Evidence map›Paper›PMID 41715286›Full record

ArticleBiopharmaceutics & drug disposition2026

Ampicillin Is a Substrate of Organic Anion Transporters 3.

Yu-Ting Liu, Xue-Yan Gou, Lu Gan, Yi-Mai MaLiu, Yan-Rong Ma, Xin-An Wu

Abstract read
In one paragraph

Article in Biopharmaceutics & drug disposition, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yu-Ting LiuSchool of Pharmacy, Lanzhou University, Lanzhou, Gansu, China.
Xue-Yan GouThe First Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Lu GanSchool of Pharmacy, Lanzhou University, Lanzhou, Gansu, China.
Yi-Mai MaLiuSchool of Basic Medical Sciences, Lanzhou University, Lanzhou, Gansu, China.
Yan-Rong MaDepartment of Pharmacy, The First Hospital of Lanzhou University, Lanzhou, Gansu, China.
Xin-An WuDepartment of Pharmacy, The First Hospital of Lanzhou University, Lanzhou, Gansu, China.

Funding

Joint Funds of the National Natural Science Foundation of China No. U21A20424
6 · The paper itself

Abstract

Ampicillin (AMP) is an organic anion drug widely used in clinical setting as a β-lactam antibiotic. However, the specific transporter involved in mediating AMP transport remains unidentified. Thus, we investigated whether organic anion transporters1/3 (OAT1/3) mediate the renal transport of AMP in this study. Both rOAT1/OAT3 (Slc22a6/Slc22a8) double-knockout and wild-type (WT) rats were administered AMP via intraperitoneal injection simultaneously. Following the knockout, a significant increase in AMP plasma concentration and the area under the plasma concentration-time curve (AUC) was observed, accompanied by a marked reduction in cumulative urinary excretion. OAT1/3-overexpressing cell uptake experiments demonstrated that AMP is a substrate of OAT3, with a Michaelis-Menten constant (K

Indexed as

AmpicillinAnti-Bacterial AgentsOrganic Anion Transporters, Sodium-IndependentAnimalsBiological TransportHEK293 CellsHumansKidneyMaleOrganic Anion Transport Protein 1Rats, Sprague-DawleyAmpicillinAnti-Bacterial AgentsOrganic Anion Transporters, Sodium-IndependentOrganic Anion Transport Protein 1organic anion transport protein 3Slc22a6 protein, ratampicillindrug‐drug interactiongene knockoutOAT1OAT3

Identifiers

PMID41715286
PMCPMC13471976

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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.