Evidence map›Paper›PMID 29929989›Full record

ArticleJournal of the American Heart Association2018

Intestinal Mineralocorticoid Receptor Contributes to Epithelial Sodium Channel-Mediated Intestinal Sodium Absorption and Blood Pressure Regulation.

Toshifumi Nakamura, Isao Kurihara, Sakiko Kobayashi, Kenichi Yokota, Ayano Murai-Takeda, Yuko Mitsuishi, Mitsuha Morisaki, Nao Kohata, Yosuke Oshima, Yukiko Minami and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Observational
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Salt and Aldosterone - Reciprocal and Combined Effects in Preclinical Models and Humans.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2024
    Review
  12. IntestinalJournal of geriatric cardiology : JGC · 2023
    Article
  13. The Epithelial Sodium Channel-An Underestimated Drug Target.International journal of molecular sciences · 2023
    Review
  14. Article
  15. Cardiometabolic effects of DOCA-salt in male C57BL/6J mice are variably dependent on sodium and nonsodium components of diet.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Article
  16. Bile acids and salt-sensitive hypertension: a role of the gut-liver axis.American journal of physiology. Heart and circulatory physiology · 2022
    Review
  17. Lysine-specific demethylase 1 as a corepressor of mineralocorticoid receptor.Hypertension research : official journal of the Japanese Society of Hypertension · 2022
    Article
  18. Review
  19. Hyperkalemia in patients undergoing hemodialysis: Its pathophysiology and management.Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy · 2022
    Review
  20. Role of the microbiota in hypertension and antihypertensive drug metabolism.Hypertension research : official journal of the Japanese Society of Hypertension · 2022
    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

12 authors at 4 institutions in 1 country.

Toshifumi NakamuraDepartment of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Isao KuriharaDepartment of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan i-kuri@dc4.so-net.ne.jp.
Sakiko KobayashiDepartment of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Kenichi YokotaDepartment of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Ayano Murai-TakedaDepartment of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Yuko MitsuishiDepartment of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Mitsuha MorisakiDepartment of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Nao KohataDepartment of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Yosuke OshimaDepartment of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Yukiko MinamiDepartment of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Hirotaka ShibataDepartment of Endocrinology, Metabolism, Rheumatology and Nephrology, Faculty of Medicine, Oita University, Oita, Japan.
Hiroshi ItohDepartment of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Keio University · JPMitsui (Japan) · JPObayashi (Japan) · JPOita University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMineralocorticoid receptor (MR) has pathological roles in various cell types, including renal tubule cells, myocytes, and smooth muscle cells; however, the role of MR in intestinal epithelial cells (IECs) has not been sufficiently evaluated. The intestine is the sensing organ of ingested sodium; accordingly, intestinal MR is expected to have essential roles in blood pressure (BP) regulation. METHODS AND

resultsWe generated IEC-specific MR knockout (IEC-MR-KO) mice. With a standard diet, fecal sodium excretion was 1.5-fold higher in IEC-MR-KO mice, with markedly decreased colonic expression of β- and γ-epithelial sodium channel, than in control mice. Urinary sodium excretion in IEC-MR-KO mice decreased by 30%, maintaining sodium balance; however, a low-salt diet caused significant reductions in body weight and BP in IEC-MR-KO mice, and plasma aldosterone exhibited a compensatory increase. With a high-salt diet, intestinal sodium absorption markedly increased to similar levels in both genotypes, without an elevation in BP. Deoxycorticosterone/salt treatment elevated BP and increased intestinal sodium absorption in both genotypes. Notably, the increase in BP was significantly smaller in IEC-MR-KO mice than in control mice. The addition of the MR antagonist spironolactone to deoxycorticosterone/salt treatment eliminated the differences in BP and intestinal sodium absorption between genotypes.

conclusionsIntestinal MR regulates intestinal sodium absorption in the colon and contributes to BP regulation. These regulatory effects are associated with variation in epithelial sodium channel expression. These findings suggest that intestinal MR is a new target for studying the molecular mechanism of hypertension and cardiovascular diseases.

Indexed as

Blood PressureIntestinal AbsorptionAldosteroneAnimalsAntihypertensive AgentsColonDiet, Sodium-RestrictedDisease Models, AnimalEpithelial Sodium ChannelsFecesHypertensionIntestinal EliminationIntestinal MucosaMaleMice, KnockoutMineralocorticoid Receptor AntagonistsAldosteroneAntihypertensive AgentsEpithelial Sodium ChannelsMineralocorticoid Receptor AntagonistsNr3c2 protein, mouseReceptors, MineralocorticoidSodium Chloride, Dietaryaldosteronehypertensionintestinemineralocorticoidsnuclear receptorsodium channels

Identifiers

PMID29929989
PMCPMC6064907
OpenAlexW2808994892

What OpenQuestion holds

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LicenceCC BY-NC
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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.