Affiliation:
1. Division of Cardiovascular Medicine and Department of Pharmacology, University of California, Davis, California, 95616
Abstract
We sought to determine whether glutamate acting at both N-methyl-d-aspartate (NMDA) and non-NMDA receptors transmits area postrema (AP) excitatory inputs to nucleus tractus solitarii (NTS) neurons in the aortic baroreceptor or vagal afferent pathways in vivo. In α-chloralose-anesthetized rabbits, we recorded extracellular NTS neuronal responses to low-frequency aortic depressor nerve (ADN), vagus nerve, and AP stimulation and to iontophoresis of α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid and NMDA during control, iontophoresis of 2,3-dihdroxy-6-nitro-7-sulfamoylbenzo( f)quinoxaline (NBQX),dl-2-amino-5-phosphonovaleric acid (AP5), or both, and recovery conditions. In neurons receiving AP and ADN inputs, NBQX attenuated AP- and ADN-evoked responses by 46 ( P = 0.0206) and 49% ( P = 0.0042). AP5 attenuated AP- and ADN-evoked responses by 39 ( P = 0.0270) and 40% ( P = 0.0157). NBQX + AP5 attenuated AP- and ADN-evoked responses by 74 ( P = 0.0040) and 75% ( P = 0.0028). In neurons receiving AP and vagal inputs, AP transmission was attenuated by 58, 60, and 98%; vagal transmission was attenuated by 62, 35, and 83% during NBQX, AP5, and both antagonists, respectively. These data suggest that both non-NMDA and NMDA receptors transmit AP input to NTS neurons in aortic baroreceptor or vagal afferent pathways.
Publisher
American Physiological Society
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology
Cited by
28 articles.
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