Evidence map›Paper›PMID 22322976›Full record

ArticleAmerican journal of physiology. Cell physiology2012

Thyroid hormone receptor-α and vascular function.

Ayako Makino, Hong Wang, Brian T Scott, Jason X-J Yuan, Wolfgang H Dillmann

Abstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. THRA1/PGC-1α/SIRT3 pathway regulates oxidative stress and is implicated in hypertension of maternal hypothyroid rat offspring.Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    Article
  3. Article
  4. Effects of T3 Administration onTransplant international : official journal of the European Society for Organ Transplantation · 2023
    Article
  5. The Clinical Spectrum of Resistance to Thyroid Hormone Alpha in Children and AdultsJournal of clinical research in pediatric endocrinology · 2021
    Review
  6. Article
  7. SGLT inhibitors attenuate NO-dependent vascular relaxation in the pulmonary artery but not in the coronary artery.American journal of physiology. Lung cellular and molecular physiology · 2015
    Article
  8. Article
  9. Review
  10. Article
  11. Inappropriate heat dissipation ignites brown fat thermogenesis in mice with a mutant thyroid hormone receptor α1.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  12. 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

5 authors.

Ayako MakinoSection of Endocrinology, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
Hong Wang
Brian T Scott
Jason X-J Yuan
Wolfgang H Dillmann

Funding

Heart Failure and Thyroid HormoneR01HL089938 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DILLMANN, WOLFGANG H · 2007 to 2010
$1.5M
Cellular and Molecular Mechanisms of Coronary Endothelial Dysfunction in DiabetesR01HL115578 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MAKINO, AYAKO · 2012 to 2015
$1.5M
Mechanisms of coronary endothelial dysfunction in diabetesK01DK083506 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MAKINO, AYAKO · 2009 to 2011
$366k
NHLBI NIH HHS HL-89938NHLBI NIH HHS R01 HL115578NIDDK NIH HHS DK-083506
6 · The paper itself

Abstract

Thyroid hormone (TH) treatment exerts beneficial effects on the cardiovascular system: it lowers cholesterol and LDL levels and enhances cardiac contractile function. However, little is known about the effect of TH on vascular function or the functional role of TH receptors (TRs) in the regulation of vascular tone. We have investigated the contribution of TRs to vascular contractility in the heart. Among different TR subtype-specific knockout (KO) mice, vascular contraction was significantly enhanced in coronary arteries isolated from TRα KO compared with wild-type mice, while chronic TH treatment significantly attenuated coronary vascular contraction. We found that TRα is the predominant TR in mouse coronary smooth muscle cells (SMCs). Coronary SMCs isolated from TRα KO mice exhibited a significant decrease in K(+) channel activity, whereas TH treatment increased K(+) channel activity in a dose-dependent manner. These data suggest that TRα in SMCs has prominent effects on regulation of vascular tone and TH treatment helps decrease coronary vascular tone by increasing K(+) channel activity through TRα in SMCs.

Indexed as

AnimalsBlotting, WesternCoronary VesselsFluorescent Antibody TechniqueMaleMiceMice, KnockoutPatch-Clamp TechniquesPolymerase Chain ReactionThyroid Hormone Receptors alphaTriiodothyronineThyroid Hormone Receptors alphaTriiodothyronine

Identifiers

PMID22322976
PMCPMC3361953

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.