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Effects of Hypobaric Hypoxia on Rat Retina and Protective Response of Resveratrol to the Stress

High-altitude retinopathy represents retinal functional changes associated with environmental challenges imposed by hypobaric hypoxia, but the detailed cellular and molecular mechanism underlying this process remains unclear. Our current investigation was to explore the effect of hypobaric hypoxia o...

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Autores principales: Xin, Xiaorong, Dang, Hong, Zhao, Xiaojing, Wang, Haohao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599917/
https://www.ncbi.nlm.nih.gov/pubmed/28924365
http://dx.doi.org/10.7150/ijms.19391
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author Xin, Xiaorong
Dang, Hong
Zhao, Xiaojing
Wang, Haohao
author_facet Xin, Xiaorong
Dang, Hong
Zhao, Xiaojing
Wang, Haohao
author_sort Xin, Xiaorong
collection PubMed
description High-altitude retinopathy represents retinal functional changes associated with environmental challenges imposed by hypobaric hypoxia, but the detailed cellular and molecular mechanism underlying this process remains unclear. Our current investigation was to explore the effect of hypobaric hypoxia on the rat retina and determine whether resveratrol has a protective efficacy on the hypoxic damage to the retina. Experiment rats were randomly grouped as the control group, hypoxia group and resveratrol intervention group. The hypoxia group and the resveratrol intervention group were maintained in a low-pressure oxygen cabin, and the resveratrol intervention group was given daily intraperitoneal injections with resveratrol. We found that hypobaric hypoxia increased thioredoxin 1 (Trx1) and thioredoxin 2 (Trx2) expression in retinas, and resveratrol treatment significantly reversed these changes (P < 0.05, P < 0.05 respectively). In comparison with controls, hypoxia upregulated the mRNA expression levels of caspase3 (P < 0.001), caspase9 (P < 0.01), heat shock protein 70 (Hsp70) (P < 0.05), heat shock protein 90 (Hsp90) (P < 0.001) and hypoxia-inducible factor-1 (HIF-1) (P < 0.05). Resveratrol administration caused a significant decrease in the gene expression of caspase3 (P< 0.001), HSP90 (P < 0.05) and HIF-1 mRNA (P < 0.01) as well as an increase in HSP70 mRNA when compared with the hypoxia group. These findings indicated that resveratrol exerted an anti-oxidative role by modulating hypoxia stress- associated genes and an anti-apoptosis role by regulating apoptosis-related cytokines. In conclusion, hypobaric hypoxia may have a pathological impact on rat retinas. The intervention of resveratrol reverses the effect induced by hypobaric hypoxia and elicits a protective response to the stress.
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spelling pubmed-55999172017-09-18 Effects of Hypobaric Hypoxia on Rat Retina and Protective Response of Resveratrol to the Stress Xin, Xiaorong Dang, Hong Zhao, Xiaojing Wang, Haohao Int J Med Sci Research Paper High-altitude retinopathy represents retinal functional changes associated with environmental challenges imposed by hypobaric hypoxia, but the detailed cellular and molecular mechanism underlying this process remains unclear. Our current investigation was to explore the effect of hypobaric hypoxia on the rat retina and determine whether resveratrol has a protective efficacy on the hypoxic damage to the retina. Experiment rats were randomly grouped as the control group, hypoxia group and resveratrol intervention group. The hypoxia group and the resveratrol intervention group were maintained in a low-pressure oxygen cabin, and the resveratrol intervention group was given daily intraperitoneal injections with resveratrol. We found that hypobaric hypoxia increased thioredoxin 1 (Trx1) and thioredoxin 2 (Trx2) expression in retinas, and resveratrol treatment significantly reversed these changes (P < 0.05, P < 0.05 respectively). In comparison with controls, hypoxia upregulated the mRNA expression levels of caspase3 (P < 0.001), caspase9 (P < 0.01), heat shock protein 70 (Hsp70) (P < 0.05), heat shock protein 90 (Hsp90) (P < 0.001) and hypoxia-inducible factor-1 (HIF-1) (P < 0.05). Resveratrol administration caused a significant decrease in the gene expression of caspase3 (P< 0.001), HSP90 (P < 0.05) and HIF-1 mRNA (P < 0.01) as well as an increase in HSP70 mRNA when compared with the hypoxia group. These findings indicated that resveratrol exerted an anti-oxidative role by modulating hypoxia stress- associated genes and an anti-apoptosis role by regulating apoptosis-related cytokines. In conclusion, hypobaric hypoxia may have a pathological impact on rat retinas. The intervention of resveratrol reverses the effect induced by hypobaric hypoxia and elicits a protective response to the stress. Ivyspring International Publisher 2017-08-17 /pmc/articles/PMC5599917/ /pubmed/28924365 http://dx.doi.org/10.7150/ijms.19391 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Xin, Xiaorong
Dang, Hong
Zhao, Xiaojing
Wang, Haohao
Effects of Hypobaric Hypoxia on Rat Retina and Protective Response of Resveratrol to the Stress
title Effects of Hypobaric Hypoxia on Rat Retina and Protective Response of Resveratrol to the Stress
title_full Effects of Hypobaric Hypoxia on Rat Retina and Protective Response of Resveratrol to the Stress
title_fullStr Effects of Hypobaric Hypoxia on Rat Retina and Protective Response of Resveratrol to the Stress
title_full_unstemmed Effects of Hypobaric Hypoxia on Rat Retina and Protective Response of Resveratrol to the Stress
title_short Effects of Hypobaric Hypoxia on Rat Retina and Protective Response of Resveratrol to the Stress
title_sort effects of hypobaric hypoxia on rat retina and protective response of resveratrol to the stress
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599917/
https://www.ncbi.nlm.nih.gov/pubmed/28924365
http://dx.doi.org/10.7150/ijms.19391
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