Evidence map›Paper›PMID 18292185›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2008

Increased cholesterol 7alpha-hydroxylase expression and size of the bile acid pool in the lactating rat.

Clavia Ruth Wooton-Kee, David E Cohen, Mary Vore

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

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  8. ABCG5/ABCG8-independent biliary cholesterol excretion in lactating rats.American journal of physiology. Gastrointestinal and liver physiology · 2010
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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

3 authors at 1 institution in 1 country.

Clavia Ruth Wooton-KeeGraduate Ctr. for Toxicology, University of Kentucky College of Medicine, Lexington, KY 40536, USA.
David E Cohen
Mary Vore
University of Kentucky · US

Funding

Phospholipid-Mediated Metabolic Control in the Pathogenesis of NAFLDR01DK056626 · NIDDK · YESHIVA UNIVERSITY · PI COHEN, DAVID E. · 2000 to 2024
$10.3M
Regulation of Hepatic Lipid and Glucose Metabolism by Phosphatidylcholine TransfeR01DK048873 · NIDDK · YESHIVA UNIVERSITY · PI DAVID E. COHEN · 2003 to 2026
$5.8M
Regulation of Hepatic Lipid and Glucose Metabolism by PC-TP/StarD2R37DK048873 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI COHEN, DAVID E. · 2012 to 2021
$5.5M
TRAINING GRANT IN MOLECULAR MECHANISMS OF TOXICITY.T32ES007266 · NIEHS · UNIVERSITY OF KENTUCKY · PI LIU, XIAOQI, MELLON, ISABEL W · 1990 to 2020
$3.7M
PROLACTIN AND BILE SECRETORY FUNCTIONR01DK046923 · NIDDK · UNIVERSITY OF KENTUCKY · PI VORE, MARY · 1994 to 2007
$1.4M
MOLECULAR PHYSIOLOGY OF BILIARY LIPID SECRETIONR29DK048873 · NIDDK · YESHIVA UNIVERSITY · PI COHEN, DAVID E · 1996 to 2000
$147k
NIDDK NIH HHS DK-46923NIDDK NIH HHS DK-48873NIDDK NIH HHS DK-56626NIDDK NIH HHS R01 DK046923NIDDK NIH HHS R01 DK048873NIDDK NIH HHS R01 DK056626NIDDK NIH HHS R29 DK048873NIDDK NIH HHS R37 DK048873NIEHS NIH HHS T32 ES007266
6 · The paper itself

Abstract

Maximal bile acid secretory rates and expression of bile acid transporters in liver and ileum are increased in lactation, possibly to facilitate increased enterohepatic recirculation of bile acids. We determined changes in the size and composition of the bile acid pool and key enzymes of the bile acid synthetic pathway [cholesterol 7alpha-hydroxylase (Cyp7a1), sterol 27-hydroxylase (Cyp27a1), and sterol 12alpha-hydroxylase (Cyp8b1)] in lactating rats relative to female virgin controls. The bile acid pool increased 1.9 to 2.5-fold [postpartum (PP) days 10, 14, and 19-23], compared with controls. A 1.5-fold increase in cholic acids and a 14 to 20% decrease in muricholic acids in lactation significantly increased the hydrophobicity index. In contrast, the hepatic concentration of bile acids and small heterodimer partner mRNA were unchanged in lactation. A 2.8-fold increase in Cyp7a1 mRNA expression at 16 h (10 h of light) demonstrated a shift in the diurnal rhythm at day 10 PP; Cyp7a1 protein expression and cholesterol 7alpha-hydroxylase activity were significantly increased at this time and remained elevated at day 14 PP but decreased to control levels by day 21 PP. There was an overall decrease in Cyp27a1 mRNA expression and a 20% decrease in Cyp27a1 protein expression, but there was no change in Cyp8b1 mRNA or protein expression at day 10 PP. The increase in Cyp7a1 expression PP provides a mechanism for the increase in the bile acid pool.

Indexed as

Circadian RhythmAnimalsBile Acids and SaltsCholestanetriol 26-MonooxygenaseCholesterolCholesterol 7-alpha-HydroxylaseCholic AcidsEnzyme InductionFemaleHydrophobic and Hydrophilic InteractionsIntestinal MucosaLactationLiverRatsRats, Sprague-DawleyReceptors, Cytoplasmic and NuclearBile Acids and SaltsCholestanetriol 26-MonooxygenaseCholesterolCholesterol 7-alpha-HydroxylaseCholic Acidsmuricholic acidnuclear receptor subfamily 0, group B, member 2Receptors, Cytoplasmic and NuclearRNA, MessengerSteroid 12-alpha-Hydroxylase

Identifiers

PMID18292185
PMCPMC2408447
OpenAlexW2171017626

What OpenQuestion holds

Textmetadata
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.