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Review
. 2020 Aug 20;8(10):5195-5205.
doi: 10.1002/fsn3.1835. eCollection 2020 Oct.

Therapeutic and nutraceutical potentials of a brown seaweed Sargassum fusiforme

Affiliations
Review

Therapeutic and nutraceutical potentials of a brown seaweed Sargassum fusiforme

Jian Liu et al. Food Sci Nutr. .

Abstract

Sargassum fusiforme, also known as Yangqicai () in Chinese and Hijiki in Japanese, is a brown seaweed that grows abundantly along the rocky coastlines of Asian countries such as Japan, Korea, and China. The first use of S. fusiforme as a traditional Chinese medicinal plant was recorded in the Shennong Bencao Jing, dated 200 AD. It was referred to as Haizao (seaweed), renowned for treating Yinglu (tumor-like induration), dysuria, and edema. Currently, it is commonly used in traditional cuisine as it is rich in dietary fiber and minerals such as calcium, iron, and magnesium. Owing to its health benefits, S. fusiforme remains popular in China, Korea, and Japan, as well as in the UK and in North America. Currently, there is a lack of research on S. fusiforme; thus, we review the therapeutic effects of S. fusiforme, such as anticancer, antiangiogenic, and antiviral effects, in vitro and in vivo as reported during the past two decades. This review may promote further research on the therapeutic uses of S. fusiforme. Furthermore, we discuss the processes and considerations involved in using drugs produced from marine sources.

Keywords: Sargassum fusiforme; antiangiogenic; antitumor; immunomodulatory; neurodegenerative.

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Conflict of interest statement

The authors declare no conflict of interest.

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References

    1. Allen, K. D. , & Golightly, Y. M. (2015). Epidemiology of osteoarthritis: State of the evidence. Current Opinion in Rheumatology, 27, 276–283. 10.1097/BOR.0000000000000161 - DOI - PMC - PubMed
    1. Anderson, N. S. , Campbell, J. W. , Harding, M. M. , Rees, D. A. , & Samuel, J. W. B. (1969). X‐ray diffraction studies of polysaccharide sulphates: Double helix models for κ‐ and ι‐carrageenans. Journal of Molecular Biology, 45, 85–97. 10.1016/0022-2836(69)90211-3 - DOI - PubMed
    1. Barve, R. A. , Minnerly, J. C. , Weiss, D. J. , Meyer, D. M. , Aguiar, D. J. , Sullivan, P. M. , … Head, R. D. (2007). Transcriptional profiling and pathway analysis of monosodium iodoacetate‐induced experimental osteoarthritis in rats: Relevance to human disease. Osteoarthritis and Cartilage, 15, 1190–1198. 10.1016/j.joca.2007.03.014 - DOI - PubMed
    1. Bathina, S. , & Das, U. N. (2015). Brain‐derived neurotrophic factor and its clinical implications. Archives of Medical Science – AMS, 11, 1164–1178. 10.5114/aoms.2015.56342 - DOI - PMC - PubMed
    1. Bauer, J. H. , & Helfand, S. L. (2006). New tricks of an old molecule: Lifespan regulation by p53. Aging Cell, 5, 437–440. 10.1111/j.1474-9726.2006.00228.x - DOI - PMC - PubMed

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