Evidence map›Paper›PMID 12970100›Full record

ArticleBritish journal of pharmacology2003

NANC inhibitory neurotransmission in mouse isolated stomach: involvement of nitric oxide, ATP and vasoactive intestinal polypeptide.

Flavia Mulè, Rosa Serio

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in British journal of pharmacology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Roles of NaWorld journal of gastroenterology · 2019
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Inhibitory effect of schisandrin on spontaneous contraction of isolated rat colon.Phytomedicine : international journal of phytotherapy and phytopharmacology · 2011
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Intrinsic inhibitory innervation of the stomach.British journal of pharmacology · 2005
    Article
  20. Article
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

2 authors at 1 institution in 1 country.

Flavia MulèDipartimento di Biologia cellulare e dello Sviluppo, Università di Palermo - 90128, Palermo, Italia. fmule@unipa.it
Rosa Serio
University of Palermo · IT

Funding

Telethon 1134
6 · The paper itself

Abstract

1. The neurotransmitters involved in NANC relaxation and their possible interactions were investigated in mouse isolated stomach, recording the motor responses as changes of endoluminal pressure from whole organ. 2. Field stimulation produced tetrodotoxin-sensitive, frequency-dependent, biphasic responses: rapid transient relaxation followed by a delayed inhibitory component. 3. The inhibitor of the synthesis of nitric oxide (NO), l-NAME, abolished the rapid relaxation and significantly reduced the slow relaxation. Apamin, blocker of Ca2+-dependent K+ channels, or ADPbetaS, which desensitises P2y purinoceptors, reduced the slow relaxation to 2-8 Hz, without affecting that to 16-32 Hz or the fast relaxation. alpha-Chymotrypsin or vasoactive intestinal polypeptide 6-28 (VIP6-28), antagonist of VIP receptors, failed to affect the fast component or the delayed relaxation to 2-4 Hz, but antagonised the slow component to 8-32 Hz. 4. Relaxation to sodium nitroprusside was not affected by l-NAME, apamin or ADPbetaS, but was reduced by alpha-chymotrypsin or VIP6-28. Relaxation to VIP was abolished by alpha-chymotrypsin, antagonised by VIP6-28, but was not affected by l-NAME, apamin or ADPbetaS. Relaxation to ATP was abolished by apamin, antagonised by ADPbetaS, but was not affected by l-NAME or alpha-chymotrypsin. 5. The present results suggest that NO is responsible for the rapid relaxation and partly for the slow relaxation. ATP is involved in the slow relaxation evoked by low frequencies of stimulation. VIP is responsible for the slow relaxation evoked by high frequencies of stimulation. The different neurotransmitters appear to work in parallel, although NO could serve also as a neuromodulator that facilitates release of VIP.

Indexed as

Adenosine DiphosphateAdenosine TriphosphateAdrenergic FibersAnimalsApaminCholinergic FibersChymotrypsinDose-Response Relationship, DrugElectric StimulationEnzyme InhibitorsIn Vitro TechniquesMiceMice, Inbred C57BLMuscle RelaxationNG-Nitroarginine Methyl EsterNitric Oxideadenosine 5'-O-(2-thiodiphosphate)Adenosine DiphosphateAdenosine Triphosphatealpha-chymotrypsinApaminChymotrypsinEnzyme InhibitorsNG-Nitroarginine Methyl EsterNitric OxideNitric Oxide DonorsNitric Oxide SynthaseNitroprussideReceptors, Vasoactive Intestinal PeptideThionucleotidesVasoactive Intestinal Peptide

Identifiers

PMID12970100
PMCPMC1574027
OpenAlexW2055795786

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.