Attenuation of endoplasmic reticulum stress and mitochondrial injury in kidney with ischemic postconditioning application and trimetazidine treatment

<p>Abstract</p> <p>Background</p> <p>Endoplasmic reticulum (ER) and mitochondria have been implicated in the pathology of renal ischemia/reperfusion (I/R). In the present study, we investigated whether the use of ischemic postconditioning (IPostC) and trimetazidine (TMZ...

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Main Authors: Mahfoudh-Boussaid Asma, Zaouali Mohamed, Hauet Thierry, Hadj-Ayed Kaouther, Miled Abdel-Hédi, Ghoul-Mazgar Sonia, Saidane-Mosbahi Dalila, Rosello-Catafau Joan, Abdennebi Hassen
Format: Article
Language:English
Published: BMC 2012-08-01
Series:Journal of Biomedical Science
Subjects:
Online Access:http://www.jbiomedsci.com/content/19/1/71
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author Mahfoudh-Boussaid Asma
Zaouali Mohamed
Hauet Thierry
Hadj-Ayed Kaouther
Miled Abdel-Hédi
Ghoul-Mazgar Sonia
Saidane-Mosbahi Dalila
Rosello-Catafau Joan
Abdennebi Hassen
author_facet Mahfoudh-Boussaid Asma
Zaouali Mohamed
Hauet Thierry
Hadj-Ayed Kaouther
Miled Abdel-Hédi
Ghoul-Mazgar Sonia
Saidane-Mosbahi Dalila
Rosello-Catafau Joan
Abdennebi Hassen
author_sort Mahfoudh-Boussaid Asma
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Endoplasmic reticulum (ER) and mitochondria have been implicated in the pathology of renal ischemia/reperfusion (I/R). In the present study, we investigated whether the use of ischemic postconditioning (IPostC) and trimetazidine (TMZ) separately or combined could reduce ER stress and mitochondria damage after renal ischemia.</p> <p>Methods</p> <p>Kidneys of Wistar rats were subjected to 60-min of warm ischemia followed by 120-min of reperfusion (I/R group, n = 6), or to 6 cycles of ischemia/reperfusion (10-s each cycle) just after 60-min of warm ischemia (IPostC group, n = 6), or to i.p. injection of TMZ (3 mg/kg) 30-min before ischemia (TMZ group, n = 6), or to the combination of both treatments (IPostC+TMZ group, n = 6). The results of these experimental groups were compared to those of a sham-operated group in which rat renal pedicles were only dissected. Sodium reabsorption rate, creatinine clearance lactate deshydrogenase (LDH) activity in plasma, and concentration of malonedialdehyde (MDA) in tissue were determined. In addition, Western blot analysis was performed to identify the amounts of cytochrome c, c-JunNH2-terminal kinase (JNK), voltage-dependent anion channel (VDAC), glycogen synthase kinase 3-beta (GSK3-β), and ER stress parameters.</p> <p>Results</p> <p>IPostC or/and TMZ significantly decreased cytolysis, oxidative stress and improved renal function in comparison to I/R group. IPostC but not TMZ significantly attenuated ER stress parameters versus I/R group. Indeed, it down-regulated the glucose-regulated protein 78 (GRP78), the activating transcription factor 4 (ATF4), the RNA activated protein kinase (PKR)-like ER kinas (PERK), the X box binding protein-1 (XBP-1) and the caspase12 protein levels. TMZ treatment significantly augmented GSK3-β phosphorylation and reduced levels of cytochrome c and VDAC phosphorylation in comparison to IPostC application. The combination of both treatments gave a synergetic effect. It significantly improved the survival rate, attenuated cytolysis, oxidative stress and improved renal function.</p> <p>Conclusion</p> <p>This study revealed that IPostC protects kidney from I/R injury by suppressing ER stress while the beneficial effects of TMZ are mediated by mitochondria protection. The combination of both treatments ameliorated functional recovery.</p>
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spelling doaj.art-e0933317f16743a6ace0b6324073307b2022-12-22T03:17:02ZengBMCJournal of Biomedical Science1021-77701423-01272012-08-011917110.1186/1423-0127-19-71Attenuation of endoplasmic reticulum stress and mitochondrial injury in kidney with ischemic postconditioning application and trimetazidine treatmentMahfoudh-Boussaid AsmaZaouali MohamedHauet ThierryHadj-Ayed KaoutherMiled Abdel-HédiGhoul-Mazgar SoniaSaidane-Mosbahi DalilaRosello-Catafau JoanAbdennebi Hassen<p>Abstract</p> <p>Background</p> <p>Endoplasmic reticulum (ER) and mitochondria have been implicated in the pathology of renal ischemia/reperfusion (I/R). In the present study, we investigated whether the use of ischemic postconditioning (IPostC) and trimetazidine (TMZ) separately or combined could reduce ER stress and mitochondria damage after renal ischemia.</p> <p>Methods</p> <p>Kidneys of Wistar rats were subjected to 60-min of warm ischemia followed by 120-min of reperfusion (I/R group, n = 6), or to 6 cycles of ischemia/reperfusion (10-s each cycle) just after 60-min of warm ischemia (IPostC group, n = 6), or to i.p. injection of TMZ (3 mg/kg) 30-min before ischemia (TMZ group, n = 6), or to the combination of both treatments (IPostC+TMZ group, n = 6). The results of these experimental groups were compared to those of a sham-operated group in which rat renal pedicles were only dissected. Sodium reabsorption rate, creatinine clearance lactate deshydrogenase (LDH) activity in plasma, and concentration of malonedialdehyde (MDA) in tissue were determined. In addition, Western blot analysis was performed to identify the amounts of cytochrome c, c-JunNH2-terminal kinase (JNK), voltage-dependent anion channel (VDAC), glycogen synthase kinase 3-beta (GSK3-β), and ER stress parameters.</p> <p>Results</p> <p>IPostC or/and TMZ significantly decreased cytolysis, oxidative stress and improved renal function in comparison to I/R group. IPostC but not TMZ significantly attenuated ER stress parameters versus I/R group. Indeed, it down-regulated the glucose-regulated protein 78 (GRP78), the activating transcription factor 4 (ATF4), the RNA activated protein kinase (PKR)-like ER kinas (PERK), the X box binding protein-1 (XBP-1) and the caspase12 protein levels. TMZ treatment significantly augmented GSK3-β phosphorylation and reduced levels of cytochrome c and VDAC phosphorylation in comparison to IPostC application. The combination of both treatments gave a synergetic effect. It significantly improved the survival rate, attenuated cytolysis, oxidative stress and improved renal function.</p> <p>Conclusion</p> <p>This study revealed that IPostC protects kidney from I/R injury by suppressing ER stress while the beneficial effects of TMZ are mediated by mitochondria protection. The combination of both treatments ameliorated functional recovery.</p>http://www.jbiomedsci.com/content/19/1/71KidneyIschemia-reperfusionIschemic postconditioningTrimetazidineEndoplasmic reticulum stressMitochondria
spellingShingle Mahfoudh-Boussaid Asma
Zaouali Mohamed
Hauet Thierry
Hadj-Ayed Kaouther
Miled Abdel-Hédi
Ghoul-Mazgar Sonia
Saidane-Mosbahi Dalila
Rosello-Catafau Joan
Abdennebi Hassen
Attenuation of endoplasmic reticulum stress and mitochondrial injury in kidney with ischemic postconditioning application and trimetazidine treatment
Journal of Biomedical Science
Kidney
Ischemia-reperfusion
Ischemic postconditioning
Trimetazidine
Endoplasmic reticulum stress
Mitochondria
title Attenuation of endoplasmic reticulum stress and mitochondrial injury in kidney with ischemic postconditioning application and trimetazidine treatment
title_full Attenuation of endoplasmic reticulum stress and mitochondrial injury in kidney with ischemic postconditioning application and trimetazidine treatment
title_fullStr Attenuation of endoplasmic reticulum stress and mitochondrial injury in kidney with ischemic postconditioning application and trimetazidine treatment
title_full_unstemmed Attenuation of endoplasmic reticulum stress and mitochondrial injury in kidney with ischemic postconditioning application and trimetazidine treatment
title_short Attenuation of endoplasmic reticulum stress and mitochondrial injury in kidney with ischemic postconditioning application and trimetazidine treatment
title_sort attenuation of endoplasmic reticulum stress and mitochondrial injury in kidney with ischemic postconditioning application and trimetazidine treatment
topic Kidney
Ischemia-reperfusion
Ischemic postconditioning
Trimetazidine
Endoplasmic reticulum stress
Mitochondria
url http://www.jbiomedsci.com/content/19/1/71
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