کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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4326982 | 1614105 | 2010 | 11 صفحه PDF | دانلود رایگان |
A dual probing methodology was implemented so that combined in vivo voltammetric (electrochemical) and in vivo electrophysiological analysis could be carried out concomitantly in two distinct brain regions of the same anaesthetized animal, i.e., cell body such as the dorsal raphe nucleus (DRN) and related terminal region such as the hippocampus, the frontal cortex, and the amygdala.In particular, this methodology allowed:1)Monitoring the previously described inhibition of the serotonin (5-HT) transporter and the consequent increase of 5-HT at synaptic levels following treatment with the selective serotonin reuptake inhibitors (SSRIs) fluoxetine (voltammetric analysis) and2)Verifying the suggested consequent activation of the somatodendritic 5-HT1A autoreceptors of serotonergic neurons within the DRN, richest brain area of 5-HT cells (electrophysiological analysis).In addition, the dual probing methodology has been applied to verify the original proposal that a combined treatment with a potassium (SK) channel blocker such as apamin and an SSRI (i.e., fluoxetine) could overcome the slow onset of the SSRI upon central 5-HT activity that could be related to the slow onset of its therapeutic action. Briefly, the effect of apamin either alone or followed by fluoxetine upon cell firing in the DRN (in vivo electrophysiology) and concomitantly upon 5-HT levels (in vivo voltammetry) in the amygdala (forebrain structure involved in mood regulation and innervated by ascending 5-HT projections from the DRN) was studied.
Journal: Brain Research - Volume 1334, 2 June 2010, Pages 1–11