Cargando…
Acute 40% exchange-transfusion with hemoglobin-vesicles in a mouse pneumonectomy model
OBJECTIVES: Hemoglobin vesicles (HbVs) function as a red blood cell (RBC) substitute and are composed of purified hemoglobin encapsulated in a phospholipid bilayer membrane. The performance of HbVs as a substitute for RBC transfusions was examined in a mouse model of pneumonectomy following acute 40...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473544/ https://www.ncbi.nlm.nih.gov/pubmed/28622333 http://dx.doi.org/10.1371/journal.pone.0178724 |
_version_ | 1783244304999776256 |
---|---|
author | Kohno, Mitsutomo Ikeda, Tatsuhiko Hashimoto, Ryo Izumi, Yotaro Watanabe, Masazumi Horinouchi, Hirohisa Sakai, Hiromi Kobayashi, Koichi Iwazaki, Masayuki |
author_facet | Kohno, Mitsutomo Ikeda, Tatsuhiko Hashimoto, Ryo Izumi, Yotaro Watanabe, Masazumi Horinouchi, Hirohisa Sakai, Hiromi Kobayashi, Koichi Iwazaki, Masayuki |
author_sort | Kohno, Mitsutomo |
collection | PubMed |
description | OBJECTIVES: Hemoglobin vesicles (HbVs) function as a red blood cell (RBC) substitute and are composed of purified hemoglobin encapsulated in a phospholipid bilayer membrane. The performance of HbVs as a substitute for RBC transfusions was examined in a mouse model of pneumonectomy following acute 40% exchange-transfusion with HbVs. METHODS: Before performing left pneumonectomies, 40% of the blood volume of mice was replaced with a) lactated Ringer’s solution (control), b) 5% recombinant human serum albumin (rHSA), c) mouse RBCs shed in rHSA (mRBCs/rHSA), or d) HbV suspended in rHSA (HbV/rHSA). We compared postoperative a) survival, b) functional recovery, and c) histopathological, immunohistochemical, and inflammatory responses among the study groups. RESULTS: In the HbV/rHSA and mRBC/rHSA groups, all mice survived ≥7 days after pneumonectomy, whereas 100% of the control mice died within a few h and 50% of mice in the rHSA group died within 24 h after pneumonectomy. Immunohistochemical staining for hypoxia-inducible factor-1α showed that hepatic and renal hypoxic injuries were prominently mitigated by HbV and mRBCs. CONCLUSIONS: The oxygen-carrying performance of HbV was similar to that of mRBCs, even with impaired lung functions following pneumonectomy. HbV infusion did not interfere with the recovery from surgical injury. In the near future, HbVs could be used clinically as a substitute for the perioperative transfusion of RBCs, when or where donated RBCs are not immediately available. |
format | Online Article Text |
id | pubmed-5473544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54735442017-06-22 Acute 40% exchange-transfusion with hemoglobin-vesicles in a mouse pneumonectomy model Kohno, Mitsutomo Ikeda, Tatsuhiko Hashimoto, Ryo Izumi, Yotaro Watanabe, Masazumi Horinouchi, Hirohisa Sakai, Hiromi Kobayashi, Koichi Iwazaki, Masayuki PLoS One Research Article OBJECTIVES: Hemoglobin vesicles (HbVs) function as a red blood cell (RBC) substitute and are composed of purified hemoglobin encapsulated in a phospholipid bilayer membrane. The performance of HbVs as a substitute for RBC transfusions was examined in a mouse model of pneumonectomy following acute 40% exchange-transfusion with HbVs. METHODS: Before performing left pneumonectomies, 40% of the blood volume of mice was replaced with a) lactated Ringer’s solution (control), b) 5% recombinant human serum albumin (rHSA), c) mouse RBCs shed in rHSA (mRBCs/rHSA), or d) HbV suspended in rHSA (HbV/rHSA). We compared postoperative a) survival, b) functional recovery, and c) histopathological, immunohistochemical, and inflammatory responses among the study groups. RESULTS: In the HbV/rHSA and mRBC/rHSA groups, all mice survived ≥7 days after pneumonectomy, whereas 100% of the control mice died within a few h and 50% of mice in the rHSA group died within 24 h after pneumonectomy. Immunohistochemical staining for hypoxia-inducible factor-1α showed that hepatic and renal hypoxic injuries were prominently mitigated by HbV and mRBCs. CONCLUSIONS: The oxygen-carrying performance of HbV was similar to that of mRBCs, even with impaired lung functions following pneumonectomy. HbV infusion did not interfere with the recovery from surgical injury. In the near future, HbVs could be used clinically as a substitute for the perioperative transfusion of RBCs, when or where donated RBCs are not immediately available. Public Library of Science 2017-06-16 /pmc/articles/PMC5473544/ /pubmed/28622333 http://dx.doi.org/10.1371/journal.pone.0178724 Text en © 2017 Kohno et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kohno, Mitsutomo Ikeda, Tatsuhiko Hashimoto, Ryo Izumi, Yotaro Watanabe, Masazumi Horinouchi, Hirohisa Sakai, Hiromi Kobayashi, Koichi Iwazaki, Masayuki Acute 40% exchange-transfusion with hemoglobin-vesicles in a mouse pneumonectomy model |
title | Acute 40% exchange-transfusion with hemoglobin-vesicles in a mouse pneumonectomy model |
title_full | Acute 40% exchange-transfusion with hemoglobin-vesicles in a mouse pneumonectomy model |
title_fullStr | Acute 40% exchange-transfusion with hemoglobin-vesicles in a mouse pneumonectomy model |
title_full_unstemmed | Acute 40% exchange-transfusion with hemoglobin-vesicles in a mouse pneumonectomy model |
title_short | Acute 40% exchange-transfusion with hemoglobin-vesicles in a mouse pneumonectomy model |
title_sort | acute 40% exchange-transfusion with hemoglobin-vesicles in a mouse pneumonectomy model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473544/ https://www.ncbi.nlm.nih.gov/pubmed/28622333 http://dx.doi.org/10.1371/journal.pone.0178724 |
work_keys_str_mv | AT kohnomitsutomo acute40exchangetransfusionwithhemoglobinvesiclesinamousepneumonectomymodel AT ikedatatsuhiko acute40exchangetransfusionwithhemoglobinvesiclesinamousepneumonectomymodel AT hashimotoryo acute40exchangetransfusionwithhemoglobinvesiclesinamousepneumonectomymodel AT izumiyotaro acute40exchangetransfusionwithhemoglobinvesiclesinamousepneumonectomymodel AT watanabemasazumi acute40exchangetransfusionwithhemoglobinvesiclesinamousepneumonectomymodel AT horinouchihirohisa acute40exchangetransfusionwithhemoglobinvesiclesinamousepneumonectomymodel AT sakaihiromi acute40exchangetransfusionwithhemoglobinvesiclesinamousepneumonectomymodel AT kobayashikoichi acute40exchangetransfusionwithhemoglobinvesiclesinamousepneumonectomymodel AT iwazakimasayuki acute40exchangetransfusionwithhemoglobinvesiclesinamousepneumonectomymodel |