Evidence for the participation of peripheral α5 subunit-containing GABAA receptors in GABAA agonists-induced nociception in rats

Eur J Pharmacol. 2014 Jul 5:734:91-7. doi: 10.1016/j.ejphar.2014.03.051. Epub 2014 Apr 12.

Abstract

The activation of GABAA receptor by γ-amino butyric acid (GABA) in primary afferent fibers produces depolarization. In normal conditions this depolarization causes a reduction in the release of neurotransmitters. Therefore, this depolarization remains inhibitory. However, previous studies have suggested that in inflammatory pain, GABA shifts its signaling from inhibition to excitation by an increased GABA-induced depolarization. The contribution of peripheral α5 subunit-containing GABAA receptors to the inflammatory pain is unknown. The purpose of this study was to investigate the possible pronociceptive role of peripheral α5 subunit-containing GABAA receptors in the formalin test. Formalin (0.5%) injection into the dorsum of the right hind paw produced flinching behavior in rats. Ipsilateral local peripheral pre-treatment (-10min) with exogenous GABA (0.003-0.03µg/paw) or common GABAA receptor agonists muscimol (0.003-0.03µg/paw), diazepam (0.017-0.056µg/paw) or phenobarbital (1-100µg/paw) significantly increased 0.5% formalin-induced nociceptive behavior. The pronociceptive effects of GABA (0.03µg/paw), muscimol (0.03µg/paw), diazepam (0.056µg/paw) and phenobarbital (100µg/paw) were prevented by either the GABAA receptor antagonist bicuculline (0.01-0.1µg/paw) or selective α5 subunit-containing GABAA receptor inverse agonist L-655,708 (0.017-0.17µg/paw). The α5 subunit-containing GABAA receptor protein was expressed in dorsal root ganglion (DRG) and dorsal spinal cord of naïve rats. The formalin injection did not modify α5 subunit-containing GABAA receptor expression. Overall, these results suggest that peripheral α5 subunit-containing GABAA receptors play a pronociceptive role in the rat formalin test.

Keywords: Bicuculline; Bicuculline (PubChem CID: 10237); Diazepam (PubChem CID: 3016); GABA; GABA (PubChem CID: 119); GABA(A) receptors; Inflammatory pain; L-655,708; L-655,708 (PubChem CID: 5311203); Muscimol (PubChem CID: 4266); Phenobarbital (PubChem CID: 4763); α(5) Subunit-containing GABA(A) receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bicuculline / pharmacology
  • Female
  • Formaldehyde / pharmacology
  • GABA-A Receptor Agonists / pharmacology*
  • Ganglia, Spinal / drug effects
  • Ganglia, Spinal / metabolism
  • Ganglia, Spinal / physiology
  • Gene Expression Regulation / drug effects
  • Imidazoles / pharmacology
  • Nociception / drug effects*
  • Peripheral Nervous System / drug effects*
  • Peripheral Nervous System / metabolism*
  • Peripheral Nervous System / physiology
  • Protein Subunits / metabolism*
  • Rats
  • Receptors, GABA-A / chemistry*
  • Receptors, GABA-A / metabolism*
  • Spinal Cord / drug effects
  • Spinal Cord / metabolism
  • Spinal Cord / physiology

Substances

  • GABA-A Receptor Agonists
  • Imidazoles
  • L 655,708
  • Protein Subunits
  • Receptors, GABA-A
  • Formaldehyde
  • Bicuculline