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Identification of a beta2-adrenergic receptor in mammalian epidermis

dc.contributor.authorDuell, Elizabeth A.en_US
dc.date.accessioned2006-04-07T17:28:33Z
dc.date.available2006-04-07T17:28:33Z
dc.date.issued1980-01-01en_US
dc.identifier.citationDuell, Elizabeth A. (1980/01/01)."Identification of a beta2-adrenergic receptor in mammalian epidermis." Biochemical Pharmacology 29(1): 97-101. <http://hdl.handle.net/2027.42/23366>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T4P-4754H3N-2GR/2/2af4563a4fce8300bb102b8efe39f379en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/23366
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6244831&dopt=citationen_US
dc.description.abstractThe presence of a beta2-adrenergic receptor in the epidermis has been demonstrated, based on the following pieces of information: (1) the addition of salbutamol, a beta2-agonist, to slices of epidermal tissue increased the levels of cyclic AMP in the tissue above control levels in a dose-dependent manner with a maximum response after 5 min of incubation in 5 x 10-5 M salbutamol, (2) the addition of butoxamine, a beta2-antagonist, in conjunction with isoproterenol or salbutamol reduced the epidermal cyclic AMP levels when compared to levels obtained with agonist alone, (3) practolol, a beta1-antagonist. had little effect on the salbutamol-induced increases in the cyclic AMP levels and further elevated the levels of cyclic AMP obtained by the addition of isoproterenol, (4) the addition of propranolol to the tissue in conjunction with isoproterenol or salbutamol reduced the levels of cyclic AMP to near control values, and (5) Ro 20-1724, a cyclic nucleotide phosphodiesterase inhibitor, maintained the salbutamolelevated cyclic AMP levels for a longer period of time.en_US
dc.format.extent668410 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleIdentification of a beta2-adrenergic receptor in mammalian epidermisen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan Medical School. Departments of Dermatology and Biological Chemistry, Ann Arbor, MI 48109, U.S.A.en_US
dc.identifier.pmid6244831en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/23366/1/0000310.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0006-2952(80)90250-6en_US
dc.identifier.sourceBiochemical Pharmacologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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