A Brainstem-Spinal Circuit Controlling Nocifensive Behavior

Neuron. 2018 Dec 19;100(6):1491-1503.e3. doi: 10.1016/j.neuron.2018.10.037. Epub 2018 Nov 15.

Abstract

Response to danger needs to be rapid and appropriate. In humans, nocifensive behaviors often precede conscious pain perception. Much is known about local spinal cord circuits for simple reflexive responses, but the mechanisms underlying more complex behaviors remain poorly understood. We now describe a brainstem circuit that controls escape responses to select noxious stimuli. Tracing experiments characterized a highly interconnected excitatory circuit involving the dorsal spinal cord, parabrachial nucleus (PBNl), and reticular formation (MdD). A combination of chemogenetic, optogenetic, and genetic ablation approaches revealed that PBNlTac1 neurons are activated by noxious stimuli and trigger robust escape responses to heat through connections to the MdD. Remarkably, MdDTac1 neurons receive excitatory input from the PBN and target both the spinal cord and PBN; activation of these neurons phenocopies the behavioral effects of PBNlTac1 neuron stimulation. These findings identify a substrate for controlling appropriate behavioral responses to painful stimuli.

Keywords: DREADD; Tachykinen; brainstem; medulla; pain; parabrachial nucleus; pronociceptive; spinal cord; substance P.

Publication types

  • Research Support, N.I.H., Intramural
  • Video-Audio Media

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Brain Stem / physiology*
  • Calcitonin Gene-Related Peptide / genetics
  • Calcitonin Gene-Related Peptide / metabolism
  • Decerebrate State
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neural Pathways / physiology*
  • Nociceptors / physiology*
  • Optogenetics
  • Pain / pathology*
  • Pain / physiopathology
  • Pain Perception / physiology
  • Spinal Cord / physiology*
  • Tachykinins / genetics
  • Tachykinins / metabolism
  • Transduction, Genetic

Substances

  • Calca protein, mouse
  • Luminescent Proteins
  • Nerve Tissue Proteins
  • Tachykinins
  • Adenosine Triphosphate
  • Calcitonin Gene-Related Peptide