yin, Ronghua
Pan, Ying
Xu, Chen
Gao, Na
Luo, Xiaodong
Zhao, Jinhua
Source :
Marine Drugs; Dec2023, Vol. 21 Issue 12, p632, 19p
Publication Year :
2023

Abstract

A sulfated polysaccharide (AG) was extracted and isolated from the sea cucumber H. fuscopunctata, consisting of GlcNAc, GalNAc, Gal, Fuc and lacking any uronic acid residues. Importantly, several chemical depolymerization methods were used to elucidate the structure of the AG through a bottom-up strategy. A highly sulfated galactose (oAG-1) and two disaccharides labeled with 2,5-anhydro-D-mannose (oAG-2, oAG-3) were obtained from the deaminative depolymerized product along with the structures of the disaccharide derivatives (oAG-4~oAG-6) identified from the free radical depolymerized product, suggesting that the repeating building blocks in a natural AG should comprise the disaccharide β-D-GalS-1,4-D-GlcNAc<subscript>6S</subscript>. The possible disaccharide side chains (bAG-1) were obtained with mild acid hydrolysis. Thus, a natural AG may consist of a keratan sulfate-like (KS-like) glycosaminoglycan with diverse modifications, including the sulfation types of the Gal residue and the possible disaccharide branches α-D-GalNAc<subscript>4S6S</subscript>-1,2-α/β-L-Fuc<subscript>3S</subscript> linked to the KS-like chain. Additionally, the anticoagulant activities of the AG and its depolymerized products (dAG1-9) were evaluated in vitro using normal human plasma. The AG could prolong activated partial thromboplastin time (APTT) in a dose-dependent manner, and the activity potency was positively related to the chain length. The AG and dAG1-dAG3 could prolong thrombin time (TT), while they had little effect on prothrombin time (PT). The results indicate that the AG could inhibit the intrinsic and common coagulation pathways. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16603397
Volume :
21
Issue :
12
Database :
Complementary Index
Journal :
Marine Drugs
Publication Type :
Academic Journal
Accession number :
174464688
Full Text :
https://doi.org/10.3390/md21120632