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A New Apparatus for Standardized Rat Kidney Biopsy
Survival biopsies are frequently applied in rat kidney disease models, but several drawbacks such as surgical kidney trauma, bleeding risk and variable loss of kidney tissue are still unsolved. Therefore, we developed an easy-to-use core biopsy instrument and evaluated whether two consecutive kidney...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266664/ https://www.ncbi.nlm.nih.gov/pubmed/25506931 http://dx.doi.org/10.1371/journal.pone.0115368 |
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author | Schirutschke, Holger Gladrow, Lars Norkus, Christian Parmentier, Simon Paul Hohenstein, Bernd Hugo, Christian P. M. |
author_facet | Schirutschke, Holger Gladrow, Lars Norkus, Christian Parmentier, Simon Paul Hohenstein, Bernd Hugo, Christian P. M. |
author_sort | Schirutschke, Holger |
collection | PubMed |
description | Survival biopsies are frequently applied in rat kidney disease models, but several drawbacks such as surgical kidney trauma, bleeding risk and variable loss of kidney tissue are still unsolved. Therefore, we developed an easy-to-use core biopsy instrument and evaluated whether two consecutive kidney biopsies within the same kidney can be carried out in a standardized manner. On day 0, 18 Lewis rats underwent a right nephrectomy and 9 of these rats a subsequent first biopsy of the left kidney (Bx group). 9 control rats had a sham biopsy of the left kidney (Ctrl group). On day 7, a second kidney biopsy/sham biopsy was performed. On day 42, all animals were sacrificed and their kidneys were removed for histology. Biopsy cylinders contained 57±28 glomeruli per transversal section, representing an adequate sample size. PAS staining showed that the biopsy depth was limited to the renal cortex whereas surgical tissue damage was limited to the area immediately adjacent to the taken biopsy cylinder. On day 42, the reduction of functional renal mass after two biopsies was only 5.2% and no differences of body weight, blood pressure, proteinuria, serum creatinine, glomerulosclerosis, interstitial fibrosis or number of ED-1 positive macrophages were found between both groups. In summary, our apparatus offers a safe method to perform repetitive kidney biopsies with minimal trauma and sufficient sample size and quality even in experimental disease models restricted to one single kidney. |
format | Online Article Text |
id | pubmed-4266664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42666642014-12-26 A New Apparatus for Standardized Rat Kidney Biopsy Schirutschke, Holger Gladrow, Lars Norkus, Christian Parmentier, Simon Paul Hohenstein, Bernd Hugo, Christian P. M. PLoS One Research Article Survival biopsies are frequently applied in rat kidney disease models, but several drawbacks such as surgical kidney trauma, bleeding risk and variable loss of kidney tissue are still unsolved. Therefore, we developed an easy-to-use core biopsy instrument and evaluated whether two consecutive kidney biopsies within the same kidney can be carried out in a standardized manner. On day 0, 18 Lewis rats underwent a right nephrectomy and 9 of these rats a subsequent first biopsy of the left kidney (Bx group). 9 control rats had a sham biopsy of the left kidney (Ctrl group). On day 7, a second kidney biopsy/sham biopsy was performed. On day 42, all animals were sacrificed and their kidneys were removed for histology. Biopsy cylinders contained 57±28 glomeruli per transversal section, representing an adequate sample size. PAS staining showed that the biopsy depth was limited to the renal cortex whereas surgical tissue damage was limited to the area immediately adjacent to the taken biopsy cylinder. On day 42, the reduction of functional renal mass after two biopsies was only 5.2% and no differences of body weight, blood pressure, proteinuria, serum creatinine, glomerulosclerosis, interstitial fibrosis or number of ED-1 positive macrophages were found between both groups. In summary, our apparatus offers a safe method to perform repetitive kidney biopsies with minimal trauma and sufficient sample size and quality even in experimental disease models restricted to one single kidney. Public Library of Science 2014-12-15 /pmc/articles/PMC4266664/ /pubmed/25506931 http://dx.doi.org/10.1371/journal.pone.0115368 Text en © 2014 Schirutschke 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Schirutschke, Holger Gladrow, Lars Norkus, Christian Parmentier, Simon Paul Hohenstein, Bernd Hugo, Christian P. M. A New Apparatus for Standardized Rat Kidney Biopsy |
title | A New Apparatus for Standardized Rat Kidney Biopsy |
title_full | A New Apparatus for Standardized Rat Kidney Biopsy |
title_fullStr | A New Apparatus for Standardized Rat Kidney Biopsy |
title_full_unstemmed | A New Apparatus for Standardized Rat Kidney Biopsy |
title_short | A New Apparatus for Standardized Rat Kidney Biopsy |
title_sort | new apparatus for standardized rat kidney biopsy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266664/ https://www.ncbi.nlm.nih.gov/pubmed/25506931 http://dx.doi.org/10.1371/journal.pone.0115368 |
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