Cargando…

Liver Protein Expression in NASH Mice on a High-Fat Diet: Response to Multi-Mineral Intervention

Male MS-NASH mice were maintained on a high-fat diet for 16 weeks with and without red algae-derived minerals. Obeticholic acid (OCA) was used as a comparator in the same strain and diet. C57BL/6 mice maintained on a standard (low-fat) rodent chow diet were used as a control. At the end of the in-li...

Descripción completa

Detalles Bibliográficos
Autores principales: Varani, James, McClintock, Shannon D., Knibbs, Randall N., Harber, Isabelle, Zeidan, Dania, Jawad-Makki, Mohamed Ali H., Aslam, Muhammad N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130755/
https://www.ncbi.nlm.nih.gov/pubmed/35634402
http://dx.doi.org/10.3389/fnut.2022.859292
_version_ 1784713040111861760
author Varani, James
McClintock, Shannon D.
Knibbs, Randall N.
Harber, Isabelle
Zeidan, Dania
Jawad-Makki, Mohamed Ali H.
Aslam, Muhammad N.
author_facet Varani, James
McClintock, Shannon D.
Knibbs, Randall N.
Harber, Isabelle
Zeidan, Dania
Jawad-Makki, Mohamed Ali H.
Aslam, Muhammad N.
author_sort Varani, James
collection PubMed
description Male MS-NASH mice were maintained on a high-fat diet for 16 weeks with and without red algae-derived minerals. Obeticholic acid (OCA) was used as a comparator in the same strain and diet. C57BL/6 mice maintained on a standard (low-fat) rodent chow diet were used as a control. At the end of the in-life portion of the study, body weight, liver weight, liver enzyme levels and liver histology were assessed. Samples obtained from individual livers were subjected to Tandem Mass Tag labeling / mass spectroscopy for protein profile determination. As compared to mice maintained on the low-fat diet, all high-fat-fed mice had increased whole-body and liver weight, increased liver enzyme (aminotransferases) levels and widespread steatosis / ballooning hepatocyte degeneration. Histological evidence for liver inflammation and collagen deposition was also present, but changes were to a lesser extent. A moderate reduction in ballooning degeneration and collagen deposition was observed with mineral supplementation. Control mice on the high-fat diet alone demonstrated multiple protein changes associated with dysregulated fat and carbohydrate metabolism, lipotoxicity and oxidative stress. Cholesterol metabolism and bile acid formation were especially sensitive to diet. In mice receiving multi-mineral supplementation along with the high-fat diet, there was reduced liver toxicity as evidenced by a decrease in levels of several cytochrome P450 enzymes and other oxidant-generating moieties. Additionally, elevated expression of several keratins was also detected in mineral-supplemented mice. The protein changes observed with mineral supplementation were not seen with OCA. Our previous studies have shown that mice maintained on a high-fat diet for up to 18 months develop end-stage liver injury including hepatocellular carcinoma. Mineral-supplemented mice were substantially protected against tumor formation and other end-state consequences of high-fat feeding. The present study identifies early (16-week) protein changes occurring in the livers of the high-fat diet-fed mice, and how the expression of these proteins is influenced by mineral supplementation. These findings help elucidate early protein changes that contribute to end-stage liver injury and potential mechanisms by which dietary minerals may mitigate such damage.
format Online
Article
Text
id pubmed-9130755
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-91307552022-05-26 Liver Protein Expression in NASH Mice on a High-Fat Diet: Response to Multi-Mineral Intervention Varani, James McClintock, Shannon D. Knibbs, Randall N. Harber, Isabelle Zeidan, Dania Jawad-Makki, Mohamed Ali H. Aslam, Muhammad N. Front Nutr Nutrition Male MS-NASH mice were maintained on a high-fat diet for 16 weeks with and without red algae-derived minerals. Obeticholic acid (OCA) was used as a comparator in the same strain and diet. C57BL/6 mice maintained on a standard (low-fat) rodent chow diet were used as a control. At the end of the in-life portion of the study, body weight, liver weight, liver enzyme levels and liver histology were assessed. Samples obtained from individual livers were subjected to Tandem Mass Tag labeling / mass spectroscopy for protein profile determination. As compared to mice maintained on the low-fat diet, all high-fat-fed mice had increased whole-body and liver weight, increased liver enzyme (aminotransferases) levels and widespread steatosis / ballooning hepatocyte degeneration. Histological evidence for liver inflammation and collagen deposition was also present, but changes were to a lesser extent. A moderate reduction in ballooning degeneration and collagen deposition was observed with mineral supplementation. Control mice on the high-fat diet alone demonstrated multiple protein changes associated with dysregulated fat and carbohydrate metabolism, lipotoxicity and oxidative stress. Cholesterol metabolism and bile acid formation were especially sensitive to diet. In mice receiving multi-mineral supplementation along with the high-fat diet, there was reduced liver toxicity as evidenced by a decrease in levels of several cytochrome P450 enzymes and other oxidant-generating moieties. Additionally, elevated expression of several keratins was also detected in mineral-supplemented mice. The protein changes observed with mineral supplementation were not seen with OCA. Our previous studies have shown that mice maintained on a high-fat diet for up to 18 months develop end-stage liver injury including hepatocellular carcinoma. Mineral-supplemented mice were substantially protected against tumor formation and other end-state consequences of high-fat feeding. The present study identifies early (16-week) protein changes occurring in the livers of the high-fat diet-fed mice, and how the expression of these proteins is influenced by mineral supplementation. These findings help elucidate early protein changes that contribute to end-stage liver injury and potential mechanisms by which dietary minerals may mitigate such damage. Frontiers Media S.A. 2022-05-11 /pmc/articles/PMC9130755/ /pubmed/35634402 http://dx.doi.org/10.3389/fnut.2022.859292 Text en Copyright © 2022 Varani, McClintock, Knibbs, Harber, Zeidan, Jawad-Makki and Aslam. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Nutrition
Varani, James
McClintock, Shannon D.
Knibbs, Randall N.
Harber, Isabelle
Zeidan, Dania
Jawad-Makki, Mohamed Ali H.
Aslam, Muhammad N.
Liver Protein Expression in NASH Mice on a High-Fat Diet: Response to Multi-Mineral Intervention
title Liver Protein Expression in NASH Mice on a High-Fat Diet: Response to Multi-Mineral Intervention
title_full Liver Protein Expression in NASH Mice on a High-Fat Diet: Response to Multi-Mineral Intervention
title_fullStr Liver Protein Expression in NASH Mice on a High-Fat Diet: Response to Multi-Mineral Intervention
title_full_unstemmed Liver Protein Expression in NASH Mice on a High-Fat Diet: Response to Multi-Mineral Intervention
title_short Liver Protein Expression in NASH Mice on a High-Fat Diet: Response to Multi-Mineral Intervention
title_sort liver protein expression in nash mice on a high-fat diet: response to multi-mineral intervention
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130755/
https://www.ncbi.nlm.nih.gov/pubmed/35634402
http://dx.doi.org/10.3389/fnut.2022.859292
work_keys_str_mv AT varanijames liverproteinexpressioninnashmiceonahighfatdietresponsetomultimineralintervention
AT mcclintockshannond liverproteinexpressioninnashmiceonahighfatdietresponsetomultimineralintervention
AT knibbsrandalln liverproteinexpressioninnashmiceonahighfatdietresponsetomultimineralintervention
AT harberisabelle liverproteinexpressioninnashmiceonahighfatdietresponsetomultimineralintervention
AT zeidandania liverproteinexpressioninnashmiceonahighfatdietresponsetomultimineralintervention
AT jawadmakkimohamedalih liverproteinexpressioninnashmiceonahighfatdietresponsetomultimineralintervention
AT aslammuhammadn liverproteinexpressioninnashmiceonahighfatdietresponsetomultimineralintervention