Show simple item record

Secretagogue effects on intracellular calcium in pancreatic duct cells

dc.contributor.authorHootman, Seth R.en_US
dc.contributor.authorStuenkel, Edward L.en_US
dc.date.accessioned2006-09-11T18:59:58Z
dc.date.available2006-09-11T18:59:58Z
dc.date.issued1990-08en_US
dc.identifier.citationStuenkel, Edward L.; Hootman, Seth R.; (1990). "Secretagogue effects on intracellular calcium in pancreatic duct cells." Pflügers Archiv European Journal of Physiology 416(6): 652-658. <http://hdl.handle.net/2027.42/47456>en_US
dc.identifier.issn0031-6768en_US
dc.identifier.issn1432-2013en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47456
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2247336&dopt=citationen_US
dc.description.abstractRegulation of intracellular free calcium ([Ca 2+ ] i ) in single epithelial duct cells of isolated rat and guinea pig pancreatic interlobular ducts by secretin, carbachol and cholecystokinin was studied by microspectrofluorometry using the Ca 2+ -sensitive, fluorescent probe Fura-2. Rat and guinea pig duct cells exhibited mean resting [Ca 2+ ] i of 84 nM and 61 nM, respectively, which increased by 50%–100% in response to carbachol stimulation, thus demonstrating the presence of physiologically responsive cholinergic receptors in pancreatic ducts of both species. The carbachol-induced increase in [Ca 2+ ] i involved both mobilization of Ca 2+ from intracellular stores and stimulation of influx of extracellular Ca 2+ . In contrast, neither cholecystokinin nor secretin showed reproducible or sizeable increses in [Ca 2+ ] i . Both rat and guinea pig duct cells showed considerable resting Ca 2+ permeability. Lowering or raising the extracellular [Ca 2+ ] i led, respectively, to a decrease or increase in the resting [Ca 2+ ] i . Application of Mn 2+ resulted in a quenching of the fluorescence signal indicating its entry into the cell. The resting Ca 2+ and Mn 2+ permeability could be blocked by La 3+ suggesting that it is mediated by a Ca 2+ channel.en_US
dc.format.extent844812 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherIntracellular Calciumen_US
dc.subject.otherCarbacholen_US
dc.subject.otherPancreatic Ductsen_US
dc.subject.otherHuman Physiologyen_US
dc.subject.otherAcetylcholineen_US
dc.subject.otherCholecystokininen_US
dc.subject.otherSecretinen_US
dc.subject.otherBicarbonate Secretionen_US
dc.titleSecretagogue effects on intracellular calcium in pancreatic duct cellsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelKinesiology and Sportsen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Physiology, University of Michigan, 7744 Medical Sciences II Building, 48109-0622, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherDepartment of Physiology, Michigan State University, 48824, East Lansing, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid2247336en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47456/1/424_2004_Article_BF00370610.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00370610en_US
dc.identifier.sourcePflügers Archiv European Journal of Physiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.