Ischemic Postconditioning (IPostC) Protects Fibrotic and Cirrhotic Rat Livers after Warm Ischemia

Background. Decreased organ function following liver resection is a major clinical issue. The practical method of ischemic postconditioning (IPostC) has been studied in heart diseases, but no data exist regarding fibrotic livers. Aims. We aimed to determine whether IPostC could protect healthy, fibr...

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Main Authors: Julia Schewe, Marie-Christine Makeschin, Ingrid Liss, Doris Mayr, Jiang Zhang, Andrej Khandoga, Simon Rothenfußer, Max Schnurr, Alexander L. Gerbes, Christian J. Steib
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Canadian Journal of Gastroenterology and Hepatology
Online Access:http://dx.doi.org/10.1155/2019/5683479
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spelling doaj-3754649f455e477b9c4f098cf55a0f382020-11-24T21:29:14ZengHindawi LimitedCanadian Journal of Gastroenterology and Hepatology2291-27892291-27972019-01-01201910.1155/2019/56834795683479Ischemic Postconditioning (IPostC) Protects Fibrotic and Cirrhotic Rat Livers after Warm IschemiaJulia Schewe0Marie-Christine Makeschin1Ingrid Liss2Doris Mayr3Jiang Zhang4Andrej Khandoga5Simon Rothenfußer6Max Schnurr7Alexander L. Gerbes8Christian J. Steib9Berlin Institute of Health Charité – Universitätsmedizin Berlin, GermanyDepartment of Pathology, University of Munich, Campus Grosshadern, Munich, GermanyDepartment of Medicine II, University Hospital, Liver Centre Munich, LMU Munich, GermanyDepartment of Pathology, University of Munich, Campus Grosshadern, Munich, GermanyDepartment of Medicine II, University Hospital, Liver Centre Munich, LMU Munich, GermanyDepartment of Surgery, University of Munich, Campus Grosshadern, Munich, GermanyDivision of Clinical Pharmacology, University of Munich, Campus Innenstadt, Munich, GermanyDivision of Clinical Pharmacology, University of Munich, Campus Innenstadt, Munich, GermanyDepartment of Medicine II, University Hospital, Liver Centre Munich, LMU Munich, GermanyDepartment of Medicine II, University Hospital, Liver Centre Munich, LMU Munich, GermanyBackground. Decreased organ function following liver resection is a major clinical issue. The practical method of ischemic postconditioning (IPostC) has been studied in heart diseases, but no data exist regarding fibrotic livers. Aims. We aimed to determine whether IPostC could protect healthy, fibrotic, and cirrhotic livers from ischemia reperfusion injury (IRI). Methods. Fibrosis was induced in male SD rats using bile duct ligation (BDL, 4 weeks), and cirrhosis was induced using thioacetamide (TAA, 18 weeks). Fibrosis and cirrhosis were histologically confirmed using HE and EvG staining. For healthy, fibrotic, and cirrhotic livers, isolated liver perfusion with 90 min of warm ischemia was performed in three groups (each with n=8): control, IPostC 8x20 sec, and IPostC 4x60 sec. additionally, healthy livers were investigated during a follow-up study. Lactate dehydrogenase (LDH) and thromboxane B2 (TXB2) in the perfusate, as well as bile flow (healthy/TAA) and portal perfusion pressure, were measured. Results. LDH and TXB2 were reduced, and bile flow was increased by IPostC, mainly in total and in the late phase of reperfusion. The follow-up study showed that the perfusate derived from a postconditioned group had much less damaging potential than perfusate derived from the nonpostconditioned group. Conclusion. IPostC following warm ischemia protects healthy, fibrotic, and cirrhotic livers against IRI. Reduced efflux of TXB2 is one possible mechanism for this effect of IPostC and increases sinusoidal microcirculation. These findings may help to improve organ function and recovery of patients after liver resection.http://dx.doi.org/10.1155/2019/5683479
collection DOAJ
language English
format Article
sources DOAJ
author Julia Schewe
Marie-Christine Makeschin
Ingrid Liss
Doris Mayr
Jiang Zhang
Andrej Khandoga
Simon Rothenfußer
Max Schnurr
Alexander L. Gerbes
Christian J. Steib
spellingShingle Julia Schewe
Marie-Christine Makeschin
Ingrid Liss
Doris Mayr
Jiang Zhang
Andrej Khandoga
Simon Rothenfußer
Max Schnurr
Alexander L. Gerbes
Christian J. Steib
Ischemic Postconditioning (IPostC) Protects Fibrotic and Cirrhotic Rat Livers after Warm Ischemia
Canadian Journal of Gastroenterology and Hepatology
author_facet Julia Schewe
Marie-Christine Makeschin
Ingrid Liss
Doris Mayr
Jiang Zhang
Andrej Khandoga
Simon Rothenfußer
Max Schnurr
Alexander L. Gerbes
Christian J. Steib
author_sort Julia Schewe
title Ischemic Postconditioning (IPostC) Protects Fibrotic and Cirrhotic Rat Livers after Warm Ischemia
title_short Ischemic Postconditioning (IPostC) Protects Fibrotic and Cirrhotic Rat Livers after Warm Ischemia
title_full Ischemic Postconditioning (IPostC) Protects Fibrotic and Cirrhotic Rat Livers after Warm Ischemia
title_fullStr Ischemic Postconditioning (IPostC) Protects Fibrotic and Cirrhotic Rat Livers after Warm Ischemia
title_full_unstemmed Ischemic Postconditioning (IPostC) Protects Fibrotic and Cirrhotic Rat Livers after Warm Ischemia
title_sort ischemic postconditioning (ipostc) protects fibrotic and cirrhotic rat livers after warm ischemia
publisher Hindawi Limited
series Canadian Journal of Gastroenterology and Hepatology
issn 2291-2789
2291-2797
publishDate 2019-01-01
description Background. Decreased organ function following liver resection is a major clinical issue. The practical method of ischemic postconditioning (IPostC) has been studied in heart diseases, but no data exist regarding fibrotic livers. Aims. We aimed to determine whether IPostC could protect healthy, fibrotic, and cirrhotic livers from ischemia reperfusion injury (IRI). Methods. Fibrosis was induced in male SD rats using bile duct ligation (BDL, 4 weeks), and cirrhosis was induced using thioacetamide (TAA, 18 weeks). Fibrosis and cirrhosis were histologically confirmed using HE and EvG staining. For healthy, fibrotic, and cirrhotic livers, isolated liver perfusion with 90 min of warm ischemia was performed in three groups (each with n=8): control, IPostC 8x20 sec, and IPostC 4x60 sec. additionally, healthy livers were investigated during a follow-up study. Lactate dehydrogenase (LDH) and thromboxane B2 (TXB2) in the perfusate, as well as bile flow (healthy/TAA) and portal perfusion pressure, were measured. Results. LDH and TXB2 were reduced, and bile flow was increased by IPostC, mainly in total and in the late phase of reperfusion. The follow-up study showed that the perfusate derived from a postconditioned group had much less damaging potential than perfusate derived from the nonpostconditioned group. Conclusion. IPostC following warm ischemia protects healthy, fibrotic, and cirrhotic livers against IRI. Reduced efflux of TXB2 is one possible mechanism for this effect of IPostC and increases sinusoidal microcirculation. These findings may help to improve organ function and recovery of patients after liver resection.
url http://dx.doi.org/10.1155/2019/5683479
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