Role of enhanced noradrenergic transmission within the ventral bed nucleus of the stria terminalis in visceral pain-induced aversion in rats

Behav Brain Res. 2009 Feb 11;197(2):279-83. doi: 10.1016/j.bbr.2008.08.024. Epub 2008 Aug 28.

Abstract

Pain is an unpleasant sensory and emotional experience. We demonstrated the crucial role of the bed nucleus of the stria terminalis (BNST) in the negative affective component of somatic and visceral pain induced by intraplantar formalin and intraperitoneal acetic acid injections, respectively, in rats. Recently, we reported the involvement of enhanced noradrenergic transmission via beta-adrenoceptors within the ventral BNST (vBNST) in formalin-induced aversion. Here, we examined the role of intra-vBNST noradrenergic transmission in the negative affective component of visceral pain induced by intraperitoneal acetic acid injection. In vivo microdialysis showed that extracellular noradrenaline levels within the vBNST significantly increased after intraperitoneal acetic acid injection. Using a conditioned place aversion (CPA) test, we found that intra-vBNST injection of timolol, a beta-adrenoceptor antagonist, dose-dependently attenuated the acetic acid-induced CPA without reducing nociceptive behaviors. These results suggest that enhanced noradrenergic transmission via beta-adrenoceptors within the vBNST plays a pivotal role in the negative affective, but not sensory, component of visceral pain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetic Acid
  • Adrenergic beta-Antagonists / administration & dosage
  • Adrenergic beta-Antagonists / pharmacology
  • Analysis of Variance
  • Animals
  • Avoidance Learning / drug effects
  • Avoidance Learning / physiology
  • Conditioning, Psychological / drug effects
  • Conditioning, Psychological / physiology
  • Dose-Response Relationship, Drug
  • Injections, Intraperitoneal
  • Male
  • Microdialysis / methods
  • Neural Pathways / drug effects
  • Neural Pathways / physiopathology*
  • Norepinephrine / analysis
  • Norepinephrine / metabolism*
  • Pain / chemically induced
  • Pain / parasitology
  • Pain / physiopathology*
  • Pain Measurement / methods
  • Pain Threshold / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Reaction Time / drug effects
  • Reaction Time / physiology
  • Septal Nuclei / cytology
  • Septal Nuclei / drug effects
  • Septal Nuclei / metabolism*
  • Timolol / administration & dosage
  • Timolol / pharmacology

Substances

  • Adrenergic beta-Antagonists
  • Timolol
  • Acetic Acid
  • Norepinephrine