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Effect of bovine lactoferrin as a novel therapeutic agent in a rat model of sepsis-induced acute lung injury
Sepsis is a serious clinical condition resulting from severe infection. High rates of mortality and tissue damage have been reported in intensive care unit (ICU) patients with sepsis. Bovine lactoferrin (BLF) is a well-known 80-kDa glycoprotein in the transferrin family that inhibits sepsis in low-b...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823406/ https://www.ncbi.nlm.nih.gov/pubmed/31673805 http://dx.doi.org/10.1186/s13568-019-0900-8 |
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author | Han, Nannan Li, Hengjie Li, Gang Shen, Ye Fei, Min Nan, Yong |
author_facet | Han, Nannan Li, Hengjie Li, Gang Shen, Ye Fei, Min Nan, Yong |
author_sort | Han, Nannan |
collection | PubMed |
description | Sepsis is a serious clinical condition resulting from severe infection. High rates of mortality and tissue damage have been reported in intensive care unit (ICU) patients with sepsis. Bovine lactoferrin (BLF) is a well-known 80-kDa glycoprotein in the transferrin family that inhibits sepsis in low-birth-weight neonates. The present study investigated the protective effects of BLF in a rat model of sepsis-induced acute lung injury (ALI). The wet/dry ratio, lipid peroxidation, antioxidant markers, total protein, total cell count, inflammatory markers and myeloperoxidase (MPO) levels were assessed. Histopathological analysis was also carried out. BLF treatment reduced the wet/dry ratio of lung tissue by 30.7% and 61.3%, and lipid peroxidation by 22.3% and 67%, at concentrations of 100 and 200 mg/kg, respectively. Superoxide dismutase (SOD), reduced glutathione (GSH), glutathione peroxidase (Gpx) and catalase were increased by more than 50% under treatment with 200 mg/kg BLF. Inflammatory markers, neutrophils, lymphocytes and total cell count were reduced by more than 50% under treatment with 200 mg/kg BLF. BLF treatment significantly reduced MPO activity, by 28.2% and 74.3%, at concentrations of 100 and 200 mg/kg, respectively. Neutrophilic infiltration and edema were observed in control rats. However, BLF treatment restored intestinal microvilli to the normal range and reduced inflammatory cell invasion. Collectively, these results suggest that BLF is an effective therapeutic agent against sepsis-induced ALI. |
format | Online Article Text |
id | pubmed-6823406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-68234062019-11-14 Effect of bovine lactoferrin as a novel therapeutic agent in a rat model of sepsis-induced acute lung injury Han, Nannan Li, Hengjie Li, Gang Shen, Ye Fei, Min Nan, Yong AMB Express Original Article Sepsis is a serious clinical condition resulting from severe infection. High rates of mortality and tissue damage have been reported in intensive care unit (ICU) patients with sepsis. Bovine lactoferrin (BLF) is a well-known 80-kDa glycoprotein in the transferrin family that inhibits sepsis in low-birth-weight neonates. The present study investigated the protective effects of BLF in a rat model of sepsis-induced acute lung injury (ALI). The wet/dry ratio, lipid peroxidation, antioxidant markers, total protein, total cell count, inflammatory markers and myeloperoxidase (MPO) levels were assessed. Histopathological analysis was also carried out. BLF treatment reduced the wet/dry ratio of lung tissue by 30.7% and 61.3%, and lipid peroxidation by 22.3% and 67%, at concentrations of 100 and 200 mg/kg, respectively. Superoxide dismutase (SOD), reduced glutathione (GSH), glutathione peroxidase (Gpx) and catalase were increased by more than 50% under treatment with 200 mg/kg BLF. Inflammatory markers, neutrophils, lymphocytes and total cell count were reduced by more than 50% under treatment with 200 mg/kg BLF. BLF treatment significantly reduced MPO activity, by 28.2% and 74.3%, at concentrations of 100 and 200 mg/kg, respectively. Neutrophilic infiltration and edema were observed in control rats. However, BLF treatment restored intestinal microvilli to the normal range and reduced inflammatory cell invasion. Collectively, these results suggest that BLF is an effective therapeutic agent against sepsis-induced ALI. Springer Berlin Heidelberg 2019-10-31 /pmc/articles/PMC6823406/ /pubmed/31673805 http://dx.doi.org/10.1186/s13568-019-0900-8 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Han, Nannan Li, Hengjie Li, Gang Shen, Ye Fei, Min Nan, Yong Effect of bovine lactoferrin as a novel therapeutic agent in a rat model of sepsis-induced acute lung injury |
title | Effect of bovine lactoferrin as a novel therapeutic agent in a rat model of sepsis-induced acute lung injury |
title_full | Effect of bovine lactoferrin as a novel therapeutic agent in a rat model of sepsis-induced acute lung injury |
title_fullStr | Effect of bovine lactoferrin as a novel therapeutic agent in a rat model of sepsis-induced acute lung injury |
title_full_unstemmed | Effect of bovine lactoferrin as a novel therapeutic agent in a rat model of sepsis-induced acute lung injury |
title_short | Effect of bovine lactoferrin as a novel therapeutic agent in a rat model of sepsis-induced acute lung injury |
title_sort | effect of bovine lactoferrin as a novel therapeutic agent in a rat model of sepsis-induced acute lung injury |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823406/ https://www.ncbi.nlm.nih.gov/pubmed/31673805 http://dx.doi.org/10.1186/s13568-019-0900-8 |
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