Laparoscopy-Assisted Creation of a Liver Failure Model in Pigs
We created a hepatic failure pig model that was suitable for the assessment of cell therapies, such as hepatocyte transplantation and bioartificial livers, using a laparoscopic surgical technique. In our model, all of three hepatic arteries were resected, 5, 7.5, or 10 ml of carbon tetrachloride (CC...
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doaj-a4f294cadc0942d194a684b3b14ea0172020-11-25T03:20:54ZengSAGE PublishingCell Transplantation0963-68971555-38922008-01-011710.3727/000000008783906973Laparoscopy-Assisted Creation of a Liver Failure Model in PigsTakeshi Yuasa0Tsuyoshi Yamamoto1Jorge D. Rivas-Carrillo2Yong Chen3Nalú Navarro-Alvarez4Alejandro Soto-Guiterrez5Hirofumi Noguchi6Shinichi Matsumoto7Noriaki Tanaka8Naoya Kobayashi M.D., Ph.D.9Department of Gastroenterological Surgery, Transplant, and Surgical Oncology, Okayama University Graduate School of Medicine and Dentistry, Okayama, JapanDepartment of Gastroenterological Surgery, Transplant, and Surgical Oncology, Okayama University Graduate School of Medicine and Dentistry, Okayama, JapanDepartment of Gastroenterological Surgery, Transplant, and Surgical Oncology, Okayama University Graduate School of Medicine and Dentistry, Okayama, JapanDepartment of Gastroenterological Surgery, Transplant, and Surgical Oncology, Okayama University Graduate School of Medicine and Dentistry, Okayama, JapanDepartment of Gastroenterological Surgery, Transplant, and Surgical Oncology, Okayama University Graduate School of Medicine and Dentistry, Okayama, JapanDepartment of Gastroenterological Surgery, Transplant, and Surgical Oncology, Okayama University Graduate School of Medicine and Dentistry, Okayama, JapanBaylor Institution for Immunology Research, Islet Cell Transplantation Laboratory, Baylor Research Institute, Dallas, TX 75204, USABaylor Institution for Immunology Research, Islet Cell Transplantation Laboratory, Baylor Research Institute, Dallas, TX 75204, USADepartment of Gastroenterological Surgery, Transplant, and Surgical Oncology, Okayama University Graduate School of Medicine and Dentistry, Okayama, JapanDepartment of Gastroenterological Surgery, Transplant, and Surgical Oncology, Okayama University Graduate School of Medicine and Dentistry, Okayama, JapanWe created a hepatic failure pig model that was suitable for the assessment of cell therapies, such as hepatocyte transplantation and bioartificial livers, using a laparoscopic surgical technique. In our model, all of three hepatic arteries were resected, 5, 7.5, or 10 ml of carbon tetrachloride (CCL 4 ) was injected into the liver through the portal vein, and subsequently the portal vein was mechanically occluded for 30 min. After the portal occlusion was released, a liver biopsy was performed, and then the surgery was completed. Blood samples were regularly taken during the surgery in order to perform biochemical examinations. All of five pigs in which 5 ml of CCL 4 was infused recovered spontaneously and survived; in contrast, all of five pigs that received 10 ml CCL 4 died within 1.5 h after surgery. The pigs in which 7.5 ml CCL 4 was administered developed liver failure and survived for 6.4 h on average (±1.4 SD). Induction of liver failure with the use of 7.5 ml CCL 4 and 30-min hepatic ischemia fulfilled five of the six criteria that were proposed by Terblanche and Hickman: reversibility, reproducibility, death from liver failure, a therapeutic window, and a large-animal model. We believe that our model is the first report on creation of a reliable model for liver failure in pigs to assess the efficacy of liver-targeted cell therapies.https://doi.org/10.3727/000000008783906973 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Takeshi Yuasa Tsuyoshi Yamamoto Jorge D. Rivas-Carrillo Yong Chen Nalú Navarro-Alvarez Alejandro Soto-Guiterrez Hirofumi Noguchi Shinichi Matsumoto Noriaki Tanaka Naoya Kobayashi M.D., Ph.D. |
spellingShingle |
Takeshi Yuasa Tsuyoshi Yamamoto Jorge D. Rivas-Carrillo Yong Chen Nalú Navarro-Alvarez Alejandro Soto-Guiterrez Hirofumi Noguchi Shinichi Matsumoto Noriaki Tanaka Naoya Kobayashi M.D., Ph.D. Laparoscopy-Assisted Creation of a Liver Failure Model in Pigs Cell Transplantation |
author_facet |
Takeshi Yuasa Tsuyoshi Yamamoto Jorge D. Rivas-Carrillo Yong Chen Nalú Navarro-Alvarez Alejandro Soto-Guiterrez Hirofumi Noguchi Shinichi Matsumoto Noriaki Tanaka Naoya Kobayashi M.D., Ph.D. |
author_sort |
Takeshi Yuasa |
title |
Laparoscopy-Assisted Creation of a Liver Failure Model in Pigs |
title_short |
Laparoscopy-Assisted Creation of a Liver Failure Model in Pigs |
title_full |
Laparoscopy-Assisted Creation of a Liver Failure Model in Pigs |
title_fullStr |
Laparoscopy-Assisted Creation of a Liver Failure Model in Pigs |
title_full_unstemmed |
Laparoscopy-Assisted Creation of a Liver Failure Model in Pigs |
title_sort |
laparoscopy-assisted creation of a liver failure model in pigs |
publisher |
SAGE Publishing |
series |
Cell Transplantation |
issn |
0963-6897 1555-3892 |
publishDate |
2008-01-01 |
description |
We created a hepatic failure pig model that was suitable for the assessment of cell therapies, such as hepatocyte transplantation and bioartificial livers, using a laparoscopic surgical technique. In our model, all of three hepatic arteries were resected, 5, 7.5, or 10 ml of carbon tetrachloride (CCL 4 ) was injected into the liver through the portal vein, and subsequently the portal vein was mechanically occluded for 30 min. After the portal occlusion was released, a liver biopsy was performed, and then the surgery was completed. Blood samples were regularly taken during the surgery in order to perform biochemical examinations. All of five pigs in which 5 ml of CCL 4 was infused recovered spontaneously and survived; in contrast, all of five pigs that received 10 ml CCL 4 died within 1.5 h after surgery. The pigs in which 7.5 ml CCL 4 was administered developed liver failure and survived for 6.4 h on average (±1.4 SD). Induction of liver failure with the use of 7.5 ml CCL 4 and 30-min hepatic ischemia fulfilled five of the six criteria that were proposed by Terblanche and Hickman: reversibility, reproducibility, death from liver failure, a therapeutic window, and a large-animal model. We believe that our model is the first report on creation of a reliable model for liver failure in pigs to assess the efficacy of liver-targeted cell therapies. |
url |
https://doi.org/10.3727/000000008783906973 |
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