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Is silence golden? Effects of auditory stimuli and their absence on adult hippocampal neurogenesis

We have previously hypothesized that the reason why physical activity increases precursor cell proliferation in adult neurogenesis is that movement serves as non-specific signal to evoke the alertness required to meet cognitive demands. Thereby a pool of immature neurons is generated that are potent...

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Autores principales: Kirste, Imke, Nicola, Zeina, Kronenberg, Golo, Walker, Tara L., Liu, Robert C., Kempermann, Gerd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4087081/
https://www.ncbi.nlm.nih.gov/pubmed/24292324
http://dx.doi.org/10.1007/s00429-013-0679-3
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author Kirste, Imke
Nicola, Zeina
Kronenberg, Golo
Walker, Tara L.
Liu, Robert C.
Kempermann, Gerd
author_facet Kirste, Imke
Nicola, Zeina
Kronenberg, Golo
Walker, Tara L.
Liu, Robert C.
Kempermann, Gerd
author_sort Kirste, Imke
collection PubMed
description We have previously hypothesized that the reason why physical activity increases precursor cell proliferation in adult neurogenesis is that movement serves as non-specific signal to evoke the alertness required to meet cognitive demands. Thereby a pool of immature neurons is generated that are potentially recruitable by subsequent cognitive stimuli. Along these lines, we here tested whether auditory stimuli might exert a similar non-specific effect on adult neurogenesis in mice. We used the standard noise level in the animal facility as baseline and compared this condition to white noise, pup calls, and silence. In addition, as patterned auditory stimulus without ethological relevance to mice we used piano music by Mozart (KV 448). All stimuli were transposed to the frequency range of C57BL/6 and hearing was objectified with acoustic evoked potentials. We found that except for white noise all stimuli, including silence, increased precursor cell proliferation (assessed 24 h after labeling with bromodeoxyuridine, BrdU). This could be explained by significant increases in BrdU-labeled Sox2-positive cells (type-1/2a). But after 7 days, only silence remained associated with increased numbers of BrdU-labeled cells. Compared to controls at this stage, exposure to silence had generated significantly increased numbers of BrdU/NeuN-labeled neurons. Our results indicate that the unnatural absence of auditory input as well as spectrotemporally rich albeit ethological irrelevant stimuli activate precursor cells—in the case of silence also leading to greater numbers of newborn immature neurons—whereas ambient and unstructured background auditory stimuli do not.
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spelling pubmed-40870812015-03-01 Is silence golden? Effects of auditory stimuli and their absence on adult hippocampal neurogenesis Kirste, Imke Nicola, Zeina Kronenberg, Golo Walker, Tara L. Liu, Robert C. Kempermann, Gerd Brain Struct Funct Short Communication We have previously hypothesized that the reason why physical activity increases precursor cell proliferation in adult neurogenesis is that movement serves as non-specific signal to evoke the alertness required to meet cognitive demands. Thereby a pool of immature neurons is generated that are potentially recruitable by subsequent cognitive stimuli. Along these lines, we here tested whether auditory stimuli might exert a similar non-specific effect on adult neurogenesis in mice. We used the standard noise level in the animal facility as baseline and compared this condition to white noise, pup calls, and silence. In addition, as patterned auditory stimulus without ethological relevance to mice we used piano music by Mozart (KV 448). All stimuli were transposed to the frequency range of C57BL/6 and hearing was objectified with acoustic evoked potentials. We found that except for white noise all stimuli, including silence, increased precursor cell proliferation (assessed 24 h after labeling with bromodeoxyuridine, BrdU). This could be explained by significant increases in BrdU-labeled Sox2-positive cells (type-1/2a). But after 7 days, only silence remained associated with increased numbers of BrdU-labeled cells. Compared to controls at this stage, exposure to silence had generated significantly increased numbers of BrdU/NeuN-labeled neurons. Our results indicate that the unnatural absence of auditory input as well as spectrotemporally rich albeit ethological irrelevant stimuli activate precursor cells—in the case of silence also leading to greater numbers of newborn immature neurons—whereas ambient and unstructured background auditory stimuli do not. Springer Berlin Heidelberg 2013-12-01 2015 /pmc/articles/PMC4087081/ /pubmed/24292324 http://dx.doi.org/10.1007/s00429-013-0679-3 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Short Communication
Kirste, Imke
Nicola, Zeina
Kronenberg, Golo
Walker, Tara L.
Liu, Robert C.
Kempermann, Gerd
Is silence golden? Effects of auditory stimuli and their absence on adult hippocampal neurogenesis
title Is silence golden? Effects of auditory stimuli and their absence on adult hippocampal neurogenesis
title_full Is silence golden? Effects of auditory stimuli and their absence on adult hippocampal neurogenesis
title_fullStr Is silence golden? Effects of auditory stimuli and their absence on adult hippocampal neurogenesis
title_full_unstemmed Is silence golden? Effects of auditory stimuli and their absence on adult hippocampal neurogenesis
title_short Is silence golden? Effects of auditory stimuli and their absence on adult hippocampal neurogenesis
title_sort is silence golden? effects of auditory stimuli and their absence on adult hippocampal neurogenesis
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4087081/
https://www.ncbi.nlm.nih.gov/pubmed/24292324
http://dx.doi.org/10.1007/s00429-013-0679-3
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