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In Vivo Evaluation of the Ameliorating Effects of Small-Volume Resuscitation with Four Different Fluids on Endotoxemia-Induced Kidney Injury

Acute kidney injury associated with renal hypoperfusion is a frequent and severe complication during sepsis. Fluid resuscitation is the main therapy. However, heart failure is usually lethal for those patients receiving large volumes of fluids. We compared the effects of small-volume resuscitation u...

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Autores principales: Wang, Yan-ling, Chen, Jing-hui, Zhu, Qiong-fang, Yu, Gao-feng, Luo, Chen-fang, Luo, Gang-jian, Li, Shang-rong, Hei, Zi-qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529950/
https://www.ncbi.nlm.nih.gov/pubmed/26273142
http://dx.doi.org/10.1155/2015/726243
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author Wang, Yan-ling
Chen, Jing-hui
Zhu, Qiong-fang
Yu, Gao-feng
Luo, Chen-fang
Luo, Gang-jian
Li, Shang-rong
Hei, Zi-qing
author_facet Wang, Yan-ling
Chen, Jing-hui
Zhu, Qiong-fang
Yu, Gao-feng
Luo, Chen-fang
Luo, Gang-jian
Li, Shang-rong
Hei, Zi-qing
author_sort Wang, Yan-ling
collection PubMed
description Acute kidney injury associated with renal hypoperfusion is a frequent and severe complication during sepsis. Fluid resuscitation is the main therapy. However, heart failure is usually lethal for those patients receiving large volumes of fluids. We compared the effects of small-volume resuscitation using four different treatment regimens, involving saline, hypertonic saline (HTS), hydroxyethyl starch (HES), or hypertonic saline hydroxyethyl starch (HSH), on the kidneys of rats treated with lipopolysaccharide (LPS) to induce endotoxemia. LPS injection caused reduced and progressively deteriorated systemic (arterial blood pressure) and renal hemodynamics (renal blood flow and renal vascular resistance index) over time. This deterioration was accompanied by marked renal functional and pathological injury, as well as an oxidative and inflammatory response, manifesting as increased levels of tumor necrosis factor-α, nitric oxide, and malondialdehyde and decreased activity of superoxide dismutase. Small-volume perfusion with saline failed to improve renal and systemic circulation. However, small-volume perfusion with HES and HSH greatly improved the above parameters, while HTS only transiently improved systemic and renal hemodynamics with obvious renal injury. Therefore, single small-volume resuscitation with HES and HSH could be valid therapeutic approaches to ameliorate kidney injury induced by endotoxemia, while HTS transiently delays injury and saline shows no protective effects.
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spelling pubmed-45299502015-08-13 In Vivo Evaluation of the Ameliorating Effects of Small-Volume Resuscitation with Four Different Fluids on Endotoxemia-Induced Kidney Injury Wang, Yan-ling Chen, Jing-hui Zhu, Qiong-fang Yu, Gao-feng Luo, Chen-fang Luo, Gang-jian Li, Shang-rong Hei, Zi-qing Mediators Inflamm Research Article Acute kidney injury associated with renal hypoperfusion is a frequent and severe complication during sepsis. Fluid resuscitation is the main therapy. However, heart failure is usually lethal for those patients receiving large volumes of fluids. We compared the effects of small-volume resuscitation using four different treatment regimens, involving saline, hypertonic saline (HTS), hydroxyethyl starch (HES), or hypertonic saline hydroxyethyl starch (HSH), on the kidneys of rats treated with lipopolysaccharide (LPS) to induce endotoxemia. LPS injection caused reduced and progressively deteriorated systemic (arterial blood pressure) and renal hemodynamics (renal blood flow and renal vascular resistance index) over time. This deterioration was accompanied by marked renal functional and pathological injury, as well as an oxidative and inflammatory response, manifesting as increased levels of tumor necrosis factor-α, nitric oxide, and malondialdehyde and decreased activity of superoxide dismutase. Small-volume perfusion with saline failed to improve renal and systemic circulation. However, small-volume perfusion with HES and HSH greatly improved the above parameters, while HTS only transiently improved systemic and renal hemodynamics with obvious renal injury. Therefore, single small-volume resuscitation with HES and HSH could be valid therapeutic approaches to ameliorate kidney injury induced by endotoxemia, while HTS transiently delays injury and saline shows no protective effects. Hindawi Publishing Corporation 2015 2015-07-26 /pmc/articles/PMC4529950/ /pubmed/26273142 http://dx.doi.org/10.1155/2015/726243 Text en Copyright © 2015 Yan-ling Wang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Yan-ling
Chen, Jing-hui
Zhu, Qiong-fang
Yu, Gao-feng
Luo, Chen-fang
Luo, Gang-jian
Li, Shang-rong
Hei, Zi-qing
In Vivo Evaluation of the Ameliorating Effects of Small-Volume Resuscitation with Four Different Fluids on Endotoxemia-Induced Kidney Injury
title In Vivo Evaluation of the Ameliorating Effects of Small-Volume Resuscitation with Four Different Fluids on Endotoxemia-Induced Kidney Injury
title_full In Vivo Evaluation of the Ameliorating Effects of Small-Volume Resuscitation with Four Different Fluids on Endotoxemia-Induced Kidney Injury
title_fullStr In Vivo Evaluation of the Ameliorating Effects of Small-Volume Resuscitation with Four Different Fluids on Endotoxemia-Induced Kidney Injury
title_full_unstemmed In Vivo Evaluation of the Ameliorating Effects of Small-Volume Resuscitation with Four Different Fluids on Endotoxemia-Induced Kidney Injury
title_short In Vivo Evaluation of the Ameliorating Effects of Small-Volume Resuscitation with Four Different Fluids on Endotoxemia-Induced Kidney Injury
title_sort in vivo evaluation of the ameliorating effects of small-volume resuscitation with four different fluids on endotoxemia-induced kidney injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529950/
https://www.ncbi.nlm.nih.gov/pubmed/26273142
http://dx.doi.org/10.1155/2015/726243
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