Enzyme Activity and Lipogenesis Inhibition by Fermented Grain Using Natural Enzymes.


Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
26 Oct 2023
Historique:
received: 15 09 2023
revised: 20 10 2023
accepted: 23 10 2023
medline: 15 11 2023
pubmed: 14 11 2023
entrez: 14 11 2023
Statut: epublish

Résumé

This study aims to compare the effects of three enzyme-rich foods, including one fermented (grain enzyme) and two non-fermented foods (enzyme foods 1 and 2), by investigating their antioxidant, anti-inflammatory, and anti-adipogenic properties. Grain enzyme exhibited the highest radical scavenging activity and was rich in antioxidant components, including total polyphenol and total flavonoid contents. Grain enzyme and enzyme foods 1 and 2 inhibited nitric oxide production by 27, 34, and 17%, respectively, at a concentration of 200 μg/mL in LPS-stimulated macrophages. Among the tested enzymes, grain enzyme demonstrated the strongest inhibition on the expression of inducible nitric oxide synthase (INOS), cyclooxygenase-2 (COX-2), and interleukin (IL)-1β, while Enzyme Food 2 exhibited the most significant suppression of IL-6 mRNA levels. Furthermore, Grain Enzyme demonstrated a stronger inhibitory effect compared to Enzyme Food 1 and 2. Grain Enzyme decreased the mRNA expression of peroxisome proliferator-activated receptor (PPAR)γ, CCAAT/enhancer-binding protein (C/EBP)α, and fatty acid-binding protein (FABP)4 by 28, 21, and 30%, respectively, at a concentration of 400 μg/mL. In summary, fermented grain enzymes outperformed non-fermented enzymes in suppressing inflammation and adipogenesis. This study highlights the anti-inflammatory and anti-adipogenic effects of grain enzyme, suggesting its potential as a valuable dietary supplement for managing metabolic disorders.

Identifiants

pubmed: 37959705
pii: molecules28217285
doi: 10.3390/molecules28217285
pmc: PMC10647246
pii:
doi:

Substances chimiques

Antioxidants 0
Anti-Inflammatory Agents 0
Nitric Oxide Synthase Type II EC 1.14.13.39
Cyclooxygenase 2 EC 1.14.99.1
RNA, Messenger 0
Nitric Oxide 31C4KY9ESH
Lipopolysaccharides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Naraentech Co., Ltd.
ID : Not applicable

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Auteurs

Jin-Sung Jun (JS)

Naraentech Co., Ltd., Sanhangni-gil, Janggun-myeon, Sejong-si 30054, Republic of Korea.

Ye-Lim You (YL)

Department of Food Nutrition, Sangmyung University, Hongjimun 2-Gil 20, Jongno-gu, Seoul 03016, Republic of Korea.

Ha-Jun Byun (HJ)

Department of Food Nutrition, Sangmyung University, Hongjimun 2-Gil 20, Jongno-gu, Seoul 03016, Republic of Korea.

Kyung-Hoon Han (KH)

Institute of Human Behavior & Genetics, Korea University College of Medicine, Seoul 02841, Republic of Korea.

Jay Kim (J)

Institute of Human Behavior & Genetics, Korea University College of Medicine, Seoul 02841, Republic of Korea.

Jea-Bum Jung (JB)

Wisedom Science Lab, Korea University, Seoul 02841, Republic of Korea.

Hyeon-Son Choi (HS)

Department of Food Nutrition, Sangmyung University, Hongjimun 2-Gil 20, Jongno-gu, Seoul 03016, Republic of Korea.

Sung-Hee Han (SH)

Institute of Human Behavior & Genetics, Korea University College of Medicine, Seoul 02841, Republic of Korea.

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Classifications MeSH