Mitochondrial calcium uniporter blocker effectively prevents brain mitochondrial dysfunction caused by iron overload

Aims Although iron overload induces oxidative stress and brain mitochondrial dysfunction, and is associated with neurodegenerative diseases, brain mitochondrial iron uptake has not been investigated. We determined the role of mitochondrial calcium uniporter (MCU) in brain mitochondria as a major rou...

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Main Authors: Jirapas Sripetchwandee, Jantira Sanit, Nipon Chattipakorn, Siriporn C. Chattipakorn
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/52264
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-522642018-09-04T09:35:52Z Mitochondrial calcium uniporter blocker effectively prevents brain mitochondrial dysfunction caused by iron overload Jirapas Sripetchwandee Jantira Sanit Nipon Chattipakorn Siriporn C. Chattipakorn Biochemistry, Genetics and Molecular Biology Pharmacology, Toxicology and Pharmaceutics Aims Although iron overload induces oxidative stress and brain mitochondrial dysfunction, and is associated with neurodegenerative diseases, brain mitochondrial iron uptake has not been investigated. We determined the role of mitochondrial calcium uniporter (MCU) in brain mitochondria as a major route for iron entry. We hypothesized that iron overload causes brain mitochondrial dysfunction, and that the MCU blocker prevents iron entry into mitochondria, thus attenuating mitochondrial dysfunction. Main methods Isolated brain mitochondria from male Wistar rats were used. Iron (Fe2 +and Fe3 +) at 0-286 μM were applied onto mitochondria at various incubation times (5-30 min), and the mitochondrial function was determined. Effects of MCU blocker (Ru-360) and iron chelator were studied. Key findings Both Fe2 +and Fe3 +entered brain mitochondria and caused mitochondrial swelling in a dose- and time-dependent manner, and caused mitochondrial depolarization and increased ROS production. However, Fe2 +caused more severe mitochondrial dysfunction than Fe3 +. Although all drugs attenuated mitochondrial dysfunction caused by iron overload, only an MCU blocker could completely prevent ROS production and mitochondrial depolarization. Significance Our findings indicated that iron overload caused brain mitochondrial dysfunction, and that an MCU blocker effectively prevented this impairment, suggesting that MCU could be the major portal for brain mitochondrial iron uptake. © 2013 Elsevier Inc. 2018-09-04T09:22:52Z 2018-09-04T09:22:52Z 2013-03-12 Journal 18790631 00243205 2-s2.0-84873713188 10.1016/j.lfs.2013.01.004 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84873713188&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/52264
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Biochemistry, Genetics and Molecular Biology
Pharmacology, Toxicology and Pharmaceutics
spellingShingle Biochemistry, Genetics and Molecular Biology
Pharmacology, Toxicology and Pharmaceutics
Jirapas Sripetchwandee
Jantira Sanit
Nipon Chattipakorn
Siriporn C. Chattipakorn
Mitochondrial calcium uniporter blocker effectively prevents brain mitochondrial dysfunction caused by iron overload
description Aims Although iron overload induces oxidative stress and brain mitochondrial dysfunction, and is associated with neurodegenerative diseases, brain mitochondrial iron uptake has not been investigated. We determined the role of mitochondrial calcium uniporter (MCU) in brain mitochondria as a major route for iron entry. We hypothesized that iron overload causes brain mitochondrial dysfunction, and that the MCU blocker prevents iron entry into mitochondria, thus attenuating mitochondrial dysfunction. Main methods Isolated brain mitochondria from male Wistar rats were used. Iron (Fe2 +and Fe3 +) at 0-286 μM were applied onto mitochondria at various incubation times (5-30 min), and the mitochondrial function was determined. Effects of MCU blocker (Ru-360) and iron chelator were studied. Key findings Both Fe2 +and Fe3 +entered brain mitochondria and caused mitochondrial swelling in a dose- and time-dependent manner, and caused mitochondrial depolarization and increased ROS production. However, Fe2 +caused more severe mitochondrial dysfunction than Fe3 +. Although all drugs attenuated mitochondrial dysfunction caused by iron overload, only an MCU blocker could completely prevent ROS production and mitochondrial depolarization. Significance Our findings indicated that iron overload caused brain mitochondrial dysfunction, and that an MCU blocker effectively prevented this impairment, suggesting that MCU could be the major portal for brain mitochondrial iron uptake. © 2013 Elsevier Inc.
format Journal
author Jirapas Sripetchwandee
Jantira Sanit
Nipon Chattipakorn
Siriporn C. Chattipakorn
author_facet Jirapas Sripetchwandee
Jantira Sanit
Nipon Chattipakorn
Siriporn C. Chattipakorn
author_sort Jirapas Sripetchwandee
title Mitochondrial calcium uniporter blocker effectively prevents brain mitochondrial dysfunction caused by iron overload
title_short Mitochondrial calcium uniporter blocker effectively prevents brain mitochondrial dysfunction caused by iron overload
title_full Mitochondrial calcium uniporter blocker effectively prevents brain mitochondrial dysfunction caused by iron overload
title_fullStr Mitochondrial calcium uniporter blocker effectively prevents brain mitochondrial dysfunction caused by iron overload
title_full_unstemmed Mitochondrial calcium uniporter blocker effectively prevents brain mitochondrial dysfunction caused by iron overload
title_sort mitochondrial calcium uniporter blocker effectively prevents brain mitochondrial dysfunction caused by iron overload
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84873713188&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/52264
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