Striate cortex-superior colliculus projection in squirrel monkey

The corticofugal projections from the striate cortex to the superior colliculus in the squirrel monkey were electrophysiologically investigated. The cortical afferents projected to the ipsilateral superior colliculus in a point-to-point manner and were retinotopically organized. They terminated mainly in the deep layer of the stratum griseum superficiale, the stratum opticum, and the superficial layer of the stratum griseum intermediale. In these layers photic collicular units were mostly sensitive to moving objects. Convergence of afferent pathways from the retina and striate cortex on collicular neurons could not be demonstrated.     

Histochemical characterization of a neocortical projection of the nucleus locus coeruleus in the squirrel monkey

Histochemical evidence is presented for a catecholamine-containing projection from the nucleus locus coeruleus to the neocortex in the squirrel monkey. The innervation of superior temporal gyrus has been examined in particular. Glyoxylic acid-induced fluorescence shows an extensive arborization of fine, catecholamine-containing fibers with prominent varicosities in all layers of the neocortex. The nucleus locus coeruleus is identified as a source of these fibers by both ortho- and retrograde axonal tracing techniques. After injection of horseradish peroxidase into the neocortex, labelled cell bodies are localized throughout the major portions of the locus coeruleus. Conversely, after microinjection into the nucleus locus coeruleus, tritiated proline is transported into the neocortex where it appears within fibers similar in distribution to those revealed by fluorescence histochemistry. Both transport techniques indicate that cortical projections of the locus coeruleus originate from both ipsilateral and contralateral nuclei.     

Synaptic innervation of midbrain dopaminergic neurons by glutamate-enriched terminals in the squirrel monkey

The excitatory amino acid, glutamate, has long been thought to be a transmitter that plays a major role in the control of the firing pattern of midbrain dopaminergic neurons. The present study was aimed at elucidating the anatomical substrate that underlies the functional interaction between glutamatergic afferents and midbrain dopaminergic neurons in the squirrel monkey. To do this, we combined preembedding immunocytochemistry for tyrosine hydroxylase and calbindin D-28k with postembedding immunostaining for glutamate. On the basis of their ultrastructural features, three types (so-called types I, II, and III) of glutamate-enriched terminals were found to form asymmetric synapses with dendrites and perikarya of midbrain dopaminergic neurons. The type I terminals accounted for more than 70% of the total population of glutamate-enriched boutons in contact with dopaminergic cells in the dorsal and ventral tiers of the substantia nigra pars compacta as well as in the ventral tegmental area, whereas 5–20% of the glutamatergic synapses with dopaminergic neurons involved the two other types of terminals. The major finding of our study is that the glutamate-enriched boutons were involved in 70% of the axodendritic synapses in the ventral tegmental area. In contrast, less than 40% of the boutons in contact with dopaminergic dendrites were immunoreactive for glutamate in the dorsal and ventral tiers of the substantia nigra pars compacta. Approximately 50% of the terminals in contact with the perikarya of the different populations of midbrain dopaminergic neurons displayed glutamate immunoreactivity. In conclusion, our findings provide the first evidence that glutamate-enriched terminals form synapses with midbrain dopaminergic neurons in primates. The fact that the proportion of glutamatergic boutons in contact with dopaminergic cells is higher in the ventral tegmental area than in the substantia nigra pars compacta suggests that the different groups of midbrain dopaminergic neurons are modulated differently by extrinsic glutamatergic afferents in primates. © 1996 Wiley-Liss, Inc.     

Brainstem dopaminergic, cholinergic and serotoninergic afferents to the pallidum in the squirrel monkey

The retrograde tracer cholera toxin B subunit (CTb) was used in combination with immunohistochemistry for tyrosine hydroxylase (TH), calbindin D-28k (CaBP), choline acetyltransferase (ChAT) and 5-hydroxytryptamine (5-HT) to determine the distribution and relative proportion of brainstem chemospecific neurons that project to the pallidum in the squirrel monkey (Saimiri sciureus). Large injections of CTb involving both pallidal segments produce numerous retrogradely labeled neurons in the substantia nigra (SN), the pedunculopontine tegmental nucleus (PPN) and the dorsal raphe nucleus (DR). Labeled neurons are distributed uniformly in SN with a slight numerical increase at the junction between the pars compacta (SNc) and the ventral tegmental area (VTA). Retrogradely labeled neurons abound also in PPN, principally in its pars dissipata, whereas other CTb-labeled cells are scattered throughout the rostrocaudal extent of DR. After CTb injection involving specifically the internal pallidal segment (GPi), the same pattern of cell distribution is found in SN, PPN and DR, except that the number of retrogradely labeled cells is lower than after large pallidal complex injections. Approximately 70% of all CTb-labeled neurons in SNc-VTA complex display TH immunoreactivity, whereas 20% are immunoreactive for CaBP. About 39% of all retrogradely labeled neurons in PPN are immunoreactive for ChAT, whereas approximately 38% of the labeled neurons in DR display 5-HT immunoreactivity. Following CTb injection in the external pallidal segment (GPe), the number of labeled cells is much smaller than after GPi injection. The majority of CTb-labeled cells in SNc-VTA complex are located in the lateral half of SNc and approximately 93% of these neurons display TH immunoreactivity compared to 10% that are immunoreactive for CaBP; very few CTb-labeled cells occur in PPN. Retrogradely labeled cells in DR are located more laterally than those that projects to the GPi and about 25% of them are immunoreactive for 5-HT. These results suggest that, in addition to their action at striatal and/or nigral levels, the brainstem dopaminergic, cholinergic and serotoninergic neurons influence the output of the primate basal ganglia by acting directly upon GPi neurons.     

Evidence for a direct projection from the superior temporal gyrus to the entorhinal cortex in the monkey

During the course of a larger study of the afferent and efferent connections of the entorhinal cortex in the macaque monkey we have found evidence for a hitherto undescribed projection to the entorhinal cortex from the superior temporal gyrus. The evidence is derived principally from experiments in which small volumes of wheat germ agglutinin-conjugated horseradish peroxidase (WGA-HRP) were injected into different parts of the entorhinal cortex, but has been confirmed by 3H-amino acid autoradiography. After WGA-HRP injections into the entorhinal cortex, retrogradely labeled neurons have been seen mainly in layer III, but also to some extent in layer VI, throughout much of the superior temporal gyrus. The projection appears to be topographically organized in the sense that the ventral insular cortex and the adjoining temporal operculum have been found to project to the periamygdaloid cortex and the lateral division of the entorhinal cortex; the convexity of the superior temporal gyrus and the cortex along the dorsal bank of the superior temporal gyrus project further caudally to the medial division of the entorhinal cortex; and the cortex surrounding the fundus of the superior temporal sulcus projects to the perirhinal cortex. Following an injection of 3H-amino acids into the convexity of the superior temporal gyrus, terminal labeling has been seen over layers I and II of the entorhinal cortex and over layer I in the most lateral portion of the presubiculum. While the distribution of retrogradely labeled cells in our WGA-HRP experiments encompasses several cytoarchitectonically distinguishable areas in the superior temporal gyrus, the most heavily labeled field appears to coincide with what Gross and his colleagues have termed the 'superior temporal polysensory area' on the dorsal bank of the superior temporal sulcus.     

Differential dopaminergic innervation of the two pallidal segments in the squirrel monkey (Saimiri sciureus)

Immunohistochemical studies with an antiserum raised against tyrosine hydroxylase have allowed us to demonstrate a dense dopaminergic innervation of the globus pallidus in the squirrel monkey. This innervation derived mostly from two fascicles that detached themselves from the major ascending dopaminergic bundle arising from midbrain dopamine cell bodies and running in the lateral hypothalamus. Dopaminergic fibers reached the globus pallidus by coursing along its two major output pathways: the lenticular fasciculus dorsally and the ansa lenticularis ventrally. At pallidal levels, dopaminergic fibers abounded in medullary laminae and arborized profusely within the internal pallidal segment, whereas the external pallidum displayed only few short fibers that prevailed in its dorsal portion. These findings provide the first evidence that the primate globus pallidus receives a massive and diffentially distributed dopaminergic input.     

Evidence for two distinct classes of unmyelinated nociceptive afferents in monkey

Unmyelinated nociceptive afferents, responsive to intense mechanical and heat stimuli, exhibited either a quickly adapting or slowly adapting response to step increases in skin temperature. These two classes of C fibers were found to differ also in other properties. The quickly adapting C fibers had significantly lower thresholds to mechanical and heat stimuli, and smaller receptive field areas than the slowly adapting C fibers.     

Evidence for leucine-enkephalin immunoreactive neurons in the medulla which project to spinal cord in squirrel monkey

Rhodamine-labeled latex microsphere injections were combined with horserasish peroxidase immunohistochemistry in squirrel monkeys to reveal neurons in the medullary raphe and medial reticular formation which projected to spinal cord and were positive for leucine-enkephalin-like immunoreactivity. Double-labeled cells were found primarily in nucleus raphe magnus, the reticular nucleus magnocellularis, and the lateral reticular nucleus. These results provide evidence for a descending projection from enkephalin-containing cells of the rostral ventral medulla, a region which has been strongly implicated in antinociception.     

Glutamate-induced vocalization in the squirrel monkey

In the squirrel monkey, 164 brain sites yielding vocalization when electrically stimulated were tested for their capability to produce vocalization when injected with mono-sodium-L-glutamate. The sites were located in the anterior limbic cortex, n. accumbens, substantia innominata, amygdala, n. striae terminalis, hypothalamus, midline thalamus, field H of Forel, substantia nigra, periventricular and periaqueductal gray, inferior colliculus, reticular formation of midbrain, pons and medulla, inferior olive, lateral reticular nucleus and nucleus of solitary tract. Of the 164 sites tested, 31 were positive. These were located in the substantia innominata, caudal periventricular and periaqueductal gray, lateral pontine and medullary reticular formation. While all the calls obtained from the forebrain and midbrain had a normal acoustic structure, most pontine and all medullary vocalizations had an artificial character. It is concluded that: the substantia innominata, caudal periventricular and periaqueductal gray, lateral pontine and medullary reticular formation represent relay stations of vocalization-controlling pathways; the periaqueductal gray represents the lowest relay station above the level of motor coordination; neurons responsible for motor coordination of vocalization lie in the reticular formation around the caudal brachium conjunctivum, the superior olive, n. facialis, n. ambiguus and below the n. solitarius; not all areas from which vocalization can be obtained by electrical stimulation of nerve cell bodies, dendrites and nerve endings (in contrast to fibers en passage) also yield vocalization when stimulated with glutamate.     

Calbindin D-28K in the dopaminergic mesocortical projection of a monkey (Aotus trivirgatus)

Injections of fluorescent dyes were made in the prefrontal and motor cortex of owl monkeys and retrogradely labeled neurons in the mesencephalon were analyzed for tyrosine hydroxylase and calbindin-D28K immunostaining. Numbers of mesocortical dopaminergic neurons in the dorsal substantia nigra compacta and in the ventral tegmental area also contain calbindin-D28K. This cortically projecting calbindin-D28K containing subpopulation of the dopaminergic mesencephalic cells may be characterized by different electrophysiological properties and a lesser vulnerability to cell death.     

Catecholamine neurons in the squirrel monkey hypothalamus

Summary Catecholamine neurons were found in the periventricular nucleus, arcuate nucleus, and a region around the mammillothalamic tract in the hypothalamus of the squirrel monkey. These neurons did not fluoresce in control or monoamine-oxidase-inhibited animals, and exhibited fluorescence only after intraventricular injections of alpha-methyl-norepinephrine. Dense accumulations of Catecholamine varicosities appeared in the periventricular nucleus, external contact zone of the median eminence, and perivascular region of the median eminence; the arcuate nucleus contained no more than a moderate density of Catecholamine varicosities. The median eminence fluorescence had a regional character, with greatest intensity in the caudal portion.     

Evidence for an amygdaloid projection to premotor cortex but not to motor cortex in the monkey

Previous studies in the cat have demonstrated a direct projection from the amygdaloid complex to motor and premotor regions of the neocortex. In the present study both anterograde and retrograde tracer techniques have been used to determine whether a similar projection exists in the monkey brain. We have found that the dorsal, magnocellular division of the basal nucleus of the amygdaloid complex gives rise to a projection to the premotor cortex (Area 6), which terminates principally in layers I and II, and to a lesser extent in layer VI. No component of the amygdaloid complex has been found to project to the motor cortex (Area 4). The amygdaloid projection to Area 6 in the monkey appears to be substantially weaker than other rostrally directed projections from the basal amygdaloid nucleus to orbitofrontal and medial frontal areas, and also relatively weaker than the projection that has been described in the cat.