Evidence map›Paper›PMID 11522599›Full record

ArticleBritish journal of pharmacology2001

Dependency of detrusor contractions on calcium sensitization and calcium entry through LOE-908-sensitive channels.

J R Jezior, J D Brady, D I Rosenstein, K A McCammon, A S Miner, P H Ratz

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 58 citations in OpenAlex.

  1. The role of rhoA/rho-kinase and PKC in the inhibitory effect of L-cysteine/HNaunyn-Schmiedeberg's archives of pharmacology · 2023
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Rhythmic contraction generates adjustable passive stiffness in rabbit detrusor.Journal of applied physiology (Bethesda, Md. : 1985) · 2010
    Article
  7. Article
  8. Adaptation of the length-active tension relationship in rabbit detrusor.American journal of physiology. Renal physiology · 2009
    Article
  9. Article
  10. Review
  11. Muscarinic receptors: what we know.Current urology reports · 2003
    Review
  12. Article
  13. 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

6 authors at 1 institution in 1 country.

J R JeziorDepartment of Urology, Eastern Virginia Medical School, PO Box 1980, Norfolk, Virginia, VA 23501, USA.
J D Brady
D I Rosenstein
K A McCammon
A S Miner
P H Ratz
Eastern Virginia Medical School · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

1. The subcellular mechanisms regulating stimulus-contraction coupling in detrusor remain to be determined. We used Ca(2+)-free solutions, Ca(2+) channel blockers, cyclopiazonic acid (CPA), and RhoA kinase (ROK) inhibitors to test the hypothesis that Ca(2+) influx and Ca(2+) sensitization play primary roles. 2. In rabbit detrusor, peak bethanechol (BE)-induced force was inhibited 90% by incubation for 3 min in a Ca(2+)-free solution. By comparison, a 20 min incubation of rabbit femoral artery in a Ca(2+)-free solution reduced receptor-induced force by only 5%. 3. In detrusor, inhibition of sarcoplasmic reticular (SR) Ca(2+) release by 2APB, or depletion of SR Ca(2+) by CPA, inhibited BE-induced force by only 27%. The CPA-insensitive force was abolished by LaCl3. By comparison, 2APB inhibited receptor-induced force in rabbit femoral artery by 71%. 4. In the presence of the non-selective cation channel (NSCC) inhibitor, LOE-908, BE did not produce an increase in [Ca(2+)]i but did produce weak increases in myosin phosphorylation and force. 5. Inhibitors of ROK-induced Ca(2+) sensitization, HA-1077 and Y-27632, inhibited BE-induced force by approximately 50%, and in combination with LOE-908, nearly abolished force. 6. These data suggest that two principal muscarinic receptor-stimulated detrusor contractile mechanisms include NSCC activation, that elevates [Ca(2+)]i and ROK activation, that sensitizes cross bridges to Ca(2+).

Indexed as

1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineAcetamidesAmidesAnimalsBethanecholCalciumCalcium Channel BlockersDose-Response Relationship, DrugFemaleImidazolesIndolesIn Vitro TechniquesIon ChannelsIsoquinolinesMuscle ContractionMyosin Light Chains1-(2-(3-(4-methoxyphenyl)propoxy)-4-methoxyphenylethyl)-1H-imidazole1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineAcetamidesAmidesBethanecholCalciumCalcium Channel Blockerscyclopiazonic acidfasudilImidazolesIndolesIon ChannelsIsoquinolinesLOE 908Myosin Light ChainsProtein Kinase InhibitorsPyridinesVerapamilY 27632

Identifiers

PMID11522599
PMCPMC1572931
OpenAlexW1965736605

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.