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Nephroprotective Effect of Sonchus oleraceus Extract against Kidney Injury Induced by Ischemia-Reperfusion in Wistar Rats

INTRODUCTION: Kidney ischemia-reperfusion (I/R) injury is the main cause of delayed graft function in solid organ transplantation. Sonchus oleraceus is a plant with well-known antioxidant and anti-inflammatory activities; however, its effects on renal I/R are unknown. OBJECTIVE: To evaluate whether...

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Autores principales: Torres-González, Liliana, Cienfuegos-Pecina, Eduardo, Perales-Quintana, Marlene M., Alarcon-Galvan, Gabriela, Muñoz-Espinosa, Linda E., Pérez-Rodríguez, Edelmiro, Cordero-Pérez, Paula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832116/
https://www.ncbi.nlm.nih.gov/pubmed/29643981
http://dx.doi.org/10.1155/2018/9572803
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author Torres-González, Liliana
Cienfuegos-Pecina, Eduardo
Perales-Quintana, Marlene M.
Alarcon-Galvan, Gabriela
Muñoz-Espinosa, Linda E.
Pérez-Rodríguez, Edelmiro
Cordero-Pérez, Paula
author_facet Torres-González, Liliana
Cienfuegos-Pecina, Eduardo
Perales-Quintana, Marlene M.
Alarcon-Galvan, Gabriela
Muñoz-Espinosa, Linda E.
Pérez-Rodríguez, Edelmiro
Cordero-Pérez, Paula
author_sort Torres-González, Liliana
collection PubMed
description INTRODUCTION: Kidney ischemia-reperfusion (I/R) injury is the main cause of delayed graft function in solid organ transplantation. Sonchus oleraceus is a plant with well-known antioxidant and anti-inflammatory activities; however, its effects on renal I/R are unknown. OBJECTIVE: To evaluate whether S. oleraceus extract (S.O.e.) has nephroprotective activity in an I/R model in Wistar rats. MATERIALS AND METHODS: Animal groups (n = 6): sham, I/R (45 min/15 h), S.O.e (300 mg/kg p.o.), and S.O.e + I/R (300 mg/kg, p.o.; 45 min/15 h). Renal function, proinflammatory cytokines, alanine aminotransferase, markers of oxidative stress, and histology were evaluated. RESULTS: None of the mediators evaluated differed significantly between the S.O.e and sham groups. Levels of blood urea nitrogen (BUN), creatinine, malondialdehyde (MDA), and proinflammatory cytokines were higher, and superoxide dismutase (SOD) was lower in the I/R group than in the sham group. Histology showed tubular epithelial necrosis in the medulla and cortex in the I/R group. In the S.O.e + I/R group, S.O.e pretreatment attenuated the I/R-induced increases in BUN, creatinine, MDA, and proinflammatory cytokines induced, SOD was maintained, and histology showed discontinuous necrosis in the medulla but no necrosis in the cortex. CONCLUSIONS: S.O.e was neither hepatotoxic nor nephrotoxic. S.O.e. pretreatment showed a nephroprotective effect against I/R.
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spelling pubmed-58321162018-04-11 Nephroprotective Effect of Sonchus oleraceus Extract against Kidney Injury Induced by Ischemia-Reperfusion in Wistar Rats Torres-González, Liliana Cienfuegos-Pecina, Eduardo Perales-Quintana, Marlene M. Alarcon-Galvan, Gabriela Muñoz-Espinosa, Linda E. Pérez-Rodríguez, Edelmiro Cordero-Pérez, Paula Oxid Med Cell Longev Research Article INTRODUCTION: Kidney ischemia-reperfusion (I/R) injury is the main cause of delayed graft function in solid organ transplantation. Sonchus oleraceus is a plant with well-known antioxidant and anti-inflammatory activities; however, its effects on renal I/R are unknown. OBJECTIVE: To evaluate whether S. oleraceus extract (S.O.e.) has nephroprotective activity in an I/R model in Wistar rats. MATERIALS AND METHODS: Animal groups (n = 6): sham, I/R (45 min/15 h), S.O.e (300 mg/kg p.o.), and S.O.e + I/R (300 mg/kg, p.o.; 45 min/15 h). Renal function, proinflammatory cytokines, alanine aminotransferase, markers of oxidative stress, and histology were evaluated. RESULTS: None of the mediators evaluated differed significantly between the S.O.e and sham groups. Levels of blood urea nitrogen (BUN), creatinine, malondialdehyde (MDA), and proinflammatory cytokines were higher, and superoxide dismutase (SOD) was lower in the I/R group than in the sham group. Histology showed tubular epithelial necrosis in the medulla and cortex in the I/R group. In the S.O.e + I/R group, S.O.e pretreatment attenuated the I/R-induced increases in BUN, creatinine, MDA, and proinflammatory cytokines induced, SOD was maintained, and histology showed discontinuous necrosis in the medulla but no necrosis in the cortex. CONCLUSIONS: S.O.e was neither hepatotoxic nor nephrotoxic. S.O.e. pretreatment showed a nephroprotective effect against I/R. Hindawi 2018-02-14 /pmc/articles/PMC5832116/ /pubmed/29643981 http://dx.doi.org/10.1155/2018/9572803 Text en Copyright © 2018 Liliana Torres-González et al. http://creativecommons.org/licenses/by/4.0/ 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
Torres-González, Liliana
Cienfuegos-Pecina, Eduardo
Perales-Quintana, Marlene M.
Alarcon-Galvan, Gabriela
Muñoz-Espinosa, Linda E.
Pérez-Rodríguez, Edelmiro
Cordero-Pérez, Paula
Nephroprotective Effect of Sonchus oleraceus Extract against Kidney Injury Induced by Ischemia-Reperfusion in Wistar Rats
title Nephroprotective Effect of Sonchus oleraceus Extract against Kidney Injury Induced by Ischemia-Reperfusion in Wistar Rats
title_full Nephroprotective Effect of Sonchus oleraceus Extract against Kidney Injury Induced by Ischemia-Reperfusion in Wistar Rats
title_fullStr Nephroprotective Effect of Sonchus oleraceus Extract against Kidney Injury Induced by Ischemia-Reperfusion in Wistar Rats
title_full_unstemmed Nephroprotective Effect of Sonchus oleraceus Extract against Kidney Injury Induced by Ischemia-Reperfusion in Wistar Rats
title_short Nephroprotective Effect of Sonchus oleraceus Extract against Kidney Injury Induced by Ischemia-Reperfusion in Wistar Rats
title_sort nephroprotective effect of sonchus oleraceus extract against kidney injury induced by ischemia-reperfusion in wistar rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832116/
https://www.ncbi.nlm.nih.gov/pubmed/29643981
http://dx.doi.org/10.1155/2018/9572803
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