Noradrenergic fiber sprouting and altered transduction in neuropathic prefrontal cortex

Brain Struct Funct. 2018 Apr;223(3):1149-1164. doi: 10.1007/s00429-017-1543-7. Epub 2017 Nov 1.

Abstract

Functional changes in hyperpolarization-activated and cyclic nucleotide-gated (HCN) channels have been shown to contribute to medial prefrontal (mPFC) hyperexcitability after peripheral nerve injury. A reduction in the open probability of these neuronal channels might be relevant since this can enhance membrane input resistance and synaptic summation. However, the molecular mechanisms underlying neuropathy-associated alterations in HCN channel activity remain elusive. Using the spared nerve injury model of neuropathic pain in Long-Evans rats, we first discovered a significant increase in noradrenergic innervation within the mPFC of nerve-injured compared to control animals. Patch-clamp recordings in layer II/III pyramidal neurons of the mPFC revealed that adrenoceptors, primarily the α2 subtype, can modulate the voltage-dependent activation of HCN channels and the abnormal prefrontal excitability following peripheral neuropathy. Additionally, microinfusions of the α2 adrenoceptor agonist clonidine in the mPFC of neuropathic rats provided analgesic effects, indicating the behavioral significance for this noradrenergic pathway in manifestations of the chronic pain state. Taken together, our results provide insights into the role of cortical catecholaminergic neuromodulation in neuropathic pain and suggest that altered noradrenergic transduction may play a major role in the HCN channel dysfunction and pyramidal hyperactivity observed in several chronic pain conditions.

Keywords: Clonidine; HCN channels; Monoamines; Neuromodulation; Neuropathic pain.

MeSH terms

  • Adrenergic Agents / pharmacology
  • Animals
  • Barium Compounds / pharmacology
  • Chlorides / pharmacology
  • Disease Models, Animal
  • Dopamine beta-Hydroxylase / metabolism
  • Electric Stimulation
  • Hyperalgesia / physiopathology
  • In Vitro Techniques
  • Male
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Nerve Fibers / drug effects
  • Nerve Fibers / physiology*
  • Neuralgia / drug therapy
  • Neuralgia / pathology*
  • Neurons
  • Norepinephrine / metabolism*
  • Pain Perception / drug effects
  • Pain Perception / physiology*
  • Patch-Clamp Techniques
  • Prefrontal Cortex / metabolism*
  • Prefrontal Cortex / pathology*
  • Rats
  • Rats, Long-Evans
  • Visual Cortex / pathology

Substances

  • Adrenergic Agents
  • Barium Compounds
  • Chlorides
  • barium chloride
  • Dopamine beta-Hydroxylase
  • Norepinephrine