Evidence map›Paper›PMID 40505410›Full record

ArticleDrug metabolism and disposition: the biological fate of chemicals2025

Comparative transcriptomic profiling of drug-metabolizing enzymes and drug transporters in rabbit ocular subtissues, liver, and duodenum.

Mengyue Li, Brian J Sanderson, Jennifer Leigh Hackett, Sayuri Sammanani Niyangoda, Huan Gong, Michael A Johnson, Michael Zhuo Wang

Abstract readComparative Study
In one paragraph

Article in Drug metabolism and disposition: the biological fate of chemicals, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Characterization of hydrolase activity in ocular tissues of humans and preclinical species.Drug metabolism and disposition: the biological fate of chemicals · 2025
    Article
4 · The record

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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

7 authors.

Mengyue LiDepartment of Pharmaceutical Chemistry, School of Pharmacy, University of Kansas, Lawrence, Kansas, USA.
Brian J SandersonDepartment of Molecular Biosciences, University of Kansas, Lawrence, Kansas, USA.
Jennifer Leigh HackettGenome Sequencing Core, University of Kansas, Lawrence, Kansas, USA.
Sayuri Sammanani NiyangodaDepartment of Chemistry, College of Liberal Arts & Sciences, University of Kansas, Lawrence, Kansas, USA.
Huan GongDepartment of Pharmaceutical Chemistry, School of Pharmacy, University of Kansas, Lawrence, Kansas, USA.
Michael A JohnsonDepartment of Chemistry, College of Liberal Arts & Sciences, University of Kansas, Lawrence, Kansas, USA.
Michael Zhuo WangDepartment of Pharmaceutical Chemistry, School of Pharmacy, University of Kansas, Lawrence, Kansas, USA. Electronic address: michael.wang@ku.edu.

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Douglas E Wright · 2012 to 2026
$63.0M
Synthetic Chemical Biology CoreP30GM145499 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI Susan M Lunte · 2022 to 2026
$6.9M
NIGMS NIH HHS P20 GM103418NIGMS NIH HHS P30 GM145499
6 · The paper itself

Abstract

The increasing prevalence of diabetes and the aging population have led to a growing market for ophthalmic pharmaceutical drugs. However, the development of ophthalmic drugs is hampered by the poor understanding of drug-metabolizing enzymes (DMEs) and drug transporters (DTs) in complex ocular tissues. The rabbit is the most commonly used preclinical model for human ocular diseases. The purpose of this study was to compare relative gene expression of DMEs and DTs in various rabbit ocular subtissues, including cornea, iris-ciliary body, vitreous humor, and retina-choroid complex. Rabbit liver and duodenum samples were also included to investigate gene expression differences among the eye, liver, and duodenum. The mRNA transcriptome of the 6 tissue types from 6 rabbits (3 males and 3 females) was sequenced in a single run using RNA-seq for cross-tissue gene expression comparisons. A total of 387 DME and 128 DT genes were identified across the 6 tissues, and distinct expression patterns of DME and DT genes were observed between ocular subtissues vs. liver and duodenum and among different ocular subtissues. Furthermore, specific DMEs and DTs that enriched in each tissue type were identified and relative gene expression of DMEs and DTs across the 6 tissue types was measured. These results are expected to aid ophthalmic drug development by providing a basis for ocular tissue-specific drug disposition/response and informing model-based predictions and interspecies extrapolation. SIGNIFICANCE STATEMENT: This study represents the first comprehensive comparative transcriptomic analysis of drug-metabolizing enzymes and drug transporters in rabbit ocular subtissues, with comparisons to key metabolic organs such as liver and duodenum. Our findings highlight critical tissue-specific differences that have significant implications for ophthalmic drug development and ocular drug delivery systems. The quantitative gene expression levels of drug-metabolizing enzymes and drug transporters in the rabbit eye will aid investigations into ocular drug metabolism and disposition in both preclinical and clinical settings.

Indexed as

DuodenumEyeLiverMembrane Transport ProteinsTranscriptomeAnimalsFemaleGene Expression ProfilingInactivation, MetabolicMaleRabbitsMembrane Transport ProteinsDrug metabolismDrug transporterOcularRNA-seqTranscriptomics

Identifiers

PMID40505410
PMCPMC12405909

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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.