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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007765,
umls-concept:C0020291,
umls-concept:C0031621,
umls-concept:C0032447,
umls-concept:C0033634,
umls-concept:C0034693,
umls-concept:C0034721,
umls-concept:C0040715,
umls-concept:C0443199,
umls-concept:C0596630,
umls-concept:C0599718,
umls-concept:C0599813,
umls-concept:C0599893,
umls-concept:C0678518,
umls-concept:C1280500,
umls-concept:C1522702
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pubmed:issue |
1-2
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pubmed:dateCreated |
1995-3-22
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pubmed:abstractText |
Previous reports from our laboratory have suggested that the neuroactivity of some polychlorinated biphenyl (PCB) congeners is associated with perturbations in cellular Ca(2+)-homeostasis. We have characterized further the neurochemical effects of PCBs on signal transduction in primary cultures of cerebellar granule cells. The present experiments found that neither 2,2'-dichlorobiphenyl (DCBP), an ortho-substituted congener, nor 3,3',4,4',5-pentachlorobiphenyl (PCBP), a non-ortho-substituted congener, affected basal phosphoinositide (PI) hydrolysis in cerebellar granule cells. However, at concentrations up to 50 microM, DCBP potentiated carbachol-stimulated PI hydrolysis, while decreasing it at 100 microM. PCBP, on the other hand, had no effect on carbachol-stimulated PI hydrolysis in concentrations up to 100 microM. [3H]Phorbol ester ([3H]PDBu) binding was used to determine protein kinase C (PKC) translocation. DCBP increased [3H]PDBu binding in a concentration-dependent manner and a twofold increase was observed at 100 microM in cerebellar granule cells. PCBP had no effect on [3H]PDBu binding at concentrations up to 100 microM. The effect of DCBP on [3H]PDBu binding was time-dependent and was also dependent on the presence of external Ca2+ in the medium. To test the hypothesis that DCBP increases [3H]PDBu binding by acting on receptor-activated calcium channels, the effects of DCBP were compared to those of L-glutamate. The effects of DCBP (50 microM) and glutamate (20 microM) were additive.(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/2,2'-dichlorobiphenyl,
http://linkedlifedata.com/resource/pubmed/chemical/3,4,5,3',4'-pentachlorobiphenyl,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Carbachol,
http://linkedlifedata.com/resource/pubmed/chemical/Excitatory Amino Acid Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Glutamic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Phorbol Esters,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositols,
http://linkedlifedata.com/resource/pubmed/chemical/Polychlorinated Biphenyls,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0006-8993
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
31
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pubmed:volume |
662
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
75-82
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:7859093-Animals,
pubmed-meshheading:7859093-Calcium,
pubmed-meshheading:7859093-Carbachol,
pubmed-meshheading:7859093-Cells, Cultured,
pubmed-meshheading:7859093-Cerebellum,
pubmed-meshheading:7859093-Excitatory Amino Acid Antagonists,
pubmed-meshheading:7859093-Glutamic Acid,
pubmed-meshheading:7859093-Hydrolysis,
pubmed-meshheading:7859093-Phorbol Esters,
pubmed-meshheading:7859093-Phosphatidylinositols,
pubmed-meshheading:7859093-Polychlorinated Biphenyls,
pubmed-meshheading:7859093-Protein Kinase C,
pubmed-meshheading:7859093-Rats,
pubmed-meshheading:7859093-Signal Transduction
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pubmed:year |
1994
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pubmed:articleTitle |
Differential effects of polychlorinated biphenyl congeners on phosphoinositide hydrolysis and protein kinase C translocation in rat cerebellar granule cells.
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pubmed:affiliation |
Cellular and Molecular Toxicology Branch, US Environmental Protection Agency, Research Triangle Park, NC 27711.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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