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Partial Portal Vein Ligation Plus Thioacetamide: A Method to Obtain a New Model of Cirrhosis and Chronic Portal Hypertension in the Rat
Authors:Marta Méndez-López  Magdalena Méndez  Fernando Sánchez-Patán  Isabel Casado  Maria-Angeles Aller  Laudino López  Maria-Teresa Corcuera  Maria-Jose Alonso  Maria-Paz Nava  Jaime Arias  Jorge-Luis Arias
Affiliation:(1) Psychobiology Department, Psychology School, University of Oviedo, Asturias, Spain;(2) Surgery Chair, Surgery Department I, Medical School, Complutense University, Madrid, Spain;(3) Pathology Service, Hospital Carlos III, Madrid, Spain;(4) Animal Physiology Department (Physiology II), School of Biological Sciences, Complutense University of Madrid, Madrid, Spain;(5) Cátedra de Cirugía, Facultad de Medicina, Universidad Complutense de Madrid, Pza. de Ramón y Cajal s.n., 28040 Madrid, Spain
Abstract:
To obtain a new model of chronic portal hypertension in the rat, two classical methods to produce portal hypertension, partial portal vein ligation and the oral administration of thioacetamide (TAA), have been combined. Male Wistar rats were divided into four groups: 1 (control; n?=?10), 2 [triple partial portal vein ligation (TPVL); n?=?9], 3 (TAA; n?=?11), and 4 (TPVL plus TAA; n?=?9). After 3 months, portal pressure, types of portosystemic collateral circulation, laboratory hepatic function tests (aspartate aminotransferase, alanine aminotransferase, bilirubin, alkaline phosphatase, and gamma-glutamyl transpeptidase) and liver histology were studied. The animals belonging to group 2 (TPVL) developed extrahepatic portosystemic collateral circulation, associated with mesenteric venous vasculopathy without hepatic destructurization or portal hypertension. Animals from group 3 (TAA) developed cirrhosis and portal hypertension but not extrahepatic portosystemic collateral circulation, or mesenteric venous vasculopathy. Finally, the animals from group 4 (TPVL?+?TAA) developed cirrhosis, portal hypertension, portosystemic collateral circulation, and mesenteric venous vasculopathy. The association of TPVL and TAA can be used to obtain a model of chronic portal hypertension in the rat that includes all the alterations that patients with hepatic cirrhosis usually have. This could, therefore, prove to be a useful tool to study the pathophysiological mechanisms involved in these alterations.
Keywords:Portal hypertension  Partial portal vein ligation  Thioacetamide  Cirrhosis  Portosystemic collateral circulation
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