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Astragaloside IV protects rat retinal capillary endothelial cells against high glucose-induced oxidative injury
AIM: Diabetic retinopathy is a microvascular complication of diabetes that leads to blindness. Hyperglycemia causes oxidative stress, which is an important cause in the pathogenesis of microangiopathy. The aim of this study was to investigate the potential protective effects of astragaloside IV (AS-...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732560/ https://www.ncbi.nlm.nih.gov/pubmed/29263652 http://dx.doi.org/10.2147/DDDT.S152489 |
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author | Qiao, Yuan Fan, Chun-Lan Tang, Min-Ke |
author_facet | Qiao, Yuan Fan, Chun-Lan Tang, Min-Ke |
author_sort | Qiao, Yuan |
collection | PubMed |
description | AIM: Diabetic retinopathy is a microvascular complication of diabetes that leads to blindness. Hyperglycemia causes oxidative stress, which is an important cause in the pathogenesis of microangiopathy. The aim of this study was to investigate the potential protective effects of astragaloside IV (AS-IV) in retinal capillary endothelial cells (RCECs) incubated with high glucose conditions. METHODS AND RESULTS: Based on rat RCECs cultured with high glucose (30 mM) in vitro, a significant increase in cell viability in rat RCECs incubated with both AS-IV and high glucose for 48 or 72 h by MTT assay. The increased viability was accompanied by decreased glucose transporter-1 expression using immunofluorescent assay. Meanwhile, AS-IV reduced intracellular hydrogen peroxide and superoxide, decreased mitochondrial reactive oxygen species in rat RCECs with high glucose by the fluorescent probes, and lowered malondialdehyde levels. In addition, AS-IV increased the activities of total superoxide dismutase, MnSOD, catalase, and glutathione peroxidase. The glutathione content also increased after AS-IV treatment. Furthermore, AS-IV reduced NADPH oxidase 4 expression by western blot method. CONCLUSION: These results suggest that the main mechanism underlying the protective effects of AS-IV in high glucose-injured RCECs may be related to its antioxidative function. |
format | Online Article Text |
id | pubmed-5732560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57325602017-12-20 Astragaloside IV protects rat retinal capillary endothelial cells against high glucose-induced oxidative injury Qiao, Yuan Fan, Chun-Lan Tang, Min-Ke Drug Des Devel Ther Original Research AIM: Diabetic retinopathy is a microvascular complication of diabetes that leads to blindness. Hyperglycemia causes oxidative stress, which is an important cause in the pathogenesis of microangiopathy. The aim of this study was to investigate the potential protective effects of astragaloside IV (AS-IV) in retinal capillary endothelial cells (RCECs) incubated with high glucose conditions. METHODS AND RESULTS: Based on rat RCECs cultured with high glucose (30 mM) in vitro, a significant increase in cell viability in rat RCECs incubated with both AS-IV and high glucose for 48 or 72 h by MTT assay. The increased viability was accompanied by decreased glucose transporter-1 expression using immunofluorescent assay. Meanwhile, AS-IV reduced intracellular hydrogen peroxide and superoxide, decreased mitochondrial reactive oxygen species in rat RCECs with high glucose by the fluorescent probes, and lowered malondialdehyde levels. In addition, AS-IV increased the activities of total superoxide dismutase, MnSOD, catalase, and glutathione peroxidase. The glutathione content also increased after AS-IV treatment. Furthermore, AS-IV reduced NADPH oxidase 4 expression by western blot method. CONCLUSION: These results suggest that the main mechanism underlying the protective effects of AS-IV in high glucose-injured RCECs may be related to its antioxidative function. Dove Medical Press 2017-12-13 /pmc/articles/PMC5732560/ /pubmed/29263652 http://dx.doi.org/10.2147/DDDT.S152489 Text en © 2017 Qiao et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Qiao, Yuan Fan, Chun-Lan Tang, Min-Ke Astragaloside IV protects rat retinal capillary endothelial cells against high glucose-induced oxidative injury |
title | Astragaloside IV protects rat retinal capillary endothelial cells against high glucose-induced oxidative injury |
title_full | Astragaloside IV protects rat retinal capillary endothelial cells against high glucose-induced oxidative injury |
title_fullStr | Astragaloside IV protects rat retinal capillary endothelial cells against high glucose-induced oxidative injury |
title_full_unstemmed | Astragaloside IV protects rat retinal capillary endothelial cells against high glucose-induced oxidative injury |
title_short | Astragaloside IV protects rat retinal capillary endothelial cells against high glucose-induced oxidative injury |
title_sort | astragaloside iv protects rat retinal capillary endothelial cells against high glucose-induced oxidative injury |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732560/ https://www.ncbi.nlm.nih.gov/pubmed/29263652 http://dx.doi.org/10.2147/DDDT.S152489 |
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