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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1995-9-21
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pubmed:abstractText |
1. While intracellular calcium concentrations are closely regulated, two types of ion channels in neurons allow calcium influx: both voltage-activated and NMDA-activated channels are significantly permeable to calcium. In this study we compare the effects of lead (Pb2+) on currents carried through voltage-activated calcium channels and NMDA-activated channels. 2. Pb2+ reduces voltage-activated calcium channel currents elicited by a voltage jump from -80 to 0 mV at 0.1 to 1 microM, with an IC50 of 0.64 microM and a Hill slope of 1.22. This effect was partially reversible and not voltage dependent. Sodium and potassium currents were relatively unaffected at Pb2+ concentrations sufficient to block calcium channel currents by more than 80%. Pb2+ is, thus, a potent, reversible and selective blocker of voltage-dependent calcium channel currents. 3. A fast reversible and slow irreversible blocking action of Pb2+ was found on NMDA-activated currents. When Pb2+ was applied simultaneously with aspartate and glycine (Asp/Gly), the inward currents were rapidly and reversibly reduced in a dose-dependent manner with a minimum effective concentration below 2 microM and a total blockade (> 80%) with 100 microM Pb2+. The IC50 was approximately 45 microM and the Hill coefficient 1.1. Preincubation with 50 microM Pb2+ resulted in a greater reduction in the response to Asp/Gly/Pb2+. This effect was reversed within 2 to 5 sec of wash. The lack of voltage dependence suggests that Pb2+ does not block the channel but rather alters the binding of agonists. Prolonged superfusion of a cell with the Asp/Gly/Pb(2+)-containing external solution resulted in a slow and irreversible decrease in the Asp/Gly activated current.(ABSTRACT TRUNCATED AT 250 WORDS)
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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/Aspartic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channel Blockers,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Glycine,
http://linkedlifedata.com/resource/pubmed/chemical/Lead,
http://linkedlifedata.com/resource/pubmed/chemical/N-Methylaspartate
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0272-4340
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
711-22
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7641231-Animals,
pubmed-meshheading:7641231-Animals, Newborn,
pubmed-meshheading:7641231-Aspartic Acid,
pubmed-meshheading:7641231-Calcium Channel Blockers,
pubmed-meshheading:7641231-Calcium Channels,
pubmed-meshheading:7641231-Cells, Cultured,
pubmed-meshheading:7641231-Dose-Response Relationship, Drug,
pubmed-meshheading:7641231-Ganglia, Spinal,
pubmed-meshheading:7641231-Glycine,
pubmed-meshheading:7641231-Kinetics,
pubmed-meshheading:7641231-Lead,
pubmed-meshheading:7641231-Membrane Potentials,
pubmed-meshheading:7641231-N-Methylaspartate,
pubmed-meshheading:7641231-Neurons,
pubmed-meshheading:7641231-Rats,
pubmed-meshheading:7641231-Time Factors
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pubmed:year |
1994
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pubmed:articleTitle |
Pb2+ reduces voltage- and N-methyl-D-aspartate (NMDA)-activated calcium channel currents.
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pubmed:affiliation |
Heinrich-Heine Universität Düsseldorf, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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