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Differential projections of cat medullary raphe neurons demonstrated by retrograde labelling following spinal cord lesions.

Neurons of the medullary raphe nuclei in cats were retrogradely labelled following injection of horseradish peroxidase (HRP) into the L6 spinal cord segment. Brainstems were cut in sagittal section to facilitate examination of the rostral-caudal extent of raphe neurons projecting to the spinal cord. Large numbers of HRP-labelled neurons were found in nucleus raphe magnus, nucleus raphe pallidus, and nucleus raphe obscurus (as well as a few neurons in nucleus raphe pontis). Dorsal or ventral hemisections at the T12-L1 level restricted HRP retrograde transport to those pathways within the intact portion of spinal cord, allowing a determination of the part of the cord through which raphe neurons project to the lumbar enlargement. Neurons of nucleus raphe magnus were found to project primarily in dorsolateral fasciculus. A significant number of neurons of nucleus reticularis gigantocellularis also project in dorsolateral fasciculus. Nucleus raphe obscurus neurons were found to project primarily in ventral funiculus, while nucleus raphe pallidus neurons project in the ventrolateral fasciculi and ventral funiculus. The serotonergic (5HT) fibers described by Dahlström and Fuxe ('65) to terminate in the dorsal horn, intermediolateral cell column, and ventral horn are likely to coincide with the raphe-spinal projections documented in this work.

Animals↗

Projections to the visual cortex in the golden hamster.

Retrograde transport of horseradish peroxidase (HRP) was used to determine the origins of afferent connexions to the visual cortex (areas 17, 18a and 18b) in the hamster. The distribution of neurons projecting to the visual cortex from other cortical areas, from the thalamus and from the brainstem was studied using a computer technique for three-dimensional reconstruction. There is a topographically organized projection from the dorsal lateral geniculate nucleus to area 17, but probably to no other of the areas studied. The lateral posterior nucleus of the thalamus (LP) projects to area 18a and weakly to area 17. The lateral nucleus (L) projects to area 18b and also, probably, weakly to area 17. The cortical projections from LP and L are also organized topographically but relatively grossly compared with the geniculo-cortical pathway. There are reciprocal association projections between area 17 and areas 18a and 18b. Areas 18a projects weakly to 18b. The main commissural connexions of the posterior neocortex are between the area 17/18a boundary zones in the two hemispheres, with little between the bodies of area 17. Labelled neurons were found bilaterally in the locus coeruleus, more ipsilaterally than contralaterally, after multiple injections into the visual cortex: single, small injections sometimes resulted in the labelling of a single cell body in the locus coeruleus.

Animals↗

Subcortical projections of six visual cortical areas in the owl monkey, Aotus trivirgatus.

Subcortical projections of six visual cortical areas (Areas 17 and 18, the Middle Temporal, Dorsomedial and Medial Areas, and the Posterior Parietal Region) in the owl monkey, Aotus trivigatus, were investigated with autoradiographic methods following injections of tritiated proline. No contralateral projections were demonstrated. While some brainstem structures received input from all six subdivisions of cortex, each cortical area appeared to exhibit its own unique pattern of subcortical projections. All six cortical areas were found to project to the superior and inferior divisions of the pulvinar, reticular nucleus of the thalamus, pretectum and superior colliculus. Other subcortical targets of one or more visual cortical areas were the basal ganglia, claustrum, zona incerta, one or more of the intralaminar nuclei, lateral posterior nucleus, pregeniculate nucleus, dorsal lateral geniculate nucleus, and pontine nuclei. Furthermore, details of corticofugal projections to the dorsal lateral geniculate nucleus, pretectum and superior colliculus varied with the cortical area studied. The projections to the reticular nucleus, pregeniculate nucleus, dorsal lateral geniculate nucleus, the inferior and a portion of the superior division of the pulvinar and the superior colliculus were found to be topographically organized. The targets of the subcortical projections were compared with those of the retina, as revealed by autoradiographic methods following tritiated proline injections of the eye and were found to overlap to varying extents in the superior colliculus, pretectum and dorsal lateral geniculate nucleus and to be segregated in the pregeniculate nucleus. The results substantiate the validity of previous studies in the owl monkey that suggest that the visual cortex is subdivided into several functionally distinct areas; and illustrate the complexity of corticofugal influence on visual processing.

Animals↗

The striate projection zone in the superior temporal sulcus of Macaca mulatta: location and topographic organization.

In the rhesus monkey, the caudal portion of the superior temporal sulcus (STS) receives a direct projection from lateral striate cortex, the striate are representing central vision. The present study was undertaken to determine whether STS also receives a direct projection from areas of striate cortex representing peripheral vision, with the intent of defining the entire striate projection zone in STS as well as providing information regarding a possible topographic organization within this secondary visual area. A series of five rhesus monkeys was prepared with unilateral lesions of lateral, posterior, or medial striate cortex, such that, collectively, the lesions in the series included all of striate cortex with little or no invasion of prestriate cortex. The monkeys were sacrificed seven days after surgery and their brains were processed by the Fink-Heimer procedure. An analysis of the distribution of terminal degeneration within STS indicated: (1) All areas of striate cortex project to a restricted region along the caudal portion of STS. The ventral limit of this region can be demarcated by an imaginary line connecting the ventral tips of the lunate and intraparietal sulci; from this limit the region extends dorsocaudally for approximately 12 mm to the point at which STS frequently bifurcates, sending one spur forward into the inferior parietal lobule. (2) Within this portion of STS there is an orderly mapping of the visual field; progression from central vision to the far periphery is represented by a progression down the posterior bank of STS and continuing along the entire floor, or insula-like portion, of the sulcus. (3) Projections from striate cortex to STS terminate predominantly in layer IV and the deep part of layer III. (4) There is a distinctive pattern of myelination contained within the striate projection zone of STS. These anatomical findings concerning the striate projection zone of STS in the rhesus monkey are remarkably similar to those that have been described for the middle temporal visual area (MT) in New World monkeys, and thus support earlier proposals that the two areas are homologous.

Animals↗

Origins of crossed and uncrossed retinal projections in pigmented and albino mice.

The extent of the binocular cortical field in albino mice, as revealed by recording from single cells, was almost normal; although the input from the ipsilateral eye was weaker than normal, most cells were driven from both eyes. By backfilling retinal ganglion cells from one optic tract with horseradish peroxidase we examined the origins of the retinofugal projections. Filled cells ipsilateral to the injected tract were concentrated in a crescent-shaped area bordering the inferior temperal retina. In black mice this area constituted 20% of the total retinal area, in albinos 17%. In black mice we counted nearly 1,000 labeled cells in the ipsilateral retina, or 2.6% of all cells filled in both eyes. Albinos had about one-third fewer filled cells ipsilaterally than black mice. Four percent of all ipsilaterally filled cells in black mice and 8% in albinos were scattered outside of the crescent region. The density of ipsilaterally projecting cells was uniform throughout the crescent region in black mice, but decreased toward the central retina in albinos. In retinas contralateral to the injection up to 39,000 cells were filled-about two-thirds of the cells in the ganglion-cell layer whose cytoplasm contained conspicuous Nissl substance. Depending on classification of unfilled cells as ganglion cells or interneurons, we estimated a total of 48,000 to 65,000 ganglion cells to exist in the retina. The size distribution of ipsilaterally projecting ganglion cells was similar in albinos and normals. Ipsilaterally projecting ganglion cells were on average 1.8-3 times larger in volume than contralaterally projecting ones in both types of mice. Displaced ganglion cells were relatively more common in ipsilateral retinofugal projections: 21% of all ipsilateral ganglion cells were displaced versus less than 1% of all the contralateral ganglion cells in black mice. In albinos only 13% of the ganglion cells in the ipsilateral retina were displaced. The overall reduction in ipsilaterally projecting cells in albinos was reflected twice as much in displaced ganglion cells as in normally placed ones.

Animals↗

The afferent ganglion cells and cortical projections of the retinal recipient zone (RRZ) of the cat's pulvinar complex'.

A retino-pulvinar projection in the cat was confirmed using anterograde (autoradiography) and retrograde (horseradish peroxidase (HRP)) tracing techniques. The part of the "pulvinar complex" receiving retinal afferents is referred to as the retinal recipient zone (RRZ). The cortical projections of the RRZ were studied by injecting HRP into different cortical areas. The retrograde labeling of the cell bodies and dendritic fields of the retinal ganglion cells projecting to the RRZ was accomplished by injecting HRP electrophoretically into the RRZ. Our results indicate that the RRZ projects to areas 19 and the lateral suprasylvian area (LS) but not to areas 17 or 18. Virtually all RRZ cells, including those that project to the cortex, are small (10-20 micron in diameter); they are the same size as the relay cells of the parvocellular C laminae of the lateral geniculate nuclear complex (LGNd) that project to areas 19 and LS. The majority of the ganglion cells projecting to the RRZ had medium-sized somas (15-25 micron in diameter), large (up to 800 micron in diameter), diffuse dendritic fields with a characteristic morphology, and appeared different from the alpha, beta, gama, and delta cells of Boycott and Wässle ('74). These cells provide evidence for another morphological class of ganglion cells, termed epsilon cells. Our results suggest that the RRZ relays the activity of specific types of retinal ganglion cells to extrastriate visual cortex and, thus, functions in parallel with the different subdivisions of the LGNd.

Animals↗

Cerebellothalamic projections in the rat: an autoradiographic and degeneration study.

The purpose of this study was to determine the topographical organization of cerebellothalamic projections in the rat. Following stereotaxic injections of 3H-leucine or electrolytic lesions in the cerebellar nuclei, efferent fibers were observed to emerge from the cerebellum through two discrete routes. Fibers from the fastigial nucleus decussated within the cerebellum, formed the crossed ascending limb of the uncinate fasciculus, ascended in the dorsal part of the midbrain tegmentum, and entered the thalamus. Cerebellothalamic fibers from the interpositus and dentate nuclei coursed in the ipsilateral brachium conjunctivum, decussated in the caudal midbrain, and ascended to the thalamus via the crossed ascending limb of the brachium conjunctivum. Cerebellar terminations were observed in the intralaminar, lateral, and ventral tier thalamic nuclei as well as in the medial dorsal nucleus. Projections to the intralaminar nuclei were more pronounced from the dentate and posterior interpositus than from the anterior interpositus and fastigial nuclei. The lateral thalamic nuclei received a projection from the dentate and posterior interpositus nuclei while the fastigial nucleus projected to the medial dorsal nucleus. Within the rostral ventral tier nuclei fastigiothalamic terminations were localized in the medial parts of the ventral medial and ventral lateral nuclei, whereas dentatothalamic projections were concentrated in the lateral parts of the ventral medial nucleus and the medial half of the ventral lateral nucleus. Terminations from the posterior interpositus nucleus were observed ventrally and laterally within the caudal two-thirds of the ventral medial nucleus and throughout the ventral lateral nucleus, where they were densest in the lateral part of its lateral wing and within the central part of its cap. The anterior interpositus nucleus also projected to the central and lateral parts of the ventral lateral nucleus, but these terminations were considerably less dense than those from the posterior interpositus. A few fibers from the interpositus nuclei terminated in the medial part of the rostral pole of the ventral posterior nucleus. A prominent recrossing of cerebellothalamic fibers from the fastigial, posterior interpositus, and dentate nuclei occurred through the central medial nucleus of the internal medullary lamina. These terminated within the ipsilateral ventral lateral and intralaminar nuclei. These results show that each of the cerebellar nuclei project to the thalamus and that their terminations are topographically organized in the rostral ventral tier nuclei. The clustering of autoradiographic silver grains or terminal degeneration observed in the thalamic nuclei suggests a medial-to-lateral organization of this cerebellothalamic system.

Animals↗

Short- and long-term effects of neonatal and adult visual cortex lesions on the retinal projection to the pulvinar in cats.

An increased retinal projection to th pulvinar occurred in cats following neonatal ablation of visual cortical areas 17, 18, and 19. After unilateral lesions, the retinopulvinar projection visualized with autoradiography was larger and denser on the lesioned side than on the intact side. This increased projection was first recognized when the lesioned kittens were 1 week old, when increased labeling in the pulvinar was first detected. The retinopulvinar projection on the intact side of the brain decreased in size with age over the first 3 months of life. This decrease in size was not observed on the lesioned side of the brain. The absence of this decrease on the lesioned side may represent a failure of retraction of exuberant connections, but because of the active invasion by retinal fibers immediately after the lesion, observations of the normal retraction may simply be obscured. Severe cellular degeneration in the dorsal lateral geniculate occurred a few days before the changes in the retinopulvinar projection began; this loss of a postsynaptic target for many retinal axons may trigger the reorganization of input to the pulvinar retino-recipient zone (pulivnar-RRZ). After adult visual cortex lesions, no reorganization of the retinopulvinar projection took place. The modification of the projection from the retina to the pulvinar that occurs after ablation of visual cortex in the newborn cat may contribute to the sparing of visual abilities seen after these lesions.

Aging↗

The olivocerebellar projection in the monkey. Experimental studies with the method of retrograde tracing of horseradish peroxidase.

Following injections of horseradish peroxidase (HRP) in various lobes and lobules of the macaque cerebellum the occurrence of retrogradely labeled cells in the inferior olive was mapped. Only cortical areas showing staining of the molecular layer were considered as sites of uptake of HRP. To facilitate comparisons between cases and presentation of findings, a diagram of the macaque inferior olive as imagined unfolded was constructed (Fig. 1). Attempts were made to compare the findings made with data on the olivocerebellar projection in the cat and the pattern of a longitudinal zonal subdivision of the cerebellum. In general there appears to be a remarkably close correspondence between the organization of the olivocerebellar projection in the monkey and the cat. The projection is precisely organized and appears to be purely crossed. Within the projections to some of the cerebellar cortical zones a topical pattern can be demonstrated. Olivary afferents to vermal lobules V, VII, and VIII are derived from the caudal half of the medial accessory olive, projecting to Voogd's zone A. The topical pattern resembles that in the cat (Fig. 8). after injections covering the lateral zone of the anterior lobe vermis (zone B), labeled cells are seen in the caudal part of the dorsal accessory olive. In some cases staining of the intermediate part of the anterior lobe and of the paramedian lobule is followed by labeling of cells in the rostral part of the dorsal accessory olive (zones C1 and C3) or in the rostral half of the medial accessory (zone C2). When the injected area covers lateral parts of the cerebellum, there is labeling in the principal olive (projecting to zones D1 and D2). Although not entirely decisive, the findings lend support to the view that the ventral lamella of the principal olive supplies zone D2, whereas the dorsal lamella supplies zone D1. The relatively sparse data in the literature on the afferents to the monkey olive are briefly considered. On may points the projections appear to be as in the cat. However, there is possibly a species difference between cat and monkey as concerns their receipt of afferents from the red nucleus.

Animals↗

Hypothalamic, other diencephalic, and telencephalic neurons that project to the dorsal midbrain.

Neurons in the hypothalamus, other diencephalic regions, and the telencephalon which project to the mesencephalic central gray (CG) and the region lateral to it were demonstrated, in the rat, by the horseradish peroxidase retrograde neuroanatomical tracing method with diaminobenzidine and tetramethyl benzidine visualization reactions. The greatest concentrations of neurons that project to the dorsal mesencephalon were found in the ventromedial nucleus, particularly the anterior and ventrolateral subdivisions, in the dorsal premammillary nucleus, and in the zona incerta. Neurons that project to or lateral to the CG were also found in the laterocaudal hypothalamus, the dorsomedial hypothalamus, regions of the anterior hypothalamic area, specific areas of the cerebral cortex (32, 29, 8, 8A, 13, 14), and the central nucleus of the amygdala. Some neurons that project were also found in the preoptic area, septum, bed nucleus of the stria terminals, and the habenula. More neurons in the mediocaudal quadrant of the hypothalamus project to the mesencephalon than do those in laterocaudal, mediorostral, or laterorostral quadrants. More neurons in the medial than the lateral half, and more in the caudal than the rostral half of the hypothalamus project to the mesencephalon. More neurons project to the central gray, or the region lateral to it, at the levels of the superior colliculus, or intercollicular region, than at the level of the inferior colliculus. These descending connections to the midbrain, particularly from the hypothalamus and zona incerta, are probably components of neural networks that regulate nociception, certain neuroendocrine functions, sexual and other behaviors, and certain autonomic functions.

Animals↗

Transplantation of tectal tissue in rats. II. Distribution of host neurons which project to transplants.

Tectal tissue was dissected from fetal rats and transplanted adjacent to the superior colliculus of newborn rats. The recipient animals were then allowed to survive for 6 or more weeks. Subsequent examination revealed that the transplants generally lay over the host inferior colliculus and rostral part of the cerebellum and had substantial fiber connections with the host superior colliculus. To determine which host areas projected to the transplants, horseradish peroxidase (HRP) was injected into the transplants, and the host brain was examined for the presence of retrogradely filled neurons. Labeled cells were found in nearly 50 host areas. Most of these areas are known to project to normal superior colliculus. There was a consistency between one animal and another in the frequency and density of cell label in the various areas. The projection from host cortex (particularly from visual cortical areas) was the densest and most consistent projection. Other areas which commonly projected into the transplants included pretectum, parabigeminal nucleus, superior colliculus, and the brachial region of the inferior colliculus. Sparse and infrequent projections were found from ventral lateral geniculate nucleus, substantia nigra, zona incerta, and catecholaminergic nuclei. No unequivocally labeled retinal ganglion cells were found. The results indicate that the host projection into the transplants is limited to those areas with axons in the vicinity of the host/transplant interconnection. However, the data also suggest that (1) the relative maturity of particular host pathways at the time of transplantation and (2) some form of preferential or absolute affinity expressed between host axons and transplant cells are also factors which influence the pattern of connections formed between host and transplant.

Animals↗

The organization of the thoracic spinal nerve projection in the rat dorsal horn demonstrated with transganglionic transport of horseradish peroxidase.

Transganglionic transport of horseradish peroxidase (HRP) was used to study the organization of the thoracic spinal nerve projection to the dorsal horn in rats. Labeling was found in the superficial dorsal horn 16-20 hours after application of HRP to the cut ends of various spinal nerve rami. Labeling was restricted to the outer part of the substantia gelatinosa at these stages. Longer survivals (25-48 hours) gave rise to labeling of the deep part of substantia gelatinosa and deeper parts of the dorsal horn as well. The dorsal ramus projected to the lateral third of the horn from half a segment rostral to half a segment caudal to the entry segment. The ventral ramus projected to the medial two-thirds of the horn from 1 1/2 segments rostral to half a segment caudal to the entry segment. The two branches of the ventral ramus that were examined projected to separate medial and lateral compartments for the entire ventral ramus. There was a distinct lateromedial shift of the projection found from rostral through caudal levels within the projection compartment for each nerve. The results indicate that the dorsal horn projection of thoracic spinal nerve branches is organized in longitudinal compartments which are arranged in a strictly somatotopic fashion.

Animals↗

Segmental distribution and central projections of renal afferent fibers in the cat studied by transganglionic transport of horseradish peroxidase.

The segmental and central distributions of renal nerve afferents in adults cats and kittens were studied by using retrograde and transganglionic transport of horseradish peroxidase (HRP). Transport of HRP from the central cut ends of the left renal nerves labelled afferent axons in the ipsilateral minor splanchnic nerves and sensory perikarya in the dorsal root ganglia from T12 to L4. The majority of labeled cells (85%) were located between L1 and L3. A few neurons in the contralateral dorsal root ganglia were also labeled. Labeled cells were not confined to any particular region within a dorsal root ganglion. Some examples of bifurcation of the peripheral and central processes within the ganglion were noted. A small number of preganglionic neurons, concentrated in the intermediolateral nucleus, were also identified in some experiments. In addition, many sympathetic postganglionic neurons were labeled in the renal nerve ganglia, the superior mesenteric ganglion, and the ipsilateral paravertebral ganglia from T12 to L3. Transganglionic transport of HRP labeled renal afferent projections to the spinal cord of kittens from T11 to L6, with the greatest concentrations between L1 and L3. These afferents extended rostrocaudally in Lissauer's tract and sent collaterals into lamina I. In the transverse plane, a major lateral projection and a minor medial projection were observed along the outer and inner margins of the dorsal horn, respectively. From the lateral projection many fibers extended medially in laminae V and VI forming dorsal and ventral bundles around Clarke's nucleus. The dorsal bundle was joined by collaterals from the medial afferent projection and crossed to the contralateral side. The ventral bundle extended into lamina VII along the lateroventral border of Clarke's nucleus. Some afferents in the lateral projection could be followed ventrally into the dorsolateral portion of lamina VII in the vicinity of the intermediolateral nucleus. In the contralateral spinal cord, labeled afferent fibers were mainly seen in laminae V and VI. These results provide the first anatomical evidence for sites of central termination of renal afferent axons. Renal inputs to regions (laminae I, V, and VI) containing spinoreticular and spinothalamic tract neurons may be important in the mediation of supraspinal cardiovascular reflexes as well as in the transmission of activity from nociceptors in the kidney. In addition, the identification of a bilateral renal afferent projection in close proximity to the thoracolumbar autonomic nuclei is consistent with the demonstration in physiological experiments of a spinal pathway for the renorenal sympathetic reflexes.

Animals↗

The distribution of neocortical projection neurons in the locus coeruleus.

The present study was conducted to examine the spatial organization of locus coeruleus (LC) neurons that project to rat cerebral cortex. Long-Evans hooded rats received unilateral pressure injections of horseradish peroxidase (HRP) in either frontal (n = 6) or sensorimotor (n = 11) or occipital (n = 7) cortex to determine the intranuclear location of LC neurons which project to specific neocortical regions. Coronal and sagittal sections (40-100 micron) through the LC were examined by light microscopy after carrying out the tetramethyl benzidine reaction and staining with neutral red. The locations of retrogradely labeled cells were recorded on a three-dimensional biological coordinate system maintained by a computer linked to the light microscope. LC neurons labeled from cerebrocortical injections of HRP were primarily located in the ipsilateral and to a lesser extent (fewer than 5% of total labeled cells) in the contralateral nucleus. Coeruleocortical projection neurons were concentrated in the caudal three-fifths of the dorsal division of the ipsilateral LC. Within this portion of the nucleus, HRP-filled neurons were distributed so that individual groups of cells projecting to occipital or sensorimotor or frontal cortex were coarsely aligned in a dorsal to ventral array, respectively. Moreover, in the sagittal plane of the nucleus the pattern of labeling was spatially graded so that the subset of neurons projecting to the occipital cortex was displaced more caudally in the LC than the groups of cells sending axons to sensorimotor or frontal cortex. Only the frontal area of the cortex received a projection from both dorsal and ventral divisions of the ipsilateral LC. Computer-assisted analysis of the data further suggested that neocortical projection neurons in the dorsal LC are loosely organized into two groups which run rostrocaudally through the core of the caudal nucleus. The zone of labeling resulting from injections confined to the neocortical gray matter overlapped with but was not coextensive with that observed following injections into the caudate, hippocampus, and cerebellum. These results suggest that partially overlapping subsets of LC cells might independently influence separate populations of neurons within noradrenergic terminal fields of the neocortex.

Afferent Pathways↗

The development and postnatal organization of primary afferent projections to the rat thoracic spinal cord.

Primary afferent projections to the thoracic spinal cord in fetal and postnatal rats were labelled by applying horseradish peroxidase (HRP) to the central stumps of cut peripheral nerves. Diaminobenzidine (DAB) and tetramethyl benzidine (TMB) histochemical processing procedures were used to reveal the HRP reaction product. In postnatal rats, individual muscle nerves were labelled to reveal the organization of muscle afferent projections to the motor nuclei. The terminals of muscle afferents were distributed widely across the dendritic arbors of motoneurons supplying the same muscles. No spatial segregation of the terminations of different populations of muscle afferents was discernable. Afferents supplying different regions of the skin were labelled by applying HRP to the dorsal and ventral primary rami of the spinal nerves. Afferents in the dorsal rami projected to lateral portions of both the ipsilateral and contralateral dorsal horns while afferents in the ventral rami projected to the medial portions of both dorsal horns. The projections of the dorsal rami were shifted caudally relative to those of the ventral rami. This relationship reflects the fact that the regions of skin innervated by the dorsal rami are displaced caudally relative to those innervated by the corresponding ventral rami. In fetuses, dorsal rami were labelled alone or in combination with ventral rami. These experiments disclosed the time course of development of the projections to different laminae of the spinal gray matter and revealed that afferents in the two primary rami project to appropriate regions in the ipsilateral and contralateral dorsal horns from the very outset.

Afferent Pathways↗

Olivary projections from the mesodiencephalic structures in the cat studied by means of axonal transport of horseradish peroxidase and tritiated amino acids.

By means of horseradish peroxidase (HRP) and autoradiographic methods, olivary projections from mesodiencephalic structures were studied in the cat. Following HRP injections in various parts of the inferior olive, many cells were labeled ipsilaterally in the nucleus of Darkschewitsch, the nucleus accessorius medialis of Bechterew, the nucleus of the fields of Forel, and the subnucleus dorsomedialis and ventrolateralis of the parvocellular red nucleus. Some labeled cells also occurred ipsilaterally in the suprarubral reticular formation and a few labeled cells in the interstitial nucleus of Cajal. After injection of tritiated amino acids in different parts of the mesodiencephalic region mentioned above, labeled fibers were found in different parts of the inferior olive, presenting a high degree of the topographic correlation within the mesodiencephalo-olivary projection, which was exclusively ipsilateral. That is, the nucleus of Darkschewitsch was found to project to the rostral half of the medial accessory olive and the dorsomedial cell column. There was mediolateral topographic relation in this projection. The nucleus accessorius medialis of Bechterew was found to project to the ventral lamella and the lateral part of the dorsal lamella as well as to small rostromedial part of the caudal half of the medial accessory olive. The subnucleus dorsomedialis and ventrolateralis of the parvocellular red nucleus projected to the rostral and caudal halves, respectively, of the medial part of the dorsal lamella. The subnucleus ventrolateralis of the parvocellular red nucleus also sent fibers to the lateral part of the ventrolateral outgrowth. The nucleus of the fields of Forel, suprarubral reticular formation, and interstitial nucleus of Cajal appeared to project to the caudal half of the medial accessory olive, the medial part of the ventrolateral outgrowth, the rostral part of the dorsal cap, and the caudal part of the dorsal accessory olive.

Animals↗

Rostral ventrolateral medulla: selective projections to the thoracic autonomic cell column from the region containing C1 adrenaline neurons.

Anterograde, retrograde, and combined axonal transport methods were used to describe the descending efferent projections of a region of rostral ventrolateral medullary reticular formation important in cardiovascular control. We have termed this region, which contains C1 adrenaline-synthesizing neurons, the nucleus reticularis rostroventrolateralis (RVL). Efferent projections from the RVL innervate all segmental levels of the thoracic intermediolateral and intermediomedial columns as shown using retrograde transport of lectin-conjugated horseradish peroxidase (HRP) or fast blue dye, and anterograde transport of either HRP or labeled amino acids. The projection is highly specific in that there are no projections to thoracic dorsal or ventral horns. This innervation corresponds to the distribution of preganglionic sympathetic neurons in the intermediolateral column. In particular, terminals surround neurons projecting to the adrenal medulla, as demonstrated by combined anterograde and retrograde transport methods at the light level. Terminals containing phenylethanolamine-N-methyl transferase (PNMT) were mapped using immunocytochemical techniques. PNMT-labeled terminals were present at all levels of thoracic intermediolateral column, in a distribution similar to that of the descending projections from the RVL. We have previously shown using double label techniques (Ross et al., '81-'83), that many of the spinal projections of the RVL originate from C1 neurons. These data support our suggestion that certain bulbospinal neurons within the RVL, in particular the C1 neurons, are crucial for tonic vasomotor control.

Animals↗

The cortical projection of the basolateral amygdaloid nucleus in the rat: a retrograde fluorescent dye study.

The fluorescent dye, retrograde labeling technique was used to determine the extent of the projection from the basolateral nucleus of the amygdala to the neocortex in the rat. Each rat received a single cortical injection of fast blue, and in one-half of the animals, a subsequent injection of nuclear yellow was placed in a different cortical region. An analysis of the results demonstrates that the projection to the midline cortex arises in the medial neurons within the caudal two-thirds of the basolateral nucleus. This projection is directed to the anterior cingulate cortex, but not to the posterior cingulate cortex. The primary motor cortex receives a basolateral amygdala projection which originates from neurons in two areas, (1) the medial part of the anterior one-third of the nucleus and (2) the center (in the lateral to medial axis) portion of the posterior two-thirds of the nucleus. The latter neurons are situated lateral to the neurons projecting to the cingulate cortex. Somatosensory cortex injections label many fewer basolateral nucleus neurons than do motor cortex injections, but these neurons are located in a position similar to that of those labeled by motor cortex injections. Finally the gustatory cortex, which lies just dorsal to the rhinal sulcus, receives a basolateral projection from neurons in the lateroventral one-half of the basolateral nucleus. These results demonstrate that the basolateral nucleus gives rise to a rather widespread and topographically organized projection to the anterior half of the neocortex of the rat.

Amidines↗