Evidence map›Paper›PMID 11689441›Full record

ArticleThe EMBO journal2001

The vasorelaxant effect of H(2)S as a novel endogenous gaseous K(ATP) channel opener.

W Zhao, J Zhang, Y Lu, R Wang

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in The EMBO journal, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06749756 (Study on the Improvement of Microcirculation in Patients With Sepsis by Vitamin B6, Vitamin B12 and Vitamin C), which is not on this map. Cited by 734 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
734citing papers in PubMed, 2 pooled it
12.7field-weighted citation impact, top 1% 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.

NCT06749756 narecruitingnot on this mapstarted 2025, after this paper: background citation

Study on the Improvement of Microcirculation in Patients With Sepsis by Vitamin B6, Vitamin B12 and Vitamin C

TypeinterventionalSponsorFan ZengRan2025 to 2026Enrolled296ConditionsSeptic ShockArmsvitamin B6+ Vitamin B12 +vitamin C, vitamin B6+ Vitamin B12, vitamin C, 0.9%Nacl
3 · Its place in the literature

Who cites it

734 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,918 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Review
  7. Inhibition of HJournal of vascular research · 2026
    Article
  8. Gas entrapping materials for damage control.Advanced drug delivery reviews · 2026
    Review
  9. Review
  10. Clonal Stabilization Reveals a DAO/3MST-Expressing MDCK Subpopulation With Robust d-Cysteine-Mediated HFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  11. HBiomedicines · 2026
    Article
  12. Review
  13. Chemogenetic Manipulation of HPrecision chemistry · 2026
    Article
  14. Review
  15. Review
  16. Naturally Occurring HHandbook of experimental pharmacology · 2026
    Review
  17. HHandbook of experimental pharmacology · 2026
    Review
  18. Hydrogen Sulfide Signaling in Neurodegenerative Movement Disorders.Handbook of experimental pharmacology · 2026
    Review
  19. Review
  20. Article

674 more citing papers are in PubMed but not listed here.

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 1 country.

W ZhaoDepartment of Physiology, University of Saskatchewan, Saskatoon, SK, Canada.
J Zhang
Y Lu
R Wang
University of Saskatchewan · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hydrogen sulfide (H(2)S) has been traditionally viewed as a toxic gas. It is also, however, endogenously generated from cysteine metabolism. We attempted to assess the physiological role of H(2)S in the regulation of vascular contractility, the modulation of H(2)S production in vascular tissues, and the underlying mechanisms. Intravenous bolus injection of H(2)S transiently decreased blood pressure of rats by 12- 30 mmHg, which was antagonized by prior blockade of K(ATP) channels. H(2)S relaxed rat aortic tissues in vitro in a K(ATP) channel-dependent manner. In isolated vascular smooth muscle cells (SMCs), H(2)S directly increased K(ATP) channel currents and hyperpolarized membrane. The expression of H(2)S-generating enzyme was identified in vascular SMCs, but not in endothelium. The endogenous production of H(2)S from different vascular tissues was also directly measured with the abundant level in the order of tail artery, aorta and mesenteric artery. Most importantly, H(2)S production from vascular tissues was enhanced by nitric oxide. Our results demonstrate that H(2)S is an important endogenous vasoactive factor and the first identified gaseous opener of K(ATP) channels in vascular SMCs.

Indexed as

AnimalsArteriesBlood PressureCardiovascular SystemCells, CulturedCell SeparationCystathionine gamma-LyaseCysteineEndothelium, VascularHydrogen SulfideInjections, IntravenousIn Situ HybridizationIn Vitro TechniquesMaleMembrane PotentialsMuscle, Smooth, VascularCystathionine gamma-LyaseCysteineHydrogen SulfideNitric OxidePotassium Channel BlockersPotassium ChannelsRNA, MessengerVasodilator Agents

Identifiers

PMID11689441
PMCPMC125693
OpenAlexW2015407072

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.