Non-NMDA and NMDA receptors in the synaptic pathway between area postrema and nucleus tractus solitarius

Am J Physiol. 1998 Oct;275(4):H1236-46. doi: 10.1152/ajpheart.1998.275.4.H1236.

Abstract

Area postrema (AP) modulates cardiovascular function through excitatory projections to neurons in nucleus tractus solitarius (NTS), which also process primary sensory (including cardiovascular-related) input via the solitary tract (TS). The neurotransmitter(s) and their receptors in the AP-NTS pathway have not been fully characterized. We used whole cell recordings in voltage- and current-clamp modes in the rat brain stem slice to examine the role of ionotropic glutamatergic receptors and alpha2-adrenergic receptors in the pathway from AP to NTS neurons receiving visceral afferent information via the TS. In neurons voltage clamped at potentials from -100 to +80 mV, AP stimulation (0. 2 Hz) evoked excitatory postsynaptic currents having a fast component blocked by the non-N-methyl-D-aspartate (NMDA) receptor antagonist 1,2,3,4-tetrahydro-6-nitro-2, 3-dioxobenzoquinoxaline-7-sulfonamide (NBQX; 3 microM, n = 7) and a slow component blocked by the NMDA receptor antagonist DL-2-amino-5-phosphonovaleric acid (APV; 50 microM, n = 8). Although NBQX (3 microM, n = 14) abolished AP-evoked action potentials, APV (50 microM, n = 9 or 500 microM, n = 6) or yohimbine, (200 nM, n = 5 or 2 microM, n = 10) did not. Thus, although AP stimulation activates both non-NMDA and NMDA receptors on NTS neurons receiving TS input, only non-NMDA receptors are required for synaptic transmission.

Publication types

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

MeSH terms

  • 2-Amino-5-phosphonovalerate / pharmacology*
  • Afferent Pathways / drug effects
  • Afferent Pathways / physiology
  • Animals
  • Brain Stem / physiology*
  • Cardiovascular System / innervation*
  • Cerebral Ventricles / physiology*
  • Electric Stimulation
  • Evoked Potentials / drug effects
  • Evoked Potentials / physiology
  • Excitatory Amino Acid Antagonists / pharmacology
  • Male
  • Neurons / drug effects
  • Neurons / physiology*
  • Patch-Clamp Techniques
  • Quinoxalines / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Adrenergic, alpha-2 / physiology*
  • Receptors, Glutamate / physiology*
  • Receptors, N-Methyl-D-Aspartate / physiology*
  • Solitary Nucleus / physiology*
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / physiology*
  • Yohimbine / pharmacology

Substances

  • Excitatory Amino Acid Antagonists
  • Quinoxalines
  • Receptors, Adrenergic, alpha-2
  • Receptors, Glutamate
  • Receptors, N-Methyl-D-Aspartate
  • 2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline
  • Yohimbine
  • 2-Amino-5-phosphonovalerate