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dc.creatorBautista Palomas, Juan Dionisio
dc.creatorCampo Castillo, José Antonio del
dc.creatorRomero Gómez, Manuel
dc.creatorRanchal Illescas, Isidora
dc.creatorCamacho Benítez, Inés
dc.creatorNuñez Hospital, David
dc.creatorDíaz Herrero, María del Mar
dc.creatorRojas, Ángela
dc.creatorMaraver Zamora, Marta
dc.creatorAmpuero Herrojo, Javier
dc.creatorFigueruela, Blanca
dc.date.accessioned2015-02-02T19:40:03Z
dc.date.available2015-02-02T19:40:03Z
dc.date.issued2012
dc.identifier.citationBautista Palomas, J.D., Campo Castillo, J.A.d., Romero Gómez, M., Ranchal Illescas, I., Camacho Benítez, I., Nuñez Hospital, D.,...,Figueruela, B. (2012). Metformin inhibits glutaminase activity and protects against hepatic encephalopathy. PLoS ONE, 7 (11), e49279.
dc.identifier.issn1932-6203es
dc.identifier.urihttp://hdl.handle.net/11441/18246
dc.description.abstractAim: To investigate the influence of metformin use on liver dysfunction and hepatic encephalopathy in a retrospective cohort of diabetic cirrhotic patients. To analyze the impact of metformin on glutaminase activity and ammonia production in vitro. Methods: Eighty-two cirrhotic patients with type 2 diabetes were included. Forty-one patients were classified as insulin sensitizers experienced (metformin) and 41 as controls (cirrhotic patients with type 2 diabetes mellitus without metformin treatment). Baseline analysis included: insulin, glucose, glucagon, leptin, adiponectin, TNFr2, AST, ALT. HOMA-IR was calculated. Baseline HE risk was calculated according to minimal hepatic encephalopathy, oral glutamine challenge and mutations in glutaminase gene. We performed an experimental study in vitro including an enzymatic activity assay where glutaminase inhibition was measured according to different metformin concentrations. In Caco2 cells, glutaminase activity inhibition was evaluated by ammonia production at 24, 48 and 72 hours after metformina treatment. Results: Hepatic encephalopathy was diagnosed during follow-up in 23.2% (19/82): 4.9% (2/41) in patients receiving metformin and 41.5% (17/41) in patients without metformin treatment (logRank 9.81; p = 0.002). In multivariate analysis, metformin use [H.R.11.4 (95% CI: 1.2–108.8); p = 0.034], age at diagnosis [H.R.1.12 (95% CI: 1.04–1.2); p = 0.002], female sex [H.R.10.4 (95% CI: 1.5–71.6); p = 0.017] and HE risk [H.R.21.3 (95% CI: 2.8–163.4); p = 0.003] were found independently associated with hepatic encephalopathy. In the enzymatic assay, glutaminase activity inhibition reached 68% with metformin 100 mM. In Caco2 cells, metformin (20 mM) decreased glutaminase activity up to 24% at 72 hours posttreatment (p,0.05). Conclusions: Metformin was found independently related to overt hepatic encephalopathy in patients with type 2 diabetes mellitus and high risk of hepatic encephalopathy. Metformin inhibits glutaminase activity in vitro. Therefore, metformin use seems to be protective against hepatic encephalopathy in diabetic cirrhotic patients.es
dc.language.isoenges
dc.relation.ispartofPLoS ONE, 7 (11), e49279.
dc.rightsAtribución-NoComercial-SinDerivadas 4.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleMetformin inhibits glutaminase activity and protects against hepatic encephalopathyes
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Medicina
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Bioquímica Vegetal y Biología Molecular
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Bioquímica y Biología Moleculares
dc.journaltitlePLoS ONEes
dc.publication.volumen7es
dc.publication.issue11es
dc.publication.initialPagee49279es
dc.identifier.idushttps://idus.us.es/xmlui/handle/11441/18246

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