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Metformin Inhibits Glutaminase Activity and Protects against Hepatic Encephalopathy
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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499552/ https://www.ncbi.nlm.nih.gov/pubmed/23166628 http://dx.doi.org/10.1371/journal.pone.0049279 |
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author | Ampuero, Javier Ranchal, Isidora Nuñez, David Díaz-Herrero, María del Mar Maraver, Marta del Campo, José Antonio Rojas, Ángela Camacho, Inés Figueruela, Blanca Bautista, Juan D. Romero-Gómez, Manuel |
author_facet | Ampuero, Javier Ranchal, Isidora Nuñez, David Díaz-Herrero, María del Mar Maraver, Marta del Campo, José Antonio Rojas, Ángela Camacho, Inés Figueruela, Blanca Bautista, Juan D. Romero-Gómez, Manuel |
author_sort | Ampuero, Javier |
collection | PubMed |
description | 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 post-treatment (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. |
format | Online Article Text |
id | pubmed-3499552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34995522012-11-19 Metformin Inhibits Glutaminase Activity and Protects against Hepatic Encephalopathy Ampuero, Javier Ranchal, Isidora Nuñez, David Díaz-Herrero, María del Mar Maraver, Marta del Campo, José Antonio Rojas, Ángela Camacho, Inés Figueruela, Blanca Bautista, Juan D. Romero-Gómez, Manuel PLoS One Research Article 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 post-treatment (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. Public Library of Science 2012-11-15 /pmc/articles/PMC3499552/ /pubmed/23166628 http://dx.doi.org/10.1371/journal.pone.0049279 Text en © 2012 Ampuero et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ampuero, Javier Ranchal, Isidora Nuñez, David Díaz-Herrero, María del Mar Maraver, Marta del Campo, José Antonio Rojas, Ángela Camacho, Inés Figueruela, Blanca Bautista, Juan D. Romero-Gómez, Manuel Metformin Inhibits Glutaminase Activity and Protects against Hepatic Encephalopathy |
title | Metformin Inhibits Glutaminase Activity and Protects against Hepatic Encephalopathy |
title_full | Metformin Inhibits Glutaminase Activity and Protects against Hepatic Encephalopathy |
title_fullStr | Metformin Inhibits Glutaminase Activity and Protects against Hepatic Encephalopathy |
title_full_unstemmed | Metformin Inhibits Glutaminase Activity and Protects against Hepatic Encephalopathy |
title_short | Metformin Inhibits Glutaminase Activity and Protects against Hepatic Encephalopathy |
title_sort | metformin inhibits glutaminase activity and protects against hepatic encephalopathy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499552/ https://www.ncbi.nlm.nih.gov/pubmed/23166628 http://dx.doi.org/10.1371/journal.pone.0049279 |
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