Evidence map›Paper›PMID 24183703›Full record

ArticleToxicology and applied pharmacology2013

Increased bile acids in enterohepatic circulation by short-term calorie restriction in male mice.

Zidong Donna Fu, Curtis D Klaassen

Abstract read
In one paragraph

Article in Toxicology and applied pharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Article
  3. Bile acid regulation of xenobiotic nuclear receptors on the expressions of orosomucoids in the liver.American journal of physiology. Endocrinology and metabolism · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Perfluorooctanesulfonic Acid (PFOS) Thwarts the Beneficial Effects of Calorie Restriction and Metformin.Toxicological sciences : an official journal of the Society of Toxicology · 2021
    Article
  14. Article
  15. Effect of Gender and Various Diets on Bile Acid Profile and Related Genes in Mice.Drug metabolism and disposition: the biological fate of chemicals · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Zidong Donna FuDepartment of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
Curtis D Klaassen
University of Kansas Medical Center · US

Funding

Regulation of Hepatic Uptake of Endogenous Signaling Molecules and XenobioticsR01ES009649 · NIEHS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI CSANAKY, IVAN · 2000 to 2014
$4.0M
NIEHS NIH HHS R01 ES009649
6 · The paper itself

Abstract

Previous studies showed glucose and insulin signaling can regulate bile acid (BA) metabolism during fasting or feeding. However, limited knowledge is available on the effect of calorie restriction (CR), a well-known anti-aging intervention, on BA homeostasis. To address this, the present study utilized a "dose-response" model of CR, where male C57BL/6 mice were fed 0, 15, 30, or 40% CR diets for one month, followed by BA profiling in various compartments of the enterohepatic circulation by UPLC-MS/MS technique. This study showed that 40% CR increased the BA pool size (162%) as well as total BAs in serum, gallbladder, and small intestinal contents. In addition, CR "dose-dependently" increased the concentrations of tauro-cholic acid (TCA) and many secondary BAs (produced by intestinal bacteria) in serum, such as tauro-deoxycholic acid (TDCA), DCA, lithocholic acid, ω-muricholic acid (ωMCA), and hyodeoxycholic acid. Notably, 40% CR increased TDCA by over 1000% (serum, liver, and gallbladder). Interestingly, 40% CR increased the proportion of 12α-hydroxylated BAs (CA and DCA), which correlated with improved glucose tolerance and lipid parameters. The CR-induced increase in BAs correlated with increased expression of BA-synthetic (Cyp7a1) and conjugating enzymes (BAL), and the ileal BA-binding protein (Ibabp). These results suggest that CR increases BAs in male mice possibly through orchestrated increases in BA synthesis and conjugation in liver as well as intracellular transport in ileum.

Indexed as

Caloric RestrictionAnimalsBile Acids and SaltsBlood GlucoseBody WeightCarrier ProteinsCholesterol 7-alpha-HydroxylaseCholic AcidsDeoxycholic AcidDose-Response Relationship, DrugEnterohepatic CirculationHomeostasisIntestinesLipidsLiverMaleBile Acids and SaltsBlood GlucoseCarrier ProteinsCholesterol 7-alpha-HydroxylaseCholic AcidsCyp7a1 protein, mouseDeoxycholic Acidhyodeoxycholic acidLipidsmuricholic acidRNA, Messenger12α-hydroxylated BAsad libitumALapical sodium-dependent bile acid transporterAsbtBABALBA profilingBATbile acidbile acid-CoA: amino acid N-acyltransferasebile acid-CoA ligaseBile acidsbile salt export pumpBsepCAcalorie restrictionCalorie restrictionCDCAchenodeoxycholic acidcholic acidCRDCAdeoxycholic acidEHCenterohepatic circulationEnterohepatic circulationfarnesoid X receptorFgffibroblast growth factorFXRgallbladderGBHDCAhyodeoxycholic acidIbabpileal bile acid binding proteinlarge intestineLCALIlithocholic acidMCAMDCAmuricholic acidmurideoxycholic acidNa(+)/taurocholate cotransporting polypeptideNtcpOatporganic anion transporting polypeptideorganic solute transporterOstSHPSIsmall heterodimer partnersmall intestinetaurine-conjugated bile acidT-BAU-BAUDCAultra-performance liquid chromatography-tandem mass spectrometryunconjugated bile acidUPLC-MS/MSursodeoxycholic acid

Identifiers

PMID24183703
PMCPMC4132937
OpenAlexW2144275775

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.