EXCITATORY AMINO-ACID RECEPTORS CONTRIBUTE TO CAROTID-SINUS AND VAGUSNERVE EVOKED EXCITATION OF NEURONS IN THE NUCLEUS OF THE TRACTUS-SOLITARIUS

Citation
W. Zhang et Sw. Mifflin, EXCITATORY AMINO-ACID RECEPTORS CONTRIBUTE TO CAROTID-SINUS AND VAGUSNERVE EVOKED EXCITATION OF NEURONS IN THE NUCLEUS OF THE TRACTUS-SOLITARIUS, Journal of the autonomic nervous system, 55(1-2), 1995, pp. 50-56
Citations number
21
Categorie Soggetti
Neurosciences
ISSN journal
01651838
Volume
55
Issue
1-2
Year of publication
1995
Pages
50 - 56
Database
ISI
SICI code
0165-1838(1995)55:1-2<50:EARCTC>2.0.ZU;2-O
Abstract
To determine the role of excitatory amino-acid (EAA) receptors in affe rent evoked excitation of neurons in the nucleus of the solitarius (NT S), responses of NTS neurons to activation of visceral afferent inputs were examined before and during iontophoretic application of the broa d spectrum EAA receptor antagonist kynurenate (KYN). Iontophoretic app lication of KYN, at doses which attenuated glutamate but not substance P or acetylcholine evoked discharge, inhibited carotid sinus nerve (C SN) and vagus nerve evoked discharge. KYN attenuation of evoked respon ses was similar whether the evoked input was monosynaptic (CSN evoked discharge reduced by 50 +/- 6% (mean +/- SE; n = 5); vagus nerve evoke d discharge reduced by 45 +/- 4%, n = 6) or polysynaptic (CSN evoked d ischarge reduced by 48 +/- 6%,n = 6; vagus nerve evoked discharge redu ced by 43 +/- 3%, n = 8). Spontaneous action potential discharge rate was reduced during KYN iontophoresis in 6 cells (1.8 +/- 0.4 spikes/s vs. 0.7 +/- 0.2 spikes/s). Iontophoretic application of a structural a nalogue of KYN which has no EAA receptor antagonist properties, xanthu renic acid, had no effect on glutamate, CSN or vagus nerve evoked disc harge. Iontophoretic application of KYN reduced the action potential d ischarge evoked by activation of the carotid body chemoreceptors by 52 +/- 2% in 5 cells tested. The results demonstrate that excitatory ami no-acid receptors are involved in visceral afferent evoked activation of NTS neurons. Furthermore, since both mono- and poly-synaptic inputs were attenuated, these receptors appear to be utilized at multiple le vels of afferent integration within NTS.