Evidence map›Paper›PMID 38106229›Full record

ArticlebioRxiv : the preprint server for biology2023

Epithelial N-methyl-D-aspartate (NMDA) receptors mediate renal vasodilation by affecting kidney autoregulation.

Cesar A Romero, Jasmine Lim, Hong Wang, Brandi M Wynne, Peipei Ma, Yao Jing, Dennis C Liotta, Michael D'Erasmo, Stephen F Traynelis, Douglas C Eaton and 1 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 3 institutions in 1 country.

Cesar A RomeroRenal Division, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
Jasmine LimRenal Division, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
Hong WangHypertension and Vascular Research Division, Department of Medicine, Henry Ford Health Systems, Detroit, Michigan, USA.
Brandi M WynneDivision of Nephrology, Department of Internal Medicine, School of Medicine, Department of Nutrition and Integrative Physiology, and Immunology, Inflammation and Infectious Disease Initiative, University of Utah, Salt Lake City, Utah, USA.
Peipei MaDepartment of Chemistry, Emory College of Arts and Sciences, Emory University, Atlanta, Georgia, USA.
Yao JingDepartment of Chemistry, Emory College of Arts and Sciences, Emory University, Atlanta, Georgia, USA.
Dennis C LiottaDepartment of Chemistry, Emory College of Arts and Sciences, Emory University, Atlanta, Georgia, USA.
Michael D'ErasmoDepartment of Chemistry, Emory College of Arts and Sciences, Emory University, Atlanta, Georgia, USA.
Stephen F TraynelisDepartment of Pharmacology and Chemical Biology, School of Medicine, Emory University, Atlanta, Georgia, USA.
Douglas C EatonRenal Division, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
Susan M WallRenal Division, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
Emory University · USHenry Ford Health System · USUniversity of Utah · US

Funding

Neuro HPA Project 1U54AG062334 · NIA · EMORY UNIVERSITY · PI Ighovwerha Ofotokun · 2018 to 2026
$12.2M
Regulation of intercalated cell function by the mineralocorticoid receptorR01DK119793 · NIDDK · EMORY UNIVERSITY · PI WALL, SUSAN MARIE · 2019 to 2022
$1.6M
Regulation of Sodium Transport in Tight EpitheliaR01DK110409 · NIDDK · EMORY UNIVERSITY · PI EATON, DOUGLAS C. · 2018 to 2021
$1.4M
Aldosterone Independent Activation of the Mineralocorticoid Receptor via IL-6 and Rac1 Induces Sodium Retention and HypertensionK01DK115660 · NIDDK · UNIVERSITY OF UTAH · PI WYNNE, BRANDI MICHELE · 2018 to 2022
$1.0M
N-methyl-D-aspartate receptors (NMDAr) participates in renal hemodynamic regulation and blood pressure homeostasisK01HL155235 · NHLBI · EMORY UNIVERSITY · PI ROMERO, CESAR ANDRES · 2021 to 2025
$559k
NHLBI NIH HHS K01 HL155235NIA NIH HHS U54 AG062334NIDDK NIH HHS K01 DK115660NIDDK NIH HHS R01 DK110409NIDDK NIH HHS R01 DK119793
6 · The paper itself

Abstract

Background: N-methyl-D-aspartate receptor (NMDAR) are amino acid receptors that are well studied in brain physiology; however, their role in kidney is poorly understood. Nonetheless, NMDAR inhibitors can increase serum K+ and reduce GFR, which suggests they have an important physiological role in the kidney. We hypothesized that NMDARs in the distal nephron induce afferent-arteriole vasodilation through the vasodilator mechanism connecting-tubule-glomerular feedback (CNTGF) that involves ENaC activation. Methods and results: Using a tubule-specific transcriptome database combined with molecular biology and microscopy techniques, we showed kidney expression of NMDAR subunits along the nephron and specifically in ENaC-positive cells. This receptor is expressed in both male and female mice, with higher abundance in females (p=0.02). Microperfusing NMDAR agonists into the connecting tubule induced afferent-arteriole vasodilation (EC Conclusion: NMDARs are expressed along the nephron, including ENaC-positive cells, with higher expression in females. Epithelial NMDAR mediates renal vasodilation through the connecting-tubule-glomerular feedback, by increasing ENaC activity.

Indexed as

Acute Kidney InjuryConnecting tubule-glomerular feedbackENaCKidney AutoregulationNMDA receptors

Identifiers

PMID38106229
PMCPMC10723319
OpenAlexW4389409119

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.