Evidence map›Paper›PMID 17615099›Full record

ArticleThe Journal of physiology2007

Properties of spontaneous Ca2+ transients recorded from interstitial cells of Cajal-like cells of the rabbit urethra in situ.

Hikaru Hashitani, Hikaru Suzuki

Open access · greenAbstract readComparative Study
In one paragraph

Article in The Journal of physiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.6field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Orai storeoperated CaChannels (Austin, Tex.) · 2025
    Review
  3. Article
  4. What do we really know about the external urethral sphincter?Continence (Amsterdam, Netherlands) · 2024
    Review
  5. CaCell calcium · 2021
    Article
  6. The intracellular CaProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  7. CaThe Journal of physiology · 2018
    Article
  8. Article
  9. Review
  10. Review
  11. T-type Ca2+ channels and the urinary and male genital tracts.Pflugers Archiv : European journal of physiology · 2014
    Review
  12. Article
  13. Article
  14. Article
  15. Functions of ICC-like cells in the urinary tract and male genital organs.Journal of cellular and molecular medicine · 2010
    Review
  16. Smooth muscle cell calcium activation mechanisms.The Journal of physiology · 2008
    Review
  17. Article
  18. 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.

Hikaru HashitaniDepartment of Regulatory Cell Physiology, Nagoya City University, Graduate School of Medical Sciences, Nagoya 467-8601, Japan. hasitani@med.nagoya-cu.ac.jp
Hikaru Suzuki
Nagoya City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interstitial cells of Cajal-like cells (ICC-LCs) in the urethra may act as electrical pacemakers of spontaneous contractions. However, their properties in situ and their interaction with neighbouring urethral smooth muscle cells (USMCs) remain to be elucidated. To further explore the physiological role of ICC-LCs, spontaneous changes in [Ca(2+)](i) (Ca(2+) transients) were visualized in fluo-4 loaded preparations of rabbit urethral smooth muscle. ICC-LCs were sparsely distributed, rather than forming an extensive network. Ca(2+) transients in ICC-LCs had a lower frequency and a longer half-width than those of USMCs. ICC-LCs often exhibited Ca(2+) transients synchronously with each other, but did not often show a close temporal relationship with Ca(2+) transients in USMCs. Nicardipine (1 microm) suppressed Ca(2+) transients in USMCs but not in ICC-LCs. Ca(2+) transients in ICC-LCs were abolished by cyclopiazonic acid (10 microm), ryanodine (50 microm) and caffeine (10 mm) or by removing extracellular Ca(2+), and inhibited by 2-aminoethoxydiphenyl borate (50 microm) and 3-morpholino-sydnonimine (SIN-1; 10 microm), but facilitated by increasing extracellular Ca(2+) or phenylephrine (1-10 microm). These results indicated that Ca(2+) transients in urethral ICC-LCs in situ rely on both Ca(2+) release from intracellular Ca(2+) stores and Ca(2+) influx through non-L-type Ca(2+) channel pathways. ICC-LCs may not act as a coordinated pacemaker electrical network as do ICC in the gastrointestinal (GI) tract. Rather they may randomly increase excitability of USMCs to maintain the tone of urethral smooth muscles.

Indexed as

Calcium SignalingMuscle ContractionAdrenergic alpha-AgonistsAnimalsBoron CompoundsCaffeineCalcium Channel BlockersCalcium ChannelsCalcium Channels, L-TypeCalcium-Transporting ATPasesEnzyme InhibitorsIndolesInositol 1,4,5-Trisphosphate ReceptorsMaleMembrane PotentialsMolsidomine2-aminoethoxydiphenyl borateAdrenergic alpha-AgonistsBoron CompoundsCaffeineCalcium Channel BlockersCalcium ChannelsCalcium Channels, L-TypeCalcium-Transporting ATPasescyclopiazonic acidEnzyme InhibitorsIndolesInositol 1,4,5-Trisphosphate ReceptorslinsidomineMolsidomineNicardipineNitric OxideNitric Oxide DonorsPhenylephrineReceptors, Adrenergic, alphaRyanodineRyanodine Receptor Calcium Release Channel

Identifiers

PMID17615099
PMCPMC2277017
OpenAlexW1562673139

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.