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Novel Rat Model of Repetitive Portal Venous Embolization Mimicking Human Non-Cirrhotic Idiopathic Portal Hypertension.
- Source :
-
PloS one [PLoS One] 2016 Sep 02; Vol. 11 (9), pp. e0162144. Date of Electronic Publication: 2016 Sep 02 (Print Publication: 2016). - Publication Year :
- 2016
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Abstract
- Background: Non-cirrhotic idiopathic portal hypertension (NCIPH) is characterized by splenomegaly, anemia and portal hypertension, while liver function is preserved. However, no animal models have been established yet. This study assessed a rat model of NCIPH and characterized the hemodynamics, and compared it to human NCIPH.<br />Methods: Portal pressure (PP) was measured invasively and coloured microspheres were injected in the ileocecal vein in rats. This procedure was performed weekly for 3 weeks (weekly embolization). Rats without and with single embolization served as controls. After four weeks (one week after last embolization), hemodynamics were investigated, hepatic fibrosis and accumulation of myofibroblasts were analysed. General characteristics, laboratory analyses and liver histology were collected in patients with NCIPH.<br />Results: Weekly embolization induced a hyperdynamic circulation, with increased PP. The mesenteric flow and hepatic hydroxyproline content was significantly higher in weekly embolized compared to single embolized rats (mesenteric flow +54.1%, hydroxyproline +41.7%). Mesenteric blood flow and shunt volumes increased, whereas splanchnic vascular resistance was decreased in the weekly embolization group. Fibrotic markers αSMA and Desmin were upregulated in weekly embolized rats.<br />Discussion: This study establishes a model using repetitive embolization via portal veins, comparable with human NCIPH and may serve to test new therapies.<br />Competing Interests: The authors have declared that no competing interests exist.
- Subjects :
- Actins metabolism
Animals
Disease Models, Animal
Endoglin metabolism
Hemodynamics physiology
Humans
Hypertension, Portal metabolism
Hypertension, Portal pathology
Hypertension, Portal physiopathology
Liver pathology
Liver Cirrhosis metabolism
Liver Cirrhosis pathology
Liver Cirrhosis physiopathology
Male
Mesentery blood supply
Rats
Rats, Sprague-Dawley
Hypertension, Portal etiology
Liver Circulation physiology
Portal Vein physiopathology
Vascular Resistance physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 11
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 27589391
- Full Text :
- https://doi.org/10.1371/journal.pone.0162144