Effects of tetrahydroxy stilbene glycoside derivatives on free radical damage and apoptosis in APP695V717I transgenic mice

ABSTRACTMitochondrial dysfunction leading to overproduction of oxygen free radicals is an important event in the development of Alzheimer's disease. Tetrahydroxy stilbene glycoside (TSG) is one of the main effective components of Polygonum multiflorum and has a certain free radical scavenging e...

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Main Authors: Jun Qian, Yun Li, Yanyun Wang, Qunying Ye, Hongbo Luo
Format: Article
Language:English
Published: Taylor & Francis Group 2023-12-01
Series:Redox Report
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/13510002.2023.2259246
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author Jun Qian
Yun Li
Yanyun Wang
Qunying Ye
Hongbo Luo
author_facet Jun Qian
Yun Li
Yanyun Wang
Qunying Ye
Hongbo Luo
author_sort Jun Qian
collection DOAJ
description ABSTRACTMitochondrial dysfunction leading to overproduction of oxygen free radicals is an important event in the development of Alzheimer's disease. Tetrahydroxy stilbene glycoside (TSG) is one of the main effective components of Polygonum multiflorum and has a certain free radical scavenging effect. We synthesized tetrahydroxy stilbene glycoside derivatives (Mito-TSGs) that can cross the mitochondrial membrane and may provide effective protection against Alzheimer's disease. This experiment investigates the protective mechanism of tetrahydroxy stilbene glycoside derivatives against mitochondrial free radical damage and apoptosis in APP695V717I transgenic model mice. The experimental subjects were healthy 3-month-old APP695V717I transgenic model mice, while C57BL/6J mice of the same age and genetic background served as controls. The results demonstrated that the tetrahydroxy stilbene glycoside derivatives significantly improved mouse behavioral performance. It also led to a decrease in the levels of H2O2, NO, MDA, and LD, along with an increase in LDH activity and in the antioxidant enzyme activity of SOD, CAT, and GSH-Px. Moreover, it elevated the mitochondrial membrane potential, decreased the gene and protein expression of Caspase-3 and Bax, and increased the gene and protein expression of Bcl-2. Notably, the effectiveness of tetrahydroxy stilbene glycoside derivatives was superior to that of traditional tetrahydroxy stilbene glycoside.
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spelling doaj.art-f58c69ec0a2b4817afb7087afae5fadf2023-12-09T20:05:02ZengTaylor & Francis GroupRedox Report1351-00021743-29282023-12-0128110.1080/13510002.2023.2259246Effects of tetrahydroxy stilbene glycoside derivatives on free radical damage and apoptosis in APP695V717I transgenic miceJun Qian0Yun Li1Yanyun Wang2Qunying Ye3Hongbo Luo4Department of Neurology, Fifth Affiliated Hospital of Zunyi Medical University, Zhuhai, People’s Republic of ChinaDepartment of Nephrology, Fifth Affiliated Hospital of Zunyi Medical University, Zhuhai, People’s Republic of ChinaDepartment of Neurology, Fifth Affiliated Hospital of Zunyi Medical University, Zhuhai, People’s Republic of ChinaDepartment of Neurology, Fifth Affiliated Hospital of Zunyi Medical University, Zhuhai, People’s Republic of ChinaDepartment of Neurology, Fifth Affiliated Hospital of Zunyi Medical University, Zhuhai, People’s Republic of ChinaABSTRACTMitochondrial dysfunction leading to overproduction of oxygen free radicals is an important event in the development of Alzheimer's disease. Tetrahydroxy stilbene glycoside (TSG) is one of the main effective components of Polygonum multiflorum and has a certain free radical scavenging effect. We synthesized tetrahydroxy stilbene glycoside derivatives (Mito-TSGs) that can cross the mitochondrial membrane and may provide effective protection against Alzheimer's disease. This experiment investigates the protective mechanism of tetrahydroxy stilbene glycoside derivatives against mitochondrial free radical damage and apoptosis in APP695V717I transgenic model mice. The experimental subjects were healthy 3-month-old APP695V717I transgenic model mice, while C57BL/6J mice of the same age and genetic background served as controls. The results demonstrated that the tetrahydroxy stilbene glycoside derivatives significantly improved mouse behavioral performance. It also led to a decrease in the levels of H2O2, NO, MDA, and LD, along with an increase in LDH activity and in the antioxidant enzyme activity of SOD, CAT, and GSH-Px. Moreover, it elevated the mitochondrial membrane potential, decreased the gene and protein expression of Caspase-3 and Bax, and increased the gene and protein expression of Bcl-2. Notably, the effectiveness of tetrahydroxy stilbene glycoside derivatives was superior to that of traditional tetrahydroxy stilbene glycoside.https://www.tandfonline.com/doi/10.1080/13510002.2023.2259246Alzheimer’s diseasetetrahydroxy stilbene glycoside derivativesfree radical damagemitochondrial targeting compoundsoxidative stressapoptosis
spellingShingle Jun Qian
Yun Li
Yanyun Wang
Qunying Ye
Hongbo Luo
Effects of tetrahydroxy stilbene glycoside derivatives on free radical damage and apoptosis in APP695V717I transgenic mice
Redox Report
Alzheimer’s disease
tetrahydroxy stilbene glycoside derivatives
free radical damage
mitochondrial targeting compounds
oxidative stress
apoptosis
title Effects of tetrahydroxy stilbene glycoside derivatives on free radical damage and apoptosis in APP695V717I transgenic mice
title_full Effects of tetrahydroxy stilbene glycoside derivatives on free radical damage and apoptosis in APP695V717I transgenic mice
title_fullStr Effects of tetrahydroxy stilbene glycoside derivatives on free radical damage and apoptosis in APP695V717I transgenic mice
title_full_unstemmed Effects of tetrahydroxy stilbene glycoside derivatives on free radical damage and apoptosis in APP695V717I transgenic mice
title_short Effects of tetrahydroxy stilbene glycoside derivatives on free radical damage and apoptosis in APP695V717I transgenic mice
title_sort effects of tetrahydroxy stilbene glycoside derivatives on free radical damage and apoptosis in app695v717i transgenic mice
topic Alzheimer’s disease
tetrahydroxy stilbene glycoside derivatives
free radical damage
mitochondrial targeting compounds
oxidative stress
apoptosis
url https://www.tandfonline.com/doi/10.1080/13510002.2023.2259246
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