Evidence map›Paper›PMID 42213650›Full record

ArticleAmerican journal of physiology. Renal physiology2026

Transcriptomics of S3 segment in mice: response to type 1 diabetes, SGLT1/2 inhibition, or GLP1 receptor agonism.

Young Chul Kim, Chen Meng, Sadhana Kanoo, Scott Thomson, Anil Karihaloo, Volker Vallon

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

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.

Young Chul KimDivision of Nephrology and Hypertension, Department of Medicine, University of California San Diego, La Jolla, California, United States.ORCID 0000-0002-6782-2186
Chen MengNovo Nordisk A/S, Måløv, Denmark.
Sadhana KanooDivision of Nephrology and Hypertension, Department of Medicine, University of California San Diego, La Jolla, California, United States.
Scott ThomsonDivision of Nephrology and Hypertension, Department of Medicine, University of California San Diego, La Jolla, California, United States.ORCID 0000-0001-8853-0505
Anil KarihalooNovo Nordisk, Lexington, Massachusetts, United States.
Volker VallonDivision of Nephrology and Hypertension, Department of Medicine, University of California San Diego, La Jolla, California, United States.ORCID 0000-0002-9211-2063

Funding

UAB-UCSD O'Brien Center for Acute Kidney Injury ResearchU54DK137307 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Javier A. Neyra · 2023 to 2026
$4.4M
Glomerular and Tubular Function in the Diabetic KidneyR01DK112042 · NIDDK · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI SCOTT Culver THOMSON, Volker Vallon · 2017 to 2026
$4.1M
Resource-based Center for the study of the joint microenvironment in rheumatology (Overall Application)P30AR073761 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CORR, MARY P · 2018 to 2022
$3.9M
Illumina NovaSeq 6000 Sequencing SystemS10OD026929 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JEPSEN, KRISTEN LYNN · 2019 to 2019
$600k
HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) R01DK112042HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) U54DK137307NIAMS NIH HHS P30 AR073761NIDDK NIH HHS R01 DK112042NIDDK NIH HHS U54 DK137307NIH HHS S10 OD026929
6 · The paper itself

Abstract

Inhibitors of SGLT2 (SGLT2is) and diabetes enhance glucose delivery and reabsorption in late proximal tubule S3 segments. Molecular consequences remain poorly understood. Here, we determined transcriptomic changes in S3 segments of male adult DBA wild-type (WT) and littermate diabetic Akita mice ± Sglt1 knockout (Sglt1-KO) given vehicle or SGLT2i dapagliflozin for 2 wk, and in Akita mice receiving glucagon-like peptide-1 receptor (GLP1R) agonist (GLP1RA) semaglutide. RNA sequencing was performed in S3 segments isolated by immunostaining-guided laser-capture-microdissection in deep cortex/outer medulla. Among 19,068 detected annotated genes, 838 genes were differentially expressed by SGLT2is in WT (differentially expressed genes; DEGs;

Indexed as

Diabetes Mellitus, Type 1Glucagon-Like Peptide-1 Receptor AgonistsKidney Tubules, ProximalSodium-Glucose Transporter 2 InhibitorsTranscriptomeAnimalsBlood GlucoseCell ProliferationDisease Models, AnimalGene Expression ProfilingGlucagon-Like Peptide-1 ReceptorGlucagon-Like PeptidesMaleMiceMice, KnockoutSemaglutideBlood GlucoseGlp1r protein, mouseGlucagon-Like Peptide-1 ReceptorGlucagon-Like Peptide-1 Receptor AgonistsGlucagon-Like PeptidesSemaglutideSlc5a1 protein, mouseSlc5a2 protein, mouseSodium-Glucose Transporter 1Sodium-Glucose Transporter 2Sodium-Glucose Transporter 2 InhibitorsGLP1 receptor agonistlate proximal tubuleRNA-seqSGLT1SGLT2 inhibitor

Identifiers

PMID42213650
PMCPMC13339211

What OpenQuestion holds

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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.