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Wiley InterScience | ||
![]() Journal of NeurochemistryVolume 103 Issue 1, Pages 57 - 66 Published Online: 20 Jul 2007 Journal compilation © 2010 International Society for Neurochemistry Published for the International Society for Neurochemistry
Abstract | References | Full Text: HTML, PDF (Size: 383K) | Related Articles | Citation Tracking Effects of noradrenaline on the GABA response in rat isolated spiral ganglion neurons in culture Copyright 2007 The Authors Journal Compilation 2007 International Society for Neurochemistry KEYWORDS gamma-aminobutyric acid • noradrenaline • protein kinase A • rat • spiral ganglion neuron ABSTRACTIn the present study, the modulatory effects of noradrenaline (NA) on the GABA response were investigated in the isolated cultured spiral ganglion neurons of rat by using nystatin perforated patch recording configuration under voltage-clamp conditions. NA reversibly depressed GABA response in a concentration-dependent manner and neither changed the reversal potential of the GABA response nor affected the apparent affinity of GABA to its receptor. α2-adrenoceptor agonist and antagonist, clonidine and yohimbine mimicked and blocked the NA action on the GABA response, respectively. N-[2(methylamino)ethyl]-5-isoquinoline sulfonamide dihydrochloride (H-89), a protein kinase A inhibitor, mimicked the effect of NA on the GABA response. NA failed to affect the GABA response in the presence of both cAMP and protein kinase A modulator. However, NA still depressed the GABA response even in the presence of both phorbol-12-myristate-13-acetate, a protein kinase C activator and chelerythrine, a protein kinase C inhibitor. These results suggest that the NA suppression of the GABA response is mediated by α2-adrenoceptor which reduces intracellular cAMP formation through the inhibition of adenylyl cyclase. Therefore, NA input to the spiral ganglion neurons may modulate the auditory transmission by affecting the GABA response. Received November 28, 2006; revised manuscript received March 27, 2007; accepted: May 2, 2007. |