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Metabolic Maturation of Auditory Neurones in the Superior Olivary Complex

Neuronal activity is energetically costly, but despite its importance, energy production and consumption have been studied in only a few neurone types. Neuroenergetics is of special importance in auditory brainstem nuclei, where neurones exhibit various biophysical adaptations for extraordinary temp...

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Autores principales: Trattner, Barbara, Gravot, Céline Marie, Grothe, Benedikt, Kunz, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694961/
https://www.ncbi.nlm.nih.gov/pubmed/23826275
http://dx.doi.org/10.1371/journal.pone.0067351
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author Trattner, Barbara
Gravot, Céline Marie
Grothe, Benedikt
Kunz, Lars
author_facet Trattner, Barbara
Gravot, Céline Marie
Grothe, Benedikt
Kunz, Lars
author_sort Trattner, Barbara
collection PubMed
description Neuronal activity is energetically costly, but despite its importance, energy production and consumption have been studied in only a few neurone types. Neuroenergetics is of special importance in auditory brainstem nuclei, where neurones exhibit various biophysical adaptations for extraordinary temporal precision and show particularly high firing rates. We have studied the development of energy metabolism in three principal nuclei of the superior olivary complex (SOC) involved in precise binaural processing in the Mongolian gerbil (Meriones unguiculatus). We used immunohistochemistry to quantify metabolic markers for energy consumption (Na(+)/K(+)-ATPase) and production (mitochondria, cytochrome c oxidase activity and glucose transporter 3 (GLUT3)). In addition, we calculated neuronal ATP consumption for different postnatal ages (P0–90) based upon published electrophysiological and morphological data. Our calculations relate neuronal processes to the regeneration of Na(+) gradients perturbed by neuronal firing, and thus to ATP consumption by Na(+)/K(+)-ATPase. The developmental changes of calculated energy consumption closely resemble those of metabolic markers. Both increase before and after hearing onset occurring at P12–13 and reach a plateau thereafter. The increase in Na(+)/K(+)-ATPase and mitochondria precedes the rise in GLUT3 levels and is already substantial before hearing onset, whilst GLUT3 levels are scarcely detectable at this age. Based on these findings we assume that auditory inputs crucially contribute to metabolic maturation. In one nucleus, the medial nucleus of the trapezoid body (MNTB), the initial rise in marker levels and calculated ATP consumption occurs distinctly earlier than in the other nuclei investigated, and is almost completed by hearing onset. Our study shows that the mathematical model used is applicable to brainstem neurones. Energy consumption varies markedly between SOC nuclei with their different neuronal properties. Especially for the medial superior olive (MSO), we propose that temporally precise input integration is energetically more costly than the high firing frequencies typical for all SOC nuclei.
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spelling pubmed-36949612013-07-03 Metabolic Maturation of Auditory Neurones in the Superior Olivary Complex Trattner, Barbara Gravot, Céline Marie Grothe, Benedikt Kunz, Lars PLoS One Research Article Neuronal activity is energetically costly, but despite its importance, energy production and consumption have been studied in only a few neurone types. Neuroenergetics is of special importance in auditory brainstem nuclei, where neurones exhibit various biophysical adaptations for extraordinary temporal precision and show particularly high firing rates. We have studied the development of energy metabolism in three principal nuclei of the superior olivary complex (SOC) involved in precise binaural processing in the Mongolian gerbil (Meriones unguiculatus). We used immunohistochemistry to quantify metabolic markers for energy consumption (Na(+)/K(+)-ATPase) and production (mitochondria, cytochrome c oxidase activity and glucose transporter 3 (GLUT3)). In addition, we calculated neuronal ATP consumption for different postnatal ages (P0–90) based upon published electrophysiological and morphological data. Our calculations relate neuronal processes to the regeneration of Na(+) gradients perturbed by neuronal firing, and thus to ATP consumption by Na(+)/K(+)-ATPase. The developmental changes of calculated energy consumption closely resemble those of metabolic markers. Both increase before and after hearing onset occurring at P12–13 and reach a plateau thereafter. The increase in Na(+)/K(+)-ATPase and mitochondria precedes the rise in GLUT3 levels and is already substantial before hearing onset, whilst GLUT3 levels are scarcely detectable at this age. Based on these findings we assume that auditory inputs crucially contribute to metabolic maturation. In one nucleus, the medial nucleus of the trapezoid body (MNTB), the initial rise in marker levels and calculated ATP consumption occurs distinctly earlier than in the other nuclei investigated, and is almost completed by hearing onset. Our study shows that the mathematical model used is applicable to brainstem neurones. Energy consumption varies markedly between SOC nuclei with their different neuronal properties. Especially for the medial superior olive (MSO), we propose that temporally precise input integration is energetically more costly than the high firing frequencies typical for all SOC nuclei. Public Library of Science 2013-06-27 /pmc/articles/PMC3694961/ /pubmed/23826275 http://dx.doi.org/10.1371/journal.pone.0067351 Text en © 2013 Trattner et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Trattner, Barbara
Gravot, Céline Marie
Grothe, Benedikt
Kunz, Lars
Metabolic Maturation of Auditory Neurones in the Superior Olivary Complex
title Metabolic Maturation of Auditory Neurones in the Superior Olivary Complex
title_full Metabolic Maturation of Auditory Neurones in the Superior Olivary Complex
title_fullStr Metabolic Maturation of Auditory Neurones in the Superior Olivary Complex
title_full_unstemmed Metabolic Maturation of Auditory Neurones in the Superior Olivary Complex
title_short Metabolic Maturation of Auditory Neurones in the Superior Olivary Complex
title_sort metabolic maturation of auditory neurones in the superior olivary complex
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694961/
https://www.ncbi.nlm.nih.gov/pubmed/23826275
http://dx.doi.org/10.1371/journal.pone.0067351
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