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Accelerated ethanol elimination via the lungs
Ethanol poisoning is endemic the world over. Morbidity and mortality depend on blood ethanol levels which in turn depend on the balance between its rates of absorption and clearance. Clearance of ethanol is mostly at a constant rate via enzymatic metabolism. We hypothesized that isocapnic hyperpnea...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7665168/ https://www.ncbi.nlm.nih.gov/pubmed/33184355 http://dx.doi.org/10.1038/s41598-020-76233-9 |
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author | Klostranec, Jesse M. Vucevic, Diana Crawley, Adrian P. Venkatraghavan, Lashmi Sobczyk, Olivia Duffin, James Sam, Kevin Holmes, Royce Fedorko, Ludwik Mikulis, David J. Fisher, Joseph A. |
author_facet | Klostranec, Jesse M. Vucevic, Diana Crawley, Adrian P. Venkatraghavan, Lashmi Sobczyk, Olivia Duffin, James Sam, Kevin Holmes, Royce Fedorko, Ludwik Mikulis, David J. Fisher, Joseph A. |
author_sort | Klostranec, Jesse M. |
collection | PubMed |
description | Ethanol poisoning is endemic the world over. Morbidity and mortality depend on blood ethanol levels which in turn depend on the balance between its rates of absorption and clearance. Clearance of ethanol is mostly at a constant rate via enzymatic metabolism. We hypothesized that isocapnic hyperpnea (IH), previously shown to be effective in acceleration of clearance of vapour anesthetics and carbon monoxide, would also accelerate the clearance of ethanol. In this proof-of-concept pilot study, five healthy male subjects were brought to a mildly elevated blood ethanol concentration (~ 0.1%) and ethanol clearance monitored during normal ventilation and IH on different days. IH increased elimination rate of ethanol in proportion to blood levels, increasing the elimination rate more than three-fold. Increased veno-arterial ethanol concentration differences during IH verified the efficacy of ethanol clearance via the lung. These data indicate that IH is a nonpharmacologic means to accelerate the elimination of ethanol by superimposing first order elimination kinetics on underlying zero order liver metabolism. Such kinetics may prove useful in treating acute severe ethanol intoxication. |
format | Online Article Text |
id | pubmed-7665168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76651682020-11-16 Accelerated ethanol elimination via the lungs Klostranec, Jesse M. Vucevic, Diana Crawley, Adrian P. Venkatraghavan, Lashmi Sobczyk, Olivia Duffin, James Sam, Kevin Holmes, Royce Fedorko, Ludwik Mikulis, David J. Fisher, Joseph A. Sci Rep Article Ethanol poisoning is endemic the world over. Morbidity and mortality depend on blood ethanol levels which in turn depend on the balance between its rates of absorption and clearance. Clearance of ethanol is mostly at a constant rate via enzymatic metabolism. We hypothesized that isocapnic hyperpnea (IH), previously shown to be effective in acceleration of clearance of vapour anesthetics and carbon monoxide, would also accelerate the clearance of ethanol. In this proof-of-concept pilot study, five healthy male subjects were brought to a mildly elevated blood ethanol concentration (~ 0.1%) and ethanol clearance monitored during normal ventilation and IH on different days. IH increased elimination rate of ethanol in proportion to blood levels, increasing the elimination rate more than three-fold. Increased veno-arterial ethanol concentration differences during IH verified the efficacy of ethanol clearance via the lung. These data indicate that IH is a nonpharmacologic means to accelerate the elimination of ethanol by superimposing first order elimination kinetics on underlying zero order liver metabolism. Such kinetics may prove useful in treating acute severe ethanol intoxication. Nature Publishing Group UK 2020-11-12 /pmc/articles/PMC7665168/ /pubmed/33184355 http://dx.doi.org/10.1038/s41598-020-76233-9 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Klostranec, Jesse M. Vucevic, Diana Crawley, Adrian P. Venkatraghavan, Lashmi Sobczyk, Olivia Duffin, James Sam, Kevin Holmes, Royce Fedorko, Ludwik Mikulis, David J. Fisher, Joseph A. Accelerated ethanol elimination via the lungs |
title | Accelerated ethanol elimination via the lungs |
title_full | Accelerated ethanol elimination via the lungs |
title_fullStr | Accelerated ethanol elimination via the lungs |
title_full_unstemmed | Accelerated ethanol elimination via the lungs |
title_short | Accelerated ethanol elimination via the lungs |
title_sort | accelerated ethanol elimination via the lungs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7665168/ https://www.ncbi.nlm.nih.gov/pubmed/33184355 http://dx.doi.org/10.1038/s41598-020-76233-9 |
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