Skip to content Skip to navigation
University of Warwick
  • Study
  • |
  • Research
  • |
  • Business
  • |
  • Alumni
  • |
  • News
  • |
  • About

University of Warwick
Publications service & WRAP

Highlight your research

  • WRAP
    • Home
    • Search WRAP
    • Browse by Warwick Author
    • Browse WRAP by Year
    • Browse WRAP by Subject
    • Browse WRAP by Department
    • Browse WRAP by Funder
    • Browse Theses by Department
  • Publications Service
    • Home
    • Search Publications Service
    • Browse by Warwick Author
    • Browse Publications service by Year
    • Browse Publications service by Subject
    • Browse Publications service by Department
    • Browse Publications service by Funder
  • Statistics
  • Help & Advice
University of Warwick

The Library

  • Login

Evidence that a Ca2+ sparks/STOCs coupling mechanism is responsible for the inhibitory effect of caffeine on electro-mechanical coupling in guinea pig ureteric smooth muscle

Tools
- Tools
+ Tools

Borisova, L., Shmygol, A., Wray, Susan and Burdyga, T.. (2007) Evidence that a Ca2+ sparks/STOCs coupling mechanism is responsible for the inhibitory effect of caffeine on electro-mechanical coupling in guinea pig ureteric smooth muscle. Cell Calcium, Vol.42 (No.3). pp. 303-311. ISSN 0143-4160

Full text not available from this repository.
Official URL: http://dx.doi.org/10.1016/j.ceca.2006.12.005

Abstract

Recent studies have highlighted the role of the sarcoplasmic reticulurn (SR) in controlling excitability, Ca2+, signalling and contractility in smooth muscle. Caffeine, an agonist of ryanodine receptors (RyRs) on the SR has been previously shown to effect Ca2+, signalling but its effects on excitability and contractility are not so clear. We have studied the effects of low concentration of caffeine (I mM) on Ca2+ signalling, action potential and contractility of guinea pig ureteric smooth muscle. Caffeine produced reversible inhibition of the action potentials, Ca2+, transients and phasic contractions evoked by electrical stimulation. It had no effect on the inward Ca2+ current or Ca 21 transient but increased the amplitude and the frequency of spontaneous transient outward currents (STOCs) in voltage clamped ureteric myocytes, suggesting Ca2+ activated K+ channels (BK) are affected by it. In isolated cells and cells in situ caffeine produced an increase in the frequency and the amplitude of Ca2+ sparks as well the number of spark discharging sites per cell. Inhibition of Ca 2, sparks by ryanodine (50 mu M) or SR Ca2+ ATPase (SERCA) cyclopiazonic acid (CPA, 20 mu M) or BKCa channels by iberiotoxin (200 nM) or TEA (I mM), fully reversed the inhibitory effect of caffeine on Ca2+ transients and force evoked by electrical field stimulation (EFS). These data suggest that the inhibitory effect of caffeine on the action potential, Ca2+ transients and force in ureteric smooth muscle is caused by activation of Ca 2, sparks/STOCs coupling mechanism. (c) 2007 Elsevier Ltd. All rights reserved.

Item Type: Journal Article
Subjects: Q Science > QH Natural history > QH301 Biology
Divisions: Faculty of Medicine > Warwick Medical School > Clinical Sciences Research Institute (CSRI)
Journal or Publication Title: Cell Calcium
Publisher: Churchill Livingstone
ISSN: 0143-4160
Date: September 2007
Volume: Vol.42
Number: No.3
Number of Pages: 9
Page Range: pp. 303-311
Identification Number: 10.1016/j.ceca.2006.12.005
Status: Peer Reviewed
Publication Status: Published
Access rights to Published version: Restricted or Subscription Access
URI: http://wrap.warwick.ac.uk/id/eprint/31572

Data sourced from Thomson Reuters' Web of Knowledge

Request changes to a record

Actions (login required)

View Item View Item
twitter

Email us: publications@warwick.ac.uk
Contact Details
About Us