Evidence map›Paper›PMID 39927881›Full record

ArticleJournal of hypertension2025

Thermoneutral-housed rats demonstrate impaired perivascular adipose tissue and vascular crosstalk.

Melissa M Henckel, Ji Hye Chun, Leslie A Knaub, Gregory B Pott, Georgia E James, Kendall S Hunter, Robin Shandas, Lori A Walker, Jane E-B Reusch, Amy C Keller

Abstract read
In one paragraph

Article in Journal of hypertension, 2025. 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
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.

  1. Review
  2. Mechanotransduction in the Perivascular Adipose Tissue.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Melissa M HenckelDivision of Endocrinology, Metabolism & Diabetes, University of Colorado Anschutz Medical Campus.
Ji Hye ChunDivision of Endocrinology, Metabolism & Diabetes, University of Colorado Anschutz Medical Campus.
Leslie A KnaubDivision of Endocrinology, Metabolism & Diabetes, University of Colorado Anschutz Medical Campus.
Gregory B PottDivision of Endocrinology, Metabolism & Diabetes, University of Colorado Anschutz Medical Campus.
Georgia E JamesUniversity of Iowa, Iowa City, Iowa.
Kendall S HunterDepartment of Bioengineering.
Robin ShandasDepartment of Bioengineering.
Lori A WalkerDivision of Cardiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Jane E-B ReuschDivision of Endocrinology, Metabolism & Diabetes, University of Colorado Anschutz Medical Campus.
Amy C KellerDivision of Endocrinology, Metabolism & Diabetes, University of Colorado Anschutz Medical Campus.

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025780 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2008 to 2011
$61.3M
PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI BRYAN C BERGMAN · 1995 to 2026
$32.6M
Role of Microvascular insulin resistance and cardiorespiratory fitness in diabetesR01DK124344 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI ZHENQI LIU, JUDITH G. REGENSTEINER · 2021 to 2026
$3.5M
BLRD VA I01 BX002046BLRD VA I01 BX005840BLRD VA IK2 BX003185NCRR NIH HHS UL1 RR025780NIDDK NIH HHS P30 DK048520NIDDK NIH HHS R01 DK124344
6 · The paper itself

Abstract

objectiveVascular pathology, characterized by impaired vasoreactivity and mitochondrial respiration, differs between the sexes. Housing rats under thermoneutral (TN) conditions causes vascular dysfunction and perturbed metabolism. We hypothesized that thoracic perivascular adipose tissue (tPVAT), a vasoregulatory adipose depot known to have a brown adipose tissue (BAT) phenotype, remodels to a mainly white adipose (WAT) phenotype in rats housed at TN, driving diminished vasoreactivity in a sex-dependent manner.

methodsMale and female Wistar rats were housed at either room temperature (RT) or TN. We measured changes in tPVAT morphology, vasoreactivity in vessels with intact tPVAT or transferred to tPVAT of the oppositely-housed animal, vessel stiffness, vessel mitochondrial respiration and cellular signaling.

resultsRemodeling of tPVAT was observed in rats housed at TN; animals in this environment showed tPVAT whitening and displayed diminished aortae vasodilation ( P  < 0.05), different between the sexes. Juxtaposing tPVAT from RT rats onto aortae from TN rats in females corrected vasodilation ( P  < 0.05); this did not occur in males. In aortae of all animals housed at TN, mitochondrial respiration was significantly diminished in lipid substrate experiments ( P  < 0.05), and there was significantly less expression of phosphorylated endothelial nitric oxide synthase (peNOS) ( P  < 0.001).

conclusionsThese data are consistent with TN-induced remodeling of tPVAT, notably associated with sex-specific blunting of vasoreactivity, diminished mitochondrial respiration, and altered cellular signaling.

Indexed as

Adipose TissueAdipose Tissue, BrownAnimalsFemaleMaleMitochondriaNitric Oxide Synthase Type IIIRatsRats, WistarTemperatureVasodilationNitric Oxide Synthase Type III

Identifiers

PMID39927881
PMCPMC11970602

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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.