In Vitro Mechanistic Studies of a Standardized Sustainable Grape Seed Extract for Potential Application as a Mood-Modulating and Cognition-Enhancing Supplement.


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
12 Oct 2024
Historique:
received: 30 08 2024
revised: 30 09 2024
accepted: 08 10 2024
medline: 26 10 2024
pubmed: 26 10 2024
entrez: 26 10 2024
Statut: epublish

Résumé

Grape seed extract (GSE) from In vitro assays were conducted to assess GSEe's inhibitory effects on γ-aminobutyric acid transaminase (GABA-T) and monoamine oxidase A (MAO-A), its binding affinity to the GABA site of GABA-A receptors, and its effects on acetylcholinesterase (AChE). Its neuroprotective effects on human SH-SY5Y neuroblastoma cells under oxidative stress (induced by H GSEe showed significant GABA-T inhibitory activity. It also exhibited MAO-A and AChE inhibition, along with moderate binding affinity to the GABA-A receptor. In neuroprotective assays, GSEe provided significant protection to SH-SY5Y cells against oxidative stress. GSEe demonstrated robust antioxidant activity in all assays, including scavenging of DPPH and ABTS radicals, high ferric-reducing power, high polyphenolic contents, and a substantial total antioxidant capacity. GSEe exhibits promising bioactivities, highlighting its potential as a supplement for modulating mood and enhancing cognitive function. Overall, the promising results from these in vitro studies provide a strong foundation for the continued exploration and development of GSEe as a viable natural supplement for enhancing mental health and cognitive function.

Sections du résumé

BACKGROUND BACKGROUND
Grape seed extract (GSE) from
METHODS METHODS
In vitro assays were conducted to assess GSEe's inhibitory effects on γ-aminobutyric acid transaminase (GABA-T) and monoamine oxidase A (MAO-A), its binding affinity to the GABA site of GABA-A receptors, and its effects on acetylcholinesterase (AChE). Its neuroprotective effects on human SH-SY5Y neuroblastoma cells under oxidative stress (induced by H
RESULTS RESULTS
GSEe showed significant GABA-T inhibitory activity. It also exhibited MAO-A and AChE inhibition, along with moderate binding affinity to the GABA-A receptor. In neuroprotective assays, GSEe provided significant protection to SH-SY5Y cells against oxidative stress. GSEe demonstrated robust antioxidant activity in all assays, including scavenging of DPPH and ABTS radicals, high ferric-reducing power, high polyphenolic contents, and a substantial total antioxidant capacity.
CONCLUSIONS CONCLUSIONS
GSEe exhibits promising bioactivities, highlighting its potential as a supplement for modulating mood and enhancing cognitive function. Overall, the promising results from these in vitro studies provide a strong foundation for the continued exploration and development of GSEe as a viable natural supplement for enhancing mental health and cognitive function.

Identifiants

pubmed: 39458455
pii: nu16203459
doi: 10.3390/nu16203459
pii:
doi:

Substances chimiques

Grape Seed Extract 0
Antioxidants 0
Neuroprotective Agents 0
Proanthocyanidins 0
Acetylcholinesterase EC 3.1.1.7
Monoamine Oxidase EC 1.4.3.4
Receptors, GABA-A 0
Monoamine Oxidase Inhibitors 0
monoamine oxidase A, human EC 1.4.3.4.
Nootropic Agents 0
Polyphenols 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : This study was partially funded by Scientific Research Projects Coordination Unit of Istanbul University (Project number: TSA-2024-40906 Project ID: 40906)
ID : Project number: TSA-2024-40906 Project ID: 40906

Auteurs

Gozde Hasbal-Celikok (G)

Department of Biochemistry, Faculty of Pharmacy, Istanbul University, Istanbul 34452, Türkiye.

Mehtap Kara (M)

Department of Pharmaceutical Toxicology, Faculty of Pharmacy, Istanbul University, Istanbul 34452, Türkiye.

Marta Sánchez (M)

Department of Pharmacology, Pharmacognosy and Botany, Faculty of Pharmacy, Complutense University of Madrid, 28040 Madrid, Spain.

Claudia Owsianik (C)

Department of Pharmacology, Pharmacognosy and Botany, Faculty of Pharmacy, Complutense University of Madrid, 28040 Madrid, Spain.

Pilar Gómez-Serranillos (P)

Department of Pharmacology, Pharmacognosy and Botany, Faculty of Pharmacy, Complutense University of Madrid, 28040 Madrid, Spain.

Tugba Yilmaz-Ozden (T)

Department of Biochemistry, Faculty of Pharmacy, Istanbul University, Istanbul 34452, Türkiye.

Ezgi Öztaş (E)

Department of Pharmaceutical Toxicology, Faculty of Pharmacy, Istanbul University, Istanbul 34452, Türkiye.

Özge Sultan Zengin (ÖS)

Department of Pharmaceutical Toxicology, Faculty of Pharmacy, Istanbul University, Istanbul 34452, Türkiye.

Gul Ozhan (G)

Department of Pharmaceutical Toxicology, Faculty of Pharmacy, Istanbul University, Istanbul 34452, Türkiye.

Nazli Arda (N)

Department of Molecular Biology and Genetics, Faculty of Science, Istanbul University, Istanbul 34452, Türkiye.

Merve Tunc (M)

Department of Molecular Biology and Genetics, Faculty of Science, Istanbul University, Istanbul 34452, Türkiye.

Sumeyye Sahin (S)

Department of Food Engineering, Ordu University, Ordu 52200, Türkiye.

Areaba Shafiq (A)

Department of Psychiatry, Lady Reading Hospital, Peshawar 25000, Pakistan.

Ayesha Kanwal (A)

Department of Psychiatry, Lady Reading Hospital, Peshawar 25000, Pakistan.

Hunaiba I Ujjan (HI)

Department of Pathology, Liaquat University of Health Sciences, Jamshoro 76090, Pakistan.

Fazle Rabbani (F)

Department of Psychiatry, Lady Reading Hospital, Peshawar 25000, Pakistan.

Giovanna Petrangolini (G)

Medical Department, Indena SpA, 20139 Milan, Italy.

Amjad Khan (A)

Department of Oncology, University of Oxford, Oxford OX3 7DQ, UK.
Department of Biochemistry, Liaquat University of Medical & Health Sciences, Jamshoro 76090, Pakistan.

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Classifications MeSH