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Disrupted brain mitochondrial morphology after in vivo hydrogen sulfide exposure
Changes in mitochondrial dynamics are often associated with dietary patterns, medical treatments, xenobiotics, and diseases. Toxic exposures to hydrogen sulfide (H(2)S) harm mitochondria by inhibiting Complex IV and via other mechanisms. However, changes in mitochondrial dynamics, including morpholo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598273/ https://www.ncbi.nlm.nih.gov/pubmed/37875542 http://dx.doi.org/10.1038/s41598-023-44807-y |
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author | Rumbeiha, Wilson K. Kim, Dong-Suk Min, Angela Nair, Maya Giulivi, Cecilia |
author_facet | Rumbeiha, Wilson K. Kim, Dong-Suk Min, Angela Nair, Maya Giulivi, Cecilia |
author_sort | Rumbeiha, Wilson K. |
collection | PubMed |
description | Changes in mitochondrial dynamics are often associated with dietary patterns, medical treatments, xenobiotics, and diseases. Toxic exposures to hydrogen sulfide (H(2)S) harm mitochondria by inhibiting Complex IV and via other mechanisms. However, changes in mitochondrial dynamics, including morphology following acute exposure to H(2)S, are not yet fully understood. This study followed mitochondrial morphology changes over time after a single acute LCt(50) dose of H(2)S by examining electron microscopy thalami images of surviving mice. Our findings revealed that within the initial 48 h after H(2)S exposure, mitochondrial morphology was impaired by H(2)S, supported by the disruption and scarcity of the cristae, which are required to enhance the surface area for ATP production. At the 72-h mark point, a spectrum of morphological cellular changes was observed, and the disordered mitochondrial network, accompanied by the probable disruption of mitophagy, was tied to changes in mitochondrial shape. In summary, this study sheds light on how acute exposure to high levels of H(2)S triggers alterations in mitochondrial shape and structure as early as 24 h that become more evident at 72 h post-exposure. These findings underscore the impact of H(2)S on mitochondrial function and overall cellular health. |
format | Online Article Text |
id | pubmed-10598273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105982732023-10-26 Disrupted brain mitochondrial morphology after in vivo hydrogen sulfide exposure Rumbeiha, Wilson K. Kim, Dong-Suk Min, Angela Nair, Maya Giulivi, Cecilia Sci Rep Article Changes in mitochondrial dynamics are often associated with dietary patterns, medical treatments, xenobiotics, and diseases. Toxic exposures to hydrogen sulfide (H(2)S) harm mitochondria by inhibiting Complex IV and via other mechanisms. However, changes in mitochondrial dynamics, including morphology following acute exposure to H(2)S, are not yet fully understood. This study followed mitochondrial morphology changes over time after a single acute LCt(50) dose of H(2)S by examining electron microscopy thalami images of surviving mice. Our findings revealed that within the initial 48 h after H(2)S exposure, mitochondrial morphology was impaired by H(2)S, supported by the disruption and scarcity of the cristae, which are required to enhance the surface area for ATP production. At the 72-h mark point, a spectrum of morphological cellular changes was observed, and the disordered mitochondrial network, accompanied by the probable disruption of mitophagy, was tied to changes in mitochondrial shape. In summary, this study sheds light on how acute exposure to high levels of H(2)S triggers alterations in mitochondrial shape and structure as early as 24 h that become more evident at 72 h post-exposure. These findings underscore the impact of H(2)S on mitochondrial function and overall cellular health. Nature Publishing Group UK 2023-10-24 /pmc/articles/PMC10598273/ /pubmed/37875542 http://dx.doi.org/10.1038/s41598-023-44807-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Rumbeiha, Wilson K. Kim, Dong-Suk Min, Angela Nair, Maya Giulivi, Cecilia Disrupted brain mitochondrial morphology after in vivo hydrogen sulfide exposure |
title | Disrupted brain mitochondrial morphology after in vivo hydrogen sulfide exposure |
title_full | Disrupted brain mitochondrial morphology after in vivo hydrogen sulfide exposure |
title_fullStr | Disrupted brain mitochondrial morphology after in vivo hydrogen sulfide exposure |
title_full_unstemmed | Disrupted brain mitochondrial morphology after in vivo hydrogen sulfide exposure |
title_short | Disrupted brain mitochondrial morphology after in vivo hydrogen sulfide exposure |
title_sort | disrupted brain mitochondrial morphology after in vivo hydrogen sulfide exposure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598273/ https://www.ncbi.nlm.nih.gov/pubmed/37875542 http://dx.doi.org/10.1038/s41598-023-44807-y |
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