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Effects of splanchnic vasoconstrictors on liver regeneration and survival after 90% rat hepatectomy

PURPOSE: Posthepatectomy liver failure is a serious complication and considered to be caused by increased portal pressure and flow. Splanchnic vasoactive agents and propranolol are known to decrease portal pressure. The aim of this study was to identify optimal candidates with potential for clinical...

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Autores principales: Kim, Dong-Sik, Ji, Woong Bae, Han, Jae Hyun, Choi, Yoon Young, Park, Hyun-Jin, Yu, Young-Dong, Kim, Ju Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Surgical Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842083/
https://www.ncbi.nlm.nih.gov/pubmed/29520345
http://dx.doi.org/10.4174/astr.2018.94.3.118
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author Kim, Dong-Sik
Ji, Woong Bae
Han, Jae Hyun
Choi, Yoon Young
Park, Hyun-Jin
Yu, Young-Dong
Kim, Ju Young
author_facet Kim, Dong-Sik
Ji, Woong Bae
Han, Jae Hyun
Choi, Yoon Young
Park, Hyun-Jin
Yu, Young-Dong
Kim, Ju Young
author_sort Kim, Dong-Sik
collection PubMed
description PURPOSE: Posthepatectomy liver failure is a serious complication and considered to be caused by increased portal pressure and flow. Splanchnic vasoactive agents and propranolol are known to decrease portal pressure. The aim of this study was to identify optimal candidates with potential for clinical use among somatostatin, terlipressin, and propranolol using rats with 90% hepatectomy. METHODS: Rats were divided into 5 groups: sham operation (n = 6), control (n = 20), propranolol (n = 20), somatostatin (n = 20), and terlipressin group (n = 20). Seven-day survival rates and portal pressure change were measured, and biochemical, histologic, and molecular analyses were performed. RESULTS: Portal pressure was significantly decreased in all 3 treatment groups compared to control. All treatment groups showed a tendency of decreased liver injury markers, and somatostatin showed the most prominent effect at 24 hours postoperatively. Histologic liver injury at 24 hours was significantly decreased in propranolol and terlipressin groups (P = 0.016, respectively) and somatostatin group showed borderline significance (P = 0.056). Hepatocyte proliferation was significantly increased after 24 hours in all treatment groups. Median survival was significantly increased in terlipressin group compared to control group (P < 0.01). CONCLUSION: Terlipressin is considered as the best candidate, while somatostatin has good potential for clinical use, considering their effects on portal pressure and subsequent decrease in liver injury and increase in liver regeneration.
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spelling pubmed-58420832018-03-08 Effects of splanchnic vasoconstrictors on liver regeneration and survival after 90% rat hepatectomy Kim, Dong-Sik Ji, Woong Bae Han, Jae Hyun Choi, Yoon Young Park, Hyun-Jin Yu, Young-Dong Kim, Ju Young Ann Surg Treat Res Original Article PURPOSE: Posthepatectomy liver failure is a serious complication and considered to be caused by increased portal pressure and flow. Splanchnic vasoactive agents and propranolol are known to decrease portal pressure. The aim of this study was to identify optimal candidates with potential for clinical use among somatostatin, terlipressin, and propranolol using rats with 90% hepatectomy. METHODS: Rats were divided into 5 groups: sham operation (n = 6), control (n = 20), propranolol (n = 20), somatostatin (n = 20), and terlipressin group (n = 20). Seven-day survival rates and portal pressure change were measured, and biochemical, histologic, and molecular analyses were performed. RESULTS: Portal pressure was significantly decreased in all 3 treatment groups compared to control. All treatment groups showed a tendency of decreased liver injury markers, and somatostatin showed the most prominent effect at 24 hours postoperatively. Histologic liver injury at 24 hours was significantly decreased in propranolol and terlipressin groups (P = 0.016, respectively) and somatostatin group showed borderline significance (P = 0.056). Hepatocyte proliferation was significantly increased after 24 hours in all treatment groups. Median survival was significantly increased in terlipressin group compared to control group (P < 0.01). CONCLUSION: Terlipressin is considered as the best candidate, while somatostatin has good potential for clinical use, considering their effects on portal pressure and subsequent decrease in liver injury and increase in liver regeneration. The Korean Surgical Society 2018-03 2018-02-28 /pmc/articles/PMC5842083/ /pubmed/29520345 http://dx.doi.org/10.4174/astr.2018.94.3.118 Text en Copyright © 2018, the Korean Surgical Society http://creativecommons.org/licenses/by-nc/4.0/ Annals of Surgical Treatment and Research is an Open Access Journal. All articles are distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Dong-Sik
Ji, Woong Bae
Han, Jae Hyun
Choi, Yoon Young
Park, Hyun-Jin
Yu, Young-Dong
Kim, Ju Young
Effects of splanchnic vasoconstrictors on liver regeneration and survival after 90% rat hepatectomy
title Effects of splanchnic vasoconstrictors on liver regeneration and survival after 90% rat hepatectomy
title_full Effects of splanchnic vasoconstrictors on liver regeneration and survival after 90% rat hepatectomy
title_fullStr Effects of splanchnic vasoconstrictors on liver regeneration and survival after 90% rat hepatectomy
title_full_unstemmed Effects of splanchnic vasoconstrictors on liver regeneration and survival after 90% rat hepatectomy
title_short Effects of splanchnic vasoconstrictors on liver regeneration and survival after 90% rat hepatectomy
title_sort effects of splanchnic vasoconstrictors on liver regeneration and survival after 90% rat hepatectomy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842083/
https://www.ncbi.nlm.nih.gov/pubmed/29520345
http://dx.doi.org/10.4174/astr.2018.94.3.118
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