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Ameliorating Effect of Fermented Perilla frutescens on Sleep Deprivation-Induced Cognitive Impairment Through Antioxidant and BDNF Signaling in Miceoa mark
  • Seo, Chae Ryeong ;
  • Lee, Bo Kyung ;
  • Jee, Hye Jin ;
  • Yoo, Jae Ryeong ;
  • Lee, Chul Kyu ;
  • Park, Jin Wook ;
  • Jung, Yi Sook
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Publication Year
2024-12-01
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Citation
Nutrients, Vol.16
Keyword
brain-derived neurotrophic factorcognitive impairmentfermentationoxidative stressPerilla frutescenssleep-deprivation
Mesh Keyword
AnimalsAntioxidantsBrain-Derived Neurotrophic FactorCognitive DysfunctionCyclic AMP Response Element-Binding ProteinDisease Models, AnimalFermentationGlutathioneHippocampusMaleMaze LearningMiceOxidative StressPerilla frutescensPlant ExtractsReceptor, trkBSignal TransductionSleep Deprivation
All Science Classification Codes (ASJC)
Food ScienceNutrition and Dietetics
Abstract
Background: Adequate sleep is essential for maintaining cognitive function, as evidenced by literature. Perilla frutescens var. acuta Kudo (PF) is a traditional medicinal herb reported to improve vascular cognitive impairment and induce sedation. However, the effects of PF on cognitive impairment caused by sleep deprivation (SD) have not yet been evaluated. This study aims to evaluate the effects of fermented PF (FPF) and its underlying mechanisms in a model of SD-induced cognitive impairment. Methods: Mice were subjected to SD to establish cognitive impairment, and FPF was administered once daily for 3 days. Cognitive performance was assessed using Y-maze and passive avoidance tests, followed by molecular mechanisms analyses. Results: FPF treatment improved SD-induced cognitive impairment, as evidenced by increased spontaneous alternation and extended latency time. Histological analysis revealed that SD impaired the hippocampus, and this impairment was alleviated by FPF treatment. FPF demonstrated antioxidant activity by increasing glutathione levels and decreasing malondialdehyde levels. Furthermore, the decreased levels of brain-derived neurotrophic factor (BDNF) observed in sleep-deprived mice were restored with FPF treatment. FPF also enhanced the phosphorylation of tropomyosin receptor kinase B, extracellular signal-regulated kinase, and cAMP response element-binding protein. Conclusions: These results indicate that FPF may have beneficial effects on SD-induced cognitive impairment by protecting against oxidative stress and increasing BDNF expression.
ISSN
2072-6643
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/34660
DOI
https://doi.org/10.3390/nu16234224
Fulltext

Type
Article
Funding
This research was supported by the GRRC program of Gyeonggi Province (GRRCAjou2023-B01), Republic of Korea.
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