Organization of sensory input to the nociceptive-specific cutaneous trunk muscle reflex in rat, an effective experimental system for examining nociception and plasticity

J Comp Neurol. 2014 Apr 1;522(5):1048-71. doi: 10.1002/cne.23461.

Abstract

Detailed characterization of neural circuitries furthers our understanding of how nervous systems perform specific functions and allows the use of those systems to test hypotheses. We have characterized the sensory input to the cutaneous trunk muscle (CTM; also cutaneus trunci [rat] or cutaneus maximus [mouse]) reflex (CTMR), which manifests as a puckering of the dorsal thoracolumbar skin and is selectively driven by noxious stimuli. CTM electromyography and neurogram recordings in naïve rats revealed that CTMR responses were elicited by natural stimuli and electrical stimulation of all segments from C4 to L6, a much greater extent of segmental drive to the CTMR than previously described. Stimulation of some subcutaneous paraspinal tissue can also elicit this reflex. Using a selective neurotoxin, we also demonstrate differential drive of the CTMR by trkA-expressing and nonexpressing small-diameter afferents. These observations highlight aspects of the organization of the CTMR system that make it attractive for studies of nociception and anesthesiology and plasticity of primary afferents, motoneurons, and the propriospinal system. We use the CTMR system to demonstrate qualitatively and quantitatively that experimental pharmacological treatments can be compared with controls applied either to the contralateral side or to another segment, with the remaining segments providing controls for systemic or other treatment effects. These data indicate the potential for using the CTMR system as both an invasive and a noninvasive quantitative assessment tool providing improved statistical power and reduced animal use.

Keywords: anesthesiology; animal models; pain; pharmacology; plasticity; sensory neurons; spinal cord.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Afferent Pathways / physiology*
  • Analgesics, Non-Narcotic / pharmacology
  • Animals
  • Bupivacaine / pharmacology
  • Dexmedetomidine / pharmacology
  • Evoked Potentials, Somatosensory / drug effects
  • Evoked Potentials, Somatosensory / physiology
  • Female
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / physiology*
  • Neural Conduction / drug effects
  • Neuronal Plasticity / drug effects
  • Neuronal Plasticity / physiology*
  • Nociception / drug effects
  • Nociception / physiology*
  • Physical Stimulation / adverse effects
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Nerve Growth Factor / metabolism
  • Reflex / drug effects
  • Reflex / physiology*
  • Skin / innervation*
  • Somatostatin / metabolism
  • Spinal Cord / drug effects
  • Spinal Cord / metabolism
  • Ubiquitin Thiolesterase / metabolism

Substances

  • Analgesics, Non-Narcotic
  • Receptors, Nerve Growth Factor
  • Somatostatin
  • Dexmedetomidine
  • UCHL1 protein, rat
  • Ubiquitin Thiolesterase
  • Bupivacaine