Evidence mapPaperPMID 34110521Full record

ReviewCurrent hypertension reports2021

New Insights into the Critical Importance of Intratubular Na

Jia Long Zhuo, Manoocher Soleimani, Xiao Chun Li

Open access · greenAbstract readReview
In one paragraph

Review in Current hypertension reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Identification of potential biomarkers for hypertension based on transcriptomic analysis in rats.Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    Article
  3. Article
  4. [Detection of pathogenic gene mutations in thirteen cases of congenital bilateral absence of vas deferens infertility patients].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2024
    Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. The Remaining Conundrum of the Role of the NaReviews in cardiovascular medicine · 2022
    Review
  10. The NaFrontiers in physiology · 2022
    Review
  11. Review
  12. 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

3 authors at 2 institutions in 1 country.

Jia Long ZhuoTulane Hypertension and Renal Center of Excellence and Department of Physiology, Tulane University School of Medicine, 1430 Tulane Avenue, New Orleans, LA, 70112, USA. jzhuo@tulane.edu.ORCID http://orcid.org/0000-0001-9477-9075
Manoocher SoleimaniDivision of Nephrology, Department of Internal Medicine, University of New Mexico College of Medicine, Albuquerque, NM, 87131, USA.
Xiao Chun LiTulane Hypertension and Renal Center of Excellence and Department of Physiology, Tulane University School of Medicine, 1430 Tulane Avenue, New Orleans, LA, 70112, USA. xli68@tulane.edu.
Tulane University · USUniversity of New Mexico · US

Funding

Role of Intracrine Angiotensin II in Kidney CellsR01DK067299 · TULANE UNIVERSITY OF LOUISIANA · 2004 to 2025
$1.2M
NHLBI NIH HHS R56 HL130988NIDDK NIH HHS R01 DK067299NIDDK NIH HHS R01 DK102429NIDDK NIH HHS R01 DK123144
6 · The paper itself

Abstract

purpose of reviewThe sodium (Na RECENT

findingsRecently, our and other laboratories have generated or used novel genetically modified mouse models with whole-body, kidney-specific, or proximal tubule-specific deletion of NHE3 to determine the critical roles and underlying mechanisms of NHE3 in maintaining basal BP homeostasis and the development of Ang II-induced hypertension at the whole-body, kidney, or proximal tubule levels. The new findings demonstrate that NHE3 contributes to about 10 to 15 mmHg to basal blood pressure levels, and that deletion of NHE3 at the whole-kidney or proximal tubule level, or pharmacological inhibition of NHE3 at the kidney level with an orally absorbable NHE3 inhibitor AVE-0657, attenuates ~ 50% of Ang II-induced hypertension in mice. The results support the proof-of-concept hypothesis that NHE3 plays critical roles in physiologically maintaining normal BP and in the development of Ang II-dependent hypertension. Our results also strongly suggest that NHE3 in the proximal tubules of the kidney may be therapeutically targeted to treat poorly controlled hypertension in humans.

Indexed as

HypertensionAngiotensin IIAnimalsHumansKidney Tubules, ProximalMiceSodium-Hydrogen Exchanger 3Sodium-Hydrogen ExchangersAngiotensin IISodium-Hydrogen Exchanger 3Sodium-Hydrogen ExchangersAngiotensin IIBlood pressureHypertensionNa+/H+ exchanger 3Proximal tubule

Identifiers

PMID34110521
PMCPMC8314783
OpenAlexW3170369116

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.