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Suppressive effects of the neutrophil elastase inhibitor sivelestat sodium hydrate on interleukin-1β production in lipopolysaccharide-stimulated porcine whole blood
OBJECTIVE: Sivelestat sodium hydrate (Siv) is expected to be an effective therapy for acute respiratory distress syndrome, although its mechanism of action is not understood. In this study, we investigated which myeloid cells-derived cytokines were suppressed by Siv. METHODS: Continuous hemofiltrati...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Fujita Medical Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766654/ https://www.ncbi.nlm.nih.gov/pubmed/35111515 http://dx.doi.org/10.20407/fmj.2019-002 |
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author | Kurimoto, Yasuyoshi Shimomura, Yasuyo Moriyama, Kazuhiro Nakamura, Tomoyuki Kuriyama, Naohide Hara, Yoshitaka Komura, Hidefumi Hasegawa, Daisuke Kawaji, Takahiro Nishida, Osamu |
author_facet | Kurimoto, Yasuyoshi Shimomura, Yasuyo Moriyama, Kazuhiro Nakamura, Tomoyuki Kuriyama, Naohide Hara, Yoshitaka Komura, Hidefumi Hasegawa, Daisuke Kawaji, Takahiro Nishida, Osamu |
author_sort | Kurimoto, Yasuyoshi |
collection | PubMed |
description | OBJECTIVE: Sivelestat sodium hydrate (Siv) is expected to be an effective therapy for acute respiratory distress syndrome, although its mechanism of action is not understood. In this study, we investigated which myeloid cells-derived cytokines were suppressed by Siv. METHODS: Continuous hemofiltration was performed by circulating fresh porcine blood through a semi-closed circuit. To ensure that leukocytes survived for 360 min, 5% glucose, heparin, and air were continuously injected. The control group received continuous administration of lipopolysaccharide (LPS) only, whereas the Siv group received LPS and Siv. Complete blood count, levels of various cytokines, and other variables were compared between the groups. RESULTS: Interleukin (IL)-1β level was significantly suppressed in the Siv group compared with that in the control group (p<0.05). CONCLUSIONS: The results suggested that Siv suppressed the production of IL-1β and possibly other cytokines by myeloid cells. Whether this suppression of cytokine production is caused directly by Siv or mediated via suppression of granulocyte elastase should be evaluated in the future. |
format | Online Article Text |
id | pubmed-8766654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Fujita Medical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-87666542022-02-01 Suppressive effects of the neutrophil elastase inhibitor sivelestat sodium hydrate on interleukin-1β production in lipopolysaccharide-stimulated porcine whole blood Kurimoto, Yasuyoshi Shimomura, Yasuyo Moriyama, Kazuhiro Nakamura, Tomoyuki Kuriyama, Naohide Hara, Yoshitaka Komura, Hidefumi Hasegawa, Daisuke Kawaji, Takahiro Nishida, Osamu Fujita Med J Original Article OBJECTIVE: Sivelestat sodium hydrate (Siv) is expected to be an effective therapy for acute respiratory distress syndrome, although its mechanism of action is not understood. In this study, we investigated which myeloid cells-derived cytokines were suppressed by Siv. METHODS: Continuous hemofiltration was performed by circulating fresh porcine blood through a semi-closed circuit. To ensure that leukocytes survived for 360 min, 5% glucose, heparin, and air were continuously injected. The control group received continuous administration of lipopolysaccharide (LPS) only, whereas the Siv group received LPS and Siv. Complete blood count, levels of various cytokines, and other variables were compared between the groups. RESULTS: Interleukin (IL)-1β level was significantly suppressed in the Siv group compared with that in the control group (p<0.05). CONCLUSIONS: The results suggested that Siv suppressed the production of IL-1β and possibly other cytokines by myeloid cells. Whether this suppression of cytokine production is caused directly by Siv or mediated via suppression of granulocyte elastase should be evaluated in the future. Fujita Medical Society 2020 2019-11-02 /pmc/articles/PMC8766654/ /pubmed/35111515 http://dx.doi.org/10.20407/fmj.2019-002 Text en https://creativecommons.org/licenses/by/4.0/This is an Open access article distributed under the Terms of Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Article Kurimoto, Yasuyoshi Shimomura, Yasuyo Moriyama, Kazuhiro Nakamura, Tomoyuki Kuriyama, Naohide Hara, Yoshitaka Komura, Hidefumi Hasegawa, Daisuke Kawaji, Takahiro Nishida, Osamu Suppressive effects of the neutrophil elastase inhibitor sivelestat sodium hydrate on interleukin-1β production in lipopolysaccharide-stimulated porcine whole blood |
title | Suppressive effects of the neutrophil elastase inhibitor sivelestat
sodium hydrate on interleukin-1β production in lipopolysaccharide-stimulated porcine whole
blood |
title_full | Suppressive effects of the neutrophil elastase inhibitor sivelestat
sodium hydrate on interleukin-1β production in lipopolysaccharide-stimulated porcine whole
blood |
title_fullStr | Suppressive effects of the neutrophil elastase inhibitor sivelestat
sodium hydrate on interleukin-1β production in lipopolysaccharide-stimulated porcine whole
blood |
title_full_unstemmed | Suppressive effects of the neutrophil elastase inhibitor sivelestat
sodium hydrate on interleukin-1β production in lipopolysaccharide-stimulated porcine whole
blood |
title_short | Suppressive effects of the neutrophil elastase inhibitor sivelestat
sodium hydrate on interleukin-1β production in lipopolysaccharide-stimulated porcine whole
blood |
title_sort | suppressive effects of the neutrophil elastase inhibitor sivelestat
sodium hydrate on interleukin-1β production in lipopolysaccharide-stimulated porcine whole
blood |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766654/ https://www.ncbi.nlm.nih.gov/pubmed/35111515 http://dx.doi.org/10.20407/fmj.2019-002 |
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