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Nebivolol treatment increases splanchnic blood flow and portal pressure in cirrhotic rats via modulation of nitric oxide signalling

Background We evaluated the effects of nebivolol, a third generation beta‐blocker capable of increasing NO‐bioavailability on portal pressure, and on splachnic and systemic haemodynamics in a cirrhotic portal hypertensive rat model. Methods Male Sprague–Dawley rats underwent sham operation (SO) or b...

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Published in:Liver international 2013-04, Vol.33 (4), p.561-568
Main Authors: Reiberger, Thomas, Payer, Berit Anna, Schwabl, Philipp, Hayden, Hubert, Horvatits, Thomas, Jäger, Bernhard, Hummel, Thomas, Mitterhauser, Markus, Trauner, Michael, Fuhrmann, Valentin, Angermayr, Bernhard, Peck-Radosavljevic, Markus
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Language:English
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Summary:Background We evaluated the effects of nebivolol, a third generation beta‐blocker capable of increasing NO‐bioavailability on portal pressure, and on splachnic and systemic haemodynamics in a cirrhotic portal hypertensive rat model. Methods Male Sprague–Dawley rats underwent sham operation (SO) or bile duct ligation (BDL). When cirrhosis was fully developed, the animals were orally treated with low‐dose (5 mg/kg) or high‐dose (10 mg/kg) nebivolol (NEBI) or vehicle (VEH) for 7 days. Heart rate (HR), mean arterial pressure (MAP), portal pressure (PP) and superior mesenteric artery blood flow (SMABF) were measured. Portosystemic collateral blood flow (PSCBF) was quantified using radioactive microspheres. Hepatic and splanchnic NOx levels and GSH/GSSG ratios (RedOx state) were determined using commercially available kits. Results BDL‐VEH rats showed increased HR, PP and PSCBF, whereas MAP was decreased compared to SO‐VEH rats. Nebivolol significantly reduced HR both in SO (P 
ISSN:1478-3223
1478-3231
DOI:10.1111/liv.12101