Skip to main content
Advertisement

Main menu

  • Home
  • Articles
    • Current Issue
    • Fast Forward
    • Latest Articles
    • Special Sections
    • Archive
  • Information
    • Instructions to Authors
    • Submit a Manuscript
    • FAQs
    • For Subscribers
    • Terms & Conditions of Use
    • Permissions
  • Editorial Board
  • Alerts
    • Alerts
    • RSS Feeds
  • Virtual Issues
  • Feedback
  • Submit
  • Other Publications
    • Drug Metabolism and Disposition
    • Journal of Pharmacology and Experimental Therapeutics
    • Molecular Pharmacology
    • Pharmacological Reviews
    • Pharmacology Research & Perspectives
    • ASPET

User menu

  • My alerts
  • Log in
  • My Cart

Search

  • Advanced search
Drug Metabolism & Disposition
  • Other Publications
    • Drug Metabolism and Disposition
    • Journal of Pharmacology and Experimental Therapeutics
    • Molecular Pharmacology
    • Pharmacological Reviews
    • Pharmacology Research & Perspectives
    • ASPET
  • My alerts
  • Log in
  • My Cart
Drug Metabolism & Disposition

Advanced Search

  • Home
  • Articles
    • Current Issue
    • Fast Forward
    • Latest Articles
    • Special Sections
    • Archive
  • Information
    • Instructions to Authors
    • Submit a Manuscript
    • FAQs
    • For Subscribers
    • Terms & Conditions of Use
    • Permissions
  • Editorial Board
  • Alerts
    • Alerts
    • RSS Feeds
  • Virtual Issues
  • Feedback
  • Submit
  • Visit dmd on Facebook
  • Follow dmd on Twitter
  • Follow ASPET on LinkedIn
Research ArticleArticle

Effect of Gender and Various Diets on Bile Acid Profile and Related Genes in Mice

Chong Ma, Ying Guo and Curtis D. Klaassen
Drug Metabolism and Disposition January 2021, 49 (1) 62-71; DOI: https://doi.org/10.1124/dmd.120.000166
Chong Ma
Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, P. R. China (C.M., Y.G.); Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha, P. R. China (C.M., Y.G.); Engineering Research Center of Applied Technology of Pharmacogenomics, Ministry of Education, Changsha, P. R. China (C.M., Y.G.); National Clinical Research Center for Geriatric Disorders,Xiangya Hospital, Central South University, Changsha, Hunan, P.R. China (C.M., Y.G.); and Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, Kansas (C.D.K.)
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Ying Guo
Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, P. R. China (C.M., Y.G.); Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha, P. R. China (C.M., Y.G.); Engineering Research Center of Applied Technology of Pharmacogenomics, Ministry of Education, Changsha, P. R. China (C.M., Y.G.); National Clinical Research Center for Geriatric Disorders,Xiangya Hospital, Central South University, Changsha, Hunan, P.R. China (C.M., Y.G.); and Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, Kansas (C.D.K.)
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Ying Guo
  • For correspondence: guoying881212@csu.edu.cn
Curtis D. Klaassen
Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, P. R. China (C.M., Y.G.); Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha, P. R. China (C.M., Y.G.); Engineering Research Center of Applied Technology of Pharmacogenomics, Ministry of Education, Changsha, P. R. China (C.M., Y.G.); National Clinical Research Center for Geriatric Disorders,Xiangya Hospital, Central South University, Changsha, Hunan, P.R. China (C.M., Y.G.); and Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, Kansas (C.D.K.)
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: curtisklaassenphd@gmail.com
  • Article
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF + SI
  • PDF
Loading

Article Figures & Data

Figures

  • Tables
  • Additional Files
  • Fig. 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 1.

    Bile acid biosynthesis, transport, and metabolism. Ath r epresents "atherogenic diet" and DR respresents "diet restriction". The left arrow (solid line) shows the trend of male mice, and the right arrow (dashed line) shows the trend of female mice.

  • Fig. 2.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 2.

    Three-dimensional scatter plots of the PCA for the influence of different diets on liver BA profile and BA-related gene mRNA expression in both genders of mice. (A) PCA based on the BA-related gene mRNA expression in livers of male mice (R2 = 0.797, Q2 = 0.532). (B) PCA based on the BA-related gene mRNA expression in livers of female mice (R2 = 0.828, Q2 = 0.584). (C) PCA based on liver BA concentrations of male mice (R2 = 0.988, Q2 = 0.664). (D) PCA based on liver BA concentrations of female mice (R2 = 0.956, Q2 = 0.618). Each color represents a single diet. PCA was performed using the software SIMCA.

  • Fig. 3.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 3.

    Effect of nine diets on the concentrations of BAs in the serum of mice. (A) The amount of T-conjugated, unconjugated, and total BAs in the serum of mice were quantified. (B) Heatmap of BAs in the serum of mice fed nine various diets. Average values of five replicates per diet are given by colored squares. High BA concentration is represented in red, whereas low BA concentration is in blue. *P < 0.05 compared with control (AIN-93M purified diet) in male and female mice, respectively; #P < 0.05 compared between genders fed the same diet.

  • Fig. 4.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 4.

    Effect of nine diets on the concentrations of BAs in the livers of mice. (A) The amount of T-conjugated, unconjugated, and total BAs in the livers of mice were quantified. (B) Heatmap of BAs in the livers of mice fed nine various diets. Average values of five replicates per diet are given by colored squares. High BA concentration is represented in red, whereas low BA concentration is in blue. *P < 0.05 compared with control (AIN-93M purified diet) in male and female mice, respectively; #P < 0.05 compared between genders fed the same diet.

  • Fig. 5.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 5.

    Effect of nine diets on mRNA expression of BA-related genes in the livers and ileum of mice. Heatmap of BA-related genes in the livers and ileum of mice fed nine various diets. Average values of five replicates per diet are given by colored squares. High mRNA abundance is represented in red, whereas low mRNA abundance is in blue. Relative mRNA levels were calculated with male controls (male, AIN-93M purified diet) set as 100%. Data were analyzed by two-way ANOVA. *P < 0.05 compared with control (AIN-93M purified diet) in male and female mice, respectively; #P < 0.05 when data from the two genders fed the same diet are compared.

Tables

  • Figures
  • Additional Files
    • View popup
    TABLE 1

    The ratio of 12α-OH BAs to non–12α-OH BAs in livers and serum of two genders

    12α-OH BAs: CA, DCA, TCA, TDCA; non–12α-OH BAs: CDCA, LCA, UDCA, HDCA, MDCA, TCDCA, TLCA, TUDCA, TMDCA, THDCA, MCAs and TMCAs.

    DietMaleFemale
    LiverSerumLiverSerum
    AIN-93M purified0.24 ± 0.050.53 ± 0.150.57 ± 0.051.55 ± 0.2
    Laboratory chow0.61 ± 0.10.69 ± 0.150.8 ± 0.11.28 ± 0.25
    Diet-restriction2.12 ± 0.55*2.14 ± 0.6*1.65 ± 0.15*2.02 ± 0.35
    High fructose0.47 ± 0.450.33 ± 0.150.8 ± 0.051.5 ± 0.15
    High fat0.29 ± 0.050.5 ± 0.200.8 ± 0.251.51 ± 0.35
    Atherogenic30.09 ± 3.25*48.47 ± 9.8*21.73 ± 8.75*41.24 ± 16.35*
    Western0.26 ± 0.10.61 ± 0.20.3 ± 0.050.82 ± 0.2
    Low n-3 FA0.23 ± 0.050.56 ± 0.250.51 ± 0.21.53 ± 0.35
    EFA deficient0.28 ± 0.10.22 ± 0.10.56 ± 0.151.05 ± 0.3
    • ↵* Indicates P < 0.05 when compared with the AIN-93M purified diet. Mean values ± S.D. are shown.

Additional Files

  • Figures
  • Tables
  • Data Supplement

    • Supplemental Tables -

      Supplementary Table 1 - Standard curve data of the different bile acids.

      Supplementary Table 2 - The effects of nine diets on serum individual, total, T-conjugated, unconjugated BAs.

      Supplementary Table 3 - The effects of nine diets on liver individual, total, T-conjugated, unconjugated BAs.

      Supplementary Table 4 - The effects of nine diets on BA-related genes in liver and ileum.

      Supplementary Table 5 - The correlation analysis of BAs (total, conjugated and unconjugated) and BA-related genes involved in the synthesis, metabolism and transport of BAs in the livers of mice fed the 9 diets.

PreviousNext
Back to top

In this issue

Drug Metabolism and Disposition: 49 (1)
Drug Metabolism and Disposition
Vol. 49, Issue 1
1 Jan 2021
  • Table of Contents
  • Table of Contents (PDF)
  • About the Cover
  • Index by author
  • Editorial Board (PDF)
  • Front Matter (PDF)
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for sharing this Drug Metabolism & Disposition article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
Effect of Gender and Various Diets on Bile Acid Profile and Related Genes in Mice
(Your Name) has forwarded a page to you from Drug Metabolism & Disposition
(Your Name) thought you would be interested in this article in Drug Metabolism & Disposition.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Citation Tools
Research ArticleArticle

Effect of Gender and Various Diets on Bile Acid Homeostasis

Chong Ma, Ying Guo and Curtis D. Klaassen
Drug Metabolism and Disposition January 1, 2021, 49 (1) 62-71; DOI: https://doi.org/10.1124/dmd.120.000166

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero

Share
Research ArticleArticle

Effect of Gender and Various Diets on Bile Acid Homeostasis

Chong Ma, Ying Guo and Curtis D. Klaassen
Drug Metabolism and Disposition January 1, 2021, 49 (1) 62-71; DOI: https://doi.org/10.1124/dmd.120.000166
Reddit logo Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Introduction
    • Materials and Methods
    • Results
    • Discussion
    • Acknowledgments
    • Authorship Contributions
    • Footnotes
    • Abbreviations
    • References
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF + SI
  • PDF

Related Articles

Cited By...

More in this TOC Section

  • Adipocyte PXR does not play an essential role in obesity.
  • CYP3A-mediated oxidation of DABE and BIBR0951
  • Biodistribution of Lipid in Rats
Show more Articles

Similar Articles

Advertisement
  • Home
  • Alerts
Facebook   Twitter   LinkedIn   RSS

Navigate

  • Current Issue
  • Fast Forward by date
  • Fast Forward by section
  • Latest Articles
  • Archive
  • Search for Articles
  • Feedback
  • ASPET

More Information

  • About DMD
  • Editorial Board
  • Instructions to Authors
  • Submit a Manuscript
  • Customized Alerts
  • RSS Feeds
  • Subscriptions
  • Permissions
  • Terms & Conditions of Use

ASPET's Other Journals

  • Journal of Pharmacology and Experimental Therapeutics
  • Molecular Pharmacology
  • Pharmacological Reviews
  • Pharmacology Research & Perspectives
ISSN 1521-009X (Online)

Copyright © 2023 by the American Society for Pharmacology and Experimental Therapeutics