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The Eeffect of Metformin Combined with Calcium-Vitamin D(3) Against Diet-Induced Nonalcoholic Fatty Liver Disease

Purpose: Metformin is one of the most popular drugs tested against nonalcoholic fatty liver disease (NAFLD). The present study aimed to investigate whether calcium-vitamin D(3) cosupplementation will intensify the effect of metformin on the prevention of high-fat, high-fructose (HFFr) diet-induced h...

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Autores principales: Shojaei Zarghani, Sara, Abbaszadeh, Samin, Alizadeh, Mohammad, Rameshrad, Maryam, Garjani, Alireza, Soraya, Hamid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5896400/
https://www.ncbi.nlm.nih.gov/pubmed/29670844
http://dx.doi.org/10.15171/apb.2018.012
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author Shojaei Zarghani, Sara
Abbaszadeh, Samin
Alizadeh, Mohammad
Rameshrad, Maryam
Garjani, Alireza
Soraya, Hamid
author_facet Shojaei Zarghani, Sara
Abbaszadeh, Samin
Alizadeh, Mohammad
Rameshrad, Maryam
Garjani, Alireza
Soraya, Hamid
author_sort Shojaei Zarghani, Sara
collection PubMed
description Purpose: Metformin is one of the most popular drugs tested against nonalcoholic fatty liver disease (NAFLD). The present study aimed to investigate whether calcium-vitamin D(3) cosupplementation will intensify the effect of metformin on the prevention of high-fat, high-fructose (HFFr) diet-induced hepatic steatosis. Methods: Male wistar rats (210±16 g) were assigned into the following seven groups: a Control group to receive a standard chow and six HFFr-fed groups to receive diets containing either normal (0.5% calcium and 1000 IU/kg vitamin D(3)) or high amount of calcium and vitamin D(3) (2.4% calcium and 10000 IU/kg vitamin D(3)) (CaD), in combination with gastric gavage administration of either saline or 25 or 200 mg/kg body weight/day metformin. After 60 days, rats were assessed with respect to their anthropometric, metabolic and hepatic parameters, as well as their hepatic AMP-activated protein kinase (AMPK) phosphorylation. Results: Metformin and CaD, either alone or in combination, caused a significant reduction in HFFr diet-induced high serum aspartate aminotransferase (AST), hepatic steatosis and lipid accumulation without effect on insulin resistance and AMPK phosphorylation. In addition, slightly (and non-significantly) better effects of the combination in ameliorating steatosis and hepatic cholesterol content were observed. Conclusion: Taken together, our results suggest that metformin and CaD could protect against the onset of HFFr diet-induced NAFLD in an insulin and AMPK-independent manner, without any marked additional benefits of their combination.
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spelling pubmed-58964002018-04-18 The Eeffect of Metformin Combined with Calcium-Vitamin D(3) Against Diet-Induced Nonalcoholic Fatty Liver Disease Shojaei Zarghani, Sara Abbaszadeh, Samin Alizadeh, Mohammad Rameshrad, Maryam Garjani, Alireza Soraya, Hamid Adv Pharm Bull Research Article Purpose: Metformin is one of the most popular drugs tested against nonalcoholic fatty liver disease (NAFLD). The present study aimed to investigate whether calcium-vitamin D(3) cosupplementation will intensify the effect of metformin on the prevention of high-fat, high-fructose (HFFr) diet-induced hepatic steatosis. Methods: Male wistar rats (210±16 g) were assigned into the following seven groups: a Control group to receive a standard chow and six HFFr-fed groups to receive diets containing either normal (0.5% calcium and 1000 IU/kg vitamin D(3)) or high amount of calcium and vitamin D(3) (2.4% calcium and 10000 IU/kg vitamin D(3)) (CaD), in combination with gastric gavage administration of either saline or 25 or 200 mg/kg body weight/day metformin. After 60 days, rats were assessed with respect to their anthropometric, metabolic and hepatic parameters, as well as their hepatic AMP-activated protein kinase (AMPK) phosphorylation. Results: Metformin and CaD, either alone or in combination, caused a significant reduction in HFFr diet-induced high serum aspartate aminotransferase (AST), hepatic steatosis and lipid accumulation without effect on insulin resistance and AMPK phosphorylation. In addition, slightly (and non-significantly) better effects of the combination in ameliorating steatosis and hepatic cholesterol content were observed. Conclusion: Taken together, our results suggest that metformin and CaD could protect against the onset of HFFr diet-induced NAFLD in an insulin and AMPK-independent manner, without any marked additional benefits of their combination. Tabriz University of Medical Sciences 2018-03 2018-03-18 /pmc/articles/PMC5896400/ /pubmed/29670844 http://dx.doi.org/10.15171/apb.2018.012 Text en ©2018 The Authors. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, as long as the original authors and source are cited. No permission is required from the authors or the publishers.
spellingShingle Research Article
Shojaei Zarghani, Sara
Abbaszadeh, Samin
Alizadeh, Mohammad
Rameshrad, Maryam
Garjani, Alireza
Soraya, Hamid
The Eeffect of Metformin Combined with Calcium-Vitamin D(3) Against Diet-Induced Nonalcoholic Fatty Liver Disease
title The Eeffect of Metformin Combined with Calcium-Vitamin D(3) Against Diet-Induced Nonalcoholic Fatty Liver Disease
title_full The Eeffect of Metformin Combined with Calcium-Vitamin D(3) Against Diet-Induced Nonalcoholic Fatty Liver Disease
title_fullStr The Eeffect of Metformin Combined with Calcium-Vitamin D(3) Against Diet-Induced Nonalcoholic Fatty Liver Disease
title_full_unstemmed The Eeffect of Metformin Combined with Calcium-Vitamin D(3) Against Diet-Induced Nonalcoholic Fatty Liver Disease
title_short The Eeffect of Metformin Combined with Calcium-Vitamin D(3) Against Diet-Induced Nonalcoholic Fatty Liver Disease
title_sort eeffect of metformin combined with calcium-vitamin d(3) against diet-induced nonalcoholic fatty liver disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5896400/
https://www.ncbi.nlm.nih.gov/pubmed/29670844
http://dx.doi.org/10.15171/apb.2018.012
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