Evidence map›Paper›PMID 20056894›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2010

Green tea catechin EGCG inhibits ileal apical sodium bile acid transporter ASBT.

Fadi Annaba, Pradeep Kumar, Amish K Dudeja, Seema Saksena, Ravinder K Gill, Waddah A Alrefai

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Recent advances in small bowel diseases: Part II.World journal of gastroenterology · 2012
    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

6 authors at 2 institutions in 1 country.

Fadi AnnabaDepartment of Medicine, University of Illinois at Chicago, and Jesse Brown Veterans Affairs Medical Center, USA.
Pradeep Kumar
Amish K Dudeja
Seema Saksena
Ravinder K Gill
Waddah A Alrefai
Jesse Brown VA Medical Center · USUniversity of Illinois Chicago · US

Funding

Regulation of Intestinal Bile Acid TransportR01DK071596 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ALREFAI, WADDAH A. · 2005 to 2014
$2.3M
Regulation of Intestinal Bile Acid TransportR56DK071596 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ALREFAI, WADDAH A. · 2010 to 2010
$196k
Intestinal Bile Acid Transport in EPEC InfectionF32DK079542 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ANNABA, FADI · 2007 to 2009
$177k
NIDDK NIH HHS DK71596NIDDK NIH HHS DK74459NIDDK NIH HHS F32 DK79542
6 · The paper itself

Abstract

Green tea catechins exhibit hypocholesterolemic effects probably via their inhibitory effects on intestinal bile acid absorption. Ileal apical sodium-dependent bile acid transporter (ASBT) is responsible for reabsorption of bile acids. The present studies were, therefore, designed to investigate the modulation of ASBT function and membrane expression by green tea catechins in human embryonic kidney HEK-293 cells stably transfected with ASBT-V5 fusion protein and intestinal Caco-2 monolayers. Our data showed that ASBT activity was significantly decreased by (-)-epigallocatechin-3-gallate (EGCG) but not other green tea catechins. Inhibition of PKC, phosphatidylinositol 3-kinase, and MAPK-dependent pathways failed to block the reduction in ASBT activity by EGCG. Kinetics studies showed a significant decrease in the V(max) of the transporter, whereas total ASBT content on the plasma membrane was unaltered by EGCG. Concomitant with the decrease in ASBT function, EGCG significantly reduced ASBT pool in the detergent-insoluble fraction, while increasing its presence in the detergent-soluble fraction of plasma membrane. Furthermore, EGCG decreased the association of ASBT with floating lipid raft fractions of cellular membrane on Optiprep density gradient. In conclusion, our data demonstrate a novel role of lipid rafts in the modulation of ASBT function by the dietary component EGCG, which may underlie the hypocholesterolemic effects of green tea.

Indexed as

Biological TransportBiotinylationCaco-2 CellsCatechinCell LineCell MembraneEnzyme InhibitorsEpithelial CellsExtracellular Signal-Regulated MAP KinasesHumansIleumKineticsMembrane LipidsMembrane MicrodomainsMembrane ProteinsOctoxynolCatechincatechin gallateEnzyme Inhibitorsepigallocatechin gallateExtracellular Signal-Regulated MAP KinasesflotillinsMembrane LipidsMembrane ProteinsOctoxynolOrganic Anion Transporters, Sodium-DependentPhosphoinositide-3 Kinase InhibitorsProtein Kinase Csodium-bile acid cotransporterSymportersTaurocholic AcidTea

Identifiers

PMID20056894
PMCPMC2838517
OpenAlexW2071789192

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.