Evidence map›Paper›PMID 26635911›Full record

ArticleOxidative medicine and cellular longevity2016

Vasorelaxant Effect of a New Hydrogen Sulfide-Nitric Oxide Conjugated Donor in Isolated Rat Aortic Rings through cGMP Pathway.

Dan Wu, Qingxun Hu, Fenfen Ma, Yi Zhun Zhu

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 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
3.0field-weighted citation impact, top 10% 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, 40 citations in OpenAlex.

  1. Review
  2. Review
  3. HBiomolecules · 2021
    Review
  4. Article
  5. Trends in HAntioxidants (Basel, Switzerland) · 2021
    Review
  6. Highly efficient HChemical science · 2020
    Article
  7. Advances in the Protective Mechanism of NO, HFrontiers in cardiovascular medicine · 2020
    Review
  8. Review
  9. Article
  10. Role of Nitric Oxide in the Cardiovascular and Renal Systems.International journal of molecular sciences · 2018
    Review
  11. Novel HRedox biology · 2018
    Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Role of thiosulfate in hydrogen sulfide-dependent redox signaling in endothelial cells.American journal of physiology. Heart and circulatory physiology · 2017
    Article
  17. Therapeutic Role of Functional Components in Alliums for Preventive Chronic Disease in Human Being.Evidence-based complementary and alternative medicine : eCAM · 2017
    Review
  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 1 institution in 2 countries.

Dan WuDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai 201203, China.
Qingxun HuDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai 201203, China.
Fenfen MaDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai 201203, China.
Yi Zhun ZhuDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai 201203, China ; Department of Pharmacology, Loo Yong Lin School of Medicine, National University of Singapore, Singapore.
Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endothelium-dependent vasorelaxant injury leads to a lot of cardiovascular diseases. Both hydrogen sulfide (H2S) and nitric oxide (NO) are gasotransmitters, which play a critical role in regulating vascular tone. However, the interaction between H2S and NO in vasorelaxation is still unclear. ZYZ-803 was a novel H2S and NO conjugated donor developed by H2S-releasing moiety (S-propyl-L-cysteine (SPRC)) and NO-releasing moiety (furoxan). ZYZ-803 could time- and dose-dependently relax the sustained contraction induced by PE in rat aortic rings, with potencies of 1.5- to 100-fold greater than that of furoxan and SPRC. Inhibition of the generations of H2S and NO with respective inhibitors abolished the vasorelaxant effect of ZYZ-803. ZYZ-803 increased cGMP level and the activity of vasodilator stimulated phosphoprotein (VASP) in aortic rings, and those effects could be suppressed by the inhibitory generation of H2S and NO. Both the inhibitor of protein kinase G (KT5823) and the inhibitor of KATP channel (glibenclamide) suppressed the vasorelaxant effect of ZYZ-803. Our results demonstrated that H2S and NO generation from ZYZ-803 cooperatively regulated vascular tone through cGMP pathway, which indicated that ZYZ-803 had therapeutic potential in cardiovascular diseases.

Indexed as

AortaAnimalsCarbazolesCardiovascular DiseasesCell Adhesion MoleculesCyclic GMPCyclic GMP-Dependent Protein KinasesHydrogen SulfideMaleMicrofilament ProteinsNitric OxidePhosphoproteinsRatsRats, Sprague-DawleySecond Messenger SystemsVasodilator AgentsCarbazolesCell Adhesion MoleculesCyclic GMPCyclic GMP-Dependent Protein KinasesHydrogen SulfideKT 5823Microfilament ProteinsNitric OxidePhosphoproteinsVasodilator AgentsVasodilator-Stimulated Phosphoprotein

Identifiers

PMID26635911
PMCPMC4655279
OpenAlexW2171351168

What OpenQuestion holds

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LicenceCC BY
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.