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Degradation of [3H][beta]-endorphin in rat plasma is increased with chronic stress

dc.contributor.authorYoung, Elizabeth A.en_US
dc.contributor.authorHoughten, Richard A.en_US
dc.contributor.authorAkil, Hudaen_US
dc.date.accessioned2006-04-07T20:43:26Z
dc.date.available2006-04-07T20:43:26Z
dc.date.issued1989-08-22en_US
dc.identifier.citationYoung, Elizabeth A., Houghten, Richard A., Akil, Huda (1989/08/22)."Degradation of [3H][beta]-endorphin in rat plasma is increased with chronic stress." European Journal of Pharmacology 167(2): 229-236. <http://hdl.handle.net/2027.42/27801>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T1J-47466RD-CF/2/e8b631620a35193f81d54a5440455378en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/27801
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2480246&dopt=citationen_US
dc.description.abstractWith a number of acute stressors [beta]-endorphin is released into plasma. It is unclear if [beta]-endorphin is converted into any other biologically active products, nor it is clear if the rate or pathways of degradation are changed during chronic stress. To explore these issues, we incubated [3H][beta]-endorphinh labeled in positions 1 and 27 with plasma from normal and chronically footshocked rats and measured the rate of conversion of the label from [beta]-endorphin size material to smaller size material. Initial separations were done using a G-50 molecular sieving column, with subsequent characterization and identification on HPLC. By G-50 sieving, there is a time dependent formation of only one radioactive peak. HPLC identification demonstrates [gamma]-endorphin and another unidentified peak. This enzymatic activity is increased in the plasma of chronically stressed rats.en_US
dc.format.extent572959 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleDegradation of [3H][beta]-endorphin in rat plasma is increased with chronic stressen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPharmacy and Pharmacologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumMental Health Research Institute, University of Michigan, 205 Washtenaw Place, Ann Arbor, MI 48109-0720, USAen_US
dc.contributor.affiliationumScripps Clinic and Research Institute, Department of Immunopathology, 10666 N. Torrey Pines, Road, La Jolla, CA 92036, U.S.A.; Mental Health Research Institute, University of Michigan, 205 Washtenaw Place, Ann Arbor, MI 48109-0720, USA.en_US
dc.contributor.affiliationotherScripps Clinic and Research Institute, Department of Immunopathology, 10666 N. Torrey Pines, Road, La Jolla, CA 92036, U.S.A.en_US
dc.identifier.pmid2480246en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/27801/1/0000201.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0014-2999(89)90583-9en_US
dc.identifier.sourceEuropean Journal of Pharmacologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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