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D N Pandya

Publications and source records attributed to D N Pandya.

At least 37 records · Page 2Linked to original sources
PubMed1993

Prelunate, occipitotemporal, and parahippocampal projections to the basis pontis in rhesus monkey.

We used tritiated amino acids to study projections to the basilar pons from prestriate cortices in 18 rhesus monkeys to determine how connectional and functional heterogeneity of these regions are reflected in corticopontine circuitry. Fibers travelled with those from other parasensory associative cortices before terminating in the pontine nuclei. Prelunate projections were derived from area 19 (OA) at the medial convexity (including areas V3 and PO) and from the lateral convexity dorsal to the caudal tip of the Sylvian fissure (including areas DP and the dorsal part of area V4d). Pontine projections also arose from area 19 (OA), and areas TF, TL, and TH in the posterior aspect of the parahippocampal gyrus. No pontine projections arose from the prelunate convexity ventral to the caudal tip of the Sylvian fissure (ventral part of area V4d and area V4v), area TEO, the inferior temporal gyrus, or the lateral ventral temporal region. Terminations in the pons were distributed in the dorsolateral and lateral nuclei, and the lateral part of the peripeduncular nucleus. Medial convexity injections produced more extensive rostrocaudal pontine labeling, as well as terminations in the extreme dorsolateral nucleus and the nucleus reticularis tegmenti pontis. Dorsal prelunate injections had additional terminations in the ventral pontine nucleus. Posterior parahippocampal gyrus injections resulted in discrete label in the lateral and dorsolateral nuclei. Corticopontine projections destined for the cerebellum appear to be derived from extrastriate areas concerned mainly with visual spatial parameters, visual motion, and the peripheral field of vision, but not from areas subserving visual object identification and the central field of vision. Pontine afferents from the posterior parahippocampal gyrus may facilitate a cerebellar contribution to visual spatial memory, particularly when invested with motivational valence.

Animals↗
PubMed1993

Striatal connections of the parietal association cortices in rhesus monkeys.

The corticostriatal connections of the parietal association cortices were examined by the autoradiographic technique in rhesus monkeys. The results show that the rostral portion of the superior parietal lobule projects predominantly to the dorsal portion of the putamen, whereas the caudal portion of the superior parietal lobule and the cortex of the upper bank of the intraparietal sulcus have connections with the caudate nucleus as well as with the dorsal portion of the putamen. The medial parietal convexity cortex projects strongly to the caudate nucleus, and has less extensive projections to the putamen. In contrast, the medial parietal cortex within the caudal portion of the cingulate sulcus projects predominantly to the dorsal portion of the putamen, and has only minor connections with the caudate nucleus. The rostral portion of the inferior parietal lobule projects mainly to the ventral sector of the putamen, and has only minor connections with the caudate nucleus. The middle portion of the inferior parietal lobule has sizable projections to both the putamen and the caudate nucleus. The caudal portion of the inferior parietal lobule as well as the lower bank of the intraparietal sulcus project predominantly to the caudate nucleus, and have relatively minor connections with the putamen. The cortex of the parietal opercular region also shows a specific pattern of corticostriatal projections. Whereas the rostral portion projects exclusively to the ventral sector of the putamen, the caudal portion has connections to the caudate nucleus as well. Thus, it seems that parietostriatal projections show a differential topographic distribution; within both the superior and the inferior parietal region, as one progresses from rostral to caudal, there is a corresponding shift in the predominance of projections from the putamen to the caudate nucleus. In addition, with regard to the projections to the putamen, the superior parietal lobule is related mainly to the dorsal portion, and the inferior parietal lobule to the ventral portion. The striatal projections of the cortex of the caudal portion of the cingulate gyrus (corresponding in part to the supplementary sensory area) and of the rostral parietal opercular region (corresponding in part to the second somatosensory area) are directed almost exclusively to the dorsal and ventral sectors of the putamen, respectively. This pattern resembles that of the primary somatosensory cortex. The results are discussed with regard to the overall architectonic organization of the posterior parietal region. Possible functional aspects of parietostriatal connectivity are considered in the light of physiological and behavioral studies.

Animals↗
PubMed1993

Laminar termination patterns of thalamic, callosal, and association afferents in the primary auditory area of the rhesus monkey.

Thalamic, callosal, and association afferents to the primary auditory konicortex, area KA, were investigated in rhesus monkeys with the aid of anterograde tract tracing techniques (radioactively labeled amino acids, wheat germ agglutinin conjugated to horseradish peroxidase (WGA-HRP), and the Fink-Heimer silver impregnation method). Different patterns of anterograde label in KA were produced by radioactively labeled amino acid injections in the contralateral primary auditory area, the ipsilateral medial geniculate body (MGB), or auditory association cortex of the superior temporal gyrus (STG). Thalamic afferents from the MGB were found throughout KA in layers IV and III where the density waxed and waned, forming regular patches of higher density label separated by areas of less dense label. Callosal afferents from the contralateral auditory cortices were found in layers IV, III, and II in larger, more spatially separated, and irregular patches. In contrast, association afferents from the auditory association cortex of the STG were found in a continuous band in layer I. To determine the extent to which the patches of callosal afferents overlap with or interdigitate between the high-density thalamic clusters, two types of double anterograde labeling experiments were undertaken. In one set of experiments isotope injections of the MGB were made in conjunction with transection of the corpus callosum in the same animal. In another set of experiments isotope injections of the MGB were made in one hemisphere and an injection of WGA-HRP was made in the opposite supratemporal plane, including KA, in the same animal. Both approaches demonstrate that the patches of callosal afferents in KA mainly occur between the high-density patches of thalamic afferents, although there is a variable degree of overlap at their periphery. Thus it seems that thalamic and callosal inputs to KA are organized in a largely complementary fashion while input from the lateral association cortex is continuous and overlaps both. When considered in light of pertinent anatomical and physiological studies in a variety of species, it appears that the areas mainly occupied by callosal or thalamic inputs may be differentially involved in frequency analysis and sound localization, respectively.

Animals↗
PubMed1992

Course of the fiber pathways to pons from parasensory association areas in the rhesus monkey.

The course of the fiber pathways to pons from parasensory association areas in the rhesus monkey was investigated by injection of tritiated amino acids and the technique of autoradiography. Results confirm the projection to pons from parasensory association areas in the temporal, parietal, and occipital lobes and extend these observations to include the posterior parahippocampal gyrus. The findings reveal that the white matter of the posterior limb of the internal capsule above the midpoint of the lateral geniculate nucleus, and at the medial aspect of the lateral geniculate nucleus, comprise common regions through which these corticopontine fibers lead to the basis pontis. The fibers demonstrate a certain degree of topographic organization in the posterior limb of the capsule above the lateral geniculate nucleus and also in the cerebral peduncle. Taken together with previous observations concerning the termination patterns of these associative corticopontine projections, it would appear that the corticopontine system consists of segregated and partially overlapping pathways, which are to some extent distinguishable anatomically at each stage of their trajectory from origin to destination. Furthermore, the existence of a common area through which all parasensory associative input to pons is transmitted suggests that a precisely located lesion in this part of the corticopontocerebellar circuit may disrupt the cerebellar access to higher order information derived from the parasensory associative regions.

Animals↗
PubMed1992

Efferent cortical connections of multimodal cortex of the superior temporal sulcus in the rhesus monkey.

The cortex of the upper bank of the superior temporal sulcus (STS) in the rhesus monkey contains a region that receives overlapping input from post-Rolandic sensory association areas and is considered multimodal in nature. We have used the fluorescence retrograde tracing technique in order to answer the question of whether multimodal areas of the STS project back to post-Rolandic sensory association areas. Additionally, we have attempted to answer the question of whether the projections from the multimodal areas directed to the parasensory association areas originate from common neurons via axon collaterals or from individual neurons. The results show that multimodal area TPO of the STS projects back to specific unimodal parasensory association areas of the parietal lobe (somatosensory), superior temporal gyrus (auditory), and posterior parahippocampal gyrus (visual). In addition, a substantial number of projections from area TPO are directed to distal parasensory association areas, area PG-Opt in the inferior parietal lobule, areas Ts1 and Ts2 in the rostral superior temporal gyrus, and areas TF and TL in the parahippocampal gyrus. These latter regions are themselves considered to be higher-order association areas. It was also noted that the majority of the projections to these higher-order association areas originate from the middle divisions of area TPO (TPO-2 and TPO-3). These neurons are organized in a significantly overlapping manner. Despite this overlap of the projection neurons, only an occasional double labeled neuron was observed in area TPO. Thus, our observations indicate that the multimodal region of the superior temporal sulcus has reciprocal connections with the unimodal parasensory association cortices subserving somatosensory, auditory and visual modalities, as well as with other post-Rolandic higher-order association areas. These connections from area TPO to post-Rolandic association areas may have a modulating influence on the sensory association input leading to multimodal areas in the superior temporal sulcus.

Animals↗
PubMed1992

The mysterious relocation of the bundle of Türck.

The name bundle of Türck has become synonymous with the temporopontine tract. As details concerning this pathway have been confusing and incomplete we reviewed the papers of Ludwig Türck (1810-1868) to determine what in fact he originally described. Türck's pioneering degeneration studies provided great detail concerning the corticospinal tracts. Charcot recognized his contributions and used the eponym 'bundle of Türck' to denote the anterior corticospinal tract. Türck did not observe projections from the temporal lobe to the basis pontis, nor did he describe a temporopontine tract located at the most lateral aspect of the cerebral peduncle. The papers of Meynert, Flechsig and others reveal the origins of the current incorrect use of the eponym.

History, 17th Century↗
PubMed1992

Lacunar thalamic stroke with pure cerebellar and proprioceptive deficits.

Case reports of two patients with cerebellar ataxia and proprioceptive sensory loss are presented. MRI of the brain revealed lesions of the ventroposterior part of the thalamus. These patients illustrate clinically the anatomical independence of cerebellar and sensory pathways in the thalamus. We suggest that the ataxic deficit is caused by interruption of cerebellar outflow pathways in the thalamus and not secondary to sensory deafferentation.

Aged↗
PubMed1991

Prefrontal projections to the mediodorsal nucleus of the thalamus in the rhesus monkey.

The corticothalamic projections to the prefrontal cortex have been shown to be topographically organized. However, the underlying basis for this topography as it relates to the organization of the different architectonically defined areas of the prefrontal cortex has not been systematically studied. In the present investigation we have reassessed the thalamic projections from the different architectonic areas of the prefrontal cortex by using the technique of autoradiography in the rhesus monkey. The results show that the prefronto-mediodorsal projections are organized according to the architectonic differentiation of the prefrontal cortices. Thus architectonically less differentiated medial and orbital prefrontal regions project to the medial sector of the mediodorsal nucleus, the magnocellular subdivision. In contrast, highly differentiated prefrontal area 8 projects to the most lateral sector of the mediodorsal nucleus, the multiformis subdivision. Lateral prefrontal areas with intermediate architectonic features project to the central parvocellular sector of the mediodorsal nucleus. Additionally, these projections also reveal a dorsoventral topography. Thus areas in the medial and dorsolateral cortices project to the dorsal part of the mediodorsal nucleus. In contrast, areas in orbital and ventrolateral cortices project to the ventral part of the mediodorsal nucleus. The topographic organization of the corticothalamic connections described in this study corresponds to the progressive elaboration and differentiation of the architectonic features of the different prefrontal areas. This successive and dichotomous organization of prefrontothalamic connections may provide the basis for the observed differential functions of the prefrontal cortex and the mediodorsal nucleus.

Animals↗
PubMed1991

Post-rolandic cortical projections of the superior temporal sulcus in the rhesus monkey.

The efferent connections of different cytoarchitectonic areas of the superior temporal sulcus (STS) in the rhesus monkey with parieto-temporo-occipital cortex were investigated using autoradiographic methods. Four rostral-to-caudal subdivisions of cortex (area TPO) in the upper bank of the STS have distinct projection patterns. Rostral sectors (areas TPO-1 and -2) project to the rostral superior temporal gyrus (areas Ts1, Ts2, and Ts3), insula of the Sylvian fissure, and parahippocampal gyrus (perirhinal and prorhinal cortexes, areas TF, TH, and TL); caudal sectors (TPO-3 and -4) project to the caudal superior temporal gyrus (areas paAlt and Tpt), supratemporal plane (area paAc), circular sulcus of the Sylvian fissure (area reIt), as well as medial paralimbic (areas 23, 24, and retrosplenial cortex) and extrastriate (areas 18 and 19) cortexes. Area TPO-1 does not project to the parietal lobe; area TPO-2 projects to the inferior parietal lobule; area TPO-3 to the lower bank of the intraparietal sulcus (IPS) (area POa); and area TPO-4 to medial parietal cortex (area PGm). Vision-related cortex (area TEa) in the rostral lower bank of the STS sends fibers to the rostral inferotemporal region (areas TE1, -2, and -3) and parahippocampal gyrus (perirhinal cortex, areas TF and TL). Visual zones in the caudal lower bank and depth of the sulcus (area OAa, or MT and FST) project to the caudal inferotemporal region (areas TE3 and TEO), lateral preoccipital region (area V4), and lower bank of the IPS (area POa). A zone in the rostral depth of the STS (area IPa) projects to the rostral inferotemporal region, parahippocampal gyrus, insula of the Sylvian fissure, parietal operculum, and lower rim of the IPS (area PG). STS projections to parieto-temporo-occipital cortex have "feedforward," "feedbackward," and "side-to-side" laminar patterns of termination similar to those of other cortical sensory systems. The differential connectivity supports the cytoarchitectonic parcellation of the STS and suggests functional heterogeneity.

Animals↗
PubMed1991

Prefrontostriatal connections in relation to cortical architectonic organization in rhesus monkeys.

Prefrontostriatal connections were investigated in rhesus monkeys using the autoradiographic technique to examine whether there are systematic relationships with regard to the architectonic organization of the prefrontal cortex. On the basis of progressive laminar elaboration, the different regions of the prefrontal cortex can be grouped into two architectonic trends. The dorsal trend, which begins in the medial proisocortical areas, can be followed through the dorsolateral prefrontal cortex, culminating in the dorsal arcuate region. The ventral trend, which originates in the orbital proisocortex, can be traced through the inferior prefrontal convexity to the ventral arcuate region. The results show that the main connections from the prefrontal cortex to the striatum are to the head and body of the caudate nucleus. These connections are topographically organized. Medial and dorsal prefrontal areas project predominantly to the dorsal and central portion of the head and body of the caudate nucleus, whereas orbital and inferior prefrontal areas are related mainly to the ventral and central portion. Moreover, prefrontostriatal connections have a medial-lateral topography. Medial and orbital prefrontal areas project medially in the head and body of the caudate nucleus, whereas the dorsal and ventral arcuate regions project laterally, adjacent to the internal capsule. The prefrontal regions above and below the principal sulcus project mainly to the intermediate sector of the head and body of the nucleus. However, there appears to be some degree of overlap of corticostriatal projections from the dorsal and ventral prefrontal regions, as well as within each trend. Relatively minor projections are directed to the putamen as well as to the tail of the caudate nucleus from certain subregions of the prefrontal cortex. Thus the distribution of prefrontostriatal connections seems to reflect the architectonic organization of the prefrontal cortex. Possible functional aspects of prefrontostriatal connectivity are considered in the light of behavioral and physiological studies.

Animals↗
PubMed1991

Projections to the basis pontis from the superior temporal sulcus and superior temporal region in the rhesus monkey.

The present investigation was designed to determine the origins in the temporal lobe, and terminations in the pons, of the temporopontine pathway. Injections of tritiated amino acids were placed in multimodal regions in the upper bank of the superior temporal sulcus (STS), and in unimodal visual, somatosensory, and auditory areas in different sectors of the lower bank of the STS, the superior temporal gyrus (STG), and the supratemporal plane (STP). The distribution of terminal label in the nuclei of the basis pontis was studied using the autoradiographic technique. Following injections of isotope into the multimodal areas (TPO and PGa) in the upper bank of the STS, intense aggregations of label were observed in the extreme dorsolateral, dorsolateral, and lateral nuclei of the pons, and modest amounts of label were seen in the peripeduncular nucleus. The caudalmost area TPO projected in addition to the ventral and intrapeduncular pontine nuclei. The second auditory area, AII, and the adjacent auditory association areas of the STG and STP contributed modest projections to the dorsolateral, lateral, and peripedunuclar nuclei, but generally spared the extreme dorsolateral nucleus. The lower bank of the STS, which subserves central vision, the somatosensory associated region at the fundus of the rostral STS, and the primary auditory area did not project to the pons. The higher order, multimodal STS contribution to the corticopontocerebellar circuit may provide a partial anatomical substrate for the hypothesis that the cerebellum contributes to the modulation of nonmotor functions.

Amino Acids↗
PubMed1991

Corticothalamic connections of the superior temporal sulcus in rhesus monkeys.

The corticothalamic connections of the superior temporal sulcus (STS) were studied by means of the autoradiographic technique. The results indicate that corticothalamic connections of the STS in general reciprocate thalamocortical connections. The cortex of the upper bank of the STS-multimodal areas TPO and PGa-projects to four major thalamic targets: the pulvinar complex, the mediodorsal nucleus, the limitans-suprageniculate nucleus, as well as intralaminar nuclei. Within the pulvinar complex, the main projections of the upper bank of the STS are directed to the medial pulvinar (PM) nucleus. Rostral upper bank regions tend to project caudally and medially within the PM nucleus, caudal upper bank regions, more laterally and ventrally. The mid-portion of the upper bank tends to occupy the central sector of the PM nucleus. There are also relatively minor projections from upper bank regions to the lateral pulvinar (PL) and oral pulvinar (PO) nuclei. In contrast to the upper bank, the projections from the lower bank are directed primarily to the pulvinar complex, with only minor projections to intralaminar nuclei. The rostral portion of the lower bank projects mainly to caudal and medial regions of the PM nucleus, whereas the caudal lower bank projects predominantly to the lateral PM nucleus, and also to the PL, PO, and inferior pulvinar (PI) nuclei. The mid-portion of the lower bank projects mainly to central and lateral portions of the PM nucleus, and also to the PI and PL nuclei. The rostral depth of the STS projects mainly to the PM nucleus, with only minor connections to the PO, PI, and PL nuclei. The mid-portion of multimodal area TPO of the upper bank, areas TPO2 and TPO3, projects preferentially to the central sector of the PM nucleus. It is possible that this STS-thalamic connectivity has a role in behavior that is dependent upon more than one sensory modality.

Animals↗
PubMed1991

Golgi, histochemical, and immunocytochemical analyses of the neurons of auditory-related cortices of the rhesus monkey.

Morphological characteristics of the neurons of the auditory cortical areas of the rhesus monkey were investigated using Golgi and horseradish peroxidase methods. Neurons of the auditory cortices can be segregated into two categories, spinous and nonspinous, which can be further subclassified according to their dendritic arrays. The spinous neurons include pyramidal, "star pyramid," multipolar, and bipolar cells. As in other cortices, pyramidal cells are found in layers II-VI and appear to be the most numerous of all cortical neurons. The "star pyramids" have radially oriented dendrites with a less prominent apical shaft and are found mainly in the middle cortical layers. The spinous multipolar neurons are also found in the middle cortical layers and have their dendrites radially arrayed but have no apical dendrite. The spinous bipolar cells, found in the infragranular layers, occur most frequently in the lateral auditory association cortex. The nonspinous neurons include neurogliaform, multipolar, bitufted, and bipolar cells and are found in all cortical layers. The neurogliaform cells are the smallest of all neurons and have radially arrayed, recurving dendrites. The nonspinous multipolar cells also have radially arrayed dendrites but vary in size from being confined to one cortical layer to extending across four laminae. The bitufted neurons are subclassified into three groups: neurons whose primary dendrites arise radially from their somata, those whose dendrites arise from two poles of their somata, and those that have a single primary dendrite arising from one pole and multiple dendrites from another pole of their somata. The nonspinous bipolar cells also have several variants but usually have dendrites arising from two poles of the somata. The chemical characteristics of the auditory neurons were investigated using histochemical and immunocytochemical methods. Peptidergic neurons, i.e., cholecystokinin-, vasoactive intestinal polypeptide-, somatostatin-, and substance P-reactive neurons are found in the various subregions of the auditory cortices and are distributed differentially in the cortical laminae. These neurons are of the nonpyramidal type. Gamma aminobutyric acid-reactive neurons are also nonpyramidal cells and they are found in all cortical layers. Their numbers varied among the cortical laminae in the different auditory regions.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1990

Anatomical investigation of projections from thalamus to posterior parietal cortex in the rhesus monkey: a WGA-HRP and fluorescent tracer study.

The parietothalamic projections have been shown to be heterogeneous and appear to be a reflection of the detailed architectonic parcellation of the parietal lobe. In the present study WGA-HRP injections were placed in the different subdivisions of the posterior parietal cortex of the rhesus monkey to determine whether a similarly complex pattern also exists in the thalamocortical pathway. Additionally, in an attempt to determine whether there is an intranuclear specificity of projections from individual thalamic nuclei to different subdivisions of the parietal lobe, multiple retrograde fluorescent tracers were injected into the rostral to caudal sectors of the parietal lobe of the same animal. Different subdivisions of the parietal lobe appear to receive different sets of thalamic input. Thus the superior parietal lobule (SPL) projections are derived from more lateral regions in the thalamus, arising predominantly from the lateral posterior (LP) and pulvinar oralis (PO) nuclei, with additional contributions from the pulvinar lateralis (PL) and pulvinar medialis (PM) nuclei. The inferior parietal lobule (IPL), by contrast, receives its projections from more medial thalamic regions, its main thalamic input originating from PM, and aided by LP, PL, and PO. Both the SPL and IPL also receive projections from the mediodorsal (MD), ventroposterior, ventrolateral, intralaminar, and limbic nuclei, albeit from different components within these nuclei. A topographical arrangement also exists in the thalamic projections to the rostral versus the caudal subdivisions of both the SPL and the IPL. Thus, in the SPL, the ventral posterolateral nucleus, pars oralis (VPLo), ventral lateral nucleus, pars oralis (VLo), and ventral lateral nucleus, pars medialis (VLm) project to rostral regions, whereas the PM and limbic nuclei, anteroventral (AV), and anteromedial (AM), project to area PGm on the medial convexity of the SPL. With respect to projections to the IPL, the ventral posteromedial (VPM) and PO nuclei project to rostral regions, whereas the limbic nuclei lateral dorsal (LD), AM and AV project only to the caudal most area, Opt. A rostrocaudal difference is reflected also within certain nuclei (LP, PO, and PM) that project to the SPL or IPL. Thus rostral parietal subdivisions receive projections from ventral regions within these thalamic nuclei, whereas caudal parietal afferents arise from the dorsal parts of these nuclei. Intervening cortical levels receive projections from intermediate positions within the nuclei. It therefore seems that the increasing architectonic and functional complexity as one moves from rostral to caudal in the SPL and IPL appear to be reflected in the thalamic afferents.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1989

Intrinsic connections and architectonics of the superior temporal sulcus in the rhesus monkey.

The intrinsic connections of the superior temporal sulcus (STS) in the rhesus monkey were studied by anterograde and retrograde tracer techniques and correlated with a reevaluation of cortical cytoarchitecture. The polymodal region in the upper bank (area TPO) is divisible into four rostral-to-caudal architectonic sectors, exhibiting increasing degrees of laminar differentiation and cellularity as one proceeds caudally. These sectors, including the sulcal proisocortex (area Pro), are tied together in a sequence of reciprocal connections. Each rostrocaudal sector of area TPO also has reciprocal connections with the laterally adjacent area TAa, at the upper rim of the sulcus, and medially adjacent areas PGa and IPa, near the depth. A similar arachitectonic/connectional organization exists for unimodal vision-related cortex in the lower bank of the STS. Here a rostrocaudal sequence of reciprocal connections unites area Pro, rostral and caudal divisions of area TEa, and the extrastriate visual area OAa (MT). Area TEa also has reciprocal connections with adjacent segments of area TEm laterally, at the lower rim of the sulcus, and area IPa, medially, in the depth. In both upper and lower banks, caudal-to-rostral "forwardgoing" connections begin in supragranular layers of cortex and terminate in and around layer IV. Reciprocal, "backgoing" connections take origin from cells in infragranular layers and terminate mainly over the first layer of the caudally adjacent target zone. Orthogonally directed, "side-to-side" projections originate in both supra- and infragranular layers and terminate diffusely over all layers of cortex.

Animals↗
PubMed1989

Anatomical investigation of projections to the basis pontis from posterior parietal association cortices in rhesus monkey.

The projections to the basis pontis from cytoarchitectonically defined subregions of the superior (SPL) and inferior (IPL) parietal lobules were investigated in 14 rhesus monkeys by using the anterograde tracing techniques of autoradiography and horseradish peroxidase histochemistry. The results of our study confirm and complement available information regarding the parietopontine projections. The projections are found in clusters distributed in lamellae approximately concentric to the peduncle. They are directed most heavily towards the peripeduncular and lateral nuclei of the pons. There are also lesser, but nevertheless substantial projections to other nuclei including the intrapeduncular, ventral, dorsolateral, extreme dorsolateral, and dorsal nuclei. The dorsomedial, paramedian, and NRTP nuclei receive only minor projections. The SPL projections are relatively widespread with respect to the more focussed IPL projections. The IPL projections are, in general, situated more laterally and at more rostral levels of the pontine nuclei than are those of the SPL. The sulcal cortex of the SPL (area PEa) favors the dorsolateral, extreme dorsolateral, and ventral nuclei compared to the light projections to these nuclei from the convexity of the SPL. The sulcal cortex of the IPL, area POa, differs from the gyral cortex in favoring the ventral and extreme dorsolateral nuclei. The rostral IPL differs from the caudal IPL in that the intrapeduncular nucleus receives projections only from rostral regions, while the lateral nucleus receives projections preferentially from caudal regions. The pontine projections from the medial SPL, area PGm, are unique in the parietal lobe in that they include the paramedian nucleus. Projections arising from multimodal regions located caudally in the SPL (areas PEa and PGm) and IPL (areas PG and Opt) are more strongly represented and more laterally placed within the pontine nuclei than projections arising from more rostral, unimodal, posterior parietal regions. The heavy projections to the pontine nuclei from the posterior parietal cortex, and particularly from those caudal parietal regions that have prominent associative and limbic connections, seem to suggest that the corticopontocerebellar pathways permit a cerebellar contribution not only to the coordination of movement, but also to the modulation and integration of higher function.

Animals↗
PubMed1989

Architecture and intrinsic connections of the prefrontal cortex in the rhesus monkey.

An investigation of the architectonic organization and intrinsic connections of the prefrontal cortex was conducted in rhesus monkeys. Cytoarchitectonic analysis indicates that in the prefrontal cortex there are two trends of gradual change in laminar characteristics that can be traced from limbic periallocortex towards isocortical areas. The stepwise change in laminar features is characterized by the emergence and gradual increase in the width of granular layer IV, by an increase in the size of pyramidal cells in layers III and V, and by a higher cell-packing density in the supragranular layers. Myeloarchitectonic analysis reveals that the limbic areas are poorly myelinated, adjacent areas have a diffuse myelin content confined to the deep layers, and in isocortices the myelinated fibers are distributed in organized horizontal bands (of Bail-larger) and a vertical plexus. Using the above architectonic criteria, we observed that one of the architectonic trends takes a radial basoventral course from the periallocortex in the caudal orbitofrontal region to the adjacent proisocortex and then to area 13. The next stage of architectonic regions includes orbital areas 12, 11, and 14, which is followed by area 10, lateral area 12, and the rostral part of ventral area 46. The last group includes the caudal part of ventral area 46 and ventral area 8. The other trend takes a mediodorsal course from the periallocortex around the rostral portion of the corpus callosum to the adjacent proisocortical areas 24, 25, and 32 and then to the medially situated isocortical areas 9, 10, and 14. The next stage includes lateral areas 10 and 9 and the rostral part of dorsal area 46. The last group includes the caudal part of dorsal area 46 and dorsal area 8. The interconnections of subdivisions of the basoventral and mediodorsal cortices were studied with the aid of anterograde and retrograde tracers. Within each trend a given area projects in two directions: to adjoining regions belonging to succeeding architectonic stages on the one hand, and to nearby regions from the preceding architectonic stage on the other. In each direction there is more than one region involved in this projection system, paralleling the radial nature of architectonic change. Periallo- and proisocortices have widespread intrinsic connections, whereas isocortices situated at a distance from limbic areas, such as area 8, have restricted connections. Most interconnections are limited to areas within the same architectonic trend. However, there are links between cortices from the two trends, and these seem to occur between areas that are at a similar stage of architectonic differentiation.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗