Hemodynamic effects of the early and long-term administration of propranolol in rats with intrahepatic portal hypertension |
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Authors: | Lionel Fizanne Nicolas Régenet Jianhua Wang Frédéric Oberti Frédéric Moal Jerôme Roux Yves Gallois Sophie Michalak Paul Calès |
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Affiliation: | 1. Laboratoire HIFIH, UPRES EA 3859, UFR de Médecine, Université d’Angers, Angers, France 2. Animalerie Universitaire, UFR de Médecine, Université d’Angers, Angers, France 3. Laboratoire de Biochimie, UFR de Médecine, Université d’Angers, Angers, France 4. Laboratoire d’Anatomie-Pathologique, UFR de Médecine, Université d’Angers, Angers, France 5. Service d’Hépato-Gastroentérologie, CHU, 49033, Angers Cedex 01, France
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Abstract: | Background and aims The aims of this study were to evaluate a preventive effect on collateral venous circulation of long-term administration of propranolol in intrahepatic portal hypertensive rats. Methods Eighty-six Sprague–Dawley rats were allocated to two models of hepatic fibrosis, bile duct-ligated (BDL) induced and carbon tetrachloride (CCl4) induced. Each model was divided into two groups: one receiving placebo and the other propranolol (75 mg kg−1 d−1). Mean arterial pressure (MAP), heart rate (HR), portal pressure (PP), cardiac index (CI), vascular systemic resistance, and splenorenal shunt blood flow (SRS-BF) were measured in anesthetized rats. Results In the BDL model, no significant hemodynamic changes were observed in the propranolol group compared with the placebo group. In CCl4-induced rats, HR (390 ± 50 vs. 329 ± 51 beats/min, P = .001), CI (44 ± 11 vs. 34 ± 10 ml/min, P = .004), PP (15.4 ± 3.0 vs. 13.4 ± 1.9 mmHg, P = .045), and SRS-BF (1.4 ± 1.1 vs. 1.0 ± 1.0 ml/min, P = .047) were significantly lower in the propranolol group. Conclusions This study showed that propranolol has a significant hemodynamic effect only in the CCl4 model and suggested a model-dependent effect of propranolol. |
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Keywords: | Bile duct ligation Carbon tetrachloride Collateral venous circulation Propranolol Splenorenal shunt |
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