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Ulinastatin: A Potential Alternative to Glucocorticoid in the Treatment of Severe Decompression Sickness

Inflammatory reaction is the crux in various clinical critical diseases including decompression sickness (DCS). Ulinastatin (UTI), a potent anti-inflammatory agent, has been used clinically, including as a substitution for steroids. This study aimed to explore the potential effects of UTI upon DCS i...

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Autores principales: Meng, Wen-tao, Qing, Long, Li, Chun-zhen, Zhang, Kun, Yi, Hong-jie, Zhao, Xu-peng, Xu, Wei-gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113395/
https://www.ncbi.nlm.nih.gov/pubmed/32273851
http://dx.doi.org/10.3389/fphys.2020.00273
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author Meng, Wen-tao
Qing, Long
Li, Chun-zhen
Zhang, Kun
Yi, Hong-jie
Zhao, Xu-peng
Xu, Wei-gang
author_facet Meng, Wen-tao
Qing, Long
Li, Chun-zhen
Zhang, Kun
Yi, Hong-jie
Zhao, Xu-peng
Xu, Wei-gang
author_sort Meng, Wen-tao
collection PubMed
description Inflammatory reaction is the crux in various clinical critical diseases including decompression sickness (DCS). Ulinastatin (UTI), a potent anti-inflammatory agent, has been used clinically, including as a substitution for steroids. This study aimed to explore the potential effects of UTI upon DCS in a rabbit model. Eighty-eight rabbits were subjected to simulated diving to 6 atmospheres absolute (ATA) for 60 min with 2.5-minute decompression. Three doses of UTI (15/7.5/3.75 × 10(5) U/kg) or saline were intravenously administered immediately following decompression. Circulating bubbles were monitored for 3 h following decompression and DCS signs were evaluated for 24 h. Blood was sampled 8 times during 72 h after decompression for inflammatory, endothelial, oxidative and routine blood indices. Lung tissues were also sampled for evaluating endothelial function. Another six rabbits were used as Normal controls. In the high dose UTI group the mortality, general morbidity and incidence of severe DCS was decreased from 31.25 to 9.38% (P = 0.030), 84.38 to 62.50% (P = 0.048) and 46.88 to 21.88% (P = 0.035), respectively. The high dose of UTI significantly postponed the occurrence of DCS (P = 0.030) and prolonged survival time (P = 0.009) compared with the Saline group, and significantly ameliorated inflammation responses, endothelial injuries and oxidative damage. The results strongly suggest the benefit of UTI on DCS, especially for severe cases. Large doses are needed to achieve significant effects. UTI may be a potential ideal pharmacological candidate for the treatment of severe DCS.
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spelling pubmed-71133952020-04-09 Ulinastatin: A Potential Alternative to Glucocorticoid in the Treatment of Severe Decompression Sickness Meng, Wen-tao Qing, Long Li, Chun-zhen Zhang, Kun Yi, Hong-jie Zhao, Xu-peng Xu, Wei-gang Front Physiol Physiology Inflammatory reaction is the crux in various clinical critical diseases including decompression sickness (DCS). Ulinastatin (UTI), a potent anti-inflammatory agent, has been used clinically, including as a substitution for steroids. This study aimed to explore the potential effects of UTI upon DCS in a rabbit model. Eighty-eight rabbits were subjected to simulated diving to 6 atmospheres absolute (ATA) for 60 min with 2.5-minute decompression. Three doses of UTI (15/7.5/3.75 × 10(5) U/kg) or saline were intravenously administered immediately following decompression. Circulating bubbles were monitored for 3 h following decompression and DCS signs were evaluated for 24 h. Blood was sampled 8 times during 72 h after decompression for inflammatory, endothelial, oxidative and routine blood indices. Lung tissues were also sampled for evaluating endothelial function. Another six rabbits were used as Normal controls. In the high dose UTI group the mortality, general morbidity and incidence of severe DCS was decreased from 31.25 to 9.38% (P = 0.030), 84.38 to 62.50% (P = 0.048) and 46.88 to 21.88% (P = 0.035), respectively. The high dose of UTI significantly postponed the occurrence of DCS (P = 0.030) and prolonged survival time (P = 0.009) compared with the Saline group, and significantly ameliorated inflammation responses, endothelial injuries and oxidative damage. The results strongly suggest the benefit of UTI on DCS, especially for severe cases. Large doses are needed to achieve significant effects. UTI may be a potential ideal pharmacological candidate for the treatment of severe DCS. Frontiers Media S.A. 2020-03-26 /pmc/articles/PMC7113395/ /pubmed/32273851 http://dx.doi.org/10.3389/fphys.2020.00273 Text en Copyright © 2020 Meng, Qing, Li, Zhang, Yi, Zhao and Xu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Meng, Wen-tao
Qing, Long
Li, Chun-zhen
Zhang, Kun
Yi, Hong-jie
Zhao, Xu-peng
Xu, Wei-gang
Ulinastatin: A Potential Alternative to Glucocorticoid in the Treatment of Severe Decompression Sickness
title Ulinastatin: A Potential Alternative to Glucocorticoid in the Treatment of Severe Decompression Sickness
title_full Ulinastatin: A Potential Alternative to Glucocorticoid in the Treatment of Severe Decompression Sickness
title_fullStr Ulinastatin: A Potential Alternative to Glucocorticoid in the Treatment of Severe Decompression Sickness
title_full_unstemmed Ulinastatin: A Potential Alternative to Glucocorticoid in the Treatment of Severe Decompression Sickness
title_short Ulinastatin: A Potential Alternative to Glucocorticoid in the Treatment of Severe Decompression Sickness
title_sort ulinastatin: a potential alternative to glucocorticoid in the treatment of severe decompression sickness
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113395/
https://www.ncbi.nlm.nih.gov/pubmed/32273851
http://dx.doi.org/10.3389/fphys.2020.00273
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