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Isolation of Fucoxanthin from Sargassum oligocystum Montagne, 1845 Seaweed in Vietnam and Its Neuroprotective Activity

Fucoxanthin extracted and purified from Vietnamese Sargassum oligocystum Montagne, 1845 exhibits various biological activities. In this study, the ability of fucoxanthin to inhibit acetylcholinesterase (AChE), the antioxidant activities, and the expression of antioxidant enzymes were investigated. F...

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Autores principales: Hong, Dang Diem, Thom, Le Thi, Ha, Nguyen Cam, Thu, Ngo Thi Hoai, Hien, Hoang Thi Minh, Tam, Luu Thi, Dat, Nguyen Manh, Duc, Tran Mai, Tru, Nguyen Van, Hang, Nguyen Thi Minh, Ambati, Ranga Rao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452663/
https://www.ncbi.nlm.nih.gov/pubmed/37626806
http://dx.doi.org/10.3390/biomedicines11082310
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author Hong, Dang Diem
Thom, Le Thi
Ha, Nguyen Cam
Thu, Ngo Thi Hoai
Hien, Hoang Thi Minh
Tam, Luu Thi
Dat, Nguyen Manh
Duc, Tran Mai
Tru, Nguyen Van
Hang, Nguyen Thi Minh
Ambati, Ranga Rao
author_facet Hong, Dang Diem
Thom, Le Thi
Ha, Nguyen Cam
Thu, Ngo Thi Hoai
Hien, Hoang Thi Minh
Tam, Luu Thi
Dat, Nguyen Manh
Duc, Tran Mai
Tru, Nguyen Van
Hang, Nguyen Thi Minh
Ambati, Ranga Rao
author_sort Hong, Dang Diem
collection PubMed
description Fucoxanthin extracted and purified from Vietnamese Sargassum oligocystum Montagne, 1845 exhibits various biological activities. In this study, the ability of fucoxanthin to inhibit acetylcholinesterase (AChE), the antioxidant activities, and the expression of antioxidant enzymes were investigated. Fucoxanthin isolated from Vietnamese S. oligocystum showed no cytotoxic effects; moreover, it exhibited AChE inhibitory activity (with an IC(50) value of 130.12 ± 6.65 μg mL(−1)) and antioxidant activity (with an IC(50) value of 3.42 ± 0.15 mg mL(−1)). At concentrations of 50 and 100 µg mL(−1), fucoxanthin provided protection against amyloid β-protein fragment 25–35-induced neurotoxicity in a C6 neuronal cell line, and the survival of C6 cells was higher than 81.01% and 80.98%, respectively, compared to the control group (59%). Moreover, antioxidant enzyme activity and quantitative PCR analysis suggested that the neuroprotective effect of fucoxanthin resulted from regulation of the gene expression of antioxidant enzymes (CAT and GPx) and ER pathways (caspase-3 and Bax), as well as the promotion of expression of genes involved in PI3K/Akt signaling (GSK-3β), autophagy (p62 and ATG5), and the biosynthesis of ACh (VAChT and ChAT). Therefore, fucoxanthin extracted from the seaweed S. oligocystum in Vietnam is a potential feedstock source for the production of health foods that exert neuroprotective effects.
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spelling pubmed-104526632023-08-26 Isolation of Fucoxanthin from Sargassum oligocystum Montagne, 1845 Seaweed in Vietnam and Its Neuroprotective Activity Hong, Dang Diem Thom, Le Thi Ha, Nguyen Cam Thu, Ngo Thi Hoai Hien, Hoang Thi Minh Tam, Luu Thi Dat, Nguyen Manh Duc, Tran Mai Tru, Nguyen Van Hang, Nguyen Thi Minh Ambati, Ranga Rao Biomedicines Article Fucoxanthin extracted and purified from Vietnamese Sargassum oligocystum Montagne, 1845 exhibits various biological activities. In this study, the ability of fucoxanthin to inhibit acetylcholinesterase (AChE), the antioxidant activities, and the expression of antioxidant enzymes were investigated. Fucoxanthin isolated from Vietnamese S. oligocystum showed no cytotoxic effects; moreover, it exhibited AChE inhibitory activity (with an IC(50) value of 130.12 ± 6.65 μg mL(−1)) and antioxidant activity (with an IC(50) value of 3.42 ± 0.15 mg mL(−1)). At concentrations of 50 and 100 µg mL(−1), fucoxanthin provided protection against amyloid β-protein fragment 25–35-induced neurotoxicity in a C6 neuronal cell line, and the survival of C6 cells was higher than 81.01% and 80.98%, respectively, compared to the control group (59%). Moreover, antioxidant enzyme activity and quantitative PCR analysis suggested that the neuroprotective effect of fucoxanthin resulted from regulation of the gene expression of antioxidant enzymes (CAT and GPx) and ER pathways (caspase-3 and Bax), as well as the promotion of expression of genes involved in PI3K/Akt signaling (GSK-3β), autophagy (p62 and ATG5), and the biosynthesis of ACh (VAChT and ChAT). Therefore, fucoxanthin extracted from the seaweed S. oligocystum in Vietnam is a potential feedstock source for the production of health foods that exert neuroprotective effects. MDPI 2023-08-19 /pmc/articles/PMC10452663/ /pubmed/37626806 http://dx.doi.org/10.3390/biomedicines11082310 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hong, Dang Diem
Thom, Le Thi
Ha, Nguyen Cam
Thu, Ngo Thi Hoai
Hien, Hoang Thi Minh
Tam, Luu Thi
Dat, Nguyen Manh
Duc, Tran Mai
Tru, Nguyen Van
Hang, Nguyen Thi Minh
Ambati, Ranga Rao
Isolation of Fucoxanthin from Sargassum oligocystum Montagne, 1845 Seaweed in Vietnam and Its Neuroprotective Activity
title Isolation of Fucoxanthin from Sargassum oligocystum Montagne, 1845 Seaweed in Vietnam and Its Neuroprotective Activity
title_full Isolation of Fucoxanthin from Sargassum oligocystum Montagne, 1845 Seaweed in Vietnam and Its Neuroprotective Activity
title_fullStr Isolation of Fucoxanthin from Sargassum oligocystum Montagne, 1845 Seaweed in Vietnam and Its Neuroprotective Activity
title_full_unstemmed Isolation of Fucoxanthin from Sargassum oligocystum Montagne, 1845 Seaweed in Vietnam and Its Neuroprotective Activity
title_short Isolation of Fucoxanthin from Sargassum oligocystum Montagne, 1845 Seaweed in Vietnam and Its Neuroprotective Activity
title_sort isolation of fucoxanthin from sargassum oligocystum montagne, 1845 seaweed in vietnam and its neuroprotective activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452663/
https://www.ncbi.nlm.nih.gov/pubmed/37626806
http://dx.doi.org/10.3390/biomedicines11082310
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