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Superoxide dismutase gene transfer reduces portal pressure in ccl4 cirrhotic rats with portal hypertension

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dc.creator Laviña Siemsen, Bàrbara
dc.creator Gracia-Sancho, Jorge
dc.creator Rodríguez Vilarrupla, Aina
dc.creator Chu, Y.
dc.creator Heistad, D. D.
dc.creator Bosch i Genover, Jaume
dc.creator García Pagán, Juan Carlos
dc.date 2011-07-07T12:30:18Z
dc.date 2011-07-07T12:30:18Z
dc.date 2009
dc.date.accessioned 2024-12-16T10:27:14Z
dc.date.available 2024-12-16T10:27:14Z
dc.identifier 0017-5749
dc.identifier http://hdl.handle.net/2445/18648
dc.identifier 581084
dc.identifier 18829979
dc.identifier.uri http://fima-docencia.ub.edu:8080/xmlui/handle/123456789/22116
dc.description Background: Increased intrahepatic vascular tone in cirrhosis has been attributed to a decrease of hepatic nitric oxide (NO) secondary to disturbances in the post-translational regulation of the enzyme eNOS. NO scavenging by superoxide (O2−) further contributes to a reduction of NO bioavailability in cirrhotic livers. Aim: To investigate whether removing increased O2− levels could be a new therapeutic strategy to increase intrahepatic NO, improve endothelial dysfunction and reduce portal pressure in cirrhotic rats with portal hypertension. Methods: Adenoviral vectors expressing extracellular superoxide dismutase (SOD) (AdECSOD) or β-galactosidase (Adβgal) were injected intravenously in control and CCl4-induced cirrhotic rats. After 3 days, liver O2− levels were determined by dihydroethidium staining, NO bioavailability by hepatic cGMP levels, nitrotyrosinated proteins by immunohistochemistry and western blot, and endothelial function by responses to acetylcholine in perfused rat livers. Mean arterial pressure (MAP) and portal pressure were evaluated in vivo. Results: Transfection of cirrhotic livers with AdECSOD produced a significant reduction in O2− levels, a significant increase in hepatic cGMP, and a decrease in liver nitrotyrosinated proteins which were associated with a significant improvement in the endothelium-dependent vasodilatation to acetylcholine. In addition, in cirrhotic livers AdECSOD transfection produced a significant reduction in portal pressure (17.3 (SD 2) mm Hg vs 15 (SD 1.6) mm Hg; p<0.05) without significant changes in MAP. In control rats, AdECSOD transfection prevents the increase in portal perfusion pressure promoted by an ROS-generating system. Conclusions: In cirrhotic rats, reduction of O2− by AdECSOD increases NO bioavailability, improves intrahepatic endothelial function and reduces portal pressure. These findings suggest that scavenging of O2− might be a new therapeutic strategy in the management of portal hypertension.
dc.format 9 p.
dc.format application/pdf
dc.language eng
dc.publisher BMJ Group
dc.relation Reproducció digital del document publicat a: http://dx.doi.org/10.1136/gut.2008.149880
dc.relation Gut, 2009, vol. 58, núm. 1, p. 118-125
dc.relation http://dx.doi.org/10.1136/gut.2008.149880
dc.rights (c) BMJ Publishing Group Ltd and British Society of Gastroenterology, 2009
dc.rights info:eu-repo/semantics/openAccess
dc.source Articles publicats en revistes (Medicina)
dc.subject Cirrosi hepàtica
dc.subject Hipertensió portal
dc.subject Transformació genètica
dc.subject Superòxid dismutasa
dc.subject Hepatic cirrhosis
dc.subject Portal hypertension
dc.subject Genetic transformation
dc.subject Superoxide dismutase
dc.title Superoxide dismutase gene transfer reduces portal pressure in ccl4 cirrhotic rats with portal hypertension
dc.type info:eu-repo/semantics/article
dc.type info:eu-repo/semantics/publishedVersion


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