Evidence map›Paper›PMID 32034107›Full record

ArticleJournal of the American Society of Nephrology : JASN2020

Two Mineralocorticoid Receptor-Mediated Mechanisms of Pendrin Activation in Distal Nephrons.

Nobuhiro Ayuzawa, Mitsuhiro Nishimoto, Kohei Ueda, Daigoro Hirohama, Wakako Kawarazaki, Tatsuo Shimosawa, Takeshi Marumo, Toshiro Fujita

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Pendrin is upregulated by corticosterone and participates in its pressor response.American journal of physiology. Renal physiology · 2026
    Article
  4. Review
  5. Review
  6. Novel functions of the anion exchanger AE4 (SLC4A9).Pflugers Archiv : European journal of physiology · 2024
    Review
  7. Angiotensin II acts through Rac1 to upregulate pendrin: role of NADPH oxidase.American journal of physiology. Renal physiology · 2024
    Article
  8. Article
  9. Review
  10. Pendrin regulation is prioritized by anion in high-potassium diets.American journal of physiology. Renal physiology · 2023
    Article
  11. Article
  12. Review
  13. Do not take a chance! We do not tell fortunes.Hypertension research : official journal of the Japanese Society of Hypertension · 2022
    Article
  14. Review
  15. Article
  16. 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

8 authors at 3 institutions in 1 country.

Nobuhiro AyuzawaDivision of Clinical Epigenetics, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan; Toshiro.FUJITA@rcast.u-tokyo.ac.jp ayuzawa-tky@umin.ac.jp.
Mitsuhiro NishimotoDivision of Clinical Epigenetics, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Kohei UedaDivision of Clinical Epigenetics, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.ORCID 0000-0002-9411-1611
Daigoro HirohamaDivision of Clinical Epigenetics, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Wakako KawarazakiDivision of Clinical Epigenetics, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Tatsuo ShimosawaDepartment of Clinical Laboratory, School of Medicine, International University of Health and Welfare, Chiba, Japan.
Takeshi MarumoDivision of Clinical Epigenetics, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Toshiro FujitaDivision of Clinical Epigenetics, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan; Toshiro.FUJITA@rcast.u-tokyo.ac.jp ayuzawa-tky@umin.ac.jp.ORCID 0000-0001-9141-7060
The University of Tokyo · JPInternational University of Health and Welfare · JPShinshu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRegulation of sodium chloride transport in the aldosterone-sensitive distal nephron is essential for fluid homeostasis and BP control. The chloride-bicarbonate exchanger pendrin in

methodsUsing mice with mineralocorticoid receptor deletion in intercalated cells, we examined the mechanism and roles of pendrin upregulation

resultsDeletion of mineralocorticoid receptor in intercalated cells suppressed the increase in renal pendrin expression induced by either exogenous angiotensin II infusion or endogenous angiotensin II upregulation

conclusionsIn conjunction with NCC, the two pathways of pendrin upregulation, induced by angiotensin II through mineralocorticoid receptor activation in intercalated cells and by alkalosis through mineralocorticoid receptor activation in principal cells, play important roles in fluid homeostasis during salt depletion and salt-sensitive hypertension mediated by aldosterone excess.

Indexed as

AldosteroneAnimalsDisease Models, AnimalHypertensionMiceMice, KnockoutNephronsReceptors, MineralocorticoidRenin-Angiotensin SystemSodium Chloride SymportersSulfate TransportersAldosteroneReceptors, MineralocorticoidSlc26a4 protein, mouseSodium Chloride SymportersSulfate Transportersaldosteroneangiotensin IIblood pressuremineralocorticoid receptorpendrinsodium chloride cotransporter

Identifiers

PMID32034107
PMCPMC7191922
OpenAlexW3004658028

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.