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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1997-6-10
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pubmed:abstractText |
In smooth muscle cells freshly isolated from the bovine ciliary body, effects of carbachol (CCh) on the membrane potential and current were examined by the whole-cell clamp method. The resting membrane potential of the muscle cells used was -60 +/- 1 mV (n = 111). Extracellular application of CCh (2 microM) depolarized the cells to -15 +/- 5 mV (n = 50) with an apparent increase in membrane conductance. Under voltage-clamp conditions, CCh (2 microM) evoked an inward current which exhibited inward-going rectification and reversed the polarity at about 0 mV. Removal of Na+ from the external solution caused a reduction of the amplitude of the current and a shift of the reversal potential to the negative direction. CCh was able to elicit an inward current even under a condition where Ca2+ was the only cation producing an inwardly directed electrochemical gradient. The current was not affected by verapamil or by tetrodotoxin. The CCh-induced current was inhibited by antimuscarinic agents with the affinity sequence: atropine approximately 4-DAMP > > pirenzepine > AF-DX116, indicating that the response is mediated by a muscarinic cholinoceptor that belongs to the M3-subtype. Unlike the non-selective cation channel current in intestinal smooth muscles, which is activated by elevation of the intracellular Ca2+ concentration ([Ca2+]i), the current of the ciliary muscle was inactivated when the [Ca2+]i was increased. The conductance, which admits Ca2+, may serve as a pathway for Ca2+ entry required for contraction.
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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/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Carbachol,
http://linkedlifedata.com/resource/pubmed/chemical/Cations,
http://linkedlifedata.com/resource/pubmed/chemical/Ion Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Muscarinic Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Muscarinic Antagonists
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0031-6768
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
433
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
705-12
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9049160-Animals,
pubmed-meshheading:9049160-Calcium,
pubmed-meshheading:9049160-Carbachol,
pubmed-meshheading:9049160-Cations,
pubmed-meshheading:9049160-Cattle,
pubmed-meshheading:9049160-Ciliary Body,
pubmed-meshheading:9049160-Electrophysiology,
pubmed-meshheading:9049160-Ion Channels,
pubmed-meshheading:9049160-Membrane Potentials,
pubmed-meshheading:9049160-Muscarinic Agonists,
pubmed-meshheading:9049160-Muscarinic Antagonists,
pubmed-meshheading:9049160-Muscle, Smooth,
pubmed-meshheading:9049160-Muscle Contraction,
pubmed-meshheading:9049160-Patch-Clamp Techniques
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pubmed:year |
1997
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pubmed:articleTitle |
Activation of non-selective cation conductance by carbachol in freshly isolated bovine ciliary muscle cells.
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pubmed:affiliation |
Department of Ophthalmology, School of Medicine, Nagoya University, Japan.
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pubmed:publicationType |
Journal Article,
In Vitro
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