Role of Hydrogen Peroxide in Cyclosporine-Induced Renal Tubular Cell (LLC-PK1) Injury
We examined the role of hydrogen peroxide production in cyclosporine A (CsA)-induced LLC-PK1 injury. After exposure to CsA (0.1 μM – 100 μM), cytotoxicity assessed by lactate dehydrogenase release to the media increased dose-dependently. LLC-PK1 cells produced hydrogen peroxide, visualized by 2,7-di...
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doaj-80f1f028f1e64c50ae87f8867f52fe3a2020-11-25T01:10:31ZengElsevierJournal of Pharmacological Sciences1347-86132003-01-01913255258Role of Hydrogen Peroxide in Cyclosporine-Induced Renal Tubular Cell (LLC-PK1) InjuryMasashi Nishida0Hiroshi Ogawa1Megumi Tamai2Kohhei Ishiwari3Kenji Hamaoka4Division of Pediatrics, Children’s Research Hospital, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, JapanDepartment of Pediatrics, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, JapanDepartment of Pediatrics, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, JapanDivision of Pediatrics, Children’s Research Hospital, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, JapanDivision of Pediatrics, Children’s Research Hospital, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, JapanWe examined the role of hydrogen peroxide production in cyclosporine A (CsA)-induced LLC-PK1 injury. After exposure to CsA (0.1 μM – 100 μM), cytotoxicity assessed by lactate dehydrogenase release to the media increased dose-dependently. LLC-PK1 cells produced hydrogen peroxide, visualized by 2,7-dichlorodihydrofluorescein assay by the treatment with 100 μM CsA, that was blocked by the treatment with catalase. The cytotoxicity of CsA significantly decreased either by the treatment with catalase, mannitol, or deferoxamine, but not with superoxide dismutase. These results suggest the role of hydrogen peroxide as the source of hydroxyl radical, which mainly contributes to CsA-induced LLC-PK1 injury.http://www.sciencedirect.com/science/article/pii/S1347861319327410 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Masashi Nishida Hiroshi Ogawa Megumi Tamai Kohhei Ishiwari Kenji Hamaoka |
spellingShingle |
Masashi Nishida Hiroshi Ogawa Megumi Tamai Kohhei Ishiwari Kenji Hamaoka Role of Hydrogen Peroxide in Cyclosporine-Induced Renal Tubular Cell (LLC-PK1) Injury Journal of Pharmacological Sciences |
author_facet |
Masashi Nishida Hiroshi Ogawa Megumi Tamai Kohhei Ishiwari Kenji Hamaoka |
author_sort |
Masashi Nishida |
title |
Role of Hydrogen Peroxide in Cyclosporine-Induced Renal Tubular Cell (LLC-PK1) Injury |
title_short |
Role of Hydrogen Peroxide in Cyclosporine-Induced Renal Tubular Cell (LLC-PK1) Injury |
title_full |
Role of Hydrogen Peroxide in Cyclosporine-Induced Renal Tubular Cell (LLC-PK1) Injury |
title_fullStr |
Role of Hydrogen Peroxide in Cyclosporine-Induced Renal Tubular Cell (LLC-PK1) Injury |
title_full_unstemmed |
Role of Hydrogen Peroxide in Cyclosporine-Induced Renal Tubular Cell (LLC-PK1) Injury |
title_sort |
role of hydrogen peroxide in cyclosporine-induced renal tubular cell (llc-pk1) injury |
publisher |
Elsevier |
series |
Journal of Pharmacological Sciences |
issn |
1347-8613 |
publishDate |
2003-01-01 |
description |
We examined the role of hydrogen peroxide production in cyclosporine A (CsA)-induced LLC-PK1 injury. After exposure to CsA (0.1 μM – 100 μM), cytotoxicity assessed by lactate dehydrogenase release to the media increased dose-dependently. LLC-PK1 cells produced hydrogen peroxide, visualized by 2,7-dichlorodihydrofluorescein assay by the treatment with 100 μM CsA, that was blocked by the treatment with catalase. The cytotoxicity of CsA significantly decreased either by the treatment with catalase, mannitol, or deferoxamine, but not with superoxide dismutase. These results suggest the role of hydrogen peroxide as the source of hydroxyl radical, which mainly contributes to CsA-induced LLC-PK1 injury. |
url |
http://www.sciencedirect.com/science/article/pii/S1347861319327410 |
work_keys_str_mv |
AT masashinishida roleofhydrogenperoxideincyclosporineinducedrenaltubularcellllcpk1injury AT hiroshiogawa roleofhydrogenperoxideincyclosporineinducedrenaltubularcellllcpk1injury AT megumitamai roleofhydrogenperoxideincyclosporineinducedrenaltubularcellllcpk1injury AT kohheiishiwari roleofhydrogenperoxideincyclosporineinducedrenaltubularcellllcpk1injury AT kenjihamaoka roleofhydrogenperoxideincyclosporineinducedrenaltubularcellllcpk1injury |
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