Evidence map›Paper›PMID 24721511›Full record

ArticleLife sciences2014

Tissue-specific and time-dependent regulation of the endothelin axis by the circadian clock protein Per1.

Jacob Richards, Amanda K Welch, Sarah J Barilovits, Sean All, Kit-Yan Cheng, Charles S Wingo, Brian D Cain, Michelle L Gumz

Open access · hybridAbstract read
In one paragraph

Article in Life sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

32 citing papers in PubMed, 40 citations in OpenAlex.

  1. Endothelin-1 signaling in the kidney: recent advances and remaining gaps.American journal of physiology. Renal physiology · 2025
    Review
  2. Review
  3. Recent advances in understanding the kidney circadian clock mechanism.American journal of physiology. Renal physiology · 2024
    Review
  4. Endothelin signaling in development.Development (Cambridge, England) · 2023
    Review
  5. Article
  6. Clock genes rescue nphp mutations in zebrafish.Human molecular genetics · 2022
    Article
  7. Review
  8. Article
  9. A wrinkle in time: circadian biology in pulmonary vascular health and disease.American journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  10. Circadian Control of Sodium and Blood Pressure Regulation.American journal of hypertension · 2021
    Review
  11. Article
  12. Review
  13. Frontiers in physiology · 2020
    Article
  14. Article
  15. Review
  16. Female C57BL/6J mice lacking the circadian clock protein PER1 are protected from nondipping hypertension.American journal of physiology. Regulatory, integrative and comparative physiology · 2019
    Article
  17. Review
  18. Circadian rhythms and the kidney.Nature reviews. Nephrology · 2018
    Review
  19. Article
  20. Review
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

8 authors at 2 institutions in 1 country.

Jacob RichardsDepartment of Medicine, University of Florida, USA; Department of Biochemistry and Molecular Biology, University of Florida, USA.
Amanda K WelchDepartment of Medicine, University of Florida, USA; North Florida/South Georgia Veterans Health System, Gainesville, FL, USA.
Sarah J BarilovitsDepartment of Medicine, University of Florida, USA; Department of Biochemistry and Molecular Biology, University of Florida, USA.
Sean AllDepartment of Medicine, University of Florida, USA.
Kit-Yan ChengDepartment of Medicine, University of Florida, USA.
Charles S WingoDepartment of Medicine, University of Florida, USA; North Florida/South Georgia Veterans Health System, Gainesville, FL, USA.
Brian D CainDepartment of Biochemistry and Molecular Biology, University of Florida, USA.
Michelle L GumzDepartment of Medicine, University of Florida, USA; Department of Biochemistry and Molecular Biology, University of Florida, USA. Electronic address: Michelle.Gumz@medicine.ufl.edu.
University of Florida · USNorth Florida/South Georgia Veterans Health System · US

Funding

Multidisciplinary Training Program in HypertensionT32HL083810 · NHLBI · UNIVERSITY OF FLORIDA · PI WOOD, CHARLES E · 2007 to 2017
$2.5M
PRE&POST-DOCTORAL TRAINING IN NEPHROLOGY&HYPERTENSIONT32DK007518 · NIDDK · UNIVERSITY OF FLORIDA · PI SEGAL, MARK S. · 1986 to 2011
$1.7M
An Aldosterone-Endothelin Feedback Mechanism on Sodium HomeostasisR01DK082680 · NIDDK · UNIVERSITY OF FLORIDA · PI CAIN, BRIAN D., WINGO, CHARLES S · 2009 to 2012
$1.2M
A Functional Role for the Circadian Clock Protein Per1 in the Regulation of ??ENaK01DK085193 · NIDDK · UNIVERSITY OF FLORIDA · PI GUMZ, MICHELLE L · 2010 to 2014
$625k
Blood Pressure Regulation by the Circadian Clock Protein Per1R03DK098460 · NIDDK · UNIVERSITY OF FLORIDA · PI GUMZ, MICHELLE L · 2013 to 2014
$149k
NCATS NIH HHS L30 TR001247NHLBI NIH HHS 2T32HL083810NHLBI NIH HHS T32 HL083810NIDDK NIH HHS DK082680NIDDK NIH HHS DK085193NIDDK NIH HHS DK098460NIDDK NIH HHS K01 DK085193NIDDK NIH HHS L30 DK096643NIDDK NIH HHS R01 DK082680NIDDK NIH HHS R03 DK098460NIDDK NIH HHS T32 DK007518
6 · The paper itself

Abstract

aimsThe present study is designed to consider a role for the circadian clock protein Per1 in the regulation of the endothelin axis in mouse kidney, lung, liver and heart. Renal endothelin-1 (ET-1) is a regulator of the epithelial sodium channel (ENaC) and blood pressure (BP), via activation of both endothelin receptors, ETA and ETB. However, ET-1 mediates many complex events in other tissues. MAIN

methodsTissues were collected in the middle of murine rest and active phases, at noon and midnight, respectively. ET-1, ETA and ETB mRNA expressions were measured in the lung, heart, liver, renal inner medulla and renal cortex of wild type and Per1 heterozygous mice using real-time quantitative RT-PCR. KEY

findingsThe effect of reduced Per1 expression on levels of mRNAs and the time-dependent regulation of expression of the endothelin axis genes appeared to be tissue-specific. In the renal inner medulla and the liver, ETA and ETB exhibited peaks of expression in opposite circadian phases. In contrast, expressions of ET-1, ETA and ETB in the lung did not appear to vary with time, but ET-1 expression was dramatically decreased in this tissue in Per1 heterozygous mice. Interestingly, ET-1 and ETA, but not ETB, were expressed in a time-dependent manner in the heart. SIGNIFICANCE: Per1 appears to regulate expression of the endothelin axis genes in a tissue-specific and time-dependent manner. These observations have important implications for our understanding of the best time of day to deliver endothelin receptor antagonists.

Indexed as

Circadian ClocksOrgan SpecificityAnimalsEndothelin-1EndothelinsGene Expression ProfilingGene Expression RegulationKidneyMicePeriod Circadian ProteinsReceptor, Endothelin AReceptor, Endothelin BRNA, MessengerTime FactorsEndothelin-1EndothelinsPer1 protein, mousePeriod Circadian ProteinsReceptor, Endothelin AReceptor, Endothelin BRNA, MessengerEndothelin-A receptorEndothelin-B receptorETAETBGene regulation

Identifiers

PMID24721511
PMCPMC4387882
OpenAlexW2017513433

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.