Autoradiographic Tracing Method Research Articles

Ultrastuctural studies of the primate lateral geniculate nucleus: Morphology and spatial relationships of axon terminals arising from the retina, visual cortex (area 17), superior colliculus, parabigminal nucleus, and pretectum of Galago crassicaudatus

The electron microscopic autoradiographic tracing method has been used to examine the morphology and postsynaptic relationships of five projections (retina, cortical area 17, superior colliculus (tectal), parabigeminal nucleus, and pretectum) to the dorsal lateral geniculate nucleus of the greater bush baby Galago crassicaudatus. Retinal terminals have been examined in the contralaterally innervated layer of each of the three matched pairs [parvi- (X-cell), magno- (Y-cell), and koniocellular (small, W-cell)] of geniculate layers. These terminals are large and contain pale mitochondria and round vesicles (RLPs). RLPs are presynaptic to juxtasomatic regions of parvi- and magnocellular neurons. In contrast, RLPs innervate more distal regions of koniocellular neurons. Labeled cortical, tectal, and parabigeminal terminals are relatively small and contain round vesicles and dark mitochondria. Cortical terminals in each of the three representative layers are presynaptic to small diameter dendrites. No convergence of cortical and retinal terminals has been seen in any layer. Labeled tectal and parabigeminal terminals are found primarily in the koniocellular layers, but the latter are also seen in all other layers. Tectal and parabigeminal terminals have been observed converging with retinal terminals on dendrites of some koniocellular neurons. Labeled pretectogeniculate terminals contain densely packed pleomorphic vesicles, dark mitochondria, and a dark cytoplasmic matrix. These terminals, which are present in each of the representative layers, are presynaptic to conventional dendrites and profiles containing loosely dispersed pleomorphic vesicles and a pale cytoplasmic matrix.

Topographic organization of the corticonuclear projections from the paraflocculus in the albino rat: an autoradiographic orthograde tracing study.

The topographic organization of corticonuclear projections from the paraflocculus was studied in rats by an autoradiographic orthograde tracing method. The corticonuclear fibers from the paraflocculus terminated primarily in the caudoventral part of the lateral cerebellar nucleus and in the lateral part of the posterior interpositus nucleus. The rostrolateral part of the ventral paraflocculus projected only to the lateral nucleus, and the caudomedial part projected only to the posterior interpositus nucleus. Although differential projections from the dorsal and ventral paraflocculi were not clearly observed, the dorsal paraflocculus appeared to project to slightly more dorsal parts of the lateral and posterior interpositus nuclei than did the ventral paraflocculus. The lateral, medial, rostral, and caudal parts of each sublobule tended to project to the ventral, dorsal, rostral, and caudal regions within the caudoventral part of the lateral nucleus, respectively, despite massive overlap in the individual terminal fields. The corticonuclear projection from the dorsal and ventral paraflocculi to the posterior interpositus nucleus were organized in different directions; those from the dorsal paraflocculus were organized rostrocaudally, while those from the ventral paraflocculus were organized mediolaterally. These results suggest that in rats the corticonuclear projections from the paraflocculus are topographically organized in the mediolateral and rostrocaudal directions as well as in the dorsoventral direction.

Distribution of nigrothalamic projections in the dog.

The distribution of nigrothalamic projections was studied in the dog by using the autoradiographic tracing method. On the basis of a systematic series of tritiated amino acid injections into different portions of the substantia nigra, we found that the rostral three-fourths of the substantia nigra pars reticulata (SNr) gives rise to widespread thalamic projections. The nigrothalamic label occupied a longitudinal band extending from rostral ventral anterior nucleus (VA) through to caudal mediodorsal nucleus (MD). In the dog, VA is histochemically identified as an acetylthiocholinesterase (AChE)-negative region and is distinct from the adjacent ventral lateral nuclei which stain positively for AChE. In rostral thalamus, the dense autoradiographic label was observed in rostral VA within the AchE-negative region lying alongside the mammillothalamic tract (MT). The adjacent AChE-positive ventral lateral nuclei did not contain autoradiographic label. In addition, homogeneously distributed silver grains were observed throughout the ventromedial nucleus (VM) bilaterally. More caudally, as the ventral lateral thalamic compartment emerges, label was also observed within the internal medullary lamina region, including the paralaminar portion of VA, the central lateral nucleus (CL), and the paralaminar portion of MD. Finally, in caudal thalamus, the central portion of MD, as well as the parafascicular nucleus (Pf), contained autoradiographic label. The overall nigrothalamic distribution observed in the dog was similar to the distribution of nigrothalamic projections in monkeys with one exception. Unlike that of primates, the distribution of nigral efferents is to the whole extent of VM in the dog as in other non-primate species. Overall, we found that nigral efferents primarily project to three main thalamic targets: the VA/MD region, VM, and the internal medullary lamina region, which includes dorsal CL and paralaminar VA and MD. We propose that these three nigrothalamic territories may constitute critical links subserving different functional channels.

Topographic organization of the corticonuclear fibers from the tuber vermis and paramedian lobule in the albino rat.

The topographic organization of the corticonuclear fibers from the tuber vermis and paramedian lobule in the albino rat was investigated by autoradiographic anterograde tracing method. The medial portion of the tuber vermis projects to the dorsal part of the caudomedial subdivision of the medial cerebellar nucleus (MNcm), whereas the lateral portion of the tuber vermis projects to the dorsal part of the MNcm and the caudal part of the middle subdivision of the medial nucleus. The intermediate cortex of the paramedian lobule can be subdivided mediolaterally into three portions which project to the dorsolateral protuberance of the medial cerebellar nucleus, the rostrodorsal part of the posterior interpositus nucleus, and the caudodorsal part of the lateral anterior interpositus nucleus, respectively. The lateral cortex of the paramedian lobule can also be subdivided mediolaterally into two portions: the medial portion projects to the dorsolateral hump, and the lateral one to the lateral cerebellar nucleus. These results indicate that the cortical efferent fibers from the tuber vermis and paramedian lobule are clearly organized in the mediolateral direction in the albino rat.

Corticonigral projections from area 6 in the raccoon

The corticonigral projections from area 6 in the raccoon were investigated using the autoradiographic tracing method. Injections of tritiated proline and leucine were made into either medial or lateral area 6 subdivisions. Uniformly distributed silver grains were observed overlying the ipsilateral substantia nigra pars compacta (SNc) while more restricted foci of label indicative of fiber labeling were present in the substantia nigra pars reticulata (SNr). Autoradiographic label was also present in the substantia nigra pars lateralis (SNl), the retrorubral area and the ventral tegmental area of Tsai. The existence of corticonigral projections from area 6 may serve to modulate SNc activity as a whole and provide an important substrate for the cerebral control of movement.

Synapse formation in the olfactory cortex by regenerating optic axons: ultrastructural evidence for polyspecific chemoaffinity.

The optic nerve was severed at its entry into the optic chiasma and implanted into the striatal region of the ipsilateral cerebral hemisphere in adult frogs (Rana pipiens). Regenerating retinal ganglion cell axons, observed by the autoradiographic tracing method and by horseradish peroxidase (HRP) fiber filling, grew anteriorly along the olfactory tracts and posteriorly along the ipsilateral lateral forebrain bundle and stria medullaris. Many of the regenerating axons ultimately joined the ipsilateral optic tract. The optic axons formed terminal plexuses in the olfactory cortex, lateral geniculate complex, pretectum, tectum, and basal optical nucleus but not in the amygdala or other cerebral territories not postsynaptic to the olfactory bulb, nor in the cell groups associated with the lateral forebrain bundle or stria medullaris. Optic axon terminals labeled with HRP were observed by electron microscopy in the ipsilateral olfactory cortex and in the normal projection areas of the optic nerve, although they were misplaced to the ipsilateral side. They contained clear, spherical synaptic vesicles and pale mitochondria and made Gray type I, asymmetric contacts on dendrites. The retinal projection to the olfactory cortex was formed early in regeneration and was maintained to some degree for periods up to 39 weeks. It was absent in a specimen surviving 50 weeks. Retinal innervation appeared earlier in the lateral geniculate complex and pretectum than in the tectum. These observations suggest that regenerating retinal ganglion cell axons have an affinity for neurons in the olfactory cortex, as well as for the neurons in the optic pathway to which they are normally postsynaptic. Unless the apparent selectivity of the aberrant projection is regulated by principles other than those that bring about the reinnervation of the normal optic centers, the data further suggest that the nature of the molecular mechanisms conveying synaptic specificity must be broad enough to permit the formation of limited sets of alternative synaptic connections. The ability to innervate selectively targets other than those normally specified is termed, here, polyspecificity. Since polyspecificity refers to the the affinity of retinal ganglion axons, as a class, for target structures considered as unit aggregates, it is conceptually different from the graded affinity of ganglion cells in different regions of the retina for target neurons in different regions of the tectum.(ABSTRACT TRUNCATED AT 400 WORDS)

Fiber pathways of basal forebrain cholinergic neurons in monkeys

In rhesus monkeys, autoradiographic tracing methods, complemented by immunocytochemical and histochemical techniques, were used to delineate pathways by which cholinergic neurons of the nucleus basalis of Meynert (nbM) and nucleus of the diagonal band of Broca (ndbB) project to forebrain targets. Following injections of [ 3H]amino acids into these nuclei, 5 major fiber pathways were identified: axons of the nbM and ndbB prject medially, principally within the cingulum bundle, to dorsomedial portions of the hemispheres; nbM and ndbB fibers exit laterally beneath the pallidum and striatum, enter the external and extreme capsules, and pass within the corona radiata to terminate in lateral and caudal regions of neocortex; axons coursing ventrally from the nbM project to protions of the temporal lobe, including the amygdala; some fibers pass through the fibrae orbitofrontales to the orbitofrontales to the orbitofrontal cortex; and, finally, axons of the nbM/ndbB project via the fimbria/fornix and a ventral pathway to the hippocampus. The presence of these 5 radiolabeled pathways arising from basal forebrain cholinergic neurons was confirmed by acetylcholinesterase histochemistry and choline acetyltransferase immunocytochemistry.

The pretectal olivary nucleus of the cat: evidence for a two-tailed structure

The pretectal olivary nucleus of the cat was reconstructed from Nissl and myelin stained tissue. The olivary nucleus is found to have a medially placed head region and two tail regions which extend obliquely from the head region. The retino-olivary projection was also analyzed using the anterograde autoradiographic tracing method. Retinal input is found bilaterally over both the head of the nucleus and the tail regions. The distribution of silver grains, when compared bilaterally, appears slightly more dense over the contralateral nucleus.

Architectonic and hodological organization of the cerebellum in reeler mutant mice

The architectonic and hodologic organization of the reeler cerebellum has been studied by means of immunohistochemistry, general cell and fiber stains and by horseradish peroxidase and autoradiographic tracing methods. Malposition of Purkinje cells, which varies in degree, is the most salient architectonic anomaly of the mutant cerebellum. Mapping the distribution of Purkinje cells is facilitated by a monoclonal antibody which selectively stains neurons of this class in the cerebellum. Although some Purkinje cells form a normal monolayer, most lie in heterotopic positions within or below the granule cell layer. The major contingent is segregated in subcortical masses in the depths of the cerebellum. Fiber bundles continuous with the cerebellar peduncles run in septa between the subcortical Purkinje cell masses. The distribution of Purkinje cell masses as well as the roof nuclei and areas of normal cortex and fiber bundles are identical from animal to animal. These consistent architectonic variations serve to partition the reeler cerebellum into 7 sagittally oriented compartments: one medial, two intermediate, two lateral and two additional lateral lobular appendages which may correspond to paraflocculus and/or flocculus of the normal cerebellum. The topography of the reeler olivocerebellar, or climbing fiber, system is normal in that the caudal-to-rostral axis of the olivary complex maps onto the medial-to-lateral axis of the contralateral hemicerebellum. The climbing fiber projection in reeler, like that of the normal animal, appears to be organized in parasagittal strips. In the mutant, mossy fibers from the pons and spinal cord project respectively to the lateral and medial cerebellar fields, and overlap in the intermediate compartment. They thus invest different and to a large extent complementary cerebellar territories, which approximate the architectonic divisions. This segregation of the two principal mossy fiber systems is not so marked in the normal cerebellum. In terms of laminar distribution, the pontine projection is distributed principally to the granule cell stratum in the mutant. The reeler spinocerebellar afferents, by contrast, project not only to the granule cell layer but also to the heterotopic Purkinje cells. The present observations suggest that the primary defect in the reeler cerebellum is malposition of Purkinje cells. As appears to be the case during development of the forebrain in reeler, the mutation may affect the terminal phase of migration of Purkinje cells in the cerebellum. However, this mechanism alone is insufficient to account for the observation that the anomaly of Purkinje cell position varies in degree, particularly at the boundaries between architectonic compartments. Since these boundaries are also zones of overlap in the distribution of mossy fiber terminations from the brainstem and the spinal cord, abnormal interaction of young postmigratory Purkinje cells with these afferent systems may contribute to the architectonic anomaly of the reeler cerebellum.

Topographical organization of the inferior collicular projection and other connections of the ventral nucleus of the lateral lemniscus in the cat.

The topographic distribution of projections from the ventral nucleus of the lateral lemniscus (VNLL) in the cat was investigated with the autoradiographic tracing method. The origin of minor projections was verified by retrograde tracing methods. Small injections of tritiated leucine were placed in restricted zones of VNLL. A major afferent fiber system to the inferior colliculus was labeled in all cases. From the injection site labeled fibers coursed through and around the nuclei of the lateral lemniscus to enter the ipsilateral inferior colliculus. Regardless of the position or small size of the injection, labeled fibers distributed widely in the inferior colliculus. Fibers ended in the central nucleus and deeper layers of the dorsal cortex in most cases. There was also labeling in the ventrolateral nucleus, but very few fibers ended as lateral as the lateral nucleus. A small number of labeled fibers passed from the inferior colliculus into the nucleus of the brachium of the inferior colliculus and adjacent tegmental areas. Some labeled fibers entered the commissure of the inferior colliculus where they were traced into the dorsal cortex and rostral pole of the inferior colliculus on the side contralateral to the injection site. Though the projections labeled in individual cases were similar in their divergent pattern within the central nucleus of the inferior colliculus, specific variations in the pattern were found. The dorsal zone of VNLL projected more heavily to the deeper layers of the dorsal cortex and an adjacent field in the central nucleus than the other zones. Dorsal injections in the middle zone of VNLL, on the other hand, labeled the medial part of the central nucleus more heavily, whereas ventral injections in the middle zone resulted in heavier lateral labeling. The ventral zone of VNLL projected heavily to a central field in the central nucleus. In addition to this major afferent system of VNLL to the inferior colliculus, a smaller descending projection was found. The descending projection ended mainly in the dorsomedial periolivary region and ventral nucleus of the trapezoid body. However, in some cases a few fibers were traced to the cochlear nuclei. Finally, we observed projections to the medial geniculate body from the dorsal and ventral zones of VNLL that ended diffusely in the medial division of the medial geniculate body. Possibly some fibers from the dorsal zone contribute to a broader projection of the lateral tegmentum to the dorsal division of the medial geniculate body.

Interpeduncular nucleus organization in the rat: Cytoarchitecture and histochemical analysis

The organization of the interpeduncular nucleus (IPN) in the adult rat was analyzed using cytoarchitectonic, histochemical and immunohistochemical methods. Four paired and four unpaired subnuclei can be distinguished in the IPN on the basis of neuronal size, morphology, staining characteristics and packing density. The rostral portion of the IPN contains a rostral dorsal, a rostral ventral and paired rostral lateral and dorsal lateral nuclei. The dorsal lateral nuclei continue into the caudal IPN, which also contains a caudal dorsal, a caudal ventral and paired caudal lateral nuclei. The distribution of extrinsic afferents and of chemically identified intrinsic neuronal and fiber populations within subdivisions of the IPN was examined using immunohistochemistry, acetylcholinesterase histochemistry, catecholamine histofluorescence and the autoradiographic tracing method. Six immunohistochemically distinct neuronal groups are identified in the IPN. Perikarya and axons showing substance P-, leu-enkephalin-, somatostatin-, avian pancreatic polypeptide-, serotonin- and glutamic acid decarboxylase-like immunoreactivity are localized to specific IPN subnuclei. Acetylcholinesterase-positive staining, extrinsic norepinephrine-containing fibers and afferents from the dorsal tegmental nuclei are also distributed specifically to IPN subnuclei. These findings demonstrate a cytoarchitectonic and cytochemical complexity in the rat IPN that implies an important functional role for this poorly understood nuclear complex.

Ascending projections from the nucleus of the brachium of the inferior colliculus in the cat.

Ascending projections from the nucleus of the brachium of the inferior colliculus (NBIC) in the cat were studied by the autoradiographic tracing method. Many fibers from the NBIC ascend ipsilaterally in the lateral tegmentum along the medial border of the brachium of the inferior colliculus. At midbrain levels, fibers from the NBIC end in the superior colliculus, the pretectum, the central gray and the peripeduncular tegmental region bilaterally with ipsilateral predominance. NBIC fibers to the superior colliculus are distributed densely to laminae VI and III throughout the whole rostrocaudal extent of the colliculus. In the pretectum, NBIC fibers terminate in the anterior and medial nuclei and the nucleus of the posterior commissure. NBIC fibers to the dorsal thalamus are distributed largely ipsilaterally. Many NBIC fibers end in the dorsal and medial divisions of the medial geniculate body, but few in the ventral division. The NBIC also sends fibers to the suprageniculate, limitans and lateralis posterior nuclei and the lateral portion of the posterior nuclear complex; these regions of termination of NBIC fibers constitute, as a whole, a single NBIC recipient sector. Additionally, the NBIC sends fibers to the centralis lateralis, medialis dorsalis, paraventricular and subparafascicular nuclei of the thalamus.

Projections from the cortex of the superior temporal sulcus to the dorsal lateral geniculate and pregeniculate nuclei in the macaque monkey.

Cortical projections from the visual region and adjacent polysensory region of the superior temporal sulcus (STs) to the lateral geniculate body (LGb) were investigated in the macaque monkey using an autoradiographic tracing method. Solutions of tritiated aminoacids were injected into different parts of the caudal half of the STs of five animals. A survival time of 7 days was allowed. Labels were found in both subdivisions of the LGb: the dorsal lateral geniculate nucleus (DLGn) and the pregeniculate nucleus (PGn). In particular, part of the visual cortical region adjacent to the middle temporal area (MT) projects into the DLGn as well as the PGn, whereas the MT itself and the superior temporal polysensory region project into the PGn only. Afferents to the DLGn terminate in the magnocellular layers and in their adjoining interlaminar zones, completely sparing the parvocellular layers. Afferents to the PGn terminate in separate regions of this nucleus; the MT and adjacent visual cortices project into the internal layer of the PGn, whereas the polysensosy region of the STs projects into the external retinorecipient layer of the PGn. Possible functional implications of these projections are discussed.

An autoradiographic study of the postnatal development of sensorimotor and visual components of the corticopontine system.

Standard autoradiographic tracing methods which employed intracortical injections of 3H-leucine were used to describe the time course of development in those components of the corticopontine system which originate in sensorimotor (SM) or visual (VIS) cortices. These studies were performed using male or female pigmented rats ranging in age from 1 to 24 days (birth = day 0). Labeled axons could easily be recognized within the cerebral peduncle at the level of the basilar pons on postnatal day 1 following either an SM or a VIS cortical injection. Labeling over the basilar pontine neuropil suggestive of axonal ingrowth could also be seen on day 1 following SM injections but not until day 3 in cases with VIS injections. During the latter part of the first postnatal week, both SM and VIS axon terminal fields were established in the pontine neuropil in locations generally similar to those described in the adult. However, at this time they occupied a larger area and appeared more diffusely organized than in the adult. Subsequently during the second postnatal week, both SM and VIS projection fields gradually became more focused and circumscribed until by day 16 in the case of the SM system, and day 18 for the VIS projection, an adultlike configuration was attained. At no time during development was there any evidence of a more substantial contralateral projection than that described for the adult. Correlation of these events with previous Golgi observations and ongoing electron microscopic studies on pontine synaptogenesis suggest that the focusing or constriction of corticopontine axon terminal fields might be the result of a selective degeneration process in which the presynaptic (corticopontine axon) and postsynaptic (basilar pontine neurons) elements both play an active role. Furthermore, the absence of a stage in development characterized by an increase in the density of the contralateral component of the projection confirms the interpretation of earlier studies which suggested that the aberrant contralateral corticopontine projections observed following neonatal cortical lesions were the result of sprouting from the intact corticopontine system and not due to failure of retraction in one component of a system which in fact distributes bilaterally for a time during development.

Organization of the efferent projections of the medial superior olivary nucleus in the cat as revealed by HRP and autoradiographic tracing methods.

Features of the organization of the efferent axonal projections from the medial superior olivary nucleus (MSO) in the cat were studied. In order to determine the origin and distribution of projections from MSO, the retrograde horseradish peroxidase (HRP) and autoradiographic tracing methods were used. The results showed that (1) in both HRP and autoradiographic studies the projection to the inferior colliculus was largely ipsilateral, although a contralateral component was present; (2) the projection field of MSO was confined to the ventral division of the central nucleus of the inferior colliculus, and within this field the labeling was heavier in the rostral and dorsolateral parts of the ventral division; (3) the projection to the inferior colliculus was topographic with ventral parts of MSO projecting ventrally and dorsal parts of MSO projecting dorsolaterally; (4) the projection field in the central nucleus formed successive laminae oriented from ventrolateral to dorsomedial; (5) the axonal course was via the medial or internal segment of the lateral lemniscus; and (6) some fibers in this course ended additionally within the dorsal nucleus of the lateral lemniscus. This latter projection was also topographically organized. These observations supported previously described features of lamination and tonotopic order for afferents of the inferior colliculus, as well as recent suggestions that functional segregation of afferent connections exists within the laminated portion of the central nucleus of the inferior colliculus.

The organization of projections of the retinorecipient and nonretinorecipient nuclei of the pretectal complex and layers of the superior colliculus to the lateral pulvinar and medial pulvinar in the macaque monkey.

AbstractThe organization of five projections from the retinorecipient and non‐retinorecipient layers of the superior colliculus (SC) and nuclei of the pre‐tectum to the lateral pulvinar, medial pulvinar, and dorsal lateral geniculate nucleus (DLG) of the thalamus in the macaque monkey were established by using both anterograde autoradiographic and retrograde horseradish perox‐idase tracing techniques. Some projections from these midbrain regions to the inferior pulvinar are also described as are projections to the thalamus from the tectorccipient parabigeminal nucleus. First, the retinorecipient and nonretinorecipient pretectal nuclei and SC layers were determined by Nissl stains, myelin stains, and the distribution of label resulting from intraocular injections of tritiated amino acids. The possible projections of these pre‐tectal nuclei, layers of the SC (as well as the parabigeminal nucleus), to the pulvinar and DLG were then determined by both horseradish peroxidase and autoradiographic tracing methods. The retinal projections to the SC extend throughout layers II‐l, II‐2, II‐3, and dorsal III with obvious patches in layers II‐l and II‐2 as described before by others. There were a number of pretectal nuclei which also had connections with the retina. In the nomenclature adopted, these include the sublentiform nucleus, the nucleus of the optic tract (not to be confused with the thalamic limitansnucleus), the posterior (orprincipal) pretectalnucleus, and the laminatedolivary nucleus (with a head and tail). The nucleus of the posterior commissure and the nucleus of the pretectal area do not receive retinal projections.The retinorecipient midbrain regions which project to the pulvinar are as follows. Aside from a complicated multifocal projection to the inferior pulvinar, the superficial retinorecipient SC layers project to three terminal foci or zones in one or more of the lateral pulvinar subdivisions alpha, beta, and gamma (Rezak and Benevento, 1977). Focus 1 lies mainly along the dorso‐ventral lateral border of subdivisions of PL‐gamma and PL‐beta, extending ventrally to PL‐alpha, and arises from SC layers II‐3 and III. Focus 2 occu‐pies the lateral 20–50% of PL‐alpha and arises from SC layers II‐2, II‐3, and III. There is a topographical arrangement to the SC projections to foci 1 and 2 which may reflect a representation of more than two visual quadrants in the lateral pulvinar.Focus 3, which consists of several clusters, is located medially in PL‐gamma and PL‐beta and overlaps their mutual border with the medial pul‐vinar. Focus 3 is complicated as it is made up of a mixed input from the retinorecipient (superficial) and nonretinorecipient (deep) SC layers. The portion of focus 3 located along the medial edge of the lateral pulvinar arises mainly from SC layers II‐2, II‐3, and III, while the portion of the focus located along the adjacent lateral edge of the medial pulvinar arises mainly from SC layersIV, V, and VI. These projections to the pulvinar from the superficial SC differ in their origins from those to the DLG which arise mainly from smaller cells in SC sublayer II‐1. The nonretinorecipient SC projections to the pulvinar arise mainly from the deep layers, i.e., IV, V, and VI, and end in focus 4 within the medial pulvinar and the caudal oral pulvinar. The projection from the deep SC layer to the medial half of focus 3 in the medial pulvinar has already been described above.A pretectal projection to the lateral pulvinar from the retinorecipient region consisting of the nucleus of the optic tract, the sublentiform nucleus, and the posterior pretectal nucleus (collectively called SL in our previous study, Benevento et al., 1977b) was confirmed. This projection forms a focus (focus 5) in the dorsal shoulder of the rostral lateral pulvinar, which extends over foci 1 and 3. Our HRP data indicate that these pretectal nuclei might have convergent projections with the SC to foci 1 to 4 and the DLG. How‐ ever, because of the problem of interruption of fibers of passage, this inter‐ pretation of convergent projections should be viewed with caution. The HRP studies also indicate that the parabigeminal nucleus, which is inter‐ connected with the SC, projects to the thalamus, as it contained a modest number of labelled cells after injections of the inferior pulvinar and focus 2 in PL‐alpha, but only a sparse number after injections of the DLG and focus 1.These results suggest that direct retinal influences can be relayed to visually responsive association cortex via retino‐tectal‐lateral pulvinar, retino‐pretectal‐lateral pulvinar, and retino‐tecto‐parabigeminal‐lateral pulvinar routes in addition to the retino‐tectal‐geniculate and retino‐tectal‐inferior pulvinar routes. In addition, visuomotor and polysensory information influences thalamocortical systems via projections from the deep layers of the SC to the medial pulvinar. When these findings are compared with the known organization of pulvinocortical interconnections one can conclude that the cortex of all four neocortical lobes can be influenced rather directly by the midbrain. The response properties of the various cortical visual areas, thus, need not depend solely upon the corticocortical projections.

Evidence of sub-collicular auditory projections to the medial geniculate nucleus in the cat: An autoradiographic and horseradish peroxidase study

Connections of a posteromedial region of the ventral nucleus of the lateral lemniscus were examined in the cat using the autoradiographic tracing method. This sub-collicular region previously had been shown, using retrograde transport of horseradish peroxidase, to send axons to the superior colliculus 10. The autoradiographic findings revealed that many axons from the posteromedial region of the ventral nucleus of the lateral lemniscus that entered the superior colliculus continued into the midbrain reticular formation. Moreover, other axons traced rostral to the inferior colliculus into the thalamus ended in the medial geniculate nucleus, bilaterally. Experiments in which horseradish peroxidase was placed in the medial geniculate nucleus retrogradely labeled the large neurons in the posteromedial region supporting the autoradiographic observations. Other sub-collicular regions also contained labeled cells in these cases, including the main body of the ventral nucleus of the lateral lemnicus and scattered cell groups around the superior olivary complex.

Descending projections to the inferior olive from the mesencephalon and superior colliculus in the cat. An autoradiographic study.

Descending projections from the mesencephalon and superior colliculus to the inferior olive were analyzed by an autoradiographic tracing method. Injections of tritium-labelled leucine were placed in regions which had previously been identified as sources of afferents to the olive. These were located adjacent to the central gray and extended from the rostral red nucleus to the posterior thalamus. Additional injections were made in the superior colliculus. Other injections were placed in the basal ganglia and thalamus. Injections restricted to one side of the central mesencephalon resulted in predominantly ipsilateral labelling of the olive. After injections in the caudo-medial parafascicular and subparafascicular nuclei and rostral nucleus of Darkschewitsch, deposits of grains were observed in the rostral pole of the medial accessory olive and adjacent ventral lamella of the principal olive. The medial accessory olive contained grains into its middle third. More caudal injections which involved the interstitial nucleus of Cajal as well as the nucleus of Darkschewitsch and rostral red nucleus resulted in the dense labeling of the entire principal olive (except the dorsal cap), the entire medial accessory olive (except subnucleus beta and the caudo-medial pole) and the caudo-dorsal accessory olive. Injections centered in the caudal magnocellular red nucleus and extending into the rostral parvocellular division labelled the dorsal lamella of the principal olive almost exclusively. When only the caudal part of the red nucleus was involved in the injection, the olive was entirely clear of grains. Minor contralateral distributions were observed in the dorsomedial cell column, the medial tip of the dorsal lamella and in the caudal medial accessory olive. The deep layers of the superior colliculus were found to project strongly to the contralateral medial accessory olive immediately beside subnucleus beta and weakly to the same area ipsilaterally. Four pathways were identified as contributing fibers to the olivary projections. These were the medial longitudinal fasciculus, the medial tegmental tract, the central tegmental tract and tectospinal or tectobulbar fibers. The rubrospinal tract did not contribute projections to the olive. Injections in the caudate nucleus, entopeduncular nucleus and ventral anterior and ventral lateral thalamic nuclei, did not result in any labeling in the olive.

Some non-fluorescent connections of the nigro-neostriatal dopamine neurones

This study of the relationships between cells identified by their catecholamine fluorescence and their less fortunate neighbours became possible with the advent of autoradiographic tracing methods. A major output from the neostriatum returns to the substantia nigra where it fills the pars reticulata. Outputs from this area of substantia nigra are present on both sides of the brain in the thalamus, in parts of parafascicular, intralaminar, and mediodorsal nuclei, and the superior colliculi in the deeper layers. Mainly unilateral pathways reach the ventromedial nucleus of thalamus and also pass under the lateral part of the colliculus to reach the region of the nucleus pendunculo-pontinus among the fibres of the brachium conjunctivum. The roles of those areas in the transmission of the output of the basal ganglia to the motor system of the animal, however, remain obscure.

Efferent connections of the lateral hypothalamic area of the rat: An autoradiographic investigation

The efferent projections of the lateral hypothalamic area (LHA) at mid-tuberal levels were examined with the autoradiographic tracing method. Connections were observed to widespread regions of the brain, from the telencephalon to the medulla. Ascending fibers course through LHA and the lateral preoptic area and lie lateral to the diagonal band of Broca. Fibers sweep dorsally into the lateral septal nucleus, cingulum bundle and medial cortex. Although sparse projections are found to the ventromedial hypothalamic nucleus, a prominent pathway courses to the dorsal and medial parvocellular subnuclei of the paraventricular nucleus. Labeled fibers in the stria medullaris project to the lateral habenular nucleus. The central nucleus of the amygdala is encapsulated by fibers from the stria terminalis and the ventral amygdalofugal pathway. The substantia innominate, nucleus paraventricularis of the thalamus, and bed nucleus of the stria terminalis also receive LHA fibers. Three descending pathways course to the brainstem: (1) periventricular system, (2) central tegmental tract (CTT), and (3) medial forebrain bundle (MFB). Periventricular fibers travel to the ventral and lateral parts of the midbrain central gray, dorsal raphe nucleus, and laterodorsal tegmental nucleus of the pens. Dorsally coursing fibers of CTT enter the central tegmental field and the lateral and medial parabrachial nuclei. The intermediate and deep layers of the superior colliculus receive some fibers. Fibers from CTT leave the parabranchial region by descending in the ventrolateral pontine and medullary reticular formation; some of these fibers sweep dorsomedially into the nucleus tractus solitarius, dorsal motor nucleus of the vagus, and nucleus commissuralis. From MFB, fibers descend into the ventral tegmental area and to the border of the median raphe and raphe magnus nuclei.