Ginsenoside Rh1 Exerts Neuroprotective Effects by Activating the PI3K/Akt Pathway in Amyloid-β Induced SH-SY5Y Cells
Alzheimer’s disease (AD) is a neurodegenerative disorder characterized by the accumulation of β-amyloid plaques and hyperphosphorylated tau proteins in the brain. Cell signaling pathways such as PI3K/Akt are known to play an essential role in regulating cell survival, motility, transcription, metabo...
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-06-01
|
Series: | Applied Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/2076-3417/11/12/5654 |
_version_ | 1797529667345842176 |
---|---|
author | Miey Park So-Hyeun Kim Hae-Jeung Lee |
author_facet | Miey Park So-Hyeun Kim Hae-Jeung Lee |
author_sort | Miey Park |
collection | DOAJ |
description | Alzheimer’s disease (AD) is a neurodegenerative disorder characterized by the accumulation of β-amyloid plaques and hyperphosphorylated tau proteins in the brain. Cell signaling pathways such as PI3K/Akt are known to play an essential role in regulating cell survival, motility, transcription, metabolism, and progression of the cell cycle. Recent studies demonstrated that the disruption of these signaling pathways in neurodegenerative disorders leads to oxidative stress and cell death. Targeting these altered signaling pathways could be considered as the therapeutic approach for neurodegenerative disorders. Ginsenoside Rh1 is known to provide beneficial effects in various diseases such as cancer, diabetes, and inflammation. In this study, human neuroblastoma SH-SY5Y cells were treated with the β-amyloid oligomers alone or in combination with ginsenoside Rh1. We observed that ginsenoside Rh1 was able to attenuate β-amyloid induced oxidative stress and cell death by activating the PI3K/Akt signaling pathway. Based on these findings, we suggest that ginsenoside Rh1 might be an efficacious therapeutic agent for AD. |
first_indexed | 2024-03-10T10:18:01Z |
format | Article |
id | doaj.art-e269ceac8ca64f42b1136a9be339685b |
institution | Directory Open Access Journal |
issn | 2076-3417 |
language | English |
last_indexed | 2024-03-10T10:18:01Z |
publishDate | 2021-06-01 |
publisher | MDPI AG |
record_format | Article |
series | Applied Sciences |
spelling | doaj.art-e269ceac8ca64f42b1136a9be339685b2023-11-22T00:43:25ZengMDPI AGApplied Sciences2076-34172021-06-011112565410.3390/app11125654Ginsenoside Rh1 Exerts Neuroprotective Effects by Activating the PI3K/Akt Pathway in Amyloid-β Induced SH-SY5Y CellsMiey Park0So-Hyeun Kim1Hae-Jeung Lee2Department of Food and Nutrition, College of BioNano Technology, Gachon University, Seongnam-si 13120, Gyeonggi-do, KoreaDepartment of Food and Nutrition, College of BioNano Technology, Gachon University, Seongnam-si 13120, Gyeonggi-do, KoreaDepartment of Food and Nutrition, College of BioNano Technology, Gachon University, Seongnam-si 13120, Gyeonggi-do, KoreaAlzheimer’s disease (AD) is a neurodegenerative disorder characterized by the accumulation of β-amyloid plaques and hyperphosphorylated tau proteins in the brain. Cell signaling pathways such as PI3K/Akt are known to play an essential role in regulating cell survival, motility, transcription, metabolism, and progression of the cell cycle. Recent studies demonstrated that the disruption of these signaling pathways in neurodegenerative disorders leads to oxidative stress and cell death. Targeting these altered signaling pathways could be considered as the therapeutic approach for neurodegenerative disorders. Ginsenoside Rh1 is known to provide beneficial effects in various diseases such as cancer, diabetes, and inflammation. In this study, human neuroblastoma SH-SY5Y cells were treated with the β-amyloid oligomers alone or in combination with ginsenoside Rh1. We observed that ginsenoside Rh1 was able to attenuate β-amyloid induced oxidative stress and cell death by activating the PI3K/Akt signaling pathway. Based on these findings, we suggest that ginsenoside Rh1 might be an efficacious therapeutic agent for AD.https://www.mdpi.com/2076-3417/11/12/5654Alzheimer’s diseaseAmyloid-βGinsenoside Rh1SH-SY5Y cellsPI3K/Akt |
spellingShingle | Miey Park So-Hyeun Kim Hae-Jeung Lee Ginsenoside Rh1 Exerts Neuroprotective Effects by Activating the PI3K/Akt Pathway in Amyloid-β Induced SH-SY5Y Cells Applied Sciences Alzheimer’s disease Amyloid-β Ginsenoside Rh1 SH-SY5Y cells PI3K/Akt |
title | Ginsenoside Rh1 Exerts Neuroprotective Effects by Activating the PI3K/Akt Pathway in Amyloid-β Induced SH-SY5Y Cells |
title_full | Ginsenoside Rh1 Exerts Neuroprotective Effects by Activating the PI3K/Akt Pathway in Amyloid-β Induced SH-SY5Y Cells |
title_fullStr | Ginsenoside Rh1 Exerts Neuroprotective Effects by Activating the PI3K/Akt Pathway in Amyloid-β Induced SH-SY5Y Cells |
title_full_unstemmed | Ginsenoside Rh1 Exerts Neuroprotective Effects by Activating the PI3K/Akt Pathway in Amyloid-β Induced SH-SY5Y Cells |
title_short | Ginsenoside Rh1 Exerts Neuroprotective Effects by Activating the PI3K/Akt Pathway in Amyloid-β Induced SH-SY5Y Cells |
title_sort | ginsenoside rh1 exerts neuroprotective effects by activating the pi3k akt pathway in amyloid β induced sh sy5y cells |
topic | Alzheimer’s disease Amyloid-β Ginsenoside Rh1 SH-SY5Y cells PI3K/Akt |
url | https://www.mdpi.com/2076-3417/11/12/5654 |
work_keys_str_mv | AT mieypark ginsenosiderh1exertsneuroprotectiveeffectsbyactivatingthepi3kaktpathwayinamyloidbinducedshsy5ycells AT sohyeunkim ginsenosiderh1exertsneuroprotectiveeffectsbyactivatingthepi3kaktpathwayinamyloidbinducedshsy5ycells AT haejeunglee ginsenosiderh1exertsneuroprotectiveeffectsbyactivatingthepi3kaktpathwayinamyloidbinducedshsy5ycells |