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A fast and accurate mouse model for inducing non-alcoholic steatohepatitis

AIM: This study aimed to perform a head-to-head comparison of changes during NASH progression throughout 6-11 weeks of an experiment to supply a faster nutritional model in mimicking NASH to decrease the duration and cost of in vivo studies. BACKGROUND: New therapies are urgently needed because of t...

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Autores principales: Rahimi, Shahrzad, Angaji, Seyyed Abdolhamid, Majd, Ahmad, Hatami, Behzad, Baghaei, Kaveh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9876774/
https://www.ncbi.nlm.nih.gov/pubmed/36762217
http://dx.doi.org/10.22037/ghfbb.v15i4.2593
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author Rahimi, Shahrzad
Angaji, Seyyed Abdolhamid
Majd, Ahmad
Hatami, Behzad
Baghaei, Kaveh
author_facet Rahimi, Shahrzad
Angaji, Seyyed Abdolhamid
Majd, Ahmad
Hatami, Behzad
Baghaei, Kaveh
author_sort Rahimi, Shahrzad
collection PubMed
description AIM: This study aimed to perform a head-to-head comparison of changes during NASH progression throughout 6-11 weeks of an experiment to supply a faster nutritional model in mimicking NASH to decrease the duration and cost of in vivo studies. BACKGROUND: New therapies are urgently needed because of the growing prevalence of non-alcoholic steatohepatitis (NASH) and the lack of an effective treatment approach. Currently, dietary interventions are the most efficient options. METHODS: This study compared features of NASH in a murine model using protocol that combined special nutritional regimes based on the combination of 21.1% fat, 41% sucrose, and 1.25% cholesterol with weekly intraperitoneal injections of carbon tetrachloride (CCl4). Male C57BL/6J mice received either special compositions + CCl4 (NASH group) or standard chow diet (healthy control group) for 11 weeks. Liver histopathology based on hematoxylin and eosin (H&E) and Masson’s Trichrome (TC) staining and biochemical analyses were used to assess disease progression. RESULTS: In C57BL/6J mice administered a high fat, high cholesterol, high sucrose diet and CCl4 for 8 weeks, steatohepatitis with pronounced hepatocyte ballooning, inflammation, steatosis, and fibrosis was observed. According to the NAFLD activity scoring system, the maximum NAS score was manifested after 8-9 weeks (NAS score: 6.75). Following this protocol also led to a significant increase in AST and ALT, total cholesterol, and total triglyceride serum levels in the NASH group. CONCLUSION: Following the special nutritional regime based on high fat, cholesterol, and sucrose in combination with CCL4 injections resulted in a NASH model using C57BL/6J mice in a shorter time compared to similar studies. The obtained histopathological NASH features can be advantageous for preclinical drug testing.
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spelling pubmed-98767742023-02-08 A fast and accurate mouse model for inducing non-alcoholic steatohepatitis Rahimi, Shahrzad Angaji, Seyyed Abdolhamid Majd, Ahmad Hatami, Behzad Baghaei, Kaveh Gastroenterol Hepatol Bed Bench Original Article AIM: This study aimed to perform a head-to-head comparison of changes during NASH progression throughout 6-11 weeks of an experiment to supply a faster nutritional model in mimicking NASH to decrease the duration and cost of in vivo studies. BACKGROUND: New therapies are urgently needed because of the growing prevalence of non-alcoholic steatohepatitis (NASH) and the lack of an effective treatment approach. Currently, dietary interventions are the most efficient options. METHODS: This study compared features of NASH in a murine model using protocol that combined special nutritional regimes based on the combination of 21.1% fat, 41% sucrose, and 1.25% cholesterol with weekly intraperitoneal injections of carbon tetrachloride (CCl4). Male C57BL/6J mice received either special compositions + CCl4 (NASH group) or standard chow diet (healthy control group) for 11 weeks. Liver histopathology based on hematoxylin and eosin (H&E) and Masson’s Trichrome (TC) staining and biochemical analyses were used to assess disease progression. RESULTS: In C57BL/6J mice administered a high fat, high cholesterol, high sucrose diet and CCl4 for 8 weeks, steatohepatitis with pronounced hepatocyte ballooning, inflammation, steatosis, and fibrosis was observed. According to the NAFLD activity scoring system, the maximum NAS score was manifested after 8-9 weeks (NAS score: 6.75). Following this protocol also led to a significant increase in AST and ALT, total cholesterol, and total triglyceride serum levels in the NASH group. CONCLUSION: Following the special nutritional regime based on high fat, cholesterol, and sucrose in combination with CCL4 injections resulted in a NASH model using C57BL/6J mice in a shorter time compared to similar studies. The obtained histopathological NASH features can be advantageous for preclinical drug testing. Shaheed Beheshti University of Medical Sciences 2022 /pmc/articles/PMC9876774/ /pubmed/36762217 http://dx.doi.org/10.22037/ghfbb.v15i4.2593 Text en https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article, distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) which permits others to copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Original Article
Rahimi, Shahrzad
Angaji, Seyyed Abdolhamid
Majd, Ahmad
Hatami, Behzad
Baghaei, Kaveh
A fast and accurate mouse model for inducing non-alcoholic steatohepatitis
title A fast and accurate mouse model for inducing non-alcoholic steatohepatitis
title_full A fast and accurate mouse model for inducing non-alcoholic steatohepatitis
title_fullStr A fast and accurate mouse model for inducing non-alcoholic steatohepatitis
title_full_unstemmed A fast and accurate mouse model for inducing non-alcoholic steatohepatitis
title_short A fast and accurate mouse model for inducing non-alcoholic steatohepatitis
title_sort fast and accurate mouse model for inducing non-alcoholic steatohepatitis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9876774/
https://www.ncbi.nlm.nih.gov/pubmed/36762217
http://dx.doi.org/10.22037/ghfbb.v15i4.2593
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