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Ramipril pretreatment worsened renal injury and survival despite a reduction in renal inflammation in experimentally induced sepsis in mice
INTRODUCTION: The angiotensin converting enzyme inhibitor ramipril is a standard antihypertensive therapy for many patients. Because angiotensin II may promote inflammation, we were interested in whether basal pretreatment with ramipril may modify renal function and inflammation as well as systemic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232051/ https://www.ncbi.nlm.nih.gov/pubmed/32419571 http://dx.doi.org/10.1177/1470320320923977 |
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author | Bondeva, Tzvetanka Schindler, Katrin Schindler, Claudia Wolf, Gunter |
author_facet | Bondeva, Tzvetanka Schindler, Katrin Schindler, Claudia Wolf, Gunter |
author_sort | Bondeva, Tzvetanka |
collection | PubMed |
description | INTRODUCTION: The angiotensin converting enzyme inhibitor ramipril is a standard antihypertensive therapy for many patients. Because angiotensin II may promote inflammation, we were interested in whether basal pretreatment with ramipril may modify renal function and inflammation as well as systemic outcome in experimentally induced sepsis in mice. MATERIAL AND METHODS: Ramipril (10 mg/kg/day) pretreatment or placebo (NaCl) was given intraperitoneally for 5 days to C57BL6/J mice, followed by either sham operation or cecal ligation and puncture sepsis induction. Real-time polymerase chain reaction and immunological stains were used to evaluate renal gene and protein expression, respectively. Plasma creatinine, neutrophil-gelatinase associated lipocalin, and blood urea nitrogen were used as markers for renal function. A clinical severity score was determined. RESULTS: Administration of ramipril before cecal ligation and puncture surgery was associated with reduced renal inflammation but did not improved renal function and structure and even worsened the clinical status of septic mice. CONCLUSIONS: The data suggest that the effects of ramipril pretreatment are complex. Additional studies including monitoring of hemodynamic parameters are necessary to elucidate the exact mechanism(s) of this observation. In addition, the timing of the ramipril administration could be of importance. |
format | Online Article Text |
id | pubmed-7232051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-72320512020-05-29 Ramipril pretreatment worsened renal injury and survival despite a reduction in renal inflammation in experimentally induced sepsis in mice Bondeva, Tzvetanka Schindler, Katrin Schindler, Claudia Wolf, Gunter J Renin Angiotensin Aldosterone Syst Original Article INTRODUCTION: The angiotensin converting enzyme inhibitor ramipril is a standard antihypertensive therapy for many patients. Because angiotensin II may promote inflammation, we were interested in whether basal pretreatment with ramipril may modify renal function and inflammation as well as systemic outcome in experimentally induced sepsis in mice. MATERIAL AND METHODS: Ramipril (10 mg/kg/day) pretreatment or placebo (NaCl) was given intraperitoneally for 5 days to C57BL6/J mice, followed by either sham operation or cecal ligation and puncture sepsis induction. Real-time polymerase chain reaction and immunological stains were used to evaluate renal gene and protein expression, respectively. Plasma creatinine, neutrophil-gelatinase associated lipocalin, and blood urea nitrogen were used as markers for renal function. A clinical severity score was determined. RESULTS: Administration of ramipril before cecal ligation and puncture surgery was associated with reduced renal inflammation but did not improved renal function and structure and even worsened the clinical status of septic mice. CONCLUSIONS: The data suggest that the effects of ramipril pretreatment are complex. Additional studies including monitoring of hemodynamic parameters are necessary to elucidate the exact mechanism(s) of this observation. In addition, the timing of the ramipril administration could be of importance. SAGE Publications 2020-05-16 /pmc/articles/PMC7232051/ /pubmed/32419571 http://dx.doi.org/10.1177/1470320320923977 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Bondeva, Tzvetanka Schindler, Katrin Schindler, Claudia Wolf, Gunter Ramipril pretreatment worsened renal injury and survival despite a reduction in renal inflammation in experimentally induced sepsis in mice |
title | Ramipril pretreatment worsened renal injury and survival despite a
reduction in renal inflammation in experimentally induced sepsis in
mice |
title_full | Ramipril pretreatment worsened renal injury and survival despite a
reduction in renal inflammation in experimentally induced sepsis in
mice |
title_fullStr | Ramipril pretreatment worsened renal injury and survival despite a
reduction in renal inflammation in experimentally induced sepsis in
mice |
title_full_unstemmed | Ramipril pretreatment worsened renal injury and survival despite a
reduction in renal inflammation in experimentally induced sepsis in
mice |
title_short | Ramipril pretreatment worsened renal injury and survival despite a
reduction in renal inflammation in experimentally induced sepsis in
mice |
title_sort | ramipril pretreatment worsened renal injury and survival despite a
reduction in renal inflammation in experimentally induced sepsis in
mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232051/ https://www.ncbi.nlm.nih.gov/pubmed/32419571 http://dx.doi.org/10.1177/1470320320923977 |
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