Show simple item record

dc.contributor.authorTully, Keith
dc.contributor.authorKupfer, David
dc.contributor.authorDopico, Alejandro M.
dc.contributor.authorTreistman, Steven N.
dc.date2022-08-11T08:08:49.000
dc.date.accessioned2022-08-23T16:09:29Z
dc.date.available2022-08-23T16:09:29Z
dc.date.issued2000-10-24
dc.date.submitted2009-01-13
dc.identifier.citationToxicol Appl Pharmacol. 2000 Nov 1;168(3):183-8. <a href="http://dx.doi.org/10.1006/taap.2000.9036">Link to article on publisher's site</a>
dc.identifier.issn0041-008X (Print)
dc.identifier.doi10.1006/taap.2000.9036
dc.identifier.pmid11042090
dc.identifier.urihttp://hdl.handle.net/20.500.14038/32707
dc.description.abstractWe 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.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=11042090&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1006/taap.2000.9036
dc.subjectAnimals; 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
dc.subjectNeurosciences
dc.titleA plasticizer released from IV drip chambers elevates calcium levels in neurosecretory terminals
dc.typeJournal Article
dc.source.journaltitleToxicology and applied pharmacology
dc.source.volume168
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1263
dc.identifier.contextkey693175
html.description.abstract<p>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.</p>
dc.identifier.submissionpathgsbs_sp/1263
dc.contributor.departmentGraduate School of Biomedical Sciences, Neuroscience Program
dc.contributor.departmentTreistman Lab
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.source.pages183-8


This item appears in the following Collection(s)

Show simple item record