Evidence map›Paper›PMID 7769123›Full record

ArticleThe Journal of clinical investigation1995

Mast cells and histamine contribute to bile acid-stimulated secretion in the mouse colon.

C M Gelbmann, C D Schteingart, S M Thompson, A F Hofmann, K E Barrett

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

26 citing papers in PubMed, 75 citations in OpenAlex.

  1. 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
  2. Contributions of bile acids to gastrointestinal physiology as receptor agonists and modifiers of ion channels.American journal of physiology. Gastrointestinal and liver physiology · 2022
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. The Farnesoid X Receptor: Good for BAD.Cellular and molecular gastroenterology and hepatology · 2016
    Review
  8. Article
  9. Secretory diarrhoea: mechanisms and emerging therapies.Nature reviews. Gastroenterology & hepatology · 2015
    Review
  10. Article
  11. Article
  12. Article
  13. Histamine regulation of hyperplastic and neoplastic cell growth in cholangiocytes.World journal of gastrointestinal pathophysiology · 2010
    Article
  14. Bile acids in regulation of intestinal physiology.Current gastroenterology reports · 2009
    Review
  15. Article
  16. Intestinal bile acid physiology and pathophysiology.World journal of gastroenterology · 2008
    Review
  17. The effect of biliary sphincterotomy on serum cholesterol level in postcholecystectomy patients: a pilot study.Canadian journal of gastroenterology = Journal canadien de gastroenterologie · 2007
    Article
  18. Article
  19. Bile salt diarrhea.Current gastroenterology reports · 2005
    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

5 authors at 1 institution in 1 country.

C M GelbmannDepartment of Medicine, University of California, San Diego, School of Medicine 92103, USA.
C D Schteingart
S M Thompson
A F Hofmann
K E Barrett
University of California, San Diego · US

Funding

BILE ACID METABOLISM IN HEALTH AND DISEASER01DK021506 · NIDDK · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI HOFMANN, ALAN F · 1986 to 1998
–
MUCOSAL MAST CELLS AND INTESTINAL DISEASESR29AI024992 · NIAID · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI BARRETT, KIM ELAINE · 1988 to 1992
–
NIAID NIH HHS AI-24992NIDDK NIH HHS DK-21506
6 · The paper itself

Abstract

Certain dihydroxy bile acids cause secretory diarrhea when present in the colonic lumen at inappropriately high concentrations. However, the mechanism underlying the secretagogue activity has not been fully elucidated. Experiments were performed to test whether mast cells and one of their major mediators, histamine, might contribute to the secretory effect. Chenodeoxycholic acid, a secretory bile acid, and ursodeoxycholic acid, a nonsecretory, hydrophilic bile acid, were compared for their ability to induce chloride secretion across segments of mouse colon mounted in Ussing chambers. Chenodeoxycholic acid, but not ursodeoxycholic acid, induced dose-dependent, biphasic chloride secretion that was greater after serosal than mucosal addition and was greater in distal versus proximal colonic segments. The secretory effect of chenodeoxycholic acid was inhibited by H1 histamine receptor antagonists and modified by the cyclooxygenase inhibitor indomethacin. However, it was unaffected by an H2 histamine receptor antagonist or by atropine. Secretory effects of chenodeoxycholic acid were diminished in magnitude and delayed in colonic tissues from mice with a genetic deficiency of tissue mast cells. Concentrations of chenodeoxycholic acid inducing secretion also released histamine from tissue segments. These data indicate that mast cells and histamine-mediated processes contribute significantly to the secretory effects of dihydroxy bile acids in the murine colon.

Indexed as

AnimalsBile Acids and SaltsBiological TransportChenodeoxycholic AcidChloridesColonDiarrheaHistamineIn Vitro TechniquesMast CellsMiceMice, Inbred C57BLMice, Mutant StrainsPyrilamineTetrodotoxinUrsodeoxycholic AcidBile Acids and SaltsChenodeoxycholic AcidChloridesHistaminePyrilamineTetrodotoxinUrsodeoxycholic Acid

Identifiers

PMID7769123
PMCPMC295969
OpenAlexW2071879560

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.