Evidence map›Paper›PMID 12883891›Full record

ReviewPflugers Archiv : European journal of physiology2004

The SLC22 drug transporter family.

Hermann Koepsell, Hitoshi Endou

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Pflugers Archiv : European journal of physiology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02586636 (Impact of OCT1 Genotype and OCT1 Inhibiting Drugs on an Individual's Tolerance of Metformin), which is not on this map. Cited by 154 papers.

0numbers the graph read from it
0cells of the map it votes in
154citing papers in PubMed
26.7field-weighted citation impact, top 1% 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.

NCT02586636 phase4completednot on this mapstarted 2016, after this paper: background citation

Impact of OCT1 Genotype and OCT1 Inhibiting Drugs on an Individual's Tolerance of Metformin

TypeinterventionalSponsorNHS TaysideRan2016 to 2018Enrolled61ConditionsToleranceArmsMetformin, Omeprazole, Placebo
3 · Its place in the literature

Who cites it

154 citing papers in PubMed, 527 citations in OpenAlex.

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  14. Impact of genetic variants in the solute carrier (Cancer drug resistance (Alhambra, Calif.) · 2024
    Review
  15. Pharmaceutical science advances · 2023
    Article
  16. Article
  17. Article
  18. Review
  19. Caged Polyprenylated Xanthones inDrug design, development and therapy · 2023
    Review
  20. Sensitive and valid assay for reliable evaluation of drug interactions mediated by human organic anion transporter 1 and 3 using 5-carboxyfluorescein.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2022
    Article

94 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

Hermann KoepsellInstitute of Anatomy and Cell Biology, Bayerische Maximilians Universität Würzburg, Koellikerstr. 6, 97070, Würzburg, Germany. Hermann@Koepsell.de
Hitoshi Endou
Bayer (Germany) · DEKyorin University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SLC22 family comprises organic cation transporters (OCTs), zwitterion/cation transporters (OCTNs), and organic anion transporters (OATs). These transporters contain 12 predicted alpha-helical transmembrane domains (TMDs) and one large extracellular loop between TMDs 1 and 2. Transporters of the SLC22 family function in different ways: (1) as uniporters that mediate facilitated diffusion in either direction (OCTs), (2) as anion exchangers (OAT1, OAT3 and URAT1), and (3) as Na(+)/ l-carnitine cotransporter (OCTN2). They participate in the absorption and/or excretion of drugs, xenobiotics, and endogenous compounds in intestine, liver and/or kidney, and perform homeostatic functions in brain and heart. The endogenous substrates include monoamine neurotransmitters, choline, l-carnitine, alpha-ketoglutarate, cAMP, cGMP, prostaglandins, and urate. Defect mutations of transporters of the SLC22 family may cause specific diseases such as "primary systemic carnitine deficiency" or "idiopathic renal hypouricemia" or change drug absorption or excretion.

Indexed as

AnimalsBiological TransportHumansMultigene FamilyOrganic Anion TransportersOrganic Cation Transport ProteinsPharmacokineticsOrganic Anion TransportersOrganic Cation Transport Proteins

Identifiers

PMID12883891
OpenAlexW2060634509

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.