Mitochondrial alterations and apoptosis in smooth muscle from aged rats

Detalhes bibliográficos
Autor(a) principal: Lopes, G. S.
Data de Publicação: 2004
Outros Autores: Mora, O. A., Cerri, P., Faria, F. P., Jurkiewicz, N. H., Jurkiewicz, A., Smaili, S. S.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.bbabio.2004.05.011
http://hdl.handle.net/11449/16558
Resumo: We studied changes in mitochondrial morphology and function in the smooth muscle of rat colon. Under confocal microscopy, tissues loaded with potentiometric dye displayed rapid and spontaneous depolarization. Cyclosporin A (CsA), inhibitor of the permeability transition pore (PTP), caused an increase in mitochondrial membrane potential (DeltaPsi(m)) in tissues from adult young animals. In aged rats these changes were not observed. This suggests that physiological activation of PTP in aged rats is reduced. Electron microscopy showed alterations of the mitochondrial ultrastructure in tissues from aged rats involving a decreased definition of the cristae and fragmentation of the mitochondrial membranes. We also detected an increase in apoptotic cells in the smooth muscle from aged animals. Our results show that the aging process changes PTP activity, the ability to maintain DeltaPsi(m) and mitochondrial morphology. It is suggested that these can be associated with mitochondrial damage and cell death. (C) 2004 Elsevier B.V. All rights reserved.
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spelling Mitochondrial alterations and apoptosis in smooth muscle from aged ratsmitochondriacalciumsmooth muscleagingmitochondrial dysfunctionWe studied changes in mitochondrial morphology and function in the smooth muscle of rat colon. Under confocal microscopy, tissues loaded with potentiometric dye displayed rapid and spontaneous depolarization. Cyclosporin A (CsA), inhibitor of the permeability transition pore (PTP), caused an increase in mitochondrial membrane potential (DeltaPsi(m)) in tissues from adult young animals. In aged rats these changes were not observed. This suggests that physiological activation of PTP in aged rats is reduced. Electron microscopy showed alterations of the mitochondrial ultrastructure in tissues from aged rats involving a decreased definition of the cristae and fragmentation of the mitochondrial membranes. We also detected an increase in apoptotic cells in the smooth muscle from aged animals. Our results show that the aging process changes PTP activity, the ability to maintain DeltaPsi(m) and mitochondrial morphology. It is suggested that these can be associated with mitochondrial damage and cell death. (C) 2004 Elsevier B.V. All rights reserved.Univ Fed São Paulo, Nat Inst Pharmacol, Dept Pharmacol, BR-04044020 São Paulo, BrazilUniv Fed São Paulo, Dept Morphol, São Paulo, BrazilUNESP, Sch Dent, Dept Morphol, Araraquara, BrazilUNESP, Sch Dent, Dept Morphol, Araraquara, BrazilElsevier B.V.Universidade Federal de São Paulo (UNIFESP)Universidade Estadual Paulista (Unesp)Lopes, G. S.Mora, O. A.Cerri, P.Faria, F. P.Jurkiewicz, N. H.Jurkiewicz, A.Smaili, S. S.2014-05-20T13:46:44Z2014-05-20T13:46:44Z2004-10-04info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article187-194application/pdfhttp://dx.doi.org/10.1016/j.bbabio.2004.05.011Biochimica Et Biophysica Acta-bioenergetics. Amsterdam: Elsevier B.V., v. 1658, n. 3, p. 187-194, 2004.0005-2728http://hdl.handle.net/11449/1655810.1016/j.bbabio.2004.05.011WOS:000224338200002WOS000224338200002.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBiochimica et Biophysica Acta: Bioenergetics4.2802,336info:eu-repo/semantics/openAccess2024-09-27T15:15:20Zoai:repositorio.unesp.br:11449/16558Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T15:15:20Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Mitochondrial alterations and apoptosis in smooth muscle from aged rats
title Mitochondrial alterations and apoptosis in smooth muscle from aged rats
spellingShingle Mitochondrial alterations and apoptosis in smooth muscle from aged rats
Lopes, G. S.
mitochondria
calcium
smooth muscle
aging
mitochondrial dysfunction
title_short Mitochondrial alterations and apoptosis in smooth muscle from aged rats
title_full Mitochondrial alterations and apoptosis in smooth muscle from aged rats
title_fullStr Mitochondrial alterations and apoptosis in smooth muscle from aged rats
title_full_unstemmed Mitochondrial alterations and apoptosis in smooth muscle from aged rats
title_sort Mitochondrial alterations and apoptosis in smooth muscle from aged rats
author Lopes, G. S.
author_facet Lopes, G. S.
Mora, O. A.
Cerri, P.
Faria, F. P.
Jurkiewicz, N. H.
Jurkiewicz, A.
Smaili, S. S.
author_role author
author2 Mora, O. A.
Cerri, P.
Faria, F. P.
Jurkiewicz, N. H.
Jurkiewicz, A.
Smaili, S. S.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Lopes, G. S.
Mora, O. A.
Cerri, P.
Faria, F. P.
Jurkiewicz, N. H.
Jurkiewicz, A.
Smaili, S. S.
dc.subject.por.fl_str_mv mitochondria
calcium
smooth muscle
aging
mitochondrial dysfunction
topic mitochondria
calcium
smooth muscle
aging
mitochondrial dysfunction
description We studied changes in mitochondrial morphology and function in the smooth muscle of rat colon. Under confocal microscopy, tissues loaded with potentiometric dye displayed rapid and spontaneous depolarization. Cyclosporin A (CsA), inhibitor of the permeability transition pore (PTP), caused an increase in mitochondrial membrane potential (DeltaPsi(m)) in tissues from adult young animals. In aged rats these changes were not observed. This suggests that physiological activation of PTP in aged rats is reduced. Electron microscopy showed alterations of the mitochondrial ultrastructure in tissues from aged rats involving a decreased definition of the cristae and fragmentation of the mitochondrial membranes. We also detected an increase in apoptotic cells in the smooth muscle from aged animals. Our results show that the aging process changes PTP activity, the ability to maintain DeltaPsi(m) and mitochondrial morphology. It is suggested that these can be associated with mitochondrial damage and cell death. (C) 2004 Elsevier B.V. All rights reserved.
publishDate 2004
dc.date.none.fl_str_mv 2004-10-04
2014-05-20T13:46:44Z
2014-05-20T13:46:44Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.bbabio.2004.05.011
Biochimica Et Biophysica Acta-bioenergetics. Amsterdam: Elsevier B.V., v. 1658, n. 3, p. 187-194, 2004.
0005-2728
http://hdl.handle.net/11449/16558
10.1016/j.bbabio.2004.05.011
WOS:000224338200002
WOS000224338200002.pdf
url http://dx.doi.org/10.1016/j.bbabio.2004.05.011
http://hdl.handle.net/11449/16558
identifier_str_mv Biochimica Et Biophysica Acta-bioenergetics. Amsterdam: Elsevier B.V., v. 1658, n. 3, p. 187-194, 2004.
0005-2728
10.1016/j.bbabio.2004.05.011
WOS:000224338200002
WOS000224338200002.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biochimica et Biophysica Acta: Bioenergetics
4.280
2,336
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 187-194
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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