Evidence map›Paper›PMID 18071300›Full record

ArticleBritish journal of pharmacology2008

Role of the NO/cGMP/K(ATP) pathway in the protective effects of sildenafil against ethanol-induced gastric damage in rats.

J V R Medeiros, G G Gadelha, S J Lima, J A Garcia, P M G Soares, A A Santos, G A C Brito, R A Ribeiro, M H L P Souza

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.6field-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

32 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
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  7. Tablet ofMolecules (Basel, Switzerland) · 2021
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  18. Antiulcerogenic Activity and Toxicity of Bauhinia holophylla Hydroalcoholic Extract.Evidence-based complementary and alternative medicine : eCAM · 2015
    Article
  19. Article
  20. The hydrogen sulfide donor, Lawesson's reagent, prevents alendronate-induced gastric damage in rats.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2013
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

J V R MedeirosDepartment of Physiology and Pharmacology, Federal University of Ceará, Fortaleza, Ceara, Brazil.
G G Gadelha
S J Lima
J A Garcia
P M G Soares
A A Santos
G A C Brito
R A Ribeiro
M H L P Souza
Universidade Federal do Ceará · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeSildenafil is a selective inhibitor of cGMP-specific phosphodiesterase. Sildenafil, acting via NO-dependent mechanisms, prevents indomethacin-induced gastropathy. Activation of ATP-sensitive potassium channels (K(ATP)) is involved in gastric defence. Our objective was to evaluate the role of the NO/cGMP/K(ATP) pathway in the protective effects of sildenafil against ethanol-induced gastric damage. EXPERIMENTAL APPROACH: Rats were treated with L-NAME (1 or 3 mg kg(-1), i.p.) or with L-arginine (200 mg kg(-1), i.p.) + L-NAME (3 mg kg(-1), i.p.), the guanylate cyclase inhibitor, ODQ (10 mg kg(-1), i.p.), glibenclamide (0.1, 0.3, 1 or 3 mg kg(-1), i.p.) or with glibenclamide (1 mg kg(-1), i.p.) + diazoxide (3 mg kg(-1), i.p.). After thirty minutes, the rats received sildenafil (1 mg kg(-1), by gavage), followed by intragastric instillation of absolute ethanol (4 ml kg(-1)) to induce gastric damage. One hour later, gastric damage (haemorrhagic or ulcerative lesions) was measured with a planimetry programme. Samples of stomach were also taken for histopathological assessment and for assays of tissue glutathione and haemoglobin. KEY

resultsSildenafil significantly reduced ethanol-induced gastric damage in rats. L-NAME alone, without L-arginine, significantly reversed the protection afforded by sildenafil. Inhibition of guanylate cyclase by ODQ completely abolished the gastric protective effect of sildenafil against ethanol-induced gastric damage. Glibenclamide alone reversed sildenafil's gastric protective effect. However, glibenclamide plus diazoxide did not alter the effects of sildenafil.

conclusionsSildenafil had a protective effect against ethanol-induced gastric damage through the activation of the NO/cGMP/K(ATP) pathway.

Indexed as

AnimalsArginineCyclic GMPCyclic Nucleotide Phosphodiesterases, Type 5DiazoxideDisease Models, AnimalEnzyme InhibitorsEthanolGastric MucosaGlutathioneGlyburideGuanylate CyclaseHemoglobinsKATP ChannelsMaleNG-Nitroarginine Methyl Ester1H-(1,2,4)oxadiazolo(4,3-a)quinoxalin-1-oneArginineCyclic GMPCyclic Nucleotide Phosphodiesterases, Type 5DiazoxideEnzyme InhibitorsEthanolGlutathioneGlyburideGuanylate CyclaseHemoglobinsKATP ChannelsNG-Nitroarginine Methyl EsterNitric OxideNitric Oxide SynthaseOxadiazolesPhosphodiesterase 5 InhibitorsPhosphodiesterase InhibitorsPiperazinesPotassium Channel BlockersPurinesQuinoxalinesSildenafil CitrateSulfones

Identifiers

PMID18071300
PMCPMC2259210
OpenAlexW1995980971

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.