Excitatory effect of norepinephrine on neurons in the inferior vestibular nucleus and the underlying receptor mechanism

J Neurosci Res. 2016 Aug;94(8):736-48. doi: 10.1002/jnr.23745. Epub 2016 Apr 28.

Abstract

The central noradrenergic system, originating mainly from the locus coeruleus in the brainstem, plays an important role in many physiological functions, including arousal and attention, learning and memory, anxiety, and nociception. However, little is known about the roles of norepinephrine (NE) in somatic motor control. Therefore, using extracellular recordings on rat brainstem slices and quantitative real-time RT-PCR, we investigate the effect and mechanisms of NE on neuronal activity in the inferior vestibular nucleus (IVN), the largest nucleus in the vestibular nuclear complex, which holds an important position in integration of information signals controlling body posture. Here, we report that NE elicits an excitatory response on IVN neurons in a concentration-dependent manner. Activation of α1 - and β2 -adrenergic receptors (ARs) induces an increase in firing rate of IVN neurons, whereas activation of α2 -ARs evokes a decrease in firing rate of IVN neurons. Therefore, the excitation induced by NE on IVN neurons is a summation of the excitatory components mediated by coactivation of α1 - and β2 -ARs and the inhibitory component induced by α2 -ARs. Accordingly, α1 -, α2 -, and β2 -AR mRNAs are expressed in the IVN. Although β1 -AR mRNAs are also detected, they are not involved in the direct electrophysiological effect of NE on IVN neurons. All these results demonstrate that NE directly regulates the activity of IVN neurons via α1 -, α2 -, and β2 -ARs and suggest that the central noradrenergic system may actively participate in IVN-mediated vestibular reflexes and postural control. © 2016 Wiley Periodicals, Inc.

Keywords: inferior vestibular nucleus; norepinephrine; α1-adrenergic receptor; α2-adrenergic receptor; β2-adrenergic receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dose-Response Relationship, Drug
  • Electrophysiological Phenomena / genetics
  • Female
  • In Vitro Techniques
  • Male
  • Neurons / drug effects*
  • Norepinephrine / pharmacology*
  • Patch-Clamp Techniques
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Adrenergic / biosynthesis*
  • Receptors, Adrenergic / drug effects
  • Receptors, Adrenergic / genetics
  • Vestibular Nuclei / cytology*
  • Vestibular Nuclei / drug effects*

Substances

  • Receptors, Adrenergic
  • Norepinephrine