Source:http://linkedlifedata.com/resource/pubmed/id/10320737
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
1999-6-30
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pubmed:abstractText |
The intracellular magnesium and calcium concentrations in cultured dorsal root ganglion neurons were measured using a fluorescent Mg2+ indicator, Mag-Fura-2 and a Ca2+ indicator, Fura-2, respectively. The magnesium concentration in the cytoplasm was higher than that in the nuclei at rest; 0.68+/-0.10 mM (mean+/-S.E.M., n=7) in the cytoplasm and 0.11+/-0.05 mM in the nucleus. When depolarized by a 60 mM KCl solution, the magnesium concentration increased remarkably in the cytoplasm; 1.52+/-0.26 mM (n=7) in the cytoplasm and 0.25+/-0. 12 mM in the nucleus. This is in contrast to a Ca2+ increase due to depolarization in which the increase was remarkable also in the nucleus. The Mg2+ response displayed a rapid spontaneous recovery even in the presence of the high K+ solution. The Ca2+ response, on the other hand, accompanied a slow recovery 'plateau'. Simultaneous measurements of Mg2+ and Ca2+ by a double-labeling experiment revealed that the Ca2+ concentration started to rise 0.46+/-0.05 s (n=32) earlier, and it reached its peak 1.38+/-0.12 s (n=32) earlier than Mg2+. These results support the scheme of 'calcium induced magnesium release', that the depolarization-induced elevation of the Ca2+ concentration causes an increase in the Mg2+ concentration in the cytoplasm.
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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/Benzofurans,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Fluorescent Dyes,
http://linkedlifedata.com/resource/pubmed/chemical/Fura-2,
http://linkedlifedata.com/resource/pubmed/chemical/Imidazoles,
http://linkedlifedata.com/resource/pubmed/chemical/Mag-Fura-2-acetoxymethyl ester,
http://linkedlifedata.com/resource/pubmed/chemical/Magnesium,
http://linkedlifedata.com/resource/pubmed/chemical/fura red
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0006-8993
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 1999 Elsevier Science B.V.
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
828
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
163-8
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:10320737-Animals,
pubmed-meshheading:10320737-Benzofurans,
pubmed-meshheading:10320737-Calcium,
pubmed-meshheading:10320737-Cells, Cultured,
pubmed-meshheading:10320737-Fluorescent Dyes,
pubmed-meshheading:10320737-Fura-2,
pubmed-meshheading:10320737-Ganglia, Spinal,
pubmed-meshheading:10320737-Image Processing, Computer-Assisted,
pubmed-meshheading:10320737-Imidazoles,
pubmed-meshheading:10320737-Magnesium,
pubmed-meshheading:10320737-Male,
pubmed-meshheading:10320737-Membrane Potentials,
pubmed-meshheading:10320737-Microscopy, Confocal,
pubmed-meshheading:10320737-Neurons,
pubmed-meshheading:10320737-Rats,
pubmed-meshheading:10320737-Rats, Sprague-Dawley
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pubmed:year |
1999
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pubmed:articleTitle |
Intracellular Mg2+ surge follows Ca2+ increase during depolarization in cultured neurons.
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pubmed:affiliation |
Department of Bioengineering, Faculty of Engineering, Soka University, Tangicho 1-236, Hachioji, Tokyo, Japan. hideki@t.soka.ac.jp
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pubmed:publicationType |
Journal Article
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