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Protective Effects of Resveratrol against Chronic Immobilization Stress on Testis

Objective. The aim of this study was to investigate protective effects of resveratrol, a strong antioxidant, against possible negative effects of chronic immobilization stress on testes of male rats histochemically, immunohistochemically, ultrastructurally, and biochemically. Material and Methods. M...

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Detalles Bibliográficos
Autores principales: Bitgul, Gulsah, Tekmen, Isil, Keles, Didem, Oktay, Gulgun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836419/
https://www.ncbi.nlm.nih.gov/pubmed/24307953
http://dx.doi.org/10.1155/2013/278720
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author Bitgul, Gulsah
Tekmen, Isil
Keles, Didem
Oktay, Gulgun
author_facet Bitgul, Gulsah
Tekmen, Isil
Keles, Didem
Oktay, Gulgun
author_sort Bitgul, Gulsah
collection PubMed
description Objective. The aim of this study was to investigate protective effects of resveratrol, a strong antioxidant, against possible negative effects of chronic immobilization stress on testes of male rats histochemically, immunohistochemically, ultrastructurally, and biochemically. Material and Methods. Male Wistar rats were divided into 4 groups (n = 7). Group I, control group (C), was not exposed to stress. Group II, stress group (S), was exposed to chronic immobilization stress. In Group III, low dose resveratrol + stress group (LRS), rats were given 10 mg/kg/day resveratrol just before the stress application. In Group IV, high dose resveratrol + stress group (HRS), rats were given 20 mg/kg/day resveratrol just before the stress application. For chronic immobilization stress application animals were put in the plastic tubes (6 cm in diameter, 15 cm in length) during 32 days for 6 hours. All animals were sacrificed 18 hours after the last stress application. Results. Histochemical and ultrastructural investigations showed that in stress group there was germ cell deprivation in seminiferous tubules and increase of connective tissue on interstitial area. No significant changes were seen in low and high dose resveratrol groups. After immunohistochemical investigations, TUNEL (+) and Active Caspase-3 (+) cells were increased in seminiferous tubules of stress group compared with those control group, but they were decreased in low and high dose resveratrol groups. According to biochemically results, MDA, GSH, and testosterone levels in stress group showed no significant difference when compared with those of the other groups. Conclusion. The chronic immobilization stress increases oxidative stress and apoptosis and causes histological tissue damages; resveratrol can minimize the histological damage in testes significantly.
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spelling pubmed-38364192013-12-04 Protective Effects of Resveratrol against Chronic Immobilization Stress on Testis Bitgul, Gulsah Tekmen, Isil Keles, Didem Oktay, Gulgun ISRN Urol Research Article Objective. The aim of this study was to investigate protective effects of resveratrol, a strong antioxidant, against possible negative effects of chronic immobilization stress on testes of male rats histochemically, immunohistochemically, ultrastructurally, and biochemically. Material and Methods. Male Wistar rats were divided into 4 groups (n = 7). Group I, control group (C), was not exposed to stress. Group II, stress group (S), was exposed to chronic immobilization stress. In Group III, low dose resveratrol + stress group (LRS), rats were given 10 mg/kg/day resveratrol just before the stress application. In Group IV, high dose resveratrol + stress group (HRS), rats were given 20 mg/kg/day resveratrol just before the stress application. For chronic immobilization stress application animals were put in the plastic tubes (6 cm in diameter, 15 cm in length) during 32 days for 6 hours. All animals were sacrificed 18 hours after the last stress application. Results. Histochemical and ultrastructural investigations showed that in stress group there was germ cell deprivation in seminiferous tubules and increase of connective tissue on interstitial area. No significant changes were seen in low and high dose resveratrol groups. After immunohistochemical investigations, TUNEL (+) and Active Caspase-3 (+) cells were increased in seminiferous tubules of stress group compared with those control group, but they were decreased in low and high dose resveratrol groups. According to biochemically results, MDA, GSH, and testosterone levels in stress group showed no significant difference when compared with those of the other groups. Conclusion. The chronic immobilization stress increases oxidative stress and apoptosis and causes histological tissue damages; resveratrol can minimize the histological damage in testes significantly. Hindawi Publishing Corporation 2013-11-06 /pmc/articles/PMC3836419/ /pubmed/24307953 http://dx.doi.org/10.1155/2013/278720 Text en Copyright © 2013 Gulsah Bitgul et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bitgul, Gulsah
Tekmen, Isil
Keles, Didem
Oktay, Gulgun
Protective Effects of Resveratrol against Chronic Immobilization Stress on Testis
title Protective Effects of Resveratrol against Chronic Immobilization Stress on Testis
title_full Protective Effects of Resveratrol against Chronic Immobilization Stress on Testis
title_fullStr Protective Effects of Resveratrol against Chronic Immobilization Stress on Testis
title_full_unstemmed Protective Effects of Resveratrol against Chronic Immobilization Stress on Testis
title_short Protective Effects of Resveratrol against Chronic Immobilization Stress on Testis
title_sort protective effects of resveratrol against chronic immobilization stress on testis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836419/
https://www.ncbi.nlm.nih.gov/pubmed/24307953
http://dx.doi.org/10.1155/2013/278720
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