Literature DB >> 34643091

Comparative impact of dietary carbohydrates on the liver transcriptome in two strains of mice.

Yuling Chi1,2, Dou Yeon Youn1,2, Alus M Xiaoli1,2,3, Li Liu1,2, Yunping Qiu4, Irwin J Kurland1,4, Jacob B Pessin1, Fajun Yang1,2,3, Jeffrey E Pessin1,2,5.   

Abstract

Excessive long-term consumption of dietary carbohydrates, including glucose, sucrose, or fructose, has been shown to have significant impact on genome-wide gene expression, which likely results from changes in metabolic substrate flux. However, there has been no comprehensive study on the acute effects of individual sugars on the genome-wide gene expression that may reveal the genetic changes altering signaling pathways, subsequent metabolic processes, and ultimately physiological/pathological responses. Considering that gene expressions in response to acute carbohydrate ingestion might be different in nutrient sensitive and insensitive mammals, we conducted comparative studies of genome-wide gene expression by deep mRNA sequencing of the liver in nutrient sensitive C57BL/6J and nutrient insensitive BALB/cJ mice. Furthermore, to determine the temporal responses, we compared livers from mice in the fasted state and following ingestion of standard laboratory mouse chow supplemented with plain drinking water or water containing 20% glucose, sucrose, or fructose. Supplementation with these carbohydrates induced unique extents and temporal changes in gene expressions in a strain specific manner. Fructose and sucrose stimulated gene changes peaked at 3 h postprandial, whereas glucose effects peaked at 12 h and 6 h postprandial in C57BL/6J and BABL/cJ mice, respectively. Network analyses revealed that fructose changed genes were primarily involved in lipid metabolism and were more complex in C57BL/6J than in BALB/cJ mice. These data demonstrate that there are qualitative and antitative differences in the normal physiological responses of the liver between these two strains of mice and C57BL/6J is more sensitive to sugar intake than BALB/cJ.

Entities:  

Keywords:  BALB/cJ; C57BL/6J; dietary carbohydrates; mRNA-seq; transcriptome

Mesh:

Substances:

Year:  2021        PMID: 34643091      PMCID: PMC8616594          DOI: 10.1152/physiolgenomics.00053.2021

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


  58 in total

1.  Refeeding with glucose rather than fructose elicits greater hepatic inflammatory gene expression in mice.

Authors:  Motoko Oarada; Azusa Takahashi-Nakaguchi; Tomoki Abe; Takeshi Nikawa; Takashi Miki; Tohru Gonoi
Journal:  Nutrition       Date:  2014-12-19       Impact factor: 4.008

2.  Hepatic transcriptomics analysis reveals that fructose intervention down-regulated xenobiotics-metabolising enzymes through aryl hydrocarbon receptor signalling suppression in C57BL/6N mice.

Authors:  Jeong Hoon Pan; Jingsi Tang; Kaleigh E Beane; Mersady C Redding; Yun Jeong Cho; Young Jun Kim; Jiangchao Zhao; Eui-Cheol Shin; Jin Hyup Lee; Byungwhi C Kong; Jae Kyeom Kim
Journal:  Br J Nutr       Date:  2019-10-14       Impact factor: 3.718

Review 3.  The regulation of hepatic fatty acid synthesis and partitioning: the effect of nutritional state.

Authors:  Leanne Hodson; Pippa J Gunn
Journal:  Nat Rev Endocrinol       Date:  2019-12       Impact factor: 43.330

4.  Regulation of gene expression during the fasting-feeding cycle of the liver displays mouse strain specificity.

Authors:  Yuling Chi; Dou Yeon Youn; Alus M Xiaoli; Li Liu; Jacob B Pessin; Fajun Yang; Jeffrey E Pessin
Journal:  J Biol Chem       Date:  2020-02-19       Impact factor: 5.157

5.  Regulation of sterol regulatory element binding proteins in livers of fasted and refed mice.

Authors:  J D Horton; Y Bashmakov; I Shimomura; H Shimano
Journal:  Proc Natl Acad Sci U S A       Date:  1998-05-26       Impact factor: 11.205

Review 6.  Fructose as a key player in the development of fatty liver disease.

Authors:  Metin Basaranoglu; Gokcen Basaranoglu; Tevfik Sabuncu; Hakan Sentürk
Journal:  World J Gastroenterol       Date:  2013-02-28       Impact factor: 5.742

7.  Short Exposure to a High-Sucrose Diet and the First 'Hit' of Nonalcoholic Fatty Liver Disease in Mice.

Authors:  Flavia Fernandes-Lima; Thiago Luís Ribeiro Gomes Monte; Fernanda Amorim de Morais Nascimento; Bianca Martins Gregório
Journal:  Cells Tissues Organs       Date:  2016-06-17       Impact factor: 2.481

8.  Disparate metabolic response to fructose feeding between different mouse strains.

Authors:  M K Montgomery; C E Fiveash; J P Braude; B Osborne; S H J Brown; T W Mitchell; N Turner
Journal:  Sci Rep       Date:  2015-12-22       Impact factor: 4.379

9.  Nutrigenomics of high fat diet induced obesity in mice suggests relationships between susceptibility to fatty liver disease and the proteasome.

Authors:  Helen Waller-Evans; Christophe Hue; Jane Fearnside; Alice R Rothwell; Helen E Lockstone; Sophie Caldérari; Steven P Wilder; Jean-Baptiste Cazier; James Scott; Dominique Gauguier
Journal:  PLoS One       Date:  2013-12-06       Impact factor: 3.240

10.  Effect of diet on expression of genes involved in lipid metabolism, oxidative stress, and inflammation in mouse liver-insights into mechanisms of hepatic steatosis.

Authors:  Helen J Renaud; Julia Y Cui; Hong Lu; Curtis D Klaassen
Journal:  PLoS One       Date:  2014-02-14       Impact factor: 3.240

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