Characterization of alpha 2-adrenoceptors which increase potassium conductance in rat locus coeruleus neurones

Neuroscience. 1985 Jan;14(1):95-101. doi: 10.1016/0306-4522(85)90166-6.

Abstract

Intracellular recordings were made from locus coeruleus neurones in a slice of rat pons superfused in vitro. A single-electrode voltage-clamp amplifier was used to measure membrane currents. Superfusion of the slice with clonidine (3-100 nM) or noradrenaline (100 nM-100 microM), or brief application of noradrenaline from a pipette by a pressure pulse, caused dose-dependent membrane hyperpolarizations. Phenylephrine (10 microM) and isoprenaline (10 microM) were ineffective. The hyperpolarizations were accompanied by a decrease in neurone input resistance. The hyperpolarization evoked by pressure ejection of noradrenaline could be reversed by membrane polarization to -110 mV. Clonidine and noradrenaline caused a membrane current which was linearly related to membrane potential between -50 and -120 mV, being outward at resting levels and reversing at -110 mV. The concentration-response curves for clonidine and noradrenaline were shifted rightwards in a parallel manner by alpha 2-adrenoceptor antagonists. The antagonist KeS estimated from the degree of shift were: RX 781094 9 nM, yohimbine 14 nM, phentolamine 20 nM and piperoxane 49 nM. These experiments indicate that in locus coeruleus neurones an increase in potassium conductance results from activation of alpha 2-adrenoceptors similar to those characterized on peripheral neurones.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Clonidine / pharmacology
  • Electric Conductivity
  • In Vitro Techniques
  • Ion Channels / physiology*
  • Locus Coeruleus / physiology*
  • Membrane Potentials / drug effects
  • Norepinephrine / pharmacology
  • Phentolamine / pharmacology
  • Potassium / physiology*
  • Rats
  • Receptors, Adrenergic, alpha / drug effects
  • Receptors, Adrenergic, alpha / physiology*

Substances

  • Ion Channels
  • Receptors, Adrenergic, alpha
  • Clonidine
  • Potassium
  • Norepinephrine
  • Phentolamine