Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/67692
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dc.contributor.authorWu, H.C.en_US
dc.contributor.authorChang, C.H.en_US
dc.contributor.authorPeng, H.Y.en_US
dc.contributor.authorChen, G.D.en_US
dc.contributor.authorLai, C.Y.en_US
dc.contributor.authorHsieh, M.C.en_US
dc.contributor.authorLin, T.B.en_US
dc.date2011zh_TW
dc.date.accessioned2014-06-11T05:55:31Z-
dc.date.available2014-06-11T05:55:31Z-
dc.identifier.issn1931-857Xzh_TW
dc.identifier.urihttp://hdl.handle.net/11455/67692-
dc.description.abstractWu HC, Chang CH, Peng HY, Chen GD, Lai CY, Hsieh MC, Lin TB. EphrinB2 induces pelvic-urethra reflex potentiation via Src kinase-dependent tyrosine phosphorylation of NR2B. Am J Physiol Renal Physiol 300: F403-F411, 2011. First published December 8, 2010; doi:10.1152/ajprenal.00520.2010.-Recently, the role of EphB receptor (EphBR) tyrosine kinase and their ephrinB ligands in pain-related neural plasticity at the spinal cord level have been identified. To test whether Src-family tyrosine kinase-dependent glutamatergic N-methyl-D-aspartate receptor NR2B subunit phosphorylation underlies lumbosacral spinal EphBR activation to mediate pelvic-urethra reflex potentiation, we recorded external urethra sphincter electromyogram reflex activity and analyzed protein expression in the lumbosacral (L(6)-S(2)) dorsal horn in response to intrathecal ephrinB2 injections. When compared with vehicle solution, exogenous ephrinB2 (5 mu g/rat it)-induced reflex potentiation, in associated with phosphorylation of EphB1/2, Src-family kinase, NR2B Y1336 and Y1472 tyrosine residues. Both intrathecal EphB1 and EphB2 immunoglobulin fusion protein (both 10 mu g/rat it) prevented ephrinB2-dependent reflex potentiation, as well as protein phosphorylation. Pretreatment with PP2 (50 mu M, 10 mu l it), an Src-family kinase antagonist, reversed the reflex potentiation, as well as Src kinase and NR2B phosphorylation. Together, these results suggest the ephrinB2-dependent EphBR activation, which subsequently provokes Src kinase-mediated N-methyl-D-aspartate receptor NR2B phosphorylation in the lumbosacral dorsal horn, is crucial for the induction of spinal reflex potentiation contributing to the development of visceral pain and/or hyperalgesia in the pelvic area.en_US
dc.language.isoen_USzh_TW
dc.relationAmerican Journal of Physiology-Renal Physiologyen_US
dc.relation.ispartofseriesAmerican Journal of Physiology-Renal Physiology, Volume 300, Issue 2, Page(s) F403-F411.en_US
dc.relation.urihttp://dx.doi.org/10.1152/ajprenal.00520.2010en_US
dc.subjectpelvic painen_US
dc.subjecturethraen_US
dc.subjectSrc-family kinaseen_US
dc.subjectN-methyl-D-aspartateen_US
dc.subjectd-aspartate receptoren_US
dc.subjecthippocampal synaptic plasticityen_US
dc.subjectlong-termen_US
dc.subjectpotentiationen_US
dc.subjectc-fos expressionen_US
dc.subjectanesthetized ratsen_US
dc.subjectephb receptorsen_US
dc.subjectspinal-corden_US
dc.subjectnmdaen_US
dc.subjectsensitizationen_US
dc.subjectsubuniten_US
dc.titleEphrinB2 induces pelvic-urethra reflex potentiation via Src kinase-dependent tyrosine phosphorylation of NR2Ben_US
dc.typeJournal Articlezh_TW
dc.identifier.doi10.1152/ajprenal.00520.2010zh_TW
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