Source:http://linkedlifedata.com/resource/pubmed/id/17298845
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2007-7-25
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pubmed:abstractText |
Recent studies have highlighted the role of the sarcoplasmic reticulum (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 (1 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 Ca2+ 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 Ca2+ sparks by ryanodine (50 microM) or SR Ca2+-ATPase (SERCA) cyclopiazonic acid (CPA, 20 microM) or BKCa channels by iberiotoxin (200 nM) or TEA (1 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 Ca2+ sparks/STOCs coupling mechanism.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Caffeine,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels, L-Type,
http://linkedlifedata.com/resource/pubmed/chemical/Indoles,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphodiesterase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels...,
http://linkedlifedata.com/resource/pubmed/chemical/Ryanodine,
http://linkedlifedata.com/resource/pubmed/chemical/cyclopiazonic acid
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0143-4160
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
303-11
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pubmed:meshHeading |
pubmed-meshheading:17298845-Action Potentials,
pubmed-meshheading:17298845-Animals,
pubmed-meshheading:17298845-Caffeine,
pubmed-meshheading:17298845-Calcium Channels, L-Type,
pubmed-meshheading:17298845-Calcium Signaling,
pubmed-meshheading:17298845-Female,
pubmed-meshheading:17298845-Guinea Pigs,
pubmed-meshheading:17298845-Indoles,
pubmed-meshheading:17298845-Muscle, Smooth,
pubmed-meshheading:17298845-Muscle Contraction,
pubmed-meshheading:17298845-Patch-Clamp Techniques,
pubmed-meshheading:17298845-Phosphodiesterase Inhibitors,
pubmed-meshheading:17298845-Potassium Channels, Calcium-Activated,
pubmed-meshheading:17298845-Ryanodine,
pubmed-meshheading:17298845-Sarcoplasmic Reticulum,
pubmed-meshheading:17298845-Ureter
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pubmed:year |
2007
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pubmed:articleTitle |
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.
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pubmed:affiliation |
The Physiological Laboratory, University of Liverpool, Crown Street, Liverpool L69 3BX, UK.
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pubmed:publicationType |
Journal Article
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