Evidence map›Paper›PMID 18060543›Full record

ReviewNaunyn-Schmiedeberg's archives of pharmacology2008

Signal transduction underlying the control of urinary bladder smooth muscle tone by muscarinic receptors and beta-adrenoceptors.

Elfaridah P Frazier, Stephan L M Peters, Alan S Braverman, Michael R Ruggieri, Martin C Michel

Open access · hybridAbstract readReview
In one paragraph

Review in Naunyn-Schmiedeberg's archives of pharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
10.2field-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.

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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 150 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Nocturia and obstructive sleep apnoea.Nature reviews. Urology · 2024
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  6. The role of rhoA/rho-kinase and PKC in the inhibitory effect of L-cysteine/HNaunyn-Schmiedeberg's archives of pharmacology · 2023
    Article
  7. Article
  8. Review
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  10. Review
  11. Article
  12. The intracellular CaProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Spotlight on ROS andOxidative medicine and cellular longevity · 2019
    Review
  17. Article
  18. Article
  19. Article
  20. On the Site and Mechanism of Action of βInternational neurourology journal · 2017
    Review
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

5 authors at 3 institutions in 2 countries.

Elfaridah P FrazierDepartment of Pharmacology and Pharmacotherapy, Academic Medical Center, University of Amsterdam, Meibergdreef 15, 1105 AZ, Amsterdam, The Netherlands.
Stephan L M Peters
Alan S Braverman
Michael R Ruggieri
Martin C Michel
Temple University · USUniversity of Amsterdam · NLAcademic Medical Center · NL

Funding

URINARY BLADDER MUSCARINIC RECEPTOR SUBTYPESR01DK043333 · NIDDK · TEMPLE UNIVERSITY · PI RUGGIERI, MICHAEL RAYMOND · 1991 to 2003
$998k
NIDDK NIH HHS R01 DK043333
6 · The paper itself

Abstract

The normal physiological contraction of the urinary bladder, which is required for voiding, is predominantly mediated by muscarinic receptors, primarily the M3 subtype, with the M2 subtype providing a secondary backup role. Bladder relaxation, which is required for urine storage, is mediated by beta-adrenoceptors, in most species involving a strong beta3-component. An excessive stimulation of contraction or a reduced relaxation of the detrusor smooth muscle during the storage phase of the micturition cycle may contribute to bladder dysfunction known as the overactive bladder. Therefore, interference with the signal transduction of these receptors may be a viable approach to develop drugs for the treatment of overactive bladder. The prototypical signaling pathway of M3 receptors is activation of phospholipase C (PLC), and this pathway is also activated in the bladder. Nevertheless, PLC apparently contributes only in a very minor way to bladder contraction. Rather, muscarinic-receptor-mediated bladder contraction involves voltage-operated Ca2+ channels and Rho kinase. The prototypical signaling pathway of beta-adrenoceptors is an activation of adenylyl cyclase with the subsequent formation of cAMP. Nevertheless, cAMP apparently contributes in a minor way only to beta-adrenoceptor-mediated bladder relaxation. BKCa channels may play a greater role in beta-adrenoceptor-mediated bladder relaxation. We conclude that apart from muscarinic receptor antagonists and beta-adrenoceptor agonists, inhibitors of Rho kinase and activators of BKCa channels may have potential to treat an overactive bladder.

Indexed as

Adrenergic beta-AgonistsAnimalsHumansMuscarinic AntagonistsPotassium ChannelsProtein Kinase InhibitorsReceptors, Adrenergic, betaReceptors, Muscarinicrho-Associated KinasesSignal TransductionUrinary BladderUrinary Bladder, OveractiveAdrenergic beta-AgonistsMuscarinic AntagonistsPotassium ChannelsProtein Kinase InhibitorsReceptors, Adrenergic, betaReceptors, Muscarinicrho-Associated Kinases

Identifiers

PMID18060543
PMCPMC2480512
OpenAlexW2083514340

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.