Evidence map›Paper›PMID 30850755›Full record

ArticleHypertension research : official journal of the Japanese Society of Hypertension2019

Dual inhibition of NADPH oxidases and xanthine oxidase potently prevents salt-induced stroke in stroke-prone spontaneously hypertensive rats.

Davis Ngarashi, Koichi Fujikawa, Mohammed Zubaerul Ferdaus, Hasan M Zahid, Hiroki Ohara, Toru Nabika

Abstract read
PubMed Publisher
In one paragraph

Article in Hypertension research : official journal of the Japanese Society of Hypertension, 2019. 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
2.0field-weighted citation impact, top 14% 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, 18 citations in OpenAlex.

  1. Babassu (Foods (Basel, Switzerland) · 2026
    Article
  2. Risk of preeclampsia in pregnant individuals with chronic kidney disease: a framework from Chinese cohort.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Article
  3. Article
  4. Article
  5. NaAntioxidants (Basel, Switzerland) · 2022
    Article
  6. Article
  7. Review
  8. The Role of Oxidative Stress in Acute Ischemic Stroke-Related Thrombosis.Oxidative medicine and cellular longevity · 2022
    Review
  9. Review
  10. Article
  11. Low doses of folic acid can reduce hyperhomocysteinemia-induced glomerular injury in spontaneously hypertensive rats.Hypertension research : official journal of the Japanese Society of Hypertension · 2020
    Article
  12. 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

6 authors at 2 institutions in 3 countries.

Davis NgarashiDepartment of Functional Pathology, Shimane University School of Medicine, Izumo, Japan.
Koichi FujikawaDepartment of Functional Pathology, Shimane University School of Medicine, Izumo, Japan.
Mohammed Zubaerul FerdausDepartment of Functional Pathology, Shimane University School of Medicine, Izumo, Japan.
Hasan M ZahidDepartment of Functional Pathology, Shimane University School of Medicine, Izumo, Japan.
Hiroki OharaDepartment of Functional Pathology, Shimane University School of Medicine, Izumo, Japan. oharah@med.shimane-u.ac.jp.
Toru NabikaDepartment of Functional Pathology, Shimane University School of Medicine, Izumo, Japan.
Shimane University · JPBangladesh Atomic Energy Commission · BD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxidative stress has been implicated in the pathophysiology of cerebral stroke. As NADPH oxidases (NOXs) play major roles in the regulation of oxidative stress, we hypothesized that reduction of NOX activity by depletion of p22phox, an essential subunit of NOX complexes, would prevent cerebral stroke. To investigate this, we used the stroke-prone spontaneously hypertensive rat (SHRSP) and the p22phox-deleted congenic SHRSP. Although p22phox depletion reduced blood pressure under salt loading, it did not ameliorate oxidative stress or reduce the incidence of salt-induced stroke in SHRSPs. Additional pharmacological reduction of oxidative stress using antioxidant reagents with different mechanisms of action was necessary to prevent stroke, indicating that NOX was not the major target in salt-induced stroke in SHRSPs. On the other hand, oxidative stress measured based on urinary isoprostane levels showed significant correlations with blood pressure, stroke latency and urinary protein excretion under salt loading, suggesting an important role of oxidative stress per se in hypertension and hypertensive organ damage. Overall, our results imply that oxidative stress from multiple sources influences stroke susceptibility and other hypertensive disorders in salt-loaded SHRSPs.

Indexed as

AnimalsAntioxidantsBlood PressureCyclic N-OxidesEnzyme InhibitorsFebuxostatMaleNADPH OxidasesOxidative StressRatsRats, Inbred SHRRats, TransgenicReactive Oxygen SpeciesSodium ChlorideSpin LabelsStrokeAntioxidantscoenzyme Q10Cyclic N-OxidesEnzyme InhibitorsFebuxostatNADPH OxidasesReactive Oxygen SpeciesSodium ChlorideSpin LabelstempolUbiquinoneXanthine OxidaseNADPH oxidaseoxidative stressp22phoxSHRSPstroke

Identifiers

PMID30850755
OpenAlexW2922386492

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.