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    A plasticizer released from IV drip chambers elevates calcium levels in neurosecretory terminals

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    Authors
    Tully, Keith
    Kupfer, David
    Dopico, Alejandro M.
    Treistman, Steven N.
    UMass Chan Affiliations
    Graduate School of Biomedical Sciences, Neuroscience Program
    Treistman Lab
    Department of Biochemistry and Molecular Pharmacology
    Document Type
    Journal Article
    Publication Date
    2000-10-24
    Keywords
    Animals; Calcium; Chromatography, Thin Layer; Diethylhexyl Phthalate; *Drug Packaging; Humans; Infusions, Intravenous; Male; Neurosecretory Systems; PC12 Cells; Pituitary Gland, Posterior; Plasticizers; Presynaptic Terminals; Rats; Rats, Sprague-Dawley; Spectrophotometry, Ultraviolet; Tumor Cells, Cultured
    Neurosciences
    
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    Link to Full Text
    http://dx.doi.org/10.1006/taap.2000.9036
    Abstract
    We report that intracellular calcium levels rise in mammalian neurosecretory terminals and in cultured pheochromocytoma cells during acute exposure to physiological medium incubated in IV drip chambers. The agent responsible for this effect is shown to be di(2-ethylhexyl)phthalate (DEHP). DEHP (800 nM) added to saline solution caused a rise in [Ca(2+)](i) similar to that elicited by the contaminant-containing solution. The extraction of this contaminant from the IV drip chamber, as measured by spectrophotometry, was time-dependent and was markedly accelerated by the presence of 50 mM ethanol in the solution. Larger [Ca(2+)](i) increases were observed in terminals exposed to solutions incubated in IV drip chambers for greater durations. The rise in calcium requires transmembrane calcium flux through membrane channels, as the response is blocked by either 100 microM cadmium or by lowering the extracellular free Ca(2+) concentration to 10 microM. Our results suggest that acute alterations in intracellular calcium should be considered in addition to long-term effects when determining the safety of phthalate-containing plastics and that laboratory researchers using plastic perfusion materials consider this potential source of artifactual results.
    Source
    Toxicol Appl Pharmacol. 2000 Nov 1;168(3):183-8. Link to article on publisher's site
    DOI
    10.1006/taap.2000.9036
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/32707
    PubMed ID
    11042090
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1006/taap.2000.9036
    Scopus Count
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    Morningside Graduate School of Biomedical Sciences Scholarly Publications
    UMass Chan Faculty and Researcher Publications

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