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Remote ischemic conditioning protects against testicular ischemia∕reperfusion injury in rats

PURPOSE: To evaluate the effect of remote ischemic conditioning associated to N-acetylcysteine (NAC) on testicular ischemia∕reperfusion (I∕R) injury in rats. METHODS: Twenty-five adult male Wistar rats were randomly distributed into five experimental groups (n=5), as follows: Sham, I∕R, Percondition...

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Detalles Bibliográficos
Autores principales: Damasceno, Ananda Vitória Barros Suzuki, de Barros, Charles Alberto Villacorta, Percario, Sandro, Ribeiro, Rubens Fernando Gonçalves, Monteiro, Andrew Moraes, Gouveia, Eduardo Henrique Herbster, Henriques, Higor Yuri Bezerra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184938/
https://www.ncbi.nlm.nih.gov/pubmed/32348402
http://dx.doi.org/10.1590/s0102-865020200020000003
Descripción
Sumario:PURPOSE: To evaluate the effect of remote ischemic conditioning associated to N-acetylcysteine (NAC) on testicular ischemia∕reperfusion (I∕R) injury in rats. METHODS: Twenty-five adult male Wistar rats were randomly distributed into five experimental groups (n=5), as follows: Sham, I∕R, Perconditioning (PER), NAC and PER+NAC. Two-hour ischemia was induced by rotating the left testis 720° to clockwise direction, followed by 4 hours of reperfusion. Perconditioning was performed by three I/R cycles of 10 min each on the left limb, 30 min before reperfusion. N-acetylcysteine (150 mg∕kg) was administered 30 min before reperfusion. RESULTS: Statistical differences were observed in MDA levels between I/R group with all groups (p<0.01), in addition there was statistical difference between PER and Sham, and PER+ NAC groups (p<0.05) in plasma. CONCLUSIONS: The protective effect of perconditioning isolated in the reduction of lipid peroxidation related to oxidative stress was demonstrated. However, when Perconditioning was associated with NAC, there was no protective effect against testicular injury of ischemia and reperfusion.