Source:http://linkedlifedata.com/resource/pubmed/id/10022279
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1999-2-25
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pubmed:abstractText |
Lead exposure results in the selective apoptotic loss of rods and bipolar cells. During and following developmental lead exposure rod/retinal cGMP phosphodiesterase expression and activity are delayed in onset and decreased, [Ca2+] is elevated, and mitochondrial ATP synthesis is decreased. In vitro studies, using retinas incubated in Ca2+ and/or Pb2+, demonstrate that rods selectively die by apoptosis, retinal mitochondrial ATP synthesis is decreased, mitochondrial cytochrome c is released and caspase activity is increased. These results suggest that lead-induced rod and bipolar cell apoptosis is triggered by Ca2+ and Pb2+ overload due to altered cGMP phosphodiesterase activity and that mitochondrial alterations play a central role in this process.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0378-4274
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
28
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pubmed:volume |
102-103
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
359-61
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:10022279-3',5'-Cyclic-GMP Phosphodiesterases,
pubmed-meshheading:10022279-Animals,
pubmed-meshheading:10022279-Apoptosis,
pubmed-meshheading:10022279-Calcium,
pubmed-meshheading:10022279-Lead,
pubmed-meshheading:10022279-Mitochondria,
pubmed-meshheading:10022279-Rats,
pubmed-meshheading:10022279-Retina,
pubmed-meshheading:10022279-Retinal Rod Photoreceptor Cells
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pubmed:year |
1998
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pubmed:articleTitle |
Lead-induced alterations in retinal cGMP phosphodiesterase trigger calcium overload, mitochondrial dysfunction and rod photoreceptor apoptosis.
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pubmed:affiliation |
College of Optometry, University of Houston, TX 77204, USA. dafox@uh.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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