To investigate the afferent projections to the flocculus in a nonhuman primate, we injected horseradish peroxidase into one flocculus of six rhesus macaques (Macaca mulatta) and processed their brains according to the tetramethylbenzidine protocol to reveal retrogradely labeled neurons. Labeled neurons were found in a large set of nuclei within the rostral medulla and the pons. The greatest numbers of labeled neurons were in the vestibular complex and the nucleus prepositus hypoglossi. There were neurons labeled bilaterally throughout all the vestibular nuclei except the lateral vestibular nucleus, but most of the labeled neurons were in the caudal parts of the medial and inferior vestibular nuclei and in the central part of the superior vestibular nucleus; the nucleus prepositus was also labeled bilaterally, primarily caudally. Modest numbers of labeled neurons were found in the y-group, most ipsilaterally, and many neurons were labeled in the interstitial nucleus of the vestibular nerve. No labeled neurons were found in the vestibular ganglion following a large injection into the flocculus. A second large source of afferents to the flocculus was the medial, paramedial, and raphe reticular formation. Dense aggregates of labeled neurons were located in several pararaphe nuclei of the rostral medulla and the rostral pons and in the nucleus reticularis paramedianus of the medulla and several component nuclei of the nucleus reticularis tegmenti pontis bilaterally. Several groups of cells within and abutting upon the medial and rostral aspects of the abducens nucleus were labeled bilaterally. There was a modest projection from two parts of the pontine nuclei. Both a dorsal midline nucleus ventral to the nucleus reticularis tegmenti pontis and a collection of nuclei in a laminar region adjacent to the contralateral middle cerebellar peduncle contained labeled neurons whose numbers, while modest, were large compared to the projections to the flocculus in other animals. This generic difference may be due to the greater development of the smooth pursuit system in monkeys and the consequent need for a more substantial input from the cerebral cortex. As in other genera, the inferior olive projected to the flocculus via the dorsal cap of Kooy and the contiguous ventrolateral outgrowth. The projection was completely crossed and large injections labeled virtually every neuron in the dorsal cap, suggesting that the dorsal cap is the principal source of climbing fiber afferents.(ABSTRACT TRUNCATED AT 400 WORDS)
A number of questions deriving from a previous electron microscopic study of the superficial layers of the rat superior colliculus pointed out the need for a comprehensive study of the cell types of the superior colliculus and their detailed morphology. In the present Golgi study the cells of the superficial layers of the superior colliculus were found to be of five major types; marginal cells, horizontal cells, narrow field vertical cells, wide field vertical cells, and stellate cells. Some of these categories were further subdivided. Each cell type has a distinctive set of dendritic field characteristics, a regional distribution, and consistent axon characteristics. The horizontal cells were found to have a preference in the orientation of their dendrites along the vertical and horizontal axes of the visual field projection upon the superior colliculus. It is argued that the horizontal cells are the presynaptic elements in the majority of the dendrodendritic synapses.
The abducens nucleus is a central coordinating element in the generation of conjugate horizontal eye movements. As such, it should receive and combine information relevant to visual fixation, saccadic eye movements, and smooth eye movements evoked by vestibular and visual stimuli. To reveal possible sources of these signals, we retrogradely labeled the afferents to the abducens nucleus by electrophoretically injecting horseradish peroxidase into an abducens nucleus in four monkeys and two cats. The histologic material was processed by the tetramethyl benzidine (TMB) method of Mesulam. In both species the largest source of afferents to the abducens nucleus was bilateral projections from the ventrolateral vestibular nucleus and the rostral pole of the medial vestibular nucleus. Scattered neurons were also labeled in the middle and caudal levels of the medial vestibular nucleus. Large numbers of neurons were labeled in the ventral margin of the nucleus prepositus hypoglossi in the cat and in the common margin of the nucleus prepositus and the medial vestibular nucleus in the monkey, a region we call the marginal zone. Substantial numbers of retrogradely labeled neurons were found in the dorsomedial pontine reticular formation both caudal and rostral to the abducens nuclei. In the monkey, large numbers of labeled neurons were present in the contralateral medial rectus subdivision of the oculomotor complex, while smaller numbers occurred in the ipsilateral medial rectus subdivision and elsewhere in the oculomotor complex. In the cat, large numbers of retrogradely labeled cells were present in a small periaqueductal gray nucleus immediately dorsal to the caudal pole of the oculomotor complex, and a few labeled neurons were also dispersed through the caudal part of the oculomotor complex. Occasional labeled neurons were present in the contralateral superior colliculus in both species. The size and distribution of the labeled neurons within the intermediate gray differed dramatically in the two species. In the cat, the retrogradely labeled neurons were very large and occurred predominantly in the central region of the colliculus, while in the monkey, they were small to intermediate in size and were distributed more uniformly within the middle gray. Among the afferent populations present in the monkey, but not in the cat, was a group of scattered neurons in the ipsilateral rostral interstitial nucleus of the medial longitudinal fasciculus and a denser, bilateral population in the interstitial nucleus of Cajal.(ABSTRACT TRUNCATED AT 400 WORDS)
1. With the use of single-unit recording, the reticular formation immediately caudal to the abducens nucleus was searched for saccadic burst neurons in alert, trained rhesus monkeys. We recorded 80 short- and long-lead burst neurons, investigated their connections, and quantitatively analyzed their discharge characteristics. 2. Like excitatory burst neurons located rostral to the abducens, these caudal burst neurons fire optimally for ipsilaterally directed saccades, fire less for vertical saccades, and fire minimally, if at all, for contralateral saccades. The direction associated with the maximum number of spikes was approximately along the horizontal axis (1 +/- 12 degrees (SD); n = 33). 3. The first spike of the burst led the saccade by 2-120 ms, depending on the unit. Neurons were divided into short lead (45%) and long lead (55%) using a burst-lead criterion of 15 ms. In the on-direction, the discharges of both types exhibited strong correlations between number of spikes in the burst and size of the horizontal saccade component; duration of the burst and duration of the saccade; and peak frequency of the burst and peak velocity of the saccade. These relations were looser for long-lead neurons than for short-lead neurons. 4. Horseradish peroxidase injected into the abducens nucleus retrogradely labeled cells in the contralateral reticular formation where burst neurons were recorded, showing that cells in this region make crossed monosynaptic connections. There was good agreement between the limits of this region, as determined physiologically and anatomically. 5. Microstimulation at the locus of recorded burst neurons elicited EMG potentials in the contralateral lateral rectus muscle of the appropriate sign and latency for a monosynaptic inhibitory projection to abducens motoneurons. Stimulation also elicited eye movements consistent with inhibition of the contralateral lateral rectus. 6. It is argued that these characteristics make it likely that the short-lead neurons are the source of the afference which generate the pause in contralateral abducens motoneuron firing during adducting saccades. These neurons are therefore analogous to the inhibitory burst neurons (IBNs) found in the cat. The characteristics of long-lead burst neurons, particularly their lead, make them less likely to subserve this function. These cells might be better suited to providing input to omnipause neurons or to the short-lead IBNs.
To fulfill its putative role in short- and long-term modification of the vestibulo-ocular reflex, the flocculus of the cerebellum must send efferents to brainstem nuclei involved in the control of eye movements. In order to reveal the sites of these interactions, we determined the projections of the flocculus by autoradiography and orthograde transport of horseradish peroxidase in five rhesus macaques. Anterogradely labeled axons collected at the base of the injected folia and coursed caudally and medially between the middle cerebellar peduncle and the flocculus. They swept medially over the caudal surface of the middle cerebellar peduncle, over the dorsal surface of the cochlear nuclei, and then caudally along the lateral surface of the inferior cerebellar peduncle to pass over its dorsal surface in the cerebellopontine angle and terminate exclusively in the ipsilateral vestibular nuclei. Three contingents of axons could be differentiated. The axons of one group flowed caudally and medially into the y-group, which clearly received the densest floccular projection. Other, notably thicker, axons of this group continued rostrally and medially to terminate chiefly in the large-cell core of the superior vestibular nucleus. A second large contingent of thin axons streamed caudal and ventral to the y-group to form a compact tract adjacent to the lateral angle of the fourth ventricle and dorsal to the medial vestibular nucleus. Fibers from this tract (the angular bundle of Löwy) supplied a sizable projection to the rostral part of the medial vestibular nucleus and modest projection to the ventrolateral vestibular nucleus. A final group of fibers extended caudally and medially from the y-group in a plexus ventral to the dentate and interposed nuclei to terminate in the basal interstitial nucleus of the cerebellum (Langer, '85), a broadly distributed cerebellar nucleus on the roof of the fourth ventricle. The flocculus can affect vestibulo-ocular behavior only through these efferents to the vestibular nuclei and the basal interstitial nucleus of the cerebellum.
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