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Noise trauma and systemic application of the selective glucocorticoid receptor modulator compound A

BACKGROUND: Selective glucocorticoid receptor modulators (SEGRMs) comprise a novel class of drugs promising both reduced side effects and similar pharmacological potency relative to glucocorticoids, which presently serve as the only clinical treatment for many otologic disorders. In the first otolog...

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Autores principales: Landegger, Lukas D., Honeder, Clemens, Zhu, Chengjing, Schöpper, Hanna, Engleder, Elisabeth, Gabor, Franz, Gstoettner, Wolfgang, Arnoldner, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863352/
https://www.ncbi.nlm.nih.gov/pubmed/27164957
http://dx.doi.org/10.1186/s12952-016-0053-0
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author Landegger, Lukas D.
Honeder, Clemens
Zhu, Chengjing
Schöpper, Hanna
Engleder, Elisabeth
Gabor, Franz
Gstoettner, Wolfgang
Arnoldner, Christoph
author_facet Landegger, Lukas D.
Honeder, Clemens
Zhu, Chengjing
Schöpper, Hanna
Engleder, Elisabeth
Gabor, Franz
Gstoettner, Wolfgang
Arnoldner, Christoph
author_sort Landegger, Lukas D.
collection PubMed
description BACKGROUND: Selective glucocorticoid receptor modulators (SEGRMs) comprise a novel class of drugs promising both reduced side effects and similar pharmacological potency relative to glucocorticoids, which presently serve as the only clinical treatment for many otologic disorders. In the first otologic SEGRM experiment in an animal model of noise trauma, we compare the effects of Compound A (a SEGRM) and dexamethasone (potent glucocorticoid). METHODS: Forty adult guinea pigs received experimental treatment once daily for ten days. The animals were divided into four cohorts based on the treatment received: Compound A (1 mg/kg or 3 mg/kg), dexamethasone (1 mg/kg) as gold standard, or water as negative control. After five applications, animals were exposed to broadband noise (8–16 kHz) at 115 dB for three hours. Hearing thresholds were determined by recording auditory brainstem responses to clicks and noise bursts (1–32 kHz) and were assessed a week prior to and immediately after exposure, as well as on days 1, 3, 7, 14, 21, and 28. Cochleae were prepared as whole-mounts or embedded and sectioned for histological analysis. RESULTS: Relative to the control treatments, Compound A failed to preserve auditory thresholds post-noise exposure with statistical significance. Histological analyses confirm the physiological result. CONCLUSION: The present findings suggest that Compound A does not have substantial otoprotective capacities in a noise trauma model.
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spelling pubmed-48633522016-05-12 Noise trauma and systemic application of the selective glucocorticoid receptor modulator compound A Landegger, Lukas D. Honeder, Clemens Zhu, Chengjing Schöpper, Hanna Engleder, Elisabeth Gabor, Franz Gstoettner, Wolfgang Arnoldner, Christoph J Negat Results Biomed Research BACKGROUND: Selective glucocorticoid receptor modulators (SEGRMs) comprise a novel class of drugs promising both reduced side effects and similar pharmacological potency relative to glucocorticoids, which presently serve as the only clinical treatment for many otologic disorders. In the first otologic SEGRM experiment in an animal model of noise trauma, we compare the effects of Compound A (a SEGRM) and dexamethasone (potent glucocorticoid). METHODS: Forty adult guinea pigs received experimental treatment once daily for ten days. The animals were divided into four cohorts based on the treatment received: Compound A (1 mg/kg or 3 mg/kg), dexamethasone (1 mg/kg) as gold standard, or water as negative control. After five applications, animals were exposed to broadband noise (8–16 kHz) at 115 dB for three hours. Hearing thresholds were determined by recording auditory brainstem responses to clicks and noise bursts (1–32 kHz) and were assessed a week prior to and immediately after exposure, as well as on days 1, 3, 7, 14, 21, and 28. Cochleae were prepared as whole-mounts or embedded and sectioned for histological analysis. RESULTS: Relative to the control treatments, Compound A failed to preserve auditory thresholds post-noise exposure with statistical significance. Histological analyses confirm the physiological result. CONCLUSION: The present findings suggest that Compound A does not have substantial otoprotective capacities in a noise trauma model. BioMed Central 2016-05-11 /pmc/articles/PMC4863352/ /pubmed/27164957 http://dx.doi.org/10.1186/s12952-016-0053-0 Text en © Landegger et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Landegger, Lukas D.
Honeder, Clemens
Zhu, Chengjing
Schöpper, Hanna
Engleder, Elisabeth
Gabor, Franz
Gstoettner, Wolfgang
Arnoldner, Christoph
Noise trauma and systemic application of the selective glucocorticoid receptor modulator compound A
title Noise trauma and systemic application of the selective glucocorticoid receptor modulator compound A
title_full Noise trauma and systemic application of the selective glucocorticoid receptor modulator compound A
title_fullStr Noise trauma and systemic application of the selective glucocorticoid receptor modulator compound A
title_full_unstemmed Noise trauma and systemic application of the selective glucocorticoid receptor modulator compound A
title_short Noise trauma and systemic application of the selective glucocorticoid receptor modulator compound A
title_sort noise trauma and systemic application of the selective glucocorticoid receptor modulator compound a
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863352/
https://www.ncbi.nlm.nih.gov/pubmed/27164957
http://dx.doi.org/10.1186/s12952-016-0053-0
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