TY - JOUR
T1 - Comparison of the effects of the superoxide dismutase mimetics EUK-134 and tempol on paraquat-induced nephrotoxicity
AU - Samai, Mohamed
AU - Sharpe, Martyn A.
AU - Gard, Paul R.
AU - Chatterjee, Prabal K.
N1 - Funding Information:
M.S. is the recipient of a Commonwealth Scholarship provided by the Commission Scholarship Commission UK (SLCS-2004-304). P.K.C. acknowledges PABS, University of Brighton, for additional funding of this research.
Copyright:
Copyright 2009 Elsevier B.V., All rights reserved.
PY - 2007/8/15
Y1 - 2007/8/15
N2 - Paraquat-induced nephrotoxicity involves severe renal cell damage caused by reactive oxygen species (ROS), specifically via increasing concentrations of superoxide anions in the kidney. Recently, superoxide dismutase (SOD) mimetics (SODm) have been developed that display safe SOD activities but which also possess additional antioxidant enzyme (e.g., catalase) or ROS-scavenging activities. The aim of this study was to compare the effects of two such SODm, specifically, EUK-134, a SODm with catalase activity, and tempol, a SODm with ROS-scavenging properties, on paraquat-induced nephrotoxicity of renal NRK-52E cells. Incubation with paraquat (1 mM) for 24 h reduced cell viability and increased necrosis significantly. Paraquat also generated significant quantities of superoxide anions and hydroxyl radicals. Both EUK-134 (10-300 μM) and tempol (0.3-1.0 mM) were able to improve cell viability and reduced paraquat-induced cell death significantly via dismutation or scavenging of superoxide anions and reduced hydroxyl radical generation. The data presented here suggest that SODm such as EUK-134 and tempol, which possess additional catalase and/or ROS-scavenging activities, can significantly reduce renal cell damage caused by paraquat. These effects were evident at concentrations which avoid the pro-oxidant activities associated with higher concentrations of SOD. Such SODm could therefore prove to be beneficial as therapies for paraquat nephrotoxicity.
AB - Paraquat-induced nephrotoxicity involves severe renal cell damage caused by reactive oxygen species (ROS), specifically via increasing concentrations of superoxide anions in the kidney. Recently, superoxide dismutase (SOD) mimetics (SODm) have been developed that display safe SOD activities but which also possess additional antioxidant enzyme (e.g., catalase) or ROS-scavenging activities. The aim of this study was to compare the effects of two such SODm, specifically, EUK-134, a SODm with catalase activity, and tempol, a SODm with ROS-scavenging properties, on paraquat-induced nephrotoxicity of renal NRK-52E cells. Incubation with paraquat (1 mM) for 24 h reduced cell viability and increased necrosis significantly. Paraquat also generated significant quantities of superoxide anions and hydroxyl radicals. Both EUK-134 (10-300 μM) and tempol (0.3-1.0 mM) were able to improve cell viability and reduced paraquat-induced cell death significantly via dismutation or scavenging of superoxide anions and reduced hydroxyl radical generation. The data presented here suggest that SODm such as EUK-134 and tempol, which possess additional catalase and/or ROS-scavenging activities, can significantly reduce renal cell damage caused by paraquat. These effects were evident at concentrations which avoid the pro-oxidant activities associated with higher concentrations of SOD. Such SODm could therefore prove to be beneficial as therapies for paraquat nephrotoxicity.
KW - EUK-134
KW - Free radicals
KW - Kidney
KW - Nephrotoxicity
KW - NRK-52E
KW - Paraquat
KW - Reactive oxygen species
KW - Renal
KW - Superoxide
KW - Superoxide dismutase mimetic
KW - Tempol
UR - http://www.scopus.com/inward/record.url?scp=34447335058&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=34447335058&partnerID=8YFLogxK
U2 - 10.1016/j.freeradbiomed.2007.05.014
DO - 10.1016/j.freeradbiomed.2007.05.014
M3 - Article
C2 - 17640563
AN - SCOPUS:34447335058
VL - 43
SP - 528
EP - 534
JO - Free Radical Biology and Medicine
JF - Free Radical Biology and Medicine
SN - 0891-5849
IS - 4
ER -