Synaptic and nonsynaptic mitochondria demonstrate a different degree of calcium-induced mitochondrial dysfunction

Aims: Since variety in response to Ca 2+-induced mitochondrial dysfunction in different neuronal mitochondrial populations is associated with the pathogenesis of several neurological diseases, we investigated the effects of Ca 2+ overload on synaptic (SM) and nonsynaptic mitochondrial (NM) dysfuncti...

Full description

Saved in:
Bibliographic Details
Main Authors: Yarana C., Sanit J., Chattipakorn N., Chattipakorn S.
Format: Article
Language:English
Published: 2014
Online Access:http://www.ncbi.nlm.nih.gov/pubmed/22525373
http://www.scopus.com/inward/record.url?eid=2-s2.0-84860776299&partnerID=40&md5=a82824333a27180371b6347b5fd593c7
http://cmuir.cmu.ac.th/handle/6653943832/1134
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
Language: English
id th-cmuir.6653943832-1134
record_format dspace
spelling th-cmuir.6653943832-11342014-08-29T09:17:47Z Synaptic and nonsynaptic mitochondria demonstrate a different degree of calcium-induced mitochondrial dysfunction Yarana C. Sanit J. Chattipakorn N. Chattipakorn S. Aims: Since variety in response to Ca 2+-induced mitochondrial dysfunction in different neuronal mitochondrial populations is associated with the pathogenesis of several neurological diseases, we investigated the effects of Ca 2+ overload on synaptic (SM) and nonsynaptic mitochondrial (NM) dysfunction and probed the effects of cyclosporin A (CsA), 4′- chlorodiazepam (CDP) and Ru360 on relieving mitochondrial damage. Main methods: SM and NM mitochondria were isolated from rats' brains (n = 5/group) and treated with various concentrations (5, 10, 100, and 200 μM) of Ca 2+, with and without CsA (mPTP blocker), CDP (PBR/TSPO blocker) and Ru360 (MCU blocker) pretreatments. Mitochondrial function was determined by mitochondrial swelling, ROS production and mitochondrial membrane potential changes (ΔΨm). Key findings: At 200-μM Ca 2+, SM presented mitochondrial swelling to a greater extent than NM. At 100 and 200-μM Ca 2+, the ROS production of SM was higher than that of NM and ΔΨm dissipation of SM was also larger. CsA, CDP and Ru360 could reduce ROS production of SM and NM with exposure to 200-μM Ca 2+. However, only Ru360 could completely inhibit ROS generation in both SM and NM, whereas CsA and CDP could only partially reduce the ROS level in SM. Moreover, CsA and CDP pretreatments were not able to restore ΔΨm. However, Ru360 pretreatment could protect ΔΨm dissipation in both SM and NM, with complete protection observed only in NM. Significance: Our findings suggested that mitochondrial calcium uniporter is a possible major pathway for calcium uptake in both mitochondrial populations. However, SM might have additional pathways involved in the calcium uptake. © 2012 Elsevier Inc. 2014-08-29T09:17:47Z 2014-08-29T09:17:47Z 2012 Article 243205 10.1016/j.lfs.2012.04.004 22525373 LIFSA http://www.ncbi.nlm.nih.gov/pubmed/22525373 http://www.scopus.com/inward/record.url?eid=2-s2.0-84860776299&partnerID=40&md5=a82824333a27180371b6347b5fd593c7 http://cmuir.cmu.ac.th/handle/6653943832/1134 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Aims: Since variety in response to Ca 2+-induced mitochondrial dysfunction in different neuronal mitochondrial populations is associated with the pathogenesis of several neurological diseases, we investigated the effects of Ca 2+ overload on synaptic (SM) and nonsynaptic mitochondrial (NM) dysfunction and probed the effects of cyclosporin A (CsA), 4′- chlorodiazepam (CDP) and Ru360 on relieving mitochondrial damage. Main methods: SM and NM mitochondria were isolated from rats' brains (n = 5/group) and treated with various concentrations (5, 10, 100, and 200 μM) of Ca 2+, with and without CsA (mPTP blocker), CDP (PBR/TSPO blocker) and Ru360 (MCU blocker) pretreatments. Mitochondrial function was determined by mitochondrial swelling, ROS production and mitochondrial membrane potential changes (ΔΨm). Key findings: At 200-μM Ca 2+, SM presented mitochondrial swelling to a greater extent than NM. At 100 and 200-μM Ca 2+, the ROS production of SM was higher than that of NM and ΔΨm dissipation of SM was also larger. CsA, CDP and Ru360 could reduce ROS production of SM and NM with exposure to 200-μM Ca 2+. However, only Ru360 could completely inhibit ROS generation in both SM and NM, whereas CsA and CDP could only partially reduce the ROS level in SM. Moreover, CsA and CDP pretreatments were not able to restore ΔΨm. However, Ru360 pretreatment could protect ΔΨm dissipation in both SM and NM, with complete protection observed only in NM. Significance: Our findings suggested that mitochondrial calcium uniporter is a possible major pathway for calcium uptake in both mitochondrial populations. However, SM might have additional pathways involved in the calcium uptake. © 2012 Elsevier Inc.
format Article
author Yarana C.
Sanit J.
Chattipakorn N.
Chattipakorn S.
spellingShingle Yarana C.
Sanit J.
Chattipakorn N.
Chattipakorn S.
Synaptic and nonsynaptic mitochondria demonstrate a different degree of calcium-induced mitochondrial dysfunction
author_facet Yarana C.
Sanit J.
Chattipakorn N.
Chattipakorn S.
author_sort Yarana C.
title Synaptic and nonsynaptic mitochondria demonstrate a different degree of calcium-induced mitochondrial dysfunction
title_short Synaptic and nonsynaptic mitochondria demonstrate a different degree of calcium-induced mitochondrial dysfunction
title_full Synaptic and nonsynaptic mitochondria demonstrate a different degree of calcium-induced mitochondrial dysfunction
title_fullStr Synaptic and nonsynaptic mitochondria demonstrate a different degree of calcium-induced mitochondrial dysfunction
title_full_unstemmed Synaptic and nonsynaptic mitochondria demonstrate a different degree of calcium-induced mitochondrial dysfunction
title_sort synaptic and nonsynaptic mitochondria demonstrate a different degree of calcium-induced mitochondrial dysfunction
publishDate 2014
url http://www.ncbi.nlm.nih.gov/pubmed/22525373
http://www.scopus.com/inward/record.url?eid=2-s2.0-84860776299&partnerID=40&md5=a82824333a27180371b6347b5fd593c7
http://cmuir.cmu.ac.th/handle/6653943832/1134
_version_ 1681419613913481216