A Preclinical Porcine Model of Portal Vein Thrombosis in Liver Cirrhosis

Background. This study aimed at presenting a novel method of developing a porcine model of portal vein thrombosis (PVT) in cirrhosis by intravenous administration of thrombin and insertion of a fibered coil. We further investigated changes of biochemical parameters, coagulation, and proinflammatory...

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Main Authors: Rui Zhang, Shenxin Lu, Ying-yi Jiang, Jing-qin Ma, Wen Zhang, Jun-ying Gu, Jian Wang, Shi-yao Chen
Format: Article
Language:English
Published: Hindawi Limited 2020-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2020/3086906
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spelling doaj-511d712a6d4941eba2d23d9fd1e01c662020-11-25T02:54:34ZengHindawi LimitedBioMed Research International2314-61332314-61412020-01-01202010.1155/2020/30869063086906A Preclinical Porcine Model of Portal Vein Thrombosis in Liver CirrhosisRui Zhang0Shenxin Lu1Ying-yi Jiang2Jing-qin Ma3Wen Zhang4Jun-ying Gu5Jian Wang6Shi-yao Chen7Department of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan University, Shanghai, ChinaLiver Cancer Institute, Zhongshan Hospital, Fudan University and Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Shanghai, ChinaDepartment of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan University, Shanghai, ChinaDepartment of Interventional Radiology, Zhongshan Hospital, Fudan University, Shanghai, ChinaDepartment of Interventional Radiology, Zhongshan Hospital, Fudan University, Shanghai, ChinaDepartment of Radiology, Zhongshan Hospital, Shanghai, ChinaDepartment of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan University, Shanghai, ChinaDepartment of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan University, Shanghai, ChinaBackground. This study aimed at presenting a novel method of developing a porcine model of portal vein thrombosis (PVT) in cirrhosis by intravenous administration of thrombin and insertion of a fibered coil. We further investigated changes of biochemical parameters, coagulation, and proinflammatory cytokine expression in the cirrhosis-PVT group. Methods. Twelve male pigs were randomized into the control group (n=3) and cirrhosis group (n=9). In cirrhotic pigs, three were randomly selected to establish PVT by ultrasound-guided percutaneous puncture of the main portal vein (MPV) followed by intravenous thrombin administration and fibered coil insertion. Thrombosis in the MPV was detected by abdominal enhanced computer tomography (CT). The changes of hepatic function, coagulation system, and inflammation cytokines were compared among normal, cirrhosis, and cirrhosis with PVT groups. Results. As manifested by the presence of a filling defect in MPV on portal venous-phase CT angiography, fibrin thrombi were formed in the MPV in cirrhotic pigs within one week and persisted for four weeks. Five weeks after surgery, abnormal liver functions occurred in association with PVT formation in cirrhosis. Both coagulation and thromboelastography parameters showed that cirrhosis-PVT pigs exhibited a procoagulant state through hyperfunction of platelets and clotting factors. Interleukin 6 (IL-6) as a potential inflammatory marker stimulated PVT-mediated inflammation activation in cirrhosis. Conclusions. Our study provides in vivo evidence that intravenous injection of a coil and thrombin into MPV under interventional guided devices enables a feasible method in thrombus creation. Further exploration and validation of large-sample cases are required to characterize utilities of this model.http://dx.doi.org/10.1155/2020/3086906
collection DOAJ
language English
format Article
sources DOAJ
author Rui Zhang
Shenxin Lu
Ying-yi Jiang
Jing-qin Ma
Wen Zhang
Jun-ying Gu
Jian Wang
Shi-yao Chen
spellingShingle Rui Zhang
Shenxin Lu
Ying-yi Jiang
Jing-qin Ma
Wen Zhang
Jun-ying Gu
Jian Wang
Shi-yao Chen
A Preclinical Porcine Model of Portal Vein Thrombosis in Liver Cirrhosis
BioMed Research International
author_facet Rui Zhang
Shenxin Lu
Ying-yi Jiang
Jing-qin Ma
Wen Zhang
Jun-ying Gu
Jian Wang
Shi-yao Chen
author_sort Rui Zhang
title A Preclinical Porcine Model of Portal Vein Thrombosis in Liver Cirrhosis
title_short A Preclinical Porcine Model of Portal Vein Thrombosis in Liver Cirrhosis
title_full A Preclinical Porcine Model of Portal Vein Thrombosis in Liver Cirrhosis
title_fullStr A Preclinical Porcine Model of Portal Vein Thrombosis in Liver Cirrhosis
title_full_unstemmed A Preclinical Porcine Model of Portal Vein Thrombosis in Liver Cirrhosis
title_sort preclinical porcine model of portal vein thrombosis in liver cirrhosis
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2020-01-01
description Background. This study aimed at presenting a novel method of developing a porcine model of portal vein thrombosis (PVT) in cirrhosis by intravenous administration of thrombin and insertion of a fibered coil. We further investigated changes of biochemical parameters, coagulation, and proinflammatory cytokine expression in the cirrhosis-PVT group. Methods. Twelve male pigs were randomized into the control group (n=3) and cirrhosis group (n=9). In cirrhotic pigs, three were randomly selected to establish PVT by ultrasound-guided percutaneous puncture of the main portal vein (MPV) followed by intravenous thrombin administration and fibered coil insertion. Thrombosis in the MPV was detected by abdominal enhanced computer tomography (CT). The changes of hepatic function, coagulation system, and inflammation cytokines were compared among normal, cirrhosis, and cirrhosis with PVT groups. Results. As manifested by the presence of a filling defect in MPV on portal venous-phase CT angiography, fibrin thrombi were formed in the MPV in cirrhotic pigs within one week and persisted for four weeks. Five weeks after surgery, abnormal liver functions occurred in association with PVT formation in cirrhosis. Both coagulation and thromboelastography parameters showed that cirrhosis-PVT pigs exhibited a procoagulant state through hyperfunction of platelets and clotting factors. Interleukin 6 (IL-6) as a potential inflammatory marker stimulated PVT-mediated inflammation activation in cirrhosis. Conclusions. Our study provides in vivo evidence that intravenous injection of a coil and thrombin into MPV under interventional guided devices enables a feasible method in thrombus creation. Further exploration and validation of large-sample cases are required to characterize utilities of this model.
url http://dx.doi.org/10.1155/2020/3086906
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