Chemical identification, antioxidant, cholinesterase inhibitory, and cytotoxic properties of fucoidan extracted from Persian Gulf Sargassum angustifolium

Arghavan Hosseinpouri Mehdi Mohammadi Elham Ehsandoost Paria Sharafi-Badr Narges Obeidi

Arghavan Hosseinpouri, Mehdi Mohammadi, Elham Ehsandoost, Paria Sharafi-Badr, Narges Obeidi. Chemical identification, antioxidant, cholinesterase inhibitory, and cytotoxic properties of fucoidan extracted from Persian Gulf Sargassum angustifolium[J]. Acta Oceanologica Sinica, 2022, 41(12): 133-141. doi: 10.1007/s13131-021-1961-5
Citation: Arghavan Hosseinpouri, Mehdi Mohammadi, Elham Ehsandoost, Paria Sharafi-Badr, Narges Obeidi. Chemical identification, antioxidant, cholinesterase inhibitory, and cytotoxic properties of fucoidan extracted from Persian Gulf Sargassum angustifolium[J]. Acta Oceanologica Sinica, 2022, 41(12): 133-141. doi: 10.1007/s13131-021-1961-5

doi: 10.1007/s13131-021-1961-5

Chemical identification, antioxidant, cholinesterase inhibitory, and cytotoxic properties of fucoidan extracted from Persian Gulf Sargassum angustifolium

Funds: The Iran National Science Foundation under contract No. 96015033.
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  • Figure  1.  Survival of NB4 cell viability under fucoidan treatment with concentrations of 62 μg/mL, 125 μg/mL, 250 μg/mL, 500 μg/mL, 1 000 μg/mL and 2 000 μg/mL after 24 h, 48 h and 72 h incubation (**p<0.01, ***p<0.005 and ****p<0.000 5).

    Figure  2.  Real-time PCR diagram of fucoidan extracted from Sargassum angustifolium ( **p<0.01 and ****p<0.000 5).

    Figure  3.  Diagram of correlation analysis of apoptosis-inducing and inhibitory genes.

    Figure  4.  Diagram of gene susceptibility evaluation to fucoidan extracted from Sargassum angustifolium.

    Figure  5.  Diagram of PBMC cells survival after treatment with concentrations of 2 000 µg/mL, 1 000 µg/mL, 500 µg/mL, 250 µg/mL, 125 µg/mL, 62.5 µg/mL related to fucoidan extracted from Sargassum angustifolium at 24h , 48 h and 72 h incubations (**p<0.01 and ****p<0.000 5).

    Figure  6.  Diagram of the anti-cholinesterase activity of fucoidan extracted from sargassum angustifolium. The anti-cholinesterase activity of fucoidan in concentrations of 0.01 μg/mL, 0.1 μg/mL, 1 μg/mL, 10 μg/mL, and 100 μg/mL compared with the control group (10% DMSO in buffer). The values are presented as mean±SEM of 3 independent experiments (n=3) and analyzed by one-way analysis of variance (ANOVA) (*p<0.05, **p<0.01 and ***p<0.001 compared with the control group).

    Table  1.   Sequences of primers used in qRT-PCR

    Base pairForward (5'–3') Reverse (5'–3')Gene
    111TGGACAGGACTGAACGTCTTGCCAGCAGGTCAGCAAAGAATTTAHPRT
    90CGGTGGGGTCATTTGTGTGCGGTTCAGGTACTCAGTCATCCBcl-2
    118ACTCATCCGATTTGGCTCTTTCCCTAGCCCCAGGATTACAAGDnmt1
    82GATGTGCAAGCGACGACAGAGAGCAAAGGCCAGCATCCTp15
    130CCTCTCACTGTCTTGTACCCTGCGTTTGGAGTGGTAGAAATCTp21
    121TAACAGTTCCTGCATGGGCGGCAGGACAGGCACAAACACGCACCp53
    下载: 导出CSV

    Table  2.   Sugar analysis of the polysaccharide from Sargassum angustifolium

    SugarComposition/%
    Fucose53±2.0
    Galactose0.2±0.9
    Mannose0.3±0.7
    Glucose12.6±0.4
    Uronic acids0.36±0.5
    Note: Each value represents the percentage of monosaccharides obtained in the fraction.
    下载: 导出CSV
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出版历程
  • 收稿日期:  2020-08-24
  • 录用日期:  2021-11-18
  • 网络出版日期:  2022-08-30
  • 刊出日期:  2022-12-30

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