AI Article Synopsis

  • The study explores how α2-adrenergic receptors affect synaptic transmission between cerebellar parallel fibers and Purkinje cells using various experimental techniques and mouse models.
  • Findings show that noradrenaline reduces the firing rate of Purkinje cells, and this effect can be blocked by specific α2-AR antagonists, indicating the role of these receptors in modulating synaptic activity.
  • The results suggest that activation of presynaptic α2A- and α2B-adrenergic receptors leads to decreased synaptic transmission in the mouse cerebellar cortex, providing insights into neurotransmitter regulation in the brain.

Article Abstract

The mechanism by which α2-adrenergic receptors (ARs) modulate the cerebellar parallel fiber-Purkinje cell (PF-PC) synaptic transmission is unclear. We investigated this issue using electrophysiological and neuropharmacological methods. Six- to eight-week-old ICR mice were used in the study. Under in vivo conditions, PF-PC synaptic transmission was evoked by facial stimulation of ipsilateral whisker pad, and recorded using cell-attached patch from PCs. Under in-vitro conditions, PF-PC synaptic transmission was evoked by electrical stimulation of the molecular layer in cerebellar slices, and was recorded using whole-cell recording from PCs. SR95531 (20 µM) was added to the ACSF during all recordings to prevent GABAA receptor-mediated inhibition. Air-puff stimulation of the ipsilateral whisker pad in-vivo evoked simple spike (eSS) firing of cerebellar PCs. Microapplication of noradrenaline (15 µM) to the molecular layer significantly decreased the numbers and frequency of eSS, an effect abolished by the α2-AR antagonist. Microapplication of an α2-AR agonist, UK14304 (1 µM), significantly decreased the numbers of eSS in PCs, which was abolished by either α2A- or α2B-AR antagonist, but not by α2C-AR antagonist. Under in-vitro conditions, application of UK 14304 significantly decreased the amplitude of PF-PC EPSCs and increased the paired-pulse ratio, which were abolished by either α2A- or α2B-AR antagonist. The present results indicate that activation of presynaptic α2A- and α2B-AR downregulates PF-PC synaptic transmission in mouse cerebellar cortex.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10766093PMC
http://dx.doi.org/10.1097/WNR.0000000000001983DOI Listing

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