Cargando…

The protective effect of ischemic preconditioning on rat testis

BACKGROUND: It has been demonstrated that brief episodes of sublethal ischemia-reperfusion, so-called ischemic preconditioning, provide powerful tissue protection in different tissues such as heart, brain, skeletal muscle, lung, liver, intestine, kidney, retina, and endothelial cells. Although a rec...

Descripción completa

Detalles Bibliográficos
Autores principales: Sahinkanat, Tayfun, Ozkan, K Ugur, Tolun, Fatma I, Ciralik, Harun, Imrek, Secil S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2231361/
https://www.ncbi.nlm.nih.gov/pubmed/18096073
http://dx.doi.org/10.1186/1477-7827-5-47
_version_ 1782150245935742976
author Sahinkanat, Tayfun
Ozkan, K Ugur
Tolun, Fatma I
Ciralik, Harun
Imrek, Secil S
author_facet Sahinkanat, Tayfun
Ozkan, K Ugur
Tolun, Fatma I
Ciralik, Harun
Imrek, Secil S
author_sort Sahinkanat, Tayfun
collection PubMed
description BACKGROUND: It has been demonstrated that brief episodes of sublethal ischemia-reperfusion, so-called ischemic preconditioning, provide powerful tissue protection in different tissues such as heart, brain, skeletal muscle, lung, liver, intestine, kidney, retina, and endothelial cells. Although a recent study has claimed that there are no protective effects of ischemic preconditioning in rat testis, the protective effects of ischemic preconditioning on testicular tissue have not been investigated adequately. The present study was thus planned to investigate whether ischemic preconditioning has a protective effect on testicular tissue. METHODS: Rats were divided into seven groups that each contained seven rats. In group 1 (control group), only unilateral testicular ischemia was performed by creating a testicular torsion by a 720 degree clockwise rotation for 180 min. In group 2, group 3, group 4, group 5, group 6, and group 7, unilateral testicular ischemia was performed for 180 min following different periods of ischemic preconditioning. The ischemic preconditioning periods were as follows: 10 minutes of ischemia with 10 minutes of reperfusion in group 2; 20 minutes of ischemia with 10 minutes of reperfusion in group 3; 30 minutes of ischemia with 10 minutes of reperfusion in group 4; multiple preconditioning periods were used (3 × 10 min early phase transient ischemia with 10 min reperfusion in all episodes) in group 5; multiple preconditioning periods were used (5, 10, and 15 min early phase transient ischemia with 10 min reperfusion in all episodes) in group 6; and, multiple preconditioning periods were used (10, 20, and 30 min early phase transient ischemia with 10 min reperfusion in all episodes) in group 7. After the ischemic protocols were carried out, animals were sacrificed by cervical dislocation and testicular tissue samples were taken for biochemical measurements (protein, malondialdehyde, nitric oxide) and histological examination. RESULTS: Although decreased tissue malondialdehyde levels were detected in the groups of 2, 3, 4, and 5 compared to group 1, significant decreases were observed in only group 2 and group 5 (p < .05). Nitric oxide levels were numerically decreased in all groups compared to the control group but was statistically significant only in group 5 (p < .05). Histopathological examination demonstrated that all groups subjected to ischemic preconditioning had less tissue damage than group 1 (p < .05). CONCLUSION: These results suggest that ischemic preconditioning provides tissue protection in testicular tissue.
format Text
id pubmed-2231361
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-22313612008-02-06 The protective effect of ischemic preconditioning on rat testis Sahinkanat, Tayfun Ozkan, K Ugur Tolun, Fatma I Ciralik, Harun Imrek, Secil S Reprod Biol Endocrinol Research BACKGROUND: It has been demonstrated that brief episodes of sublethal ischemia-reperfusion, so-called ischemic preconditioning, provide powerful tissue protection in different tissues such as heart, brain, skeletal muscle, lung, liver, intestine, kidney, retina, and endothelial cells. Although a recent study has claimed that there are no protective effects of ischemic preconditioning in rat testis, the protective effects of ischemic preconditioning on testicular tissue have not been investigated adequately. The present study was thus planned to investigate whether ischemic preconditioning has a protective effect on testicular tissue. METHODS: Rats were divided into seven groups that each contained seven rats. In group 1 (control group), only unilateral testicular ischemia was performed by creating a testicular torsion by a 720 degree clockwise rotation for 180 min. In group 2, group 3, group 4, group 5, group 6, and group 7, unilateral testicular ischemia was performed for 180 min following different periods of ischemic preconditioning. The ischemic preconditioning periods were as follows: 10 minutes of ischemia with 10 minutes of reperfusion in group 2; 20 minutes of ischemia with 10 minutes of reperfusion in group 3; 30 minutes of ischemia with 10 minutes of reperfusion in group 4; multiple preconditioning periods were used (3 × 10 min early phase transient ischemia with 10 min reperfusion in all episodes) in group 5; multiple preconditioning periods were used (5, 10, and 15 min early phase transient ischemia with 10 min reperfusion in all episodes) in group 6; and, multiple preconditioning periods were used (10, 20, and 30 min early phase transient ischemia with 10 min reperfusion in all episodes) in group 7. After the ischemic protocols were carried out, animals were sacrificed by cervical dislocation and testicular tissue samples were taken for biochemical measurements (protein, malondialdehyde, nitric oxide) and histological examination. RESULTS: Although decreased tissue malondialdehyde levels were detected in the groups of 2, 3, 4, and 5 compared to group 1, significant decreases were observed in only group 2 and group 5 (p < .05). Nitric oxide levels were numerically decreased in all groups compared to the control group but was statistically significant only in group 5 (p < .05). Histopathological examination demonstrated that all groups subjected to ischemic preconditioning had less tissue damage than group 1 (p < .05). CONCLUSION: These results suggest that ischemic preconditioning provides tissue protection in testicular tissue. BioMed Central 2007-12-20 /pmc/articles/PMC2231361/ /pubmed/18096073 http://dx.doi.org/10.1186/1477-7827-5-47 Text en Copyright © 2007 Sahinkanat et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Sahinkanat, Tayfun
Ozkan, K Ugur
Tolun, Fatma I
Ciralik, Harun
Imrek, Secil S
The protective effect of ischemic preconditioning on rat testis
title The protective effect of ischemic preconditioning on rat testis
title_full The protective effect of ischemic preconditioning on rat testis
title_fullStr The protective effect of ischemic preconditioning on rat testis
title_full_unstemmed The protective effect of ischemic preconditioning on rat testis
title_short The protective effect of ischemic preconditioning on rat testis
title_sort protective effect of ischemic preconditioning on rat testis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2231361/
https://www.ncbi.nlm.nih.gov/pubmed/18096073
http://dx.doi.org/10.1186/1477-7827-5-47
work_keys_str_mv AT sahinkanattayfun theprotectiveeffectofischemicpreconditioningonrattestis
AT ozkankugur theprotectiveeffectofischemicpreconditioningonrattestis
AT tolunfatmai theprotectiveeffectofischemicpreconditioningonrattestis
AT ciralikharun theprotectiveeffectofischemicpreconditioningonrattestis
AT imreksecils theprotectiveeffectofischemicpreconditioningonrattestis
AT sahinkanattayfun protectiveeffectofischemicpreconditioningonrattestis
AT ozkankugur protectiveeffectofischemicpreconditioningonrattestis
AT tolunfatmai protectiveeffectofischemicpreconditioningonrattestis
AT ciralikharun protectiveeffectofischemicpreconditioningonrattestis
AT imreksecils protectiveeffectofischemicpreconditioningonrattestis