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The effects of acute renal denervation on kidney perfusion and metabolism in experimental septic shock

BACKGROUND: Perfusion deficits likely play an important role in the development of renal dysfunction in sepsis. Renal denervation may improve kidney perfusion and metabolism. METHODS: We randomized 14 female sheep to undergo bilateral surgical renal denervation (n = 7) or sham procedure (n = 7) prio...

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Autores principales: Post, Emiel Hendrik, Su, Fuhong, Hosokawa, Koji, Taccone, Fabio Silvio, Herpain, Antoine, Creteur, Jacques, De Backer, Daniel, Vincent, Jean-Louis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452298/
https://www.ncbi.nlm.nih.gov/pubmed/28569187
http://dx.doi.org/10.1186/s12882-017-0586-6
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author Post, Emiel Hendrik
Su, Fuhong
Hosokawa, Koji
Taccone, Fabio Silvio
Herpain, Antoine
Creteur, Jacques
De Backer, Daniel
Vincent, Jean-Louis
author_facet Post, Emiel Hendrik
Su, Fuhong
Hosokawa, Koji
Taccone, Fabio Silvio
Herpain, Antoine
Creteur, Jacques
De Backer, Daniel
Vincent, Jean-Louis
author_sort Post, Emiel Hendrik
collection PubMed
description BACKGROUND: Perfusion deficits likely play an important role in the development of renal dysfunction in sepsis. Renal denervation may improve kidney perfusion and metabolism. METHODS: We randomized 14 female sheep to undergo bilateral surgical renal denervation (n = 7) or sham procedure (n = 7) prior to induction of sepsis. Renal blood flow (RBF) was measured with a pre-calibrated flowprobe. Laser Doppler probes were implanted to measure cortical and medullary perfusion. Cortical glucose, lactate and pyruvate levels were measured using the microdialysis technique. Creatinine clearance was determined. Sepsis was induced by peritonitis and fluid resuscitation was provided to avoid hypovolemia. RESULTS: RBF and cortical perfusion were higher in the denervated group during the first 6 h after induction of sepsis (P < 0.001 and P < 0.05, respectively), while medullary perfusion decreased similarly in both groups. After hypotension developed, RBF decreased to similar levels in both groups. Cortical pyruvate and lactate levels were lower in the denervated animals (P < 0.001 and P < 0.001, respectively). There were no differences between groups in creatinine clearance, urine output or time to oliguria. CONCLUSION: Denervation thus caused an early increase in RBF that was distributed towards the kidney cortex. Although associated with an attenuation of early cortical metabolic alterations, denervation failed to prevent the deterioration in renal function.
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spelling pubmed-54522982017-06-01 The effects of acute renal denervation on kidney perfusion and metabolism in experimental septic shock Post, Emiel Hendrik Su, Fuhong Hosokawa, Koji Taccone, Fabio Silvio Herpain, Antoine Creteur, Jacques De Backer, Daniel Vincent, Jean-Louis BMC Nephrol Research Article BACKGROUND: Perfusion deficits likely play an important role in the development of renal dysfunction in sepsis. Renal denervation may improve kidney perfusion and metabolism. METHODS: We randomized 14 female sheep to undergo bilateral surgical renal denervation (n = 7) or sham procedure (n = 7) prior to induction of sepsis. Renal blood flow (RBF) was measured with a pre-calibrated flowprobe. Laser Doppler probes were implanted to measure cortical and medullary perfusion. Cortical glucose, lactate and pyruvate levels were measured using the microdialysis technique. Creatinine clearance was determined. Sepsis was induced by peritonitis and fluid resuscitation was provided to avoid hypovolemia. RESULTS: RBF and cortical perfusion were higher in the denervated group during the first 6 h after induction of sepsis (P < 0.001 and P < 0.05, respectively), while medullary perfusion decreased similarly in both groups. After hypotension developed, RBF decreased to similar levels in both groups. Cortical pyruvate and lactate levels were lower in the denervated animals (P < 0.001 and P < 0.001, respectively). There were no differences between groups in creatinine clearance, urine output or time to oliguria. CONCLUSION: Denervation thus caused an early increase in RBF that was distributed towards the kidney cortex. Although associated with an attenuation of early cortical metabolic alterations, denervation failed to prevent the deterioration in renal function. BioMed Central 2017-05-31 /pmc/articles/PMC5452298/ /pubmed/28569187 http://dx.doi.org/10.1186/s12882-017-0586-6 Text en © The Author(s). 2017 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Post, Emiel Hendrik
Su, Fuhong
Hosokawa, Koji
Taccone, Fabio Silvio
Herpain, Antoine
Creteur, Jacques
De Backer, Daniel
Vincent, Jean-Louis
The effects of acute renal denervation on kidney perfusion and metabolism in experimental septic shock
title The effects of acute renal denervation on kidney perfusion and metabolism in experimental septic shock
title_full The effects of acute renal denervation on kidney perfusion and metabolism in experimental septic shock
title_fullStr The effects of acute renal denervation on kidney perfusion and metabolism in experimental septic shock
title_full_unstemmed The effects of acute renal denervation on kidney perfusion and metabolism in experimental septic shock
title_short The effects of acute renal denervation on kidney perfusion and metabolism in experimental septic shock
title_sort effects of acute renal denervation on kidney perfusion and metabolism in experimental septic shock
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452298/
https://www.ncbi.nlm.nih.gov/pubmed/28569187
http://dx.doi.org/10.1186/s12882-017-0586-6
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