rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
1996-10-24
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pubmed:abstractText |
1. Whole-cell voltage-dependent Ca2+ currents recorded from chemoreceptor type I cells of the adult rat carotid body had maximum amplitudes of -94 pA in 10 mM Ca2+ and were half-inactivated at a holding potential of -38 mV. Somatostatin and dopamine inhibited whole-cell Ca2+ current in type I cells. 2. The dihydropyridine agonist (+)202-791 increased the Ca2+ current amplitude by 106% at a step potential of -18 mV. The dihydropyridine antagonist nimodipine decreased the Ca2+ current amplitude by 40% from a holding potential of -80 mV, and by 74% from a holding potential of -60 mV. The nimodipine-sensitive current had a maximum amplitude at a membrane potential of -12 mV. omega-Conotoxin GVIA (omega-CgTX GVIA) blocked the whole-cell Ca2+ current by 40%. The omega-CgTX GVIA-sensitive current had a maximum amplitude at a membrane potential of +2 mV. 3. In summary, type I cells of the adult rat carotid body have dihydropyridine-sensitive L-type and omega-conotoxin GVIA-sensitive N-type voltage-dependent Ca2+ channels. These channels may play a role in the voltage-gated entry of Ca2+ necessary for stimulus-secretion coupling in response to changes in arterial PO2, PCO2 and pH. Inhibition of the Ca2+ currents by somatostatin and dopamine may alter the chemotransduction signal in type I cells.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-1321648,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-1322510,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-1352986,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-1476161,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-1654413,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-1660968,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-1974481,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2011601,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2438698,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2443646,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2443679,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2451016,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2456613,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2544656,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2547195,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2560643,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2567963,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2720436,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2737279,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-2738574,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-3419588,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-389092,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-4950075,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-6248164,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-6270629,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-6509012,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-7182480,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-7480785,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-7506754,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-7519263,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-7519759,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-7938227,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-7965831,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-8107963,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8788934-8394721
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Barium,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channel Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channel Blockers,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Nimodipine,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Somatostatin,
http://linkedlifedata.com/resource/pubmed/chemical/Tyrosine 3-Monooxygenase,
http://linkedlifedata.com/resource/pubmed/chemical/omega-Conotoxin GVIA,
http://linkedlifedata.com/resource/pubmed/chemical/omega-Conotoxins,
http://linkedlifedata.com/resource/pubmed/chemical/omega-conotoxin-MVIIC
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0022-3751
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
489 ( Pt 3)
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
689-99
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pubmed:dateRevised |
2010-9-13
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pubmed:meshHeading |
pubmed-meshheading:8788934-Animals,
pubmed-meshheading:8788934-Barium,
pubmed-meshheading:8788934-Calcium Channel Agonists,
pubmed-meshheading:8788934-Calcium Channel Blockers,
pubmed-meshheading:8788934-Calcium Channels,
pubmed-meshheading:8788934-Carotid Body,
pubmed-meshheading:8788934-Dopamine,
pubmed-meshheading:8788934-Electrophysiology,
pubmed-meshheading:8788934-Immunohistochemistry,
pubmed-meshheading:8788934-Nimodipine,
pubmed-meshheading:8788934-Patch-Clamp Techniques,
pubmed-meshheading:8788934-Peptides,
pubmed-meshheading:8788934-Rats,
pubmed-meshheading:8788934-Rats, Wistar,
pubmed-meshheading:8788934-Somatostatin,
pubmed-meshheading:8788934-Tyrosine 3-Monooxygenase,
pubmed-meshheading:8788934-omega-Conotoxin GVIA,
pubmed-meshheading:8788934-omega-Conotoxins
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pubmed:year |
1995
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pubmed:articleTitle |
L- and N-type Ca2+ channels in adult rat carotid body chemoreceptor type I cells.
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pubmed:affiliation |
Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta 30912-2300, USA.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, U.S. Gov't, P.H.S.
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