Bioactivity of alginetin, a caramelization product of pectin: Cytometric analysis of rat thymic lymphocytes using fluorescent probes.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 30 04 2020
accepted: 12 10 2020
entrez: 2 11 2020
pubmed: 3 11 2020
medline: 29 12 2020
Statut: epublish

Résumé

Alginetin is the major product formed from pentoses and hexurionic acids. Alginetin is producted by cooking process of food including pection, a naturally-occurring polysacharride found in many plants. However, the biological interaction and toxicity of alginetin are not known at all. The aim of the present study was to investigate the cellular actions of alginetin on rat thymic lymphocytes. The effects of alginetin on the cell were examined using flow cytometry with fluorescent probes. Alginetin increased cellular content of non-protein thiols ([NPT]i) and elevated intracellular Zn2+ levels ([Zn2+]i). Chelation of intracellular Zn2+ reduced the effect of alginetin on [NPT]i, and chelation of external Zn2+ almost completely diminished alginetin-induced elevation of [Zn2+]i, indicating that alginetin treatment increased Zn2+ influx. Increased [NPT]i and [Zn2+]i levels in response to alginetin were positively correlated. Alginetin protected cells against oxidative stress induced by hydrogen peroxide and Ca2+ overload by calcium ionophore. It is considered that the increases in [NPT]i and [Zn2+]i are responsible for the cytoprotective activity of alginetin because NPT attenuates oxidative stress and Zn2+ competes with Ca2+. Alginetin may be produced during manufacturing of jam, which may provide additional health benefits of jam.

Identifiants

pubmed: 33137129
doi: 10.1371/journal.pone.0241290
pii: PONE-D-20-12715
pmc: PMC7605654
doi:

Substances chimiques

Pectins 89NA02M4RX
Alginic Acid 8C3Z4148WZ
Zinc J41CSQ7QDS

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0241290

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Sayaka Doi (S)

Faculty of Human Life Science, Osaka City University, Osaka City, Osaka, Japan.

Mina Kawamura (M)

Faculty of Bioscience and Bioindustry, Tokushima University, Tokushima City, Tokushima Japan.

Keisuke Oyama (K)

Surgery Division, Sakai City Medical Center, Sakai City, Osaka, Japan.

Tetsuya Akamatsu (T)

Faculty of Bioscience and Bioindustry, Tokushima University, Tokushima City, Tokushima Japan.

Mizuki Mizobuchi (M)

Department of Food-Nutritional Sciences, Faculty of Life Sciences, Tokushima Bunri University, Tokushima, Japan.

Yasuo Oyama (Y)

Faculty of Bioscience and Bioindustry, Tokushima University, Tokushima City, Tokushima Japan.

Toshiya Masuda (T)

Faculty of Human Life Science, Osaka City University, Osaka City, Osaka, Japan.

Norio Kamemura (N)

Department of Food-Nutritional Sciences, Faculty of Life Sciences, Tokushima Bunri University, Tokushima, Japan.

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Classifications MeSH