LUNG AND LIVER CHANGES DUE TO THE INDUCTION OF CIRRHOSIS IN TWO EXPERIMENTAL MODELS

Author:

FERRARI Renata Salatti1,TIEPPO Mauricio2,ROSA Darlan Pase da3,FORGIARINI JR Luiz Alberto4,DIAS Alexandre Simoes1,MARRONI Norma Possa3

Affiliation:

1. Hospital das Clinicas de Porto Alegre; Universidade Federal do Rio Grande do Sul, Brasil

2. Hospital das Clinicas de Porto Alegre; Universidade Luterana do Brasil

3. Hospital das Clinicas de Porto Alegre; Universidade Luterana do Brasil; Universidade Federal do Rio Grande do Sul, Brasil

4. Hospital das Clinicas de Porto Alegre

Abstract

Context To evaluate lung and liver changes in two experimental models using intraperitoneal carbon tetrachloride (CCl4) and bile duct ligation (BDL). Methods Twenty-four male Wistar rats were divided into a control group (CO) and an experimental group (EX). We evaluated the liver transaminases (AST, ALT, AP), arterial blood gases (PaO2, PCO2 and SpO2) and lipid peroxidation by TBARS (substances that react to thiobarbituric acid) and chemiluminescence. We also evaluated the antioxidant enzyme superoxide dismutase (SOD) and histology of lung tissue and liver. Results There were significant differences in AST, ALT, ALP and PaO2 between CO group and EX group (P<0.05). The levels of TBARS, chemiluminescence and activity of enzyme superoxide dismutase were increased to different degrees in the CCl4 groups: CO and in the BDL -EX (P<0.05, respectively). In the lung histology, an increase in the wall thickness of the pulmonary artery and a diameter reduction in the CCl4 animal model were observed: comparing CO group with EX group, we observed a reduction in thickness and an increase in the diameter of the artery wall lung. Conclusion Both experimental models have caused liver damage and alterations in the artery wall that are associated with major changes in pulmonary gas exchange.

Publisher

FapUNIFESP (SciELO)

Subject

Gastroenterology

Reference34 articles.

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2. Prophylactic and curative effects of purslane on bile duct ligation-induced hepatic fibrosis in albino rats;Ali SI;Ann Hepatol,2011

3. Quercetin prevents oxidative stress in cirrhotic rats;Amália PM;Dig Dis Sci,2007

4. Portopulmonary hypertension: an increasingly important complication of cirrhosis;Blendis L;Gastroenterology,2003

5. Effect of Antioxidant Treatment on Fibrogenesis in Rats with Carbon Tetrachloride-Induced Cirrhosis.;Bona S;ISRN Gastroenterol

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