Olivocochlear neurons in the brainstem of the mouse.

The locations of efferent auditory neurons in the white mouse were determined using retrograde transport of HRP from the cochlea. Labeled neurons were localized in the lateral superior olivary nucleus (LSO) and ventral nucleus of the trapezoid body (VNTB). The total number of efferent neurons was determined to be 475; of these 34.5% are medial group efferents and 65.4% are lateral group efferents. The ipsilateral LSO contains 99% of the lateral group neurons and the contralateral VNTB contains 75% of the medial group neurons.

Quantitative estimate of bilaterally projecting medial olivocochlear neurones in the guinea pig brainstem.

Bilateral intracochlear injections of the fluorescent retrograde neuronal tracers fast blue and diamidino yellow were used to identify efferent neurones in the guinea pig brainstem which project to the inner ear on both sides. Bilaterally projecting neurones, detected by their double-labelled appearance in fluorescence microscopy, were found in all the nuclei of origin of the large neurone extra-LSO system of olivocochlear neurones. No double-labelled neurones were found in the small neurone LSO system. When precautions were taken to maximize their capture, these bilaterally projecting neurones comprised 5.4% of the total extra-LSO system neurones projecting to any one cochlea. On the basis of these quantitative data, it was suggested that the bilaterally projecting neurones may correspond to the small group of binaurally activated cochlear efferents identified in physiological studies.

Anatomy of cochlear innervation.

In this review of cochlear innervation, the differences in the innervation of outer and inner hair cells are emphasized. Of the afferent neurons, 90 to 95 per cent are large, myelinated type I neurons, exclusively connected in an essentially radial unbranched manner to the inner hair cells; 5 to 10 per cent are small, mostly unmyelinated type II neurons connected to the outer hair cells with considerable spiral extension and branching. The few small type II neurons, with their thin unmyelinated axons, probably have a minor functional importance for centripetal information transfer. The functional emphasis of the outer hair cell system is likely at the level of the receptor cells where the outer hair cells monitor receptor function. The efferent innervation also consists of at least two types of neurons. Small neurons from the lateral superior olivary nucleus project to the inner hair cell area in a predominantly homolateral fashion, making almost exclusively synaptic contacts with the afferent dendrites associated with the inner hair cells. Larger neurons from the medial nucleus of the trapezoid body and periolivary nucleus provide the abundant efferent nerve supply of the outer hair cells, predominantly contralateral. They have mostly large synaptic contacts, and, in some species exclusively, with the receptor cells, indicating again the functional emphasis of the outer hair cell system at the receptor cell level.

Sympathetic preganglionic efferent and afferent neurons mediated by the greater splanchnic nerve in rabbit.

Motion sickness, a multisymptom disorder characterized by abnormal gastrointestinal motility and emesis, can be induced by vestibular effects on the sympathetic portion of the autonomic nervous system. However, the vestibular-autonomic pathways are unknown. As a first step in the analysis, we identified the locus of preganglionic sympathetic neurons (PSNs) and dorsal root afferent ganglionic neurons (DRGs) which supply sympathetic innervation to major portions of the gastrointestinal tract in the rabbit. Retrograde labeling of neurons was obtained by application of horseradish peroxidase (HRP) to the cut end of the greater splanchnic nerve. Labeled PSNs were found, ipsilaterally, within the T1 to T11 spinal cord segments, with the highest density of neurons in T6. Most PSNs were located within the intermediolateral column (IML), but a significant portion also occurred within the lateral funiculus (LF), the intercalated region (IC) and the central autonomic area (CA). The proportion of labeling between the four regions depended on the spinal cord segment. In the midthoracic levels, the distribution of labeled neurons was denser in the IML and LF, and in the caudal thoracic segments, the majority were localized in the IC and CA. Labeled cells in these four areas varied morphologically from large fusiform neurons in the IC to small fusiform neurons in the LF, small stellate neurons in the CA, and medium-size stellate neurons in the IML. The DRGs were labeled in thoracic segments T1 to T12, with the majority between T5 and T11. These labeled DRG somata of the greater splanchnic nerve were smaller in comparison with unlabeled ones.

Efferent innervation of vestibular receptors in the cat: a radioautographic visualization.

A tritiated amino acid tracing method was used to test the hypothesis that a unilateral group of vestibular efferent neurons of the brain stem may present different innervation patterns to the sensory vestibular epithelia of the ipsi- and contralateral labyrinths. Densitometric analysis of labeled efferent endings suggested a heterogeneity of the efferent projections issuing from a unilateral predominated in the maculae utriculi and cristae ampullares of the semicircular canals. These findings are discussed as a function of other data related to efferent vestibular control.

Facial nerve nucleus in the cat. Further study.

The location of efferent neurons, supplying muscles innervated by facial nerve, was studied in the brain stem of the cat using horseradish peroxidase. One to four microliters of HRP was injected in the frontalis, posterior belly of digastric, platysma, and auricularis superior muscles of the kittens. Their representative locations were determined in the facial nucleus. No direct relation between the amount of HRP injected and the numer of labeled neurons was found. The number of positive cells was between 2 and 661. No labeled neurons were found in nucleus of Vth or any other brain stem nuclei.

Efferent neurons of the rat olfactory bulb. (An experimental study using horseradish peroxidase).

1) Two efferent neurone populations - mitral and tufted cells - are present in the main structure of the rat olfactory bulb. 2) The tufted cells, whose axons leave the olfactory bulb, are scattered throughout the whole of the outer plexiform layer and some of them lie in the periglomelural layer. 3) The axons of some of the tufted cells lead to the rostral part of the prepyriform cortex (the anterior olfactory nucleus). 4) Our findings do not indicate that the tufted cells ensure monosynapltic interbulbar connection.

Autoradiographic studies of the projections of the midbrain reticular formation: ascending projections of nucleus cuneiformis.

The ascending projections of the cuneiform nucleus in the cat were traced by autoradiography in the transverse and sagittal planes following stereotaxically placed injections of (3)H-leucine. The ascending fibers are almost exclusively ipsilateral and enter the diencephalon as a wide radiation. At the mesodiencephalic junction fibers enter the nucleus of the posterior commissure and pretectal nuclei, and others cross in the posterior commissure to distribute to these structures on the contralateral side. More ventrally directed fibers distribute to the fields of Forel and then spread into the posterior hypothalamus and zona incerta. At the caudal level of the ventral thalamic group, the ascending fibers diverge and follow two separate courses. One division of fibers continues forward beneath the ventral thalamic group and distributes to the zpna incerta and dorsal hypothalamic area. It rapidly diminishes in size as it attains more rostral levels where it is found in the bed nuclei of the stria terminalis and the anterior commissure. Other fibers of this division spread laterally to innervate the ventral lateral geniculate nucleus, the lateral hypothalamus, and preoptic area, and still others follow the entire confirmation of the thalamic reticular nucleus. The second division of fiber ascends through midline and intralaminar nuclei, completely encircling the mediodorsal nucleus, which is uninnervated except for a small ventral region. The distribution of this division is heaviest to the paraventricular, parafascicular, and central dorsal nuclei. Neither division is conspicuous rostral to the anterior commissure. No projections to neostriatum or specific thalamic nuclei were evident.