Polysaccharides of Grifola frondosa ameliorate oxidative stress and hypercholesterolaemia in hamsters fed a high-fat, high-cholesterol diet.


Journal

The Journal of pharmacy and pharmacology
ISSN: 2042-7158
Titre abrégé: J Pharm Pharmacol
Pays: England
ID NLM: 0376363

Informations de publication

Date de publication:
01 Sep 2022
Historique:
received: 03 11 2021
accepted: 13 04 2022
pubmed: 15 5 2022
medline: 9 9 2022
entrez: 14 5 2022
Statut: ppublish

Résumé

This study was to evaluate the antioxidant and anti-hypercholesterolaemia activities of Grifola frondosa in hamsters fed a high-fat, high-cholesterol (HFHC) diet. G. frondosa, including fruiting bodies (FGF), fermented mycelia (MGF) and polysaccharides extracted from fruiting bodies (FPS), fermented mycelia (MIP) and fermented broth (BEP) were received intragastrically. Lipid profile and antioxidant status in the blood and liver of hamsters were assessed. FGF decreased weight gain, serum triglycerides and cholesterol and increased hepatic mRNA expression of cholesterol-7α-hydroxylase expression. FGF, MGF, FPS and MIP decreased the HFHC diet-increased area under the curve (AUC) of serum cholesterol. FGF and FPS further decreased AUC of serum triglycerides. When evaluating the redox status of erythrocytes, FPS and MIP increased non-protein sulfhydryl (NP-SH) groups, reduced glutathione (GSH) and catalase activity and FPS further increased GSH peroxidase activity. In the liver, MGF increased NP-SH groups and GSH and decreased triglycerides content. FPS, MIP and BEP decreased oxidized GSH and triglycerides content. Moreover, all treatments alleviated HFHC diet-increased LDL oxidation. Fruiting bodies of G. frondosa may improve hypercholesterolaemia via increased bile acid synthesis. Additionally, fermented biomass and polysaccharides of G. frondosa may have the potential to prevent hepatic lipid accumulation.

Identifiants

pubmed: 35567773
pii: 6585934
doi: 10.1093/jpp/rgac031
doi:

Substances chimiques

Antioxidants 0
Polysaccharides 0
Triglycerides 0
Cholesterol 97C5T2UQ7J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1296-1306

Subventions

Organisme : Changhua Christian Hospital
ID : 94-CCH-NSC-13
Organisme : Ministry of Science and Technology, Taiwan
ID : NSC94-2320-B-309-001

Informations de copyright

© Crown copyright 2022.

Auteurs

Wen-Tzu Wu (WT)

Department of Food Nutrition and Health Biotechnology, Asia University, Taichung, Taiwan (R.O.C).

Tai-Hao Hsu (TH)

Department of Food Science and Biotechnology, Da-Yeh University, Changhua County, Taiwan (R.O.C).

Woan-Ling Chen (WL)

Department of Chemical Engineering and Materials Engineering, Tunghai University, Taichung, Taiwan (R.O.C).
Department of Food Science, Tunghai University, Taichung, Taiwan (R.O.C).

Chueh-Ko Yang (CK)

Women's Health Research Laboratory, Changhua Christian Hospital, Changhua County, Taiwan (R.O.C).

Hui-Chen Lo (HC)

Department of Nutritional Science, Fu Jen Catholic University, New Taipei City, Taiwan (R.O.C).

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