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Role of prostaglandin E 2 in cholinergic-mediated glycoprotein synthesis in canine antrum

dc.contributor.authorBoland, C. Richarden_US
dc.contributor.authorShimakura, Shuyaen_US
dc.contributor.authorYoshimura, Kenjien_US
dc.contributor.authorKraus, Eugene R.en_US
dc.contributor.authorScheiman, James M.en_US
dc.date.accessioned2006-09-11T14:46:09Z
dc.date.available2006-09-11T14:46:09Z
dc.date.issued1992-07en_US
dc.identifier.citationYoshimura, Kenji; Kraus, Eugene R.; Shimakura, Shuya; Scheiman, James M.; Boland, C. Richard; (1992). "Role of prostaglandin E 2 in cholinergic-mediated glycoprotein synthesis in canine antrum." Digestive Diseases and Sciences 37(7): 1045-1050. <http://hdl.handle.net/2027.42/44416>en_US
dc.identifier.issn0163-2116en_US
dc.identifier.issn1573-2568en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44416
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1618052&dopt=citationen_US
dc.description.abstractWe studied the mechanism of cholinergic stimulation of mucin synthesis in canine antral explants, including the role of PGE 2 as an intermediate messenger. Isolated antral mucosa was incubated with 10 −5 M carbachol (Cb), 10 −5 M indomethacin (IND), 10 −5 M pirenzepine (PZ), 10 −5 M Cb+10 −5 M PZ, 10 −5 M Cb+10 −5 M IND, and 10 −5 M IND +PGE 2 (10 −8 , 10 −7 and 10 −6 M) in the presence or absence of [ 3 H]glucosamine. After 24 hr, total glycoprotein synthesis was quantitated by Sepharose-4B chromatography and by 10% TCA/1%PTA precipitation with lipid extraction. PGE 2 released into the media was measured by radioimmunoassay (RIA). Cb significantly increased total glycoprotein synthesis and produced a significant increase in PGE 2 release. The increase in glycoprotein synthesis and the release of PGE 2 was blocked by the addition of muscarinic antagonist PZ. The addition of IND significantly inhibited glycoprotein synthesis and almost entirely suppressed PGE 2 secretion. IND also inhibited the effect of Cb on glycoprotein synthesis and PGE 2 release. Moreover, PGE 2 (10 −6 and 10 −7 M) significantly increased the glycoprotein synthesis in the canine stomach. This suggests the coordinate participation of PGE 2 -releasing cell population in modulation of glycoprotein synthesis in gastric mucosa.en_US
dc.format.extent652754 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Mediaen_US
dc.subject.otherProstaglandin E 2en_US
dc.subject.otherGastroenterologyen_US
dc.subject.otherBiochemistry, Generalen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherHepatologyen_US
dc.subject.otherOncologyen_US
dc.subject.otherTransplant Surgeryen_US
dc.subject.otherAcetylcholineen_US
dc.subject.otherMuscarinic Receptorsen_US
dc.subject.otherGastric Mucinen_US
dc.titleRole of prostaglandin E 2 in cholinergic-mediated glycoprotein synthesis in canine antrumen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Internal Medicine, VA Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michigan; University of Michigan School of Medicine, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Internal Medicine, VA Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michigan; University of Michigan School of Medicine, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Internal Medicine, VA Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michigan; University of Michigan School of Medicine, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Internal Medicine, VA Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michigan; University of Michigan School of Medicine, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Internal Medicine, VA Medical Center, 2215 Fuller Road, 48105, Ann Arbor, Michigan; University of Michigan School of Medicine, Ann Arbor, Michiganen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid1618052en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44416/1/10620_2005_Article_BF01300285.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01300285en_US
dc.identifier.sourceDigestive Diseases and Sciencesen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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