Evidence map›Paper›PMID 30919600›Full record

ArticleGut and liver2019

Bile Acid Transporters Are Expressed and Heterogeneously Distributed in Rat Bile Ducts.

Zhu-Lin Luo, Long Cheng, Tao Wang, Li-Jun Tang, Fu-Zhou Tian, Ke Xiang, Lin Cui

Open access · diamondAbstract read
In one paragraph

Article in Gut and liver, 2019. 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
0.6field-weighted citation impact, top 29% 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, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. bioRxiv : the preprint server for biology · 2024
    Article
  5. Review
  6. Article
  7. Loss of apical sodium bile acid transporter alters bile acid circulation and reduces biliary damage in cholangitis.American journal of physiology. Gastrointestinal and liver physiology · 2023
    Article
  8. Article
  9. Review
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

7 authors at 1 institution in 1 country.

Zhu-Lin LuoDepartments of General Surgery, Chengdu Military General Hospital, Chengdu, China.
Long ChengDepartments of General Surgery, Chengdu Military General Hospital, Chengdu, China.ORCID 0000-0003-1240-3360
Tao WangDepartments of General Surgery, Chengdu Military General Hospital, Chengdu, China.ORCID 0000-0002-0005-0994
Li-Jun TangDepartments of General Surgery, Chengdu Military General Hospital, Chengdu, China.
Fu-Zhou TianDepartments of General Surgery, Chengdu Military General Hospital, Chengdu, China.
Ke XiangDepartments of General Surgery, Chengdu Military General Hospital, Chengdu, China.
Lin CuiDepartments of Orthopedics, Chengdu Military General Hospital, Chengdu, China.
Chengdu Military General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aims: Cholangiocytes are capable of reabsorbing bile salts from bile, but the pathophysiological significance of this process is unclear. To this end, we detected the expression and distribution of bile acid transport proteins in cholangiocytes from normal rat liver and analyzed the possible pathophysiological significance. Methods: Bile duct tissues of Sprague-Dawley rats were isolated by enzymatic digestion and mechanical isolation, and then divided into large and small bile duct tissues. Immunohistochemistry, real-time polymerase chain reaction and Western blotting were used to determine the expression of the apical sodium-dependent bile acid transporter (ASBT), ileal bile acid binding protein (IBABP), and basolateral organic solute transporter α (Ostα) in the biliary tract system of rats. Differences in the expression and distribution of these proteins were analyzed. Results: In cholangiocytes, ASBT and IBABP were mainly expressed in cholangiocytes of the large bile ducts, in which the expression of both was significantly higher than that in the small ducts (p<0.05). Ostα was simultaneously expressed in cholangiocytes of both the large and small bile ducts, showing no significant difference in expression between the two groups of bile ducts (p>0.05). Conclusions: Bile acid transporters are expressed and heterogeneously distributed in rat bile ducts, indicating that bile acid reabsorption by cholangiocytes might mainly occur in the large bile ducts. These findings may help explore the physiology of bile ducts and the pathogenesis of various cholangiopathies.

Indexed as

AnimalsBile Acids and SaltsBile DuctsCarrier ProteinsEpithelial CellsLiverMaleMembrane GlycoproteinsMembrane Transport ProteinsOrganic Anion Transporters, Sodium-DependentRats, Sprague-DawleySymportersbile acid binding proteinsBile Acids and SaltsCarrier ProteinsMembrane GlycoproteinsMembrane Transport ProteinsOrganic Anion Transporters, Sodium-DependentSlc51a protein, ratSlc51b protein, ratsodium-bile acid cotransporterSymportersBile acid transporterCholangiocyteCholangiopathiesHeterogeneity

Identifiers

PMID30919600
PMCPMC6743800
OpenAlexW2926977525

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Registered trials

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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.