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The effects of the dicarboxylic amino acid, DL-alpha-aminoadipate (DLAA) on amino acid responses have been investigated using intracellular recordings from mouse spinal cord neurons grown in dissociated cell culture. DL-alpha-Aminoadipate markedly antagonized postsynaptic responses to iontophoretically appllied aspartate; antagonism of glutamate was much less prominent. DL-alpha-Aminoadipate altered the affinity of aspartate for its receptor while having no observed effects on aspartate-receptor cooperativity. No direct effects of DLAA on membrane potentials or passive membrane properties were seen at the currents used for antagonism. Responses to the inhibitory amino acids GABA and glycine were unaffected by DLAA.

Microionophoretically applied excitatory amino acids induced firing of extracellularly recorded single units in a tissue slice preparation of the mouse cochlear nucleus, and the similarly applied antagonist 2-amino-5-phosphonovalerate (2APV) was demonstrated to be a selective N-methyl-D-aspartate (NMDA) receptor antagonist. In addition, the effect of various bath-applied excitatory amino acid receptor antagonists on auditory nerve evoked field potentials was studied. Antagonists which block NMDA type receptors, blocked auditory nerve evoked potentials in a dose-dependent manner. The 50% effective concentration (EC50) for three of the antagonists used was: D-alpha-aminoadipate, 7.8 mM; 2APV, 4.2 mM; and 2,3-cis-piperidine dicarboxylate, 1.1 mM. Glutamate diethylester (5 mM) had no effect. The results suggest that NMDA, kainate and quisqualate receptors are present in the cochlear nucleus and that auditory nerve transmission in the mouse is mediated by an NMDA type receptor. This is consistent with the concept that the auditory nerve postsynaptic receptor in mammals is of the NMDA type.

The facial nucleus of the rat can be divided into 5 morphological subdivisions. Using a method for the correlation of the observed subdivisions with antidromic field profiles, the orgins of the major muscle branches of the facial nerve in the motor nucleus were determined. The posterior auricular branch is in the medial, the cervical in the ventromedial, the inferior and superior buccolabiales in the lateral, the zygomatic in the dorsal and the temporal and digastric in the intermediate subdivision. The results are consistent with an organization of the motor nucleus reflecting a corresponding topographic organization of the facial musculature.

The cobalt sulphide precipitation technique, in conjunction with Timm's intensification procedure, was used to delineate the afferent and efferent intramedullary pathways of the seventh cranial nerve complex in the rat. The branchial motor nucleus with the accompanying first part, genu, and second part of the root are described. The motor branches to the superficial facial musculature do not contain fibres of geniculate ganglion origin or fibres which terminate in the spinal trigeminal nucleus. The motor branches to the deep facial muscles arise from the dorsal part of the branchial motor nucleus and traverse to the midline medial to the genu, then project under the genu into the lateral reticular formation before exiting with the facial nerve. The salivatory and lacrimal nuclei and their intramedullary pathways are described. Sensory fibres from the cutaneous auricular branch enter the spinal trigeminal tract and most of the chorda tympani gustatory fibres enter the fasciculus solitarius. A smaller number of gustatory fibres extend medially to the region of the salivatory nucleus. Fibres of greater superficial petrosal origin also enter the fasciculus solitarius as well as the medial reticular formation. These findings are discussed in relation to previous anatomical, physiological and clinical reports.

The spontaneous firing rates of non-prepotential (NPP) units of the anteroventral cochlear nucleus are quite low so it has not been possible to determine whether side band tones are inhibitory when presented alone. Microiontophoretically-applied excitatory amino acids can be used to excite non-spontaneous cells directly. Using this technique it can be shown that side band tone bursts 1/2 to 3/4 octave above the characteristic frequency (CF) of a NPP unit inhibit the amino acid-induced firing. Side band tones which inhibited the amino acid-induced firing were beyond the tuning curve. Side band tones within the tuning curve produced excitation. Both, however, usually reduced the activity evoked by a CF tone burst (i.e., two-tone interaction). The data suggests that lateral inhibition and two-tone interactions are separate phenomena in the auditory system and that lateral inhibition may play a critical role in determining the shape of the tuning curve of NPP units.

Experiments were performed on the nucleus magnocellularis and auditory nerve in tissue slices of 19-20-day-old chick embryos. Bath-applied kainate, quisqualate and N-methyl-D-aspartate induced dose-dependent alterations in the antidromic responses of nucleus magnocellularis neurons. The sensitivity of these agonist-induced responses to 2,3-cis-piperidine dicarboxylate, glutamate diethylester and D-alpha-aminoadipate were tested, as was the sensitivity of auditory nerve transmission. The data suggest that receptors for all three agonists are present on nucleus magnocellularis neurons and that the postsynaptic receptor of the nucleus magnocellularis-auditory nerve synapse is of the kainate type. The effects of bath-applied baclofen were also studied. Baclofen blocked orthodromic responses suggesting that an excitatory amino acid is released from the presynaptic terminal.