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dc.contributor.authorRiquelme, Raquel-
dc.contributor.authorCediel, Rafael-
dc.contributor.authorContreras, Julio-
dc.contributor.authorRodriguez-de la Rosa, Lourdes-
dc.contributor.authorMurillo-Cuesta, Silvia-
dc.contributor.authorHernández-Sánchez, Catalina-
dc.contributor.authorZubeldia, José M.-
dc.contributor.authorCerdán, Sebastián-
dc.contributor.authorVarela-Nieto, Isabel-
dc.date.accessioned2011-01-26T10:57:03Z-
dc.date.available2011-01-26T10:57:03Z-
dc.date.issued2010-07-13-
dc.identifier.citationFrontiers in Neuroanatomy 4: 27 (2010)es_ES
dc.identifier.issn1662-5129-
dc.identifier.urihttp://hdl.handle.net/10261/31549-
dc.description.abstractInsulin-like growth factor-I (IGF-I) belongs to the family of insulin-related peptides that fulfils a key role during the late development of the nervous system. Human IGF1 mutations cause profound deafness, poor growth and mental retardation. Accordingly, Igf1(-/-) null mice are dwarfs that have low survival rates, cochlear alterations and severe sensorineural deafness. Presbycusis (age-related hearing loss) is a common disorder associated with aging that causes social and cognitive problems. Aging is also associated with a decrease in circulating IGF-I levels and this reduction has been related to cognitive and brain alterations, although there is no information as yet regarding the relationship between presbycusis and IGF-I biodisponibility. Here we present a longitudinal study of wild type Igf1(+/+) and null Igf1(-/-) mice from 2 to 12 months of age comparing the temporal progression of several parameters: hearing, brain morphology, cochlear cytoarchitecture, insulin-related factors and IGF gene expression and IGF-I serum levels. Complementary invasive and non-invasive techniques were used, including auditory brainstem-evoked response (ABR) recordings and in vivo MRI brain imaging. Igf1(-/-) null mice presented profound deafness at all the ages studied, without any obvious worsening of hearing parameters with aging. Igf1(+/+) wild type mice suffered significant age-related hearing loss, their auditory thresholds and peak I latencies augmenting as they aged, in parallel with a decrease in the circulating levels of IGF-I. Accordingly, there was an age-related spiral ganglion degeneration in wild type mice that was not evident in the Igf1 null mice. However, the Igf1(-/-) null mice in turn developed a prematurely aged stria vascularis reminiscent of the diabetic strial phenotype. Our data indicate that IGF-I is required for the correct development and maintenance of hearing, supporting the idea that IGF-I-based therapies could contribute to prevent or ameliorate age-related hearing loss.es_ES
dc.description.sponsorshipThis work was partially supported by grants to IVN from DIGNA Biotech, the Ministerio de Ciencia e Innovacion (SAF2008-00470) and from the Fundacion Mutua Madrileña to IVN and JMZ.-
dc.language.isoenges_ES
dc.publisherFrontiers Mediaes_ES
dc.relation.isversionofPublisher's version-
dc.rightsopenAccesses_ES
dc.subjectAginges_ES
dc.subjectAuditory brainstem responseses_ES
dc.subjectDeafnesses_ES
dc.subjectIgf1-/- null mousees_ES
dc.subjectInsuline-like factorses_ES
dc.subjectIn vivo brain imaginges_ES
dc.subjectPresbycusises_ES
dc.subjectSensorineural deafnesses_ES
dc.titleA comparative study of age-related hearing loss in wild type and insulin-like growth factor I deficient micees_ES
dc.typeartículoes_ES
dc.identifier.doi10.3389/fnana.2010.00027-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.3389/fnana.2010.00027es_ES
dc.contributor.funderMinisterio de Ciencia e Innovación (España)-
dc.contributor.funderFundación Mutua Madrileña-
dc.contributor.funderDigna Biotech-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004837es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100008061es_ES
dc.identifier.pmid20661454-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
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