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Optimized method to harvest both kidneys from one donor rat for transplantation
BACKGROUND: Rat renal transplantation is an essential experimental model for studies of transplantation immunobiology. Harvesting both kidneys from one donor rat for transplantation is widely used to reduce the number of experimental animals. Using the conventional method, both kidneys of the donor...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114511/ https://www.ncbi.nlm.nih.gov/pubmed/30157811 http://dx.doi.org/10.1186/s12893-018-0400-9 |
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author | Ju, Chun-hua Xue, Ling-na Cheng, Hong-jia Jin, Zhong-da |
author_facet | Ju, Chun-hua Xue, Ling-na Cheng, Hong-jia Jin, Zhong-da |
author_sort | Ju, Chun-hua |
collection | PubMed |
description | BACKGROUND: Rat renal transplantation is an essential experimental model for studies of transplantation immunobiology. Harvesting both kidneys from one donor rat for transplantation is widely used to reduce the number of experimental animals. Using the conventional method, both kidneys of the donor rat are harvested simultaneously, which leads to the prolonged warm ischemic times during transplantation of the second donor kidney. Prolonged warm ischemia time is the main risk factor for delayed graft function. METHODS: Two different approaches are compared. Method 1, conventional method: both kidneys of the donor rat are harvested simultaneously and then transplanted into two recipients. During transplantation, the first and second donor kidneys were regarded as Group 1 and 2, respectively. Method 2, step-by-step method: after left nephrectomy, the donor rat survives, and we perform left renal transplantation (Group 3). Then, the right kidney of the surviving donor rat is incised and transplanted into the left side of the second recipient (Group 4). RESULTS: The success rates were 86.7, 93.3, 93.3 and 86.7% in groups 1, 2, 3 and 4, respectively. The warm ischemia times increased significantly in group 2 compared with the other 3 groups (p < 0.05) but differed non-significantly between groups 3 and 4 (p > 0.05). Serum creatinine levels, blood urea nitrogen and 24-h urine protein level obviously increased after kidney transplantation in group 2 compared with other groups (p < 0.05). CONCLUSIONS: We developed an optimized method for reducing warm ischemia time, thereby minimizing delayed graft function. |
format | Online Article Text |
id | pubmed-6114511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61145112018-09-04 Optimized method to harvest both kidneys from one donor rat for transplantation Ju, Chun-hua Xue, Ling-na Cheng, Hong-jia Jin, Zhong-da BMC Surg Research Article BACKGROUND: Rat renal transplantation is an essential experimental model for studies of transplantation immunobiology. Harvesting both kidneys from one donor rat for transplantation is widely used to reduce the number of experimental animals. Using the conventional method, both kidneys of the donor rat are harvested simultaneously, which leads to the prolonged warm ischemic times during transplantation of the second donor kidney. Prolonged warm ischemia time is the main risk factor for delayed graft function. METHODS: Two different approaches are compared. Method 1, conventional method: both kidneys of the donor rat are harvested simultaneously and then transplanted into two recipients. During transplantation, the first and second donor kidneys were regarded as Group 1 and 2, respectively. Method 2, step-by-step method: after left nephrectomy, the donor rat survives, and we perform left renal transplantation (Group 3). Then, the right kidney of the surviving donor rat is incised and transplanted into the left side of the second recipient (Group 4). RESULTS: The success rates were 86.7, 93.3, 93.3 and 86.7% in groups 1, 2, 3 and 4, respectively. The warm ischemia times increased significantly in group 2 compared with the other 3 groups (p < 0.05) but differed non-significantly between groups 3 and 4 (p > 0.05). Serum creatinine levels, blood urea nitrogen and 24-h urine protein level obviously increased after kidney transplantation in group 2 compared with other groups (p < 0.05). CONCLUSIONS: We developed an optimized method for reducing warm ischemia time, thereby minimizing delayed graft function. BioMed Central 2018-08-29 /pmc/articles/PMC6114511/ /pubmed/30157811 http://dx.doi.org/10.1186/s12893-018-0400-9 Text en © The Author(s). 2018 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 Ju, Chun-hua Xue, Ling-na Cheng, Hong-jia Jin, Zhong-da Optimized method to harvest both kidneys from one donor rat for transplantation |
title | Optimized method to harvest both kidneys from one donor rat for transplantation |
title_full | Optimized method to harvest both kidneys from one donor rat for transplantation |
title_fullStr | Optimized method to harvest both kidneys from one donor rat for transplantation |
title_full_unstemmed | Optimized method to harvest both kidneys from one donor rat for transplantation |
title_short | Optimized method to harvest both kidneys from one donor rat for transplantation |
title_sort | optimized method to harvest both kidneys from one donor rat for transplantation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114511/ https://www.ncbi.nlm.nih.gov/pubmed/30157811 http://dx.doi.org/10.1186/s12893-018-0400-9 |
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