Evidence map›Paper›PMID 26379554›Full record

ArticleFrontiers in physiology2015

Functional aortic stiffness: role of CD4(+) T lymphocytes.

Beenish A Majeed, Lance S Eberson, Supannikar Tawinwung, Nicolas Larmonier, Timothy W Secomb, Douglas F Larson

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact, top 97% of its field
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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. The role of T cells in vascular aging, hypertension, and atherosclerosis.American journal of physiology. Heart and circulatory physiology · 2024
    Review
  4. 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 at 1 institution in 1 country.

Beenish A MajeedSarver Heart Center, College of Medicine, The University of Arizona Tucson, AZ, USA ; Department of Pharmacology, College of Medicine, The University of Arizona Tucson, AZ, USA.
Lance S EbersonSarver Heart Center, College of Medicine, The University of Arizona Tucson, AZ, USA.
Supannikar TawinwungSarver Heart Center, College of Medicine, The University of Arizona Tucson, AZ, USA ; Department of Pharmacology, College of Medicine, The University of Arizona Tucson, AZ, USA.
Nicolas LarmonierDepartments of Pediatrics and Immunology, College of Medicine, The University of Arizona Tucson, AZ, USA.
Timothy W SecombDepartment of Physiology, College of Medicine, The University of Arizona Tucson, AZ, USA.
Douglas F LarsonSarver Heart Center, College of Medicine, The University of Arizona Tucson, AZ, USA ; Department of Pharmacology, College of Medicine, The University of Arizona Tucson, AZ, USA ; Department of Physiology, College of Medicine, The University of Arizona Tucson, AZ, USA ; Department of Surgery, College of Medicine, The University of Arizona Tucson, AZ, USA.
University of Arizona · US

Funding

Blocking Hypertension by Regulatory T-lymphocytesR01HL105280 · NHLBI · UNIVERSITY OF ARIZONA · PI LARSON, DOUGLAS F · 2010 to 2013
$1.5M
NHLBI NIH HHS R01 HL105280
6 · The paper itself

Abstract

The immune system is suggested to be essential in vascular remodeling and stiffening. To study the dependence upon lymphocytes in vascular stiffening, we compared an angiotensin II-model of vascular stiffening in normal C57BL/6J mice with lymphocyte-deficient RAG 1(-/-) mice and additionally characterized the component of vascular stiffness due to vasoconstriction vs. vascular remodeling. Chronic angiotensin II increased aortic pulse wave velocity, effective wall stiffness, and effective Young's modulus in C57BL/6J mice by three-fold but caused no change in the RAG 1(-/-) mice. These functional measurements were supported by aortic morphometric analysis. Adoptive transfer of CD4(+) T helper lymphocytes restored the angiotensin II-mediated aortic stiffening in the RAG 1(-/-) mice. In order to account for the hydraulic vs. material effects of angiotensin II on pulse wave velocity, subcutaneous osmotic pumps were removed after 21 days of angiotensin II-infusion in the WT mice to achieve normotensive values. The pulse wave velocity (PWV) decreased from three- to two-fold above baseline values up to 7 days following pump removal. This study supports the pivotal role of the CD4(+) T-lymphocytes in angiotensin II-mediated vascular stiffening and that angiotensin II-mediated aortic stiffening is due to the additive effect of active vascular smooth muscle vasoconstriction and vascular remodeling.

Indexed as

angiotensin IIlymphocytespulse wave velocityvascular remodelingvasoconstriction

Identifiers

PMID26379554
PMCPMC4549563
OpenAlexW1605684907

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.