Tac1-Expressing Neurons in the Periaqueductal Gray Facilitate the Itch-Scratching Cycle via Descending Regulation

Neuron. 2019 Jan 2;101(1):45-59.e9. doi: 10.1016/j.neuron.2018.11.010. Epub 2018 Dec 13.

Abstract

Uncontrollable itch-scratching cycles lead to serious skin damage in patients with chronic itch. However, the neural mechanism promoting the itch-scratching cycle remains elusive. Here, we report that tachykinin 1 (Tac1)-expressing glutamatergic neurons in the lateral and ventrolateral periaqueductal gray (l/vlPAG) facilitate the itch-scratching cycle. We found that l/vlPAG neurons exhibited scratching-behavior-related neural activity and that itch-evoked scratching behavior was impaired after suppressing the activity of l/vlPAG neurons. Furthermore, we showed that the activity of Tac1-expressing glutamatergic neurons in the l/vlPAG was elevated during itch-induced scratching behavior and that ablating or suppressing the activity of these neurons decreased itch-induced scratching behavior. Importantly, activation of Tac1-expressing neurons induced robust spontaneous scratching and grooming behaviors. The scratching behavior evoked by Tac1-expressing neuron activation was suppressed by ablation of spinal neurons expressing gastrin-releasing peptide receptor (GRPR), the key relay neurons for itch. These results suggest that Tac1-expressing neurons in the l/vlPAG promote itch-scratching cycles.

Keywords: GRPR; Tac1; extracellular recording; grooming; itch; optogenetics; periaqueductal gray; rostral ventromedial medulla; somatostatin; spinal cord.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Gene Expression
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neurokinin A / biosynthesis*
  • Neurokinin A / genetics
  • Neurons / chemistry
  • Neurons / metabolism*
  • Periaqueductal Gray / chemistry
  • Periaqueductal Gray / metabolism*
  • Pruritus / metabolism*
  • Pruritus / pathology
  • Pyramidal Tracts / chemistry
  • Pyramidal Tracts / metabolism*
  • Random Allocation
  • Receptors, Neurokinin-1 / biosynthesis*
  • Receptors, Neurokinin-1 / genetics
  • Tachykinins / biosynthesis
  • Tachykinins / genetics

Substances

  • Receptors, Neurokinin-1
  • Tachykinins
  • Neurokinin A