Evidence map›Paper›PMID 30101218›Full record

ArticleVessel plus2018

Immunohistochemistry of the circadian clock in mouse and human vascular tissues.

Ciprian B Anea, Ana M Merloiu, David J R Fulton, Vijay Patel, R Dan Rudic

Open access · diamondAbstract read
In one paragraph

Article in Vessel plus, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. A wrinkle in time: circadian biology in pulmonary vascular health and disease.American journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  5. Review
  6. Article
  7. Old and New Roles and Evolving Complexities of Cardiovascular Clocks.The Yale journal of biology and medicine · 2019
    Review
  8. 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 at 1 institution in 1 country.

Ciprian B AneaDepartment of Pharmacology & Toxicology, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.
Ana M MerloiuDepartment of Pharmacology & Toxicology, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.
David J R FultonDepartment of Pharmacology & Toxicology, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.
Vijay PatelDepartment of Surgery, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.
R Dan RudicDepartment of Pharmacology & Toxicology, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.
Augusta University · US

Funding

Galectin-3: A mediator of vascular remodeling in pulmonary arterial hypertensionR01HL125926 · NHLBI · AUGUSTA UNIVERSITY · PI BARMAN, SCOTT A, FULTON, DAVID J · 2016 to 2025
$4.9M
TACE and Clock mechanisms in aging and vascular stiffeningR01AG054651 · NIA · AUGUSTA UNIVERSITY · PI BAGI, ZSOLT, RUDIC, RADU DANIEL · 2017 to 2021
$2.6M
NHLBI NIH HHS R01 HL125926NIA NIH HHS R01 AG054651
6 · The paper itself

Abstract

Aim: The circadian clock is a molecular network that controls the body physiological rhythms. In blood vessels, the circadian clock components modulate vascular remodeling, blood pressure, and signaling. The goal in this study was to determine the pattern of expression of circadian clock proteins in the endothelium, smooth muscle, and adventitia of the vasculature of human and mouse tissues. Methods: Immunohistochemistry was performed in frozen sections of mouse aorta, common carotid artery, femoral artery, lung, and heart at 12 AM and 12 PM for Bmal1, Clock, Npas2, Per and other clock components. Studies of expression were also assessed in human saphenous vein both by immunoblotting and immunohistochemistry. Results: In this study, we identified the expression of Bmal1, Clock, Npas, Per1, Cry1, and accessory clock components by immunohistochemical staining in the endothelium, smooth muscle and adventitia of the mouse vasculature with differing temporal and cellular profiles depending on vasculature and tissue analyzed. The human saphenous vein also exhibited expression of clock genes that exhibited an oscillatory pattern in Bmal1 and Cry by immunoblotting. Conclusion: These studies show that circadian clock components display differences in expression and localization throughout the cardiovascular system, which may confer nuances of circadian clock signaling in a cell-specific manner.

Indexed as

aortaBmal1Circadian blood vesselClockCryhumanmousePersmooth musclevascular endothelium

Identifiers

PMID30101218
PMCPMC6085090
OpenAlexW2884800111

What OpenQuestion holds

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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.