Alteration of nociceptive integration in the spinal cord of a rat model of Parkinson's disease

Mov Disord. 2018 Jul;33(6):1010-1015. doi: 10.1002/mds.27377. Epub 2018 May 18.

Abstract

Background: Pain is a major non motor symptom that contributes to impaired quality of life in PD. However, its mechanism is unknown.

Objectives and methods: We sought to identify the pain phenotypes and parallel changes in spinal integration of peripheral stimuli in a rat model of PD induced by lesions of SN dopamine neurons, using behavioral plantar and von Frey tests as well as electrophysiology of the dorsal horn.

Results: We show that dopamine depletion by 6-OHDA induced hypersensitivity to mechanical and thermal stimuli. These abnormal behaviors were paralleled by increased neuronal responses and hyperexcitability of wide dynamic range neurons of lamina V of the dorsal horn of the spinal cord in response to electrical stimulation of the sciatic nerve in the 6-OHDA model as compared to sham rats.

Conclusions: These results provide evidence for alteration of nociceptive integration in the spinal dorsal horn neurons in 6-OHDA rats that can reflect changes in pain behavior. © 2018 International Parkinson and Movement Disorder Society.

Keywords: 6-hydroxydopamine; Parkinson's disease; dorsal horn; pain; rat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology
  • Animals
  • Disease Models, Animal
  • Dopamine / metabolism
  • Functional Laterality
  • Hyperalgesia / etiology*
  • Hyperalgesia / pathology
  • Hyperkinesis / chemically induced*
  • Male
  • Neurons / physiology
  • Oxidopamine / toxicity
  • Pain Measurement
  • Pain Threshold / drug effects
  • Pain Threshold / physiology
  • Parkinson Disease, Secondary / chemically induced
  • Parkinson Disease, Secondary / complications*
  • Parkinson Disease, Secondary / pathology*
  • Patch-Clamp Techniques
  • Rats
  • Rats, Sprague-Dawley
  • Spinal Cord / pathology*
  • Sympatholytics / toxicity

Substances

  • Sympatholytics
  • Oxidopamine
  • Dopamine