Cargando…
Aliskiren effect on non-alcoholic steatohepatitis in metabolic syndrome
BACKGROUND: Non-alcoholic steatohepatitis (NASH) is highly associated with metabolic syndrome, a major cause of morbidity in the globalized society. The renin–angiotensin system (RAS) influences hepatic fatty acid metabolism, inflammation and fibrosis. Thus, in the present study, we aimed to evaluat...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640954/ https://www.ncbi.nlm.nih.gov/pubmed/29046730 http://dx.doi.org/10.1186/s13098-017-0282-5 |
_version_ | 1783271127735336960 |
---|---|
author | Ramalho, F. N. Sanches, S. C. Foss, M. C. Augusto, M. J. Silva, D. M. Oliveira, A. M. Ramalho, L. N. |
author_facet | Ramalho, F. N. Sanches, S. C. Foss, M. C. Augusto, M. J. Silva, D. M. Oliveira, A. M. Ramalho, L. N. |
author_sort | Ramalho, F. N. |
collection | PubMed |
description | BACKGROUND: Non-alcoholic steatohepatitis (NASH) is highly associated with metabolic syndrome, a major cause of morbidity in the globalized society. The renin–angiotensin system (RAS) influences hepatic fatty acid metabolism, inflammation and fibrosis. Thus, in the present study, we aimed to evaluate the effect of aliskiren, a direct renin inhibitor, on metabolic syndrome-related NASH. METHODS: C57BL/6 male mice (n = 45) were divided into three groups: controls; animals inoculated with streptozotocin (STZ) (40 mg/kg/day) for 5 days and fed with high fat diet (HFD) for 8 weeks; and animals inoculated with STZ for 5 days, fed with HFD for 8 weeks and treated with aliskiren (100 mg/kg/day) for the final 2 weeks. Glycemic and insulin levels, hepatic lipid profile, histological parameters and inflammatory protein expression were analyzed. RESULTS: Aliskiren normalized plasma glucose and insulin levels, reduced cholesterol, triglycerides and total fat accumulation in liver and diminished hepatic injury, steatosis and fibrosis. These results could be explained by the ability of aliskiren to block angiotensin-II, lowering oxidative stress and inflammation in liver. Also, it exhibited a beneficial effect in increasing insulin sensitivity. CONCLUSION: These findings support the use of aliskiren in the treatment of metabolic syndrome underlying conditions. However, clinical studies are indispensable to test its effectiveness in the treatment of patients with metabolic syndrome. |
format | Online Article Text |
id | pubmed-5640954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56409542017-10-18 Aliskiren effect on non-alcoholic steatohepatitis in metabolic syndrome Ramalho, F. N. Sanches, S. C. Foss, M. C. Augusto, M. J. Silva, D. M. Oliveira, A. M. Ramalho, L. N. Diabetol Metab Syndr Research BACKGROUND: Non-alcoholic steatohepatitis (NASH) is highly associated with metabolic syndrome, a major cause of morbidity in the globalized society. The renin–angiotensin system (RAS) influences hepatic fatty acid metabolism, inflammation and fibrosis. Thus, in the present study, we aimed to evaluate the effect of aliskiren, a direct renin inhibitor, on metabolic syndrome-related NASH. METHODS: C57BL/6 male mice (n = 45) were divided into three groups: controls; animals inoculated with streptozotocin (STZ) (40 mg/kg/day) for 5 days and fed with high fat diet (HFD) for 8 weeks; and animals inoculated with STZ for 5 days, fed with HFD for 8 weeks and treated with aliskiren (100 mg/kg/day) for the final 2 weeks. Glycemic and insulin levels, hepatic lipid profile, histological parameters and inflammatory protein expression were analyzed. RESULTS: Aliskiren normalized plasma glucose and insulin levels, reduced cholesterol, triglycerides and total fat accumulation in liver and diminished hepatic injury, steatosis and fibrosis. These results could be explained by the ability of aliskiren to block angiotensin-II, lowering oxidative stress and inflammation in liver. Also, it exhibited a beneficial effect in increasing insulin sensitivity. CONCLUSION: These findings support the use of aliskiren in the treatment of metabolic syndrome underlying conditions. However, clinical studies are indispensable to test its effectiveness in the treatment of patients with metabolic syndrome. BioMed Central 2017-10-13 /pmc/articles/PMC5640954/ /pubmed/29046730 http://dx.doi.org/10.1186/s13098-017-0282-5 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ramalho, F. N. Sanches, S. C. Foss, M. C. Augusto, M. J. Silva, D. M. Oliveira, A. M. Ramalho, L. N. Aliskiren effect on non-alcoholic steatohepatitis in metabolic syndrome |
title | Aliskiren effect on non-alcoholic steatohepatitis in metabolic syndrome |
title_full | Aliskiren effect on non-alcoholic steatohepatitis in metabolic syndrome |
title_fullStr | Aliskiren effect on non-alcoholic steatohepatitis in metabolic syndrome |
title_full_unstemmed | Aliskiren effect on non-alcoholic steatohepatitis in metabolic syndrome |
title_short | Aliskiren effect on non-alcoholic steatohepatitis in metabolic syndrome |
title_sort | aliskiren effect on non-alcoholic steatohepatitis in metabolic syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640954/ https://www.ncbi.nlm.nih.gov/pubmed/29046730 http://dx.doi.org/10.1186/s13098-017-0282-5 |
work_keys_str_mv | AT ramalhofn aliskireneffectonnonalcoholicsteatohepatitisinmetabolicsyndrome AT sanchessc aliskireneffectonnonalcoholicsteatohepatitisinmetabolicsyndrome AT fossmc aliskireneffectonnonalcoholicsteatohepatitisinmetabolicsyndrome AT augustomj aliskireneffectonnonalcoholicsteatohepatitisinmetabolicsyndrome AT silvadm aliskireneffectonnonalcoholicsteatohepatitisinmetabolicsyndrome AT oliveiraam aliskireneffectonnonalcoholicsteatohepatitisinmetabolicsyndrome AT ramalholn aliskireneffectonnonalcoholicsteatohepatitisinmetabolicsyndrome |