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dc.contributor.author
Cabrillana, María Eugenia
dc.contributor.author
Uribe, Pamela
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Villegas, Juana V.
dc.contributor.author
Álvarez, Juan
dc.contributor.author
Sánchez, Raúl
dc.contributor.author
Fornes, Miguel Walter
dc.date.available
2018-06-19T18:58:08Z
dc.date.issued
2016-09
dc.identifier.citation
Cabrillana, María Eugenia; Uribe, Pamela; Villegas, Juana V.; Álvarez, Juan; Sánchez, Raúl; et al.; Thiol oxidation by nitrosative stress: Cellular localization in human spermatozoa; Informa Healthcare; Systems Biology In Reproductive Medicine; 62; 5; 9-2016; 325-334
dc.identifier.issn
1939-6368
dc.identifier.uri
http://hdl.handle.net/11336/49386
dc.description.abstract
Peroxynitrite is a highly reactive nitrogen species and when it is generated at high levels it causes nitrosative stress, an important cause of impaired sperm function. High levels of peroxynitrite have been shown to correlate with decreased semen quality in infertile men. Thiol groups in sperm are mainly found in enzymes, antioxidant molecules, and structural proteins in the axoneme. Peroxynitrite primarily reacts with thiol groups of cysteine-containing proteins. Although it is well known that peroxynitrite oxidizes sulfhydryl groups in sperm, the subcellular localization of this oxidation remains unknown. The main objective of this study was to establish the subcellular localization of peroxynitrite-induced nitrosative stress in thiol groups and its relation to sperm motility in human spermatozoa. For this purpose, spermatozoa from healthy donors were exposed in vitro to 3-morpholinosydnonimine (SIN-1), a compound which generates peroxynitrite. In order to detect peroxynitrite and reduced thiol groups, the fluorescent probes, dihydrorhodamine 123 and monobromobimane (mBBr), were used respectively. Sperm viability was analyzed by propidium iodide staining. Peroxynitrite generation and thiol redox state were monitored by confocal microscopy whereas sperm viability was evaluated by flow cytometry. Sperm motility was analyzed by CASA using the ISAS® system. The results showed that exposure of human spermatozoa to peroxynitrite results in increased thiol oxidation which is mainly localized in the sperm head and principal piece regions. Thiol oxidation was associated with motility loss. The high susceptibility of thiol groups to peroxynitrite-induced oxidation could explain, at least in part, the negative effect of reactive nitrogen species on sperm motility. Abbreviations: DHR: dihydrorhodamine 123; mBBr: monobromobimane ONOO−: peroxynitrite RNS: reactive nitrogen species RFI: relative fluorescence intensity SIN-1: 3-morpholinosydnonimine CASA: Computer-Aided Sperm Analysis PARP: poli ADP ribose polimerasa VCL: curvilinear velocity VSL: straight-line velocity VAP: average path velocity PRDXs: peroxiredoxins ODF: outer dense fiber ODF1: outer dense fiber 1 PI: propidium iodide DMSO: dimethyl sulfoxide SD: standard deviation ANOVA: analysis of variance
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Informa Healthcare
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Human Spermatozoa
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Nitrosative Stress
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Oxidative Stress
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Peroxynitrite
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Sperm Motility
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Thiol Groups
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Otras Ciencias Biológicas
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Ciencias Biológicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Thiol oxidation by nitrosative stress: Cellular localization in human spermatozoa
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2018-06-13T16:53:48Z
dc.journal.volume
62
dc.journal.number
5
dc.journal.pagination
325-334
dc.journal.pais
Reino Unido
dc.journal.ciudad
Londres
dc.description.fil
Fil: Cabrillana, María Eugenia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Cienicas Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina. Universidad del Aconcagua; Argentina
dc.description.fil
Fil: Uribe, Pamela. Universidad de La Frontera; Chile
dc.description.fil
Fil: Villegas, Juana V.. Universidad de La Frontera; Chile
dc.description.fil
Fil: Álvarez, Juan. Harvard Medical School; Estados Unidos
dc.description.fil
Fil: Sánchez, Raúl. Universidad de La Frontera; Chile
dc.description.fil
Fil: Fornes, Miguel Walter. Universidad del Aconcagua; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Cienicas Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina
dc.journal.title
Systems Biology In Reproductive Medicine
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1080/19396368.2016.1208782
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.tandfonline.com/doi/full/10.1080/19396368.2016.1208782
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