Evidence map›Paper›PMID 10098100›Full record

ArticleJournal of pharmacokinetics and biopharmaceutics1998

Competitive inhibition of p-aminohippurate transport by quinapril in rabbit renal basolateral membrane vesicles.

W Akarawut, D E Smith

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Journal of pharmacokinetics and biopharmaceutics, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 84% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Novobiocin is a potent inhibitor for human organic anion transporters.Drug metabolism and disposition: the biological fate of chemicals · 2009
    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

2 authors at 1 institution in 1 country.

W AkarawutCollege of Pharmacy, University of Michigan, Ann Arbor 48109-0504, USA.
D E Smith
University of Michigan–Ann Arbor · US

Funding

Role of PEPT2 in Peptide/Mimetic Disposition-DynamicsR01GM035498 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SMITH, DAVID E · 1988 to 2013
$3.7M
NIGMS NIH HHS R01 GM35498
6 · The paper itself

Abstract

The mechanism of quinapril's interaction with the organic anion transporter was characterized by studying its effect on the transport of p-aminohippurate (PAH) in rabbit renal basolateral membrane vesicles (BLMV). Cis-inhibition studies demonstrated that quinapril was a specific and potent inhibitor of PAH. The Ki of quinapril was about 20 microM, a value similar to that of probenecid and eight-times lower than the K(m) value of 165 microM for PAH. Even though quinapril resulted in trans-inhibition of PAH uptake during counterflow studies, kinetic studies revealed that quinapril was a competitive inhibitor of PAH transport. This latter findings suggests that quinapril and PAH share a common binding site on the transporter. Overall, the results indicate that quinapril is a high-affinity inhibitor of the organic anion transporter in renal BLMV, and that drug-drug interactions may occur with other organic anions at the basolateral membrane of proximal cells.

Indexed as

TetrahydroisoquinolinesAngiotensin-Converting Enzyme InhibitorsAnimalsBinding, CompetitiveBiological TransportCell MembraneIn Vitro TechniquesIsoquinolinesKidney CortexLiposomesMaleMolecular Structurep-Aminohippuric AcidQuinaprilRabbitsAngiotensin-Converting Enzyme InhibitorsIsoquinolinesLiposomesp-Aminohippuric AcidQuinaprilTetrahydroisoquinolines

Identifiers

PMID10098100
OpenAlexW2158203329

What OpenQuestion holds

Texttitle and abstract
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.