Acute and Chronic Dopaminergic Depletion Differently Affect Motor Thalamic Function

Int J Mol Sci. 2020 Apr 15;21(8):2734. doi: 10.3390/ijms21082734.

Abstract

The motor thalamus (MTh) plays a crucial role in the basal ganglia (BG)-cortical loop in motor information codification. Despite this, there is limited evidence of MTh functionality in normal and Parkinsonian conditions. To shed light on the functional properties of the MTh, we examined the effects of acute and chronic dopamine (DA) depletion on the neuronal firing of MTh neurons, cortical/MTh interplay and MTh extracellular concentrations of glutamate (GLU) and gamma-aminobutyric acid (GABA) in two states of DA depletion: acute depletion induced by the tetrodotoxin (TTX) and chronic denervation obtained by 6-hydroxydopamine (6-OHDA), both infused into the medial forebrain bundle (MFB) in anesthetized rats. The acute TTX DA depletion caused a clear-cut reduction in MTh neuronal activity without changes in burst content, whereas the chronic 6-OHDA depletion did not modify the firing rate but increased the burst firing. The phase correlation analysis underscored that the 6-OHDA chronic DA depletion affected the MTh-cortical activity coupling compared to the acute TTX-induced DA depletion state. The TTX acute DA depletion caused a clear-cut increase of the MTh GABA concentration and no change of GLU levels. On the other hand, the 6-OHDA-induced chronic DA depletion led to a significant reduction of local GABA and an increase of GLU levels in the MTh. These data show that MTh is affected by DA depletion and support the hypothesis that a rebalancing of MTh in the chronic condition counterbalances the profound alteration arising after acute DA depletion state.

Keywords: L-DOPA; deep brain stimulation; electrophysiology; immunohistochemistry; microdialysis.

MeSH terms

  • Adrenergic Agents / adverse effects*
  • Animals
  • Basal Ganglia / drug effects
  • Basal Ganglia / physiology
  • Cerebral Cortex / physiology
  • Deep Brain Stimulation
  • Dopamine / metabolism*
  • Dopamine Agents
  • Glutamic Acid / metabolism
  • Immunohistochemistry
  • Levodopa / pharmacology
  • Male
  • Medial Forebrain Bundle / drug effects*
  • Microdialysis
  • Neurons / drug effects
  • Neurons / physiology*
  • Oxidopamine / adverse effects*
  • Rats
  • Rats, Sprague-Dawley
  • Tetrodotoxin / toxicity
  • Thalamus / drug effects
  • Thalamus / physiopathology*
  • gamma-Aminobutyric Acid / metabolism

Substances

  • Adrenergic Agents
  • Dopamine Agents
  • Glutamic Acid
  • Tetrodotoxin
  • Levodopa
  • gamma-Aminobutyric Acid
  • Oxidopamine
  • Dopamine