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Reversible biliary occlusion in a small animal model: first description of a new technique

BACKGROUND: Experimental models with reversible biliary occlusion resulted in a high mortality of the animals, up to 20–60% according to the literature. Our aim was to assess a safe and valid technique for reversible biliary occlusion with a low mortality. METHODS: We randomized 30 rats into two gro...

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Autores principales: Richter, Beate, Khodaverdi, Semik, Bechstein, Wolf Otto, Gutt, Carsten N., Krähenbühl, Lukas, Schmandra, Thomas C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604588/
https://www.ncbi.nlm.nih.gov/pubmed/31579790
http://dx.doi.org/10.1515/iss-2018-0021
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author Richter, Beate
Khodaverdi, Semik
Bechstein, Wolf Otto
Gutt, Carsten N.
Krähenbühl, Lukas
Schmandra, Thomas C.
author_facet Richter, Beate
Khodaverdi, Semik
Bechstein, Wolf Otto
Gutt, Carsten N.
Krähenbühl, Lukas
Schmandra, Thomas C.
author_sort Richter, Beate
collection PubMed
description BACKGROUND: Experimental models with reversible biliary occlusion resulted in a high mortality of the animals, up to 20–60% according to the literature. Our aim was to assess a safe and valid technique for reversible biliary occlusion with a low mortality. METHODS: We randomized 30 rats into two groups: with bile duct occlusion (BDO, n=18) and with sham manipulation of the extrahepatic bile duct (control, n=12). We used a removable vascular clip for temporary occlusion of the extrahepatic bile duct. The clip was removed on postoperative day (POD) 2. On POD 2, 3, and 5, we measured the hepatocellular injury and metabolic function markers in serum. Activation of mononuclear cells (HIS36) and expression of regeneration markers [cytokeratin 19, hepatic growth factor (HGF)-α, and HGF-β] were determined by immunohistochemistry. RESULTS: The survival rate was 96.67% (1/30); one animal died. The mortality in the BDO group was 6% (1/18) and that in the control group was 0% (0/12). BDO resulted in a sharp increase of hepatocellular injury and cholestatic parameters on POD 2 with a rapid decline till POD 3. Significantly strongest activation of Kupffer cells and expression of proliferation markers were found until POD 5 after BDO. CONCLUSION: The clip technique is a safe, cheap, and valid method for reversible biliary occlusion with an extremely low mortality.
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spelling pubmed-66045882019-10-02 Reversible biliary occlusion in a small animal model: first description of a new technique Richter, Beate Khodaverdi, Semik Bechstein, Wolf Otto Gutt, Carsten N. Krähenbühl, Lukas Schmandra, Thomas C. Innov Surg Sci Original Articles BACKGROUND: Experimental models with reversible biliary occlusion resulted in a high mortality of the animals, up to 20–60% according to the literature. Our aim was to assess a safe and valid technique for reversible biliary occlusion with a low mortality. METHODS: We randomized 30 rats into two groups: with bile duct occlusion (BDO, n=18) and with sham manipulation of the extrahepatic bile duct (control, n=12). We used a removable vascular clip for temporary occlusion of the extrahepatic bile duct. The clip was removed on postoperative day (POD) 2. On POD 2, 3, and 5, we measured the hepatocellular injury and metabolic function markers in serum. Activation of mononuclear cells (HIS36) and expression of regeneration markers [cytokeratin 19, hepatic growth factor (HGF)-α, and HGF-β] were determined by immunohistochemistry. RESULTS: The survival rate was 96.67% (1/30); one animal died. The mortality in the BDO group was 6% (1/18) and that in the control group was 0% (0/12). BDO resulted in a sharp increase of hepatocellular injury and cholestatic parameters on POD 2 with a rapid decline till POD 3. Significantly strongest activation of Kupffer cells and expression of proliferation markers were found until POD 5 after BDO. CONCLUSION: The clip technique is a safe, cheap, and valid method for reversible biliary occlusion with an extremely low mortality. De Gruyter 2018-08-15 /pmc/articles/PMC6604588/ /pubmed/31579790 http://dx.doi.org/10.1515/iss-2018-0021 Text en ©2018 Walter de Gruyter GmbH, Berlin/Boston http://creativecommons.org/licenses/by-nc-nd/4.0 This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.
spellingShingle Original Articles
Richter, Beate
Khodaverdi, Semik
Bechstein, Wolf Otto
Gutt, Carsten N.
Krähenbühl, Lukas
Schmandra, Thomas C.
Reversible biliary occlusion in a small animal model: first description of a new technique
title Reversible biliary occlusion in a small animal model: first description of a new technique
title_full Reversible biliary occlusion in a small animal model: first description of a new technique
title_fullStr Reversible biliary occlusion in a small animal model: first description of a new technique
title_full_unstemmed Reversible biliary occlusion in a small animal model: first description of a new technique
title_short Reversible biliary occlusion in a small animal model: first description of a new technique
title_sort reversible biliary occlusion in a small animal model: first description of a new technique
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604588/
https://www.ncbi.nlm.nih.gov/pubmed/31579790
http://dx.doi.org/10.1515/iss-2018-0021
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