Neil M. Montgomery

Neural Correlates of Optokinetic Nystagmus in the Mesencephalon of Rana pipiens: A Functional Analysis

The effects of lesions of the anuran mesencephalic retinal terminal fields on horizontal optokinetic nystagmus (OKN) were examined. Lesion sites which produced effects upon OKN responses were as follows: BOR, nBOR, peri-nBOR, the large-celled pretectal nucleus, and the dorsal tegmental gray and deep tectal layers. Transection of BOR generally resulted in an increase in saccadic frequently at the lower stimulus velocities. Lesions of nBOR produced a decrease in the frequency of both head and eye saccades in the middle to high range of stimulus velocities. The only lesions which totally abolished horizontal OKN were those located medical to nBOR, in the peri-nBOR region. Lesions of the large-celled pretectal nucleus and dorsal tegmental gray substantially reduced both head and eye saccades at all stimulus velocities. Small lesions in the deep tectal layers also depressed OKN frequency. These studies indicate that horizontal OKN may be mediated by a number of structures within the anuran mesencephalon.

Thyrotropin-releasing hormone (TRH): Immunohistochemical distribution in tadpole and frog brain ☆

The anatomical localization of immunoreactive TRH (IR-TRH) was demonstrated by the peroxidase-antiperoxidase technique in the brain and pituitary gland of larval and adult Rana catesbeiana. In the adult frog main sites of IR-TRH are perikarya and neuronal fibers in the preoptic and infundibular nuclei of the hypothalamus and in the amygdala and diagonal band of Broca of the telencephalon. In addition, TRH-positive neuronal fibers and endings were found in the septum, pallium, and brain stem as well as in the preoptico-hypophyseal tract, the external zone of the median eminence (which matures during late larval stages), and the pars nervosa; fibers were less extensive in the pars intermedia, and were absent from the pars distalis. In early larval stages, the magnocellular nucleus of the posterior preoptic area is the main site of immunoreactive perikarya. During late stages the extensive adult pattern of distribution of IR-TRH becomes established. The study represents the first immunohistochemical demonstration of IR-TRH in larval anurans, and serves as a basis for clarification of the neuroendocrine regulation of metamorphosis.

Projections of the Vestibular and Cerebellar Nuclei in Rana pipiens

The efferent projections and cytoarchitecture of the vestibulocerebellar region were examined to determine the nuclear boundaries and potential homologies. The anterior portion of the vestibular complex projects to the ipsilateral oculomotor and trochlear nuclei and is the major source of commissural fibers. Neurons in the rostromedial portions of the complex project to the contralateral trochlear nucleus. Large neurons in the ventrolateral portion of the complex give rise to a bilateral vestibulospinal pathway. Medium-sized neurons in the neuropil and small neurons in the central gray giving rise to bilateral projections to the spinal cord and oculomotor nuclei as well as commissural and ipsilateral cerebellar efferents. Projections from the nucleus of the cerebellum reach the contralateral spinal cord and cerebellar nucleus and there is also a bilateral projection to the ventral rhombencephalic and mesencephalic basal plates. The medial portion of the nucleus gives rise to commissural, ipsilateral mesencephalic and contralateral spinal projections. The lateral portion of the nucleus projects to the contralateral ventral mesencephalon. On the whole, the results of this investigation substantiate the division of the anuran vestibular complex in anurans into nuclei which may be homologous to the superior nucleus and nucleus of Deiters in mammals. The case for distinct descending and medial nuclei is less compelling. Further, it appears possible to divide the nucleus of the cerebellum into medial and lateral components whose connectivity is similar to that of reptiles and to a lesser extent mammals.

Organization of ascending projections from the optic tectum and mesencephalic pretectal gray in Rana pipiens

The ascending projections from the dorsal mesencephalon to the thalamus and pretectum in Rana pipiens were investigated by using the anterograde and retrograde transport of HRP with regard to two major issues: (1) the degree of tectotopic organization in the projections, and (2) their cells of origin. The results indicate that the spatial organization of the tecto-thalamic tract is specifically related to the laminar organization of the contributing tectal efferent neurons. Axons of neurons in the superficial portion of tectal layer 8 exit the tectum through layer 9 and travel in the superficial portion of the dorsal and ventral tecto-thalamic tracts and innervate the nucleus lentiformis mesencephali, the posterior lateral dorsal nucleus, and corpus geniculatum. The distribution of terminals within these structures varied with the tectal HRP-injection site. HRP injections in the ventral tecto-thalamic tract retrogradely labeled neurons in the superficial portion of tectal layer 8 across the lateral and caudal portion of the tectal lobe. HRP injections into the dorsal tecto-thalamic tract, at the level of the pretectum, retrogradely labeled pyriform neurons in the superficial portion of tectal layer 8 in the rostral and medial portions of the tectal lobe. With regard to the deep tectal layers, axons from pyramidal neurons in layer 6 and ganglionic neurons in layer 8 leave the tectum through layer 7, travel in both the dorsal and ventral tecto-thalamic tracts, and are located internal to the axons of the pyriform neurons of superficial tectal layer 8. The majority of the ganglionic neurons project to the posterior lateral ventral nucleus and the anterior lateral nucleus. The distribution of terminals within these nuclei did not display a tectotopic organization. A second major projection to the thalamus originates from the mesencephalic pretectal gray and innervates the nucleus lentiformis mesencephali, the posterior lateral dorsal nucleus, the anterior lateral nucleus, dorsal and ventral divisions of the ventral lateral thalamus, and the nucleus of Bellonci. Other axons from the mesencephalic pretectal gray terminate in the contralateral, medial portions of the posterior lateral dorsal thalamus, the ventral lateral thalamus, and the anterior lateral nucleus. The isthmo-tectal projection was also retrogradely labeled following tectal injections of HRP. This pathway travels in the most ventral portion of the ventral tecto-thalamic tract; its axons passed over the lateral margin of the endopeduncular nucleus bilaterally, and crossed the midline in the caudal portion of the optic chiasm. Extensive, bead-like varicosities were observed on these axons both in the endopeduncular nucleus and in the posterior optic chiasm.(ABSTRACT TRUNCATED AT 400 WORDS)

Anatomical evidence for an intergeniculate leaflet in Rana pipiens

The projections of the nucleus of Bellonci and the anterior thalamic nucleus in Rana pipiens appear to be remarkably similar to those that have been described for the mammalian intergeniculate leaflet. The connections of these nuclei were examined using both the anterograde and retrograde transport of horseradish peroxidase. Afferents to the neuropil of Bellonci and its nucleus include bilateral projections from the retina, the contralateral nucleus of Bellonci, and anterior thalamic nucleus as well as bilateral projections from the pretectum and the ipsilateral suprachiasmatic nucleus. Efferent projections observed following HRP injections in the anterior thalamus consist of three components: (1) a ventral hypothalamic-suprachiasmatic and commissural projection, (2) a dorsal descending tract to the pretectum and tectum, and (3) a ventral descending tract to the somatomotor brainstem.

Organization of retinal axons within the optic nerve, optic chiasm, and the innervation of multiple central nervous system targets Rana pipiens

Light microscopic analysis of the optic nerve, chiasm, and optic tracts of Rana pipiens after the anterograde and retrograde transport of horseradish peroxidase has shown that retinal ganglion‐cell axons reach the optic nerve head in chronotopically organized fascicles that form bands across the intraocular optic nerve. These bands of fascicles are divided along the midline in a “zone of reorganization” to create two full maps of the retinal surface; however, this map is discontinuous in that nasal and temporal quadrants are adjacent to one another. In the intracranial portion of the optic nerve, axons undergo another reorganization such that peripheral retinal axons shift position and become localized laterally and ventrally, whereas centrally placed axons become localized dorsally. Within this reorganization, the nerve is reconfigured into laminae of axons, and each lamina consists of age‐related axons organized into two retinal maps.