Evidence map›Paper›PMID 41987231›Full record

ArticleBMC veterinary research2026

Erythrocyte sequestration of metformin in horses: impact on matrix-specific pharmacokinetics and detection windows.

Megan E Jacobs, Jeff Blea, Michael Hardy, Daniel S McKemie, Megan Traynham, Heather K Knych

Abstract read
In one paragraph

Article in BMC veterinary research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

  1. 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

6 authors.

Megan E JacobsK.L. Maddy Equine Analytical Chemistry Laboratory (Pharmacology Section), University of California, Davis, School of Veterinary Medicine, 620 West Health Science Drive, Davis, CA, 95616, USA.
Jeff BleaSchool of Veterinary Medicine, University of California, Davis, USA.
Michael HardyRacing Medication and Testing Consortium, Lexington, KY, USA.
Daniel S McKemieK.L. Maddy Equine Analytical Chemistry Laboratory (Pharmacology Section), University of California, Davis, School of Veterinary Medicine, 620 West Health Science Drive, Davis, CA, 95616, USA.
Megan TraynhamK.L. Maddy Equine Analytical Chemistry Laboratory (Pharmacology Section), University of California, Davis, School of Veterinary Medicine, 620 West Health Science Drive, Davis, CA, 95616, USA.
Heather K KnychK.L. Maddy Equine Analytical Chemistry Laboratory (Pharmacology Section), University of California, Davis, School of Veterinary Medicine, 620 West Health Science Drive, Davis, CA, 95616, USA. hkknych@ucdavis.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetformin is used for the treatment of type 2 diabetes and is one of the most prescribed medications in human medicine. It is less commonly prescribed in equine medicine, and its use is tightly regulated in several performance horse disciplines. In horseracing, it is considered a banned substance. A previous pharmacokinetic study of metformin in horses demonstrated a prolonged, unpredictable elimination phase. In the current study it was hypothesized that this was due to sequestration of metformin in a “deep” compartment, specifically red blood cells. This could result in pharmacokinetic differences between blood matrices (i.e. blood and serum). The objective of the current study was to assess red blood cell partitioning and the concentrations of metformin in different blood matrices following oral administration to horses. To that end, six horses received a single 15 g oral dose of metformin and plasma, serum, whole blood, red blood cells, and urine samples were collected starting at 5 min until 31 days post administration. Concentrations of metformin were determined using liquid chromatography-tandem mass spectrometry, and pharmacokinetic analysis performed.

resultsRed blood cells act as a reservoir for metformin in horses with the average blood to plasma ratio ranging from < 1 to > 10 at the later time points. The terminal half-life (mean ± SD) was 14.7 ± 7.25, 75.4 ± 32.2 and 49.1 ± 7.01 in plasma, serum, and red blood cells, respectively. The difference between serum and plasma concentrations was > 15% at several time points, especially at the later times. Concentrations in urine samples, fluctuated unpredictably over time.

conclusionRed blood cells act as a reservoir for metformin leading to a prolonged detection time, necessitating an extended withdrawal time for oral administration prior to competition in performance horses to prevent inadvertent positive drug tests. Additionally, differences in metformin concentrations across various biological matrices may preclude the extrapolation of data from one sample type to another.

Indexed as

ErythrocytesHypoglycemic AgentsMetforminAdministration, OralAnimalsFemaleHalf-LifeHorsesMaleHypoglycemic AgentsMetforminDetection windowErythrocyte partitioningMatrix effectMetforminPerformance horsePharmacokinetics

Identifiers

PMID41987231
PMCPMC13214104

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Registered trials

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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.