Evidence map›Paper›PMID 15965495›Full record

ArticleBritish journal of pharmacology2005

M(2) and M(3) muscarinic receptor-mediated contractions in longitudinal smooth muscle of the ileum studied with receptor knockout mice.

Toshihiro Unno, Hayato Matsuyama, Takashi Sakamoto, Mai Uchiyama, Yusuke Izumi, Hiroyuki Okamoto, Masahisa Yamada, Jürgen Wess, Seiichi Komori

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.6field-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

34 citing papers in PubMed, 91 citations in OpenAlex.

  1. Trial
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  4. Antispasmodic activity of a series of cyclic imides (phthalimides) derivatives.Naunyn-Schmiedeberg's archives of pharmacology · 2026
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  17. Possible antagonistic effects of the TRPC4 channel blocker ML204 on MThe Journal of veterinary medical science · 2018
    Article
  18. DoesVeterinary research forum : an international quarterly journal · 2017
    Article
  19. 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

9 authors at 2 institutions in 1 country.

Toshihiro UnnoLaboratory of Pharmacology, Department of Veterinary Medicine, Faculty of Applied Biological Science, Gifu University, Japan.
Hayato Matsuyama
Takashi Sakamoto
Mai Uchiyama
Yusuke Izumi
Hiroyuki Okamoto
Masahisa Yamada
Jürgen Wess
Seiichi Komori
Gifu University · JPRIKEN Center for Brain Science · JP

Funding

STUDIES ON NEUROTRANSMITTER RECEPTOR GENESZ01DK032003 · NIDDK · DIABETES, DIGESTIVE, KIDNEY DISEASES · PI WESS, JURGEN · 1993 to 2006
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6 · The paper itself

Abstract

Isometric contractile responses to carbachol were studied in ileal longitudinal smooth muscle strips from wild-type mice and mice genetically lacking M(2) or M(3) muscarinic receptors, in order to characterize the mechanisms involved in M(2) and M(3) receptor-mediated contractile responses. Single applications of carbachol (0.1-100 microM) produced concentration-dependent contractions in preparations from M(2)-knockout (KO) and M(3)-KO mice, mediated via M(3) and M(2) receptors, respectively, as judged by the sensitivity of contractile responses to blockade by the M(2)-preferring antagonist methoctramine (300 nM) or the M(3)-preferring antagonist 4-DAMP (30 nM). The M(2)-mediated contractions were mimicked in shape by submaximal stimulation with high K(+) concentrations (up to 35 mM), almost abolished by voltage-dependent Ca(2+) channel (VDCC) antagonists or depolarization with 140 mM K(+) medium, and greatly reduced by pertussis toxin (PTX) treatment. The M(3)-mediated contractions were only partially inhibited by VDCC antagonists or 140 mM K(+)-depolarization medium, and remained unaffected by PTX treatment. The contractions observed during high K(+) depolarization consisted of different components, either sensitive or insensitive to extracellular Ca(2+). The carbachol contractions observed with wild-type preparations consisted of PTX-sensitive and -insensitive components. The PTX-sensitive component was functionally significant only at low carbachol concentrations. The results suggest that the M(2) receptor, through PTX-sensitive mechanisms, induces ileal contractions that depend on voltage-dependent Ca(2+) entry, especially associated with action potential discharge, and that the M(3) receptor, through PTX-insensitive mechanisms, induces contractions that depend on voltage-dependent and -independent Ca(2+) entry and intracellular Ca(2+) release. In intact tissues coexpressing M(2) and M(3) receptors, M(2) receptor activity appears functionally relevant only when fractional receptor occupation is relatively small.

Indexed as

AnimalsCalcium Channel BlockersCarbacholCholinergic AgonistsDiaminesFemaleIleumIn Vitro TechniquesMaleMiceMice, KnockoutMuscarinic AntagonistsMuscle ContractionMuscle, SmoothNicardipinePertussis Toxin4-diphenylacetoxy-1,1-dimethylpiperidiniumCalcium Channel BlockersCarbacholCholinergic AgonistsDiaminesmethoctramineMuscarinic AntagonistsNicardipinePertussis ToxinPiperidinesReceptor, Muscarinic M2Receptor, Muscarinic M3

Identifiers

PMID15965495
PMCPMC1576249
OpenAlexW2008873185

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.