Article
Metformin inhibits glutaminase activity and protects against hepatic encephalopathy
Author/s | Bautista Palomas, Juan Dionisio
Campo Castillo, José Antonio del Romero Gómez, Manuel Ranchal Illescas, Isidora Camacho Benítez, Inés Nuñez Hospital, David Díaz Herrero, María del Mar Rojas, Ángela Maraver Zamora, Marta Ampuero Herrojo, Javier Figueruela, Blanca |
Department | Universidad de Sevilla. Departamento de Medicina Universidad de Sevilla. Departamento de Bioquímica Vegetal y Biología Molecular Universidad de Sevilla. Departamento de Bioquímica y Biología Molecular |
Publication Date | 2012 |
Deposit Date | 2015-02-02 |
Published in |
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Abstract | Aim: 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 ... Aim: 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. |
Citation | Bautista 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. |
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