Source:http://linkedlifedata.com/resource/pubmed/id/17267168
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2007-3-27
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pubmed:abstractText |
The effect of the antidepressant desipramine on intracellular Ca(2+) movement and viability in prostate cancer cells has not been explored previously. The present study examined whether desipramine could alter Ca(2+) handling and viability in human prostate PC3 cancer cells. Cytosolic free Ca(2+) levels ([Ca(2+)](i)) in populations of cells were measured using fura-2 as a probe. Desipramine at concentrations above 10 microM increased [Ca(2+)](i) in a concentration-dependent manner. The responses saturated at 300 microM desipramine. The Ca(2+) signal was reduced by half by removing extracellular Ca(2+), but was unaffected by nifedipine, nicardipine, nimodipine, diltiazem or verapamil. In Ca(2+)-free medium, after treatment with 300 microM desipramine, 1 microM thapsigargin (an endoplasmic reticulum Ca(2+) pump inhibitor) failed to release Ca(2+) from endoplasmic reticulum. Conversely, desipramine failed to release more Ca(2+) after thapsigargin treatment. Inhibition of phospholipase C with U73122 did not affect desipramine-induced Ca(2+) release. Overnight incubation with 10-800 microM desipramine decreased viability in a concentration-dependent manner. Chelation of cytosolic Ca(2+) with BAPTA did not reverse the decreased cell viability. Collectively, the data suggest that in PC3 cells, desipramine induced a [Ca(2+)](i) increase by causing Ca(2+) release from endoplasmic reticulum in a phospholipase C-independent fashion and by inducing Ca(2+) influx. Desipramine decreased cell viability in a concentration-dependent, Ca(2+)-independent manner.
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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/Antidepressive Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Chelating Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Desipramine,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Fura-2,
http://linkedlifedata.com/resource/pubmed/chemical/Thapsigargin
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0887-2333
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pubmed:author |
pubmed-author:ChenI-ShuIS,
pubmed-author:ChengHe-HsiungHH,
pubmed-author:ChouChiang-TingCT,
pubmed-author:ChuSau-TungST,
pubmed-author:HsuShu-ShongSS,
pubmed-author:HuangChun-JenCJ,
pubmed-author:JanChung-RenCR,
pubmed-author:KuoChun-ChiCC,
pubmed-author:LinKo-LongKL,
pubmed-author:LiuShiuh-InnSI,
pubmed-author:LuYih-ChauYC,
pubmed-author:TsengLi-LingLL,
pubmed-author:WangJue-LongJL
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pubmed:issnType |
Print
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pubmed:volume |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
449-56
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pubmed:dateRevised |
2009-4-10
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pubmed:meshHeading |
pubmed-meshheading:17267168-Antidepressive Agents,
pubmed-meshheading:17267168-Calcium,
pubmed-meshheading:17267168-Calcium Signaling,
pubmed-meshheading:17267168-Cell Survival,
pubmed-meshheading:17267168-Chelating Agents,
pubmed-meshheading:17267168-Desipramine,
pubmed-meshheading:17267168-Dose-Response Relationship, Drug,
pubmed-meshheading:17267168-Enzyme Inhibitors,
pubmed-meshheading:17267168-Fura-2,
pubmed-meshheading:17267168-Humans,
pubmed-meshheading:17267168-Male,
pubmed-meshheading:17267168-Prostatic Neoplasms,
pubmed-meshheading:17267168-Thapsigargin
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pubmed:year |
2007
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pubmed:articleTitle |
Desipramine-induced Ca2+ movement and cytotoxicity in PC3 human prostate cancer cells.
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pubmed:affiliation |
Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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