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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2 Pt 1
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pubmed:dateCreated |
1997-4-24
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pubmed:abstractText |
Ureteral myocytes of guinea pigs have L-type Ca2+ channels (I(Ca)). In 3 mM Ca2+, maximum I(Ca) was 3.38 microA/cm2. Voltage at which conductance is 50% of maximum (V0.5) of I(Ca) was -1.0 mV in 3 mM Ca2+ and +22 mV in 30 mM Ca2+, with slope factors of 8 mV. V0.5 of steady-state inactivation of I(Ca) was -16.2 and +1.1 mV in 3 and 30 mM Ca2+, respectively, with similar slope factors of about -6 mV. A window current reaching 20-25% of the maximum I(Ca) was active between -20 and 0 mV. I(Ca) inactivated very slowly, with time constants of 217.6 and 2,455.9 ms with no voltage dependency. When Ba2+ was used as the charge carrier, the amplitude and inactivation kinetics of the Ba2+ current were similar to those for I(Ca). These results indicate that the ureteral myocyte has little Ca2+-mediated Ca2+ channel inactivation, a feature significantly associated with the slow I(Ca) inactivation. The slow inactivation and the window current are essential for the sustained membrane depolarization during the plateau of ureteral action potentials.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0002-9513
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
272
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
C543-9
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:9124297-Animals,
pubmed-meshheading:9124297-Calcium,
pubmed-meshheading:9124297-Electric Conductivity,
pubmed-meshheading:9124297-Guinea Pigs,
pubmed-meshheading:9124297-Homeostasis,
pubmed-meshheading:9124297-Kinetics,
pubmed-meshheading:9124297-Muscle, Smooth,
pubmed-meshheading:9124297-Patch-Clamp Techniques,
pubmed-meshheading:9124297-Ureter
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pubmed:year |
1997
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pubmed:articleTitle |
Properties of inward calcium current in guinea pig ureteral myocytes.
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pubmed:affiliation |
Department of Pharmacology, State University of New York Health Science Center at Brooklyn, 11203, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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