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A Comparative Study of Age-Related Hearing Loss in Wild Type and Insulin-Like Growth Factor I Deficient Mice

Insulin-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 lo...

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Autores principales: Riquelme, Raquel, Cediel, Rafael, Contreras, Julio, Lourdes, Rodriguez-de la Rosa, Murillo-Cuesta, Silvia, Hernandez-Sanchez, Catalina, Zubeldia, Jose M., Cerdan, Sebastian, Varela-Nieto, Isabel
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907134/
https://www.ncbi.nlm.nih.gov/pubmed/20661454
http://dx.doi.org/10.3389/fnana.2010.00027
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author Riquelme, Raquel
Cediel, Rafael
Contreras, Julio
Lourdes, Rodriguez-de la Rosa
Murillo-Cuesta, Silvia
Hernandez-Sanchez, Catalina
Zubeldia, Jose M.
Cerdan, Sebastian
Varela-Nieto, Isabel
author_facet Riquelme, Raquel
Cediel, Rafael
Contreras, Julio
Lourdes, Rodriguez-de la Rosa
Murillo-Cuesta, Silvia
Hernandez-Sanchez, Catalina
Zubeldia, Jose M.
Cerdan, Sebastian
Varela-Nieto, Isabel
author_sort Riquelme, Raquel
collection PubMed
description Insulin-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.
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spelling pubmed-29071342010-07-26 A Comparative Study of Age-Related Hearing Loss in Wild Type and Insulin-Like Growth Factor I Deficient Mice Riquelme, Raquel Cediel, Rafael Contreras, Julio Lourdes, Rodriguez-de la Rosa Murillo-Cuesta, Silvia Hernandez-Sanchez, Catalina Zubeldia, Jose M. Cerdan, Sebastian Varela-Nieto, Isabel Front Neuroanat Neuroscience Insulin-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. Frontiers Research Foundation 2010-06-23 /pmc/articles/PMC2907134/ /pubmed/20661454 http://dx.doi.org/10.3389/fnana.2010.00027 Text en Copyright © 2010 Riquelme, Cediel, Contreras, Rodriguez-de la Rosa, Murillo-Cuesta, Hernandez-Sanchez, Zubeldia, Cerdan and Varela-Nieto. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Riquelme, Raquel
Cediel, Rafael
Contreras, Julio
Lourdes, Rodriguez-de la Rosa
Murillo-Cuesta, Silvia
Hernandez-Sanchez, Catalina
Zubeldia, Jose M.
Cerdan, Sebastian
Varela-Nieto, Isabel
A Comparative Study of Age-Related Hearing Loss in Wild Type and Insulin-Like Growth Factor I Deficient Mice
title A Comparative Study of Age-Related Hearing Loss in Wild Type and Insulin-Like Growth Factor I Deficient Mice
title_full A Comparative Study of Age-Related Hearing Loss in Wild Type and Insulin-Like Growth Factor I Deficient Mice
title_fullStr A Comparative Study of Age-Related Hearing Loss in Wild Type and Insulin-Like Growth Factor I Deficient Mice
title_full_unstemmed A Comparative Study of Age-Related Hearing Loss in Wild Type and Insulin-Like Growth Factor I Deficient Mice
title_short A Comparative Study of Age-Related Hearing Loss in Wild Type and Insulin-Like Growth Factor I Deficient Mice
title_sort comparative study of age-related hearing loss in wild type and insulin-like growth factor i deficient mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907134/
https://www.ncbi.nlm.nih.gov/pubmed/20661454
http://dx.doi.org/10.3389/fnana.2010.00027
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