Evidence map›Paper›PMID 24154698›Full record

ArticleAmerican journal of physiology. Renal physiology2013

A role for the circadian clock protein Per1 in the regulation of aldosterone levels and renal Na+ retention.

Jacob Richards, Kit-Yan Cheng, Sean All, George Skopis, Lauren Jeffers, I Jeanette Lynch, Charles S Wingo, Michelle L Gumz

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

36 citing papers in PubMed, 64 citations in OpenAlex.

  1. Current perspective on circadian function of the kidney.American journal of physiology. Renal physiology · 2024
    Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Circadian Control of Sodium and Blood Pressure Regulation.American journal of hypertension · 2021
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Loss of circadian geneAmerican journal of physiology. Renal physiology · 2020
    Article
  17. Review
  18. Article
  19. 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
  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 1 institution in 1 country.

Jacob Richards1600 SW Archer Rd., Box 100224, Gainesville, FL 32610. Michelle.Gumz@medicine.ufl.edu.
Kit-Yan Cheng
Sean All
George Skopis
Lauren Jeffers
I Jeanette Lynch
Charles S Wingo
Michelle L Gumz
University of Florida · US

Funding

PRE&POST-DOCTORAL TRAINING IN NEPHROLOGY&HYPERTENSIONT32DK007518 · NIDDK · UNIVERSITY OF FLORIDA · PI SEGAL, MARK S. · 1986 to 2011
$1.7M
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
NIDDK NIH HHS DK-085193NIDDK NIH HHS DK-098460NIDDK NIH HHS K01 DK085193NIDDK NIH HHS L30 DK096643NIDDK NIH HHS R03 DK098460NIDDK NIH HHS T32 DK007518
6 · The paper itself

Abstract

The circadian clock plays an important role in the regulation of physiological processes, including renal function and blood pressure. We have previously shown that the circadian protein period (Per)1 regulates the expression of multiple Na(+) transport genes in the collecting duct, including the α-subunit of the renal epithelial Na(+) channel. Consistent with this finding, Per1 knockout mice exhibit dramatically lower blood pressure than wild-type mice. We have also recently demonstrated the potential opposing actions of cryptochrome (Cry)2 on Per1 target genes. Recent work by others has demonstrated that Cry1/2 regulates aldosterone production through increased expression of the adrenal gland-specific rate-limiting enzyme 3β-dehydrogenase isomerase (3β-HSD). Therefore, we tested the hypothesis that Per1 plays a role in the regulation of aldosterone levels and renal Na(+) retention. Using RNA silencing and pharmacological blockade of Per1 nuclear entry in the NCI-H295R human adrenal cell line, we showed that Per1 regulates 3β-HSD expression in vitro. These results were confirmed in vivo: mice with reduced levels of Per1 had decreased levels of plasma aldosterone and decreased mRNA expression of 3β-HSD. We postulated that mice with reduced Per1 would have a renal Na(+)-retaining defect. Indeed, metabolic cage experiments demonstrated that Per1 heterozygotes excreted more urinary Na(+) compared with wild-type mice. Taken together, these data support the hypothesis that Per1 regulates aldosterone levels and that Per1 plays an integral role in the regulation of Na(+) retention.

Indexed as

3-Hydroxysteroid DehydrogenasesAdrenal GlandsAldosteroneAnimalsCell LineCells, CulturedCryptochromesHumansIn Vitro TechniquesKidneyMaleMiceMice, KnockoutModels, AnimalPeriod Circadian ProteinsRNA, Small Interfering3-Hydroxysteroid DehydrogenasesAldosteroneCRY2 protein, humanCry2 protein, mouseCryptochromesPER1 protein, humanPer1 protein, mousePeriod Circadian ProteinsRNA, Small InterferingSodiumaldosteronecircadian clockkidneyperiod 1sodium transport

Identifiers

PMID24154698
PMCPMC3882450
OpenAlexW2100229060

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.