Cited by 47Liver physiology and pathologyOrgan Transplantation Techniques and OutcomesTissue Engineering and Regenerative Medicine

Elevated Liver Regeneration in Response to Pharmacological Reduction of Elevated Portal Venous Pressure by Terlipressin After Partial Hepatectomy

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Fahrner, René, Patsenker, Eleonora, Gottardi, Andrea de, Stickel, Felix, Montani, Matteo, Stroka, Deborah, Candinas, Daniel, Beldi, Guido·2014·Transplantation

Abstract

Background Liver regeneration is of crucial importance for patients undergoing living liver transplantations or extended liver resections and can be associated with elevated portal venous pressure, impaired hepatic regeneration, and postoperative morbidity. The aim of this study was to assess whether reduction of portal venous pressure by terlipressin improves postoperative liver regeneration in normal and steatotic livers after partial hepatectomy in a rodent model. Methods Portal venous pressure was assessed after minor (30%), standard (60%), or extended (80%) partial hepatectomy (PH) in mice with and without liver steatosis. Liver regeneration was assessed by BrdU incorporation and Ki-67 immunostaining. Results Portal venous pressure was significantly elevated post-PH in mice with normal and steatotic livers compared to sham-operated mice. Reduction of elevated portal pressure after 80% PH by terlipressin was associated with an increase of hepatocellular proliferation. In steatotic livers, animals treated with terlipressin had an increase in liver regeneration after 30% PH and increased survival after 60% PH. Mechanistically, terlipressin alleviated IL-6 mRNA expression following PH and down-regulated p21 and GADD45 mRNA suggesting a reduction of cell cycle inhibition and cellular stress. Conclusions Reduction of elevated portal pressure post-PH by the use of terlipressin improves liver regeneration after PH in lean and steatotic mouse livers.

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Crossref · 10.1097/tp.0000000000000045

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  • Hyperplasia-driven regeneration occurs only when a significant portion of liver mass is lost, and is not dependent on the size of the dissection plane.

    “Based on this, it is generally accepted that hyperplasia-driven regeneration occurs only when a significant portion of liver mass is lost, and is not dependent on the size of the dissection plane.”
  • The direction of regenerative processes following liver tissue damage is determined by changes in portal pressure and flow.

    “Our long-term studies, supported by literature data, indicate that the direction of regenerative processes following liver tissue damage is determined by changes in portal pressure and flow—which act as mechanical and physiological determinants[4,9,11,12].”
  • Pharmacological reduction of postoperative portal pressure, such as with Terlipressin, prevents hepatocyte necrosis and promotes proliferative activity, ultimately improving survival rates in operated animals.

    “Additionally, pharmacological reduction of postoperative portal pressure, such as with Terlipressin, has been shown to prevent hepatocyte necrosis and promote proliferative activity, ultimately improving survival rates in operated animals.”

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Authors
Fahrner, R., Patsenker, E., Gottardi, A. D., Stickel, F., Montani, M., Stroka, D., Candinas, D., & Beldi, G.
Affiliations
University Hospital of Bern (CH)
Corresponding author
Beldi, Guido
Venue
Transplantation
Published
2014-05-15
Volume
97
Issue
9
Pages
892-900
ISSN
0041-1337 (ISSN-L)
OpenAlex
W2006895517
Cited by
47
References
0
Citations by year
2025: 2 · 2024: 3 · 2023: 2 · 2022: 2 · 2021: 4 · 2020: 6 · 2019: 5 · 2018: 5 · 2017: 6 · 2016: 5 · 2015: 5 · 2014: 2
FWCI
3.36
Type
journal article
Language
en
Open access
Licence
other-oa
Locations
  • Transplantation (publishedVersion)
  • PubMed (publishedVersion)
  • Bern Open Repository and Information System (University of Bern) (submittedVersion, other-oa)
  • Open Access CRIS of the University of Bern
Funders
  • National Science Foundation
  • University of Bern
  • Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (146986, 130816)
Topics
  • Health Sciences › Medicine › Hepatology › Liver physiology and pathology
  • Health Sciences › Medicine › Surgery › Organ Transplantation Techniques and Outcomes
  • Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
Keywords
terlipressin, liver regeneration, partial hepatectomy, portal pressure, hepatic steatosis, hepatocyte proliferation, interleukin-6, p21, GADD45, cell cycle inhibition, postoperative survival, extended liver resection
MeSH terms
Terlipressin, GADD45 Proteins, Animals, Cell Cycle, Fatty Liver, Hepatectomy, Liver, Liver Regeneration, Lypressin, Mice, Inbred C57BL, Nuclear Proteins, Portal Vein, Regeneration, Vasoconstrictor Agents, Interleukin-6, Portal Pressure, Cell Cycle Proteins, Ki-67 Antigen, Cyclin-Dependent Kinase Inhibitor p21, Mice

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