Evidence map›Paper›PMID 26887831›Full record

ArticleAmerican journal of physiology. Renal physiology2016

Angiotensin II-mediated hypertension impairs nitric oxide-induced NKCC2 inhibition in thick ascending limbs.

Vanesa D Ramseyer, Pablo A Ortiz, Oscar A Carretero, Jeffrey L Garvin

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. The non-steroidal mineralocorticoid receptor blocker esaxerenone reduces glomerular hyperfiltration and albuminuria.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2026
    Article
  2. Review
  3. Review
  4. Vascular control of kidney epithelial transporters.American journal of physiology. Renal physiology · 2021
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Potassium-sparing effects of furosemide in mice on high-potassium diets.American journal of physiology. Renal physiology · 2019
    Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Macrophages under pressure: the role of macrophage polarization in hypertension.Translational research : the journal of laboratory and clinical medicine · 2018
    Review
  15. Review
  16. Renal sodium handling and sodium sensitivity.Kidney research and clinical practice · 2017
    Review
  17. Article
  18. 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

4 authors at 3 institutions in 1 country.

Vanesa D RamseyerHypertension and Vascular Research Division, Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan; vramseye@med.wayne.edu.
Pablo A OrtizHypertension and Vascular Research Division, Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan.
Oscar A CarreteroHypertension and Vascular Research Division, Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan.
Jeffrey L GarvinHypertension and Vascular Research Division, Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan.
Henry Ford Health System · USCase Western Reserve University · USWayne State University · US

Funding

VASOACTIVE HORMONES IN THE REGULATION OF BLOOD PRESSUREP01HL028982 · NHLBI · HENRY FORD HOSPITAL · PI GARVIN, JEFFREY L. · 1985 to 2017
$39.8M
NHLBI NIH HHS P01 HL028982
6 · The paper itself

Abstract

In thick ascending limbs (THALs), nitric oxide (NO) decreases NaCl reabsorption via cGMP-mediated inhibition of Na-K-2Cl cotransporter (NKCC2). In angiotensin (ANG II)-induced hypertension, endothelin-1 (ET-1)-induced NO production by THALs is impaired. However, whether this alters NO's natriuretic effects and the mechanisms involved are unknown. In other cell types, ANG II augments phosphodiesterase 5 (PDE5)-mediated cGMP degradation. We hypothesized that NO-mediated inhibition of NKCC2 activity and stimulation of cGMP synthesis are blunted via PDE5 in ANG II-induced hypertension. Sprague-Dawley rats were infused with vehicle or ANG II (200 ng·kg ANG II: Δ-41 ± 10%). NO increased cGMP by 2.08 ± 0.36 fmol/μg protein in THALs from vehicle-treated rats but only 1.06 ± 0.25 fmol/μg protein in ANG II-hypertensive rats (

Indexed as

Angiotensin IIAnimalsCyclic CMPCyclic GMPCyclic Nucleotide Phosphodiesterases, Type 5Endothelin-1HypertensionLoop of HenleMaleNitric OxideNitric Oxide DonorsPhosphodiesterase 5 InhibitorsRatsRats, Sprague-DawleySolute Carrier Family 12, Member 1Vardenafil DihydrochlorideAngiotensin IICyclic CMPCyclic GMPCyclic Nucleotide Phosphodiesterases, Type 5dibutyryl cyclic-3',5'-cytidine monophosphateEndothelin-1Nitric OxideNitric Oxide DonorsPde5a protein, ratPhosphodiesterase 5 InhibitorsSolute Carrier Family 12, Member 1Vardenafil DihydrochloridecGMPendothelin-1kidneyphosphodiesterase 5sodium transport

Identifiers

PMID26887831
PMCPMC4835923
OpenAlexW2276370194

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.