Biomedical subjects

W M Cowan

Publications and source records attributed to W M Cowan.

At least 19 recordsLinked to original sources

PubMed1990

Quantitative, three-dimensional analysis of granule cell dendrites in the rat dentate gyrus.

The three-dimensional organization of dentate granule cell dendritic trees has been quantitatively analyzed with the aid of a computerized microscope system. The dendrites were visualized by iontophoretic injection of horseradish peroxidase into individual granule cells in the in vitro hippocampal slice preparation. Selection criteria insured that the analyzed cells were completely stained and that only neurons with two or fewer cut dendrites in the distal portion of the molecular layer were analyzed. Twenty-nine of the 48 sampled granule cells had no cut dendrites. The granule cells had between one and four primary dendrites. Granule cell dendritic branches were covered with spines and most extended to the hippocampal fissure or pial surface. The mean total dendritic length was 3,221 microns with a range from 2,324 microns to 4,582 microns. The dendrites formed an elliptical plexus with the transverse spread averaging 325 microns and the spread in the septotemporal axis averaging 176 microns. On individual neurons, the maximum branch order ranged from four to eight and the number of dendritic segments ranged from 22 to 40. Approximately 63% of the dendritic branch points occurred in a zone that included the granule cell layer and the inner one-third of the molecular layer. The dendritic tree was organized so that, on average, 30% of the length was in the granule cell layer and proximal third of the molecular layer, 30% was in the middle third, and 40% was in the distal third. Comparisons were made between the dendrites of granule cells in the suprapyramidal and infrapyramidal blades of the dentate gyrus. Suprapyramidal cells had a significantly greater total dendritic length than infrapyramidal cells, their transverse spread was higher, and they had a greater number of dendritic segments. When neurons in the suprapyramidal blade were further subdivided on the basis of somal position within the depth of the cell body layer, superficial neurons were found to have a greater number of primary dendrites, more elliptical trees, and larger transverse spreads of their dendrites. There were no significant differences in dendritic segment number or total dendritic length between superficial and deep cells.

Animals↗

PubMed1988

Observations on the development of certain ascending inputs to the thalamus in rats. I. Postnatal development.

We have studied the postnatal development of the major ascending afferents to the thalamus in postnatal rats using tetramethylbenzidine histochemistry following wheat germ agglutinin-conjugated horseradish peroxidase injections into either the dorsal column nuclei, the deep cerebellar nuclei, or the inferior colliculus. By the day of birth, the efferents from each of these regions have already entered, and arborized extensively within, their appropriate thalamic relay nuclei. However, the overall distribution of each of these ascending afferent systems differs dramatically from that seen in mature rats. In neonatal rats, a substantial proportion of the ascending axons extend beyond the thalamus and often enter the internal capsule, some bypassing the thalamus altogether. In addition, some of the axons which enter and arborize within the thalamus extend beyond their appropriate terminal field into adjoining thalamic nuclei. Retrograde tracing experiments utilizing Fast blue indicate that the cells of origin of these overshooting axons are distributed similarly to the cells of origin of the definitive thalamic afferents. These early erroneous projections are all subsequently eliminated and the characteristically restricted adult distribution of each afferent system is evident by P30. These results indicate that developmental overgrowths and targeting errors of thalamic afferent fibers are not unique to the visual system (where they have been documented previously), but may be a general feature in the development of these pathways.

Afferent Pathways↗

PubMed1988

pp60c-src expression in the developing rat brain.

We have studied pp60c-src expression in the striatum, hippocampus, and cerebellum of the developing rat brain. In the striatum, pp60c-src protein kinase activity peaks during embryonic development and then declines in the adult. The peak activity occurs in the striatum on embryonic day 20 (E20) when it is 18- to 20-fold higher than the activity in fibroblasts and 4- to 5-fold higher than the activity in the striatum at E15 or in the adult striatum. In the hippocampal region, pp60c-src activity reaches a maximum shortly after birth but remains high throughout life. On postnatal day 2 (P2) the activity in the hippocampus is 9- to 13-fold higher than the activity in fibroblasts and twice as high as the activity in the hippocampus at E18. In the cerebellum, the kinase activity remains constant from E20 onward and is 6- to 10-fold higher than that observed in fibroblasts. The increase in pp60c-src kinase activity observed during the development of the striatum and hippocampus is due to an increase in the amount of pp60c-src protein and to an increase in the specific activity of the kinase. The increase in specific activity in these regions coincides with the peak periods of neurogenesis and neuronal growth. In the striatum, we have found that the increase in pp60c-src activity also parallels the increase observed in culture as embryonic striatal neurons differentiate. Taken together, our results are consonant with the idea that pp60c-src is the product of a developmentally regulated gene that is important for the differentiation and/or the continuing function of neurons.

Aging↗

PubMed1987

The survival of dentate gyrus neurons in dissociated culture.

Using a technique for dissociating cells from the area dentata of postnatal rats, we have been able to routinely establish low density cultures of dentate granule neurons that can be grown in the presence or absence of serum. Non-granule neurons from the hilar region and glial cells (both astrocytes and oligodendrocytes) are also present, but can be readily distinguished from the granule cells in these cultures. Unlike dissociated hippocampal pyramidal cells, which frequently resemble their in vivo morphology, dissociated dentate granule cells bear little resemblance to their normal in vivo counterparts, but are very similar in appearance to the ectopic granule cells seen in the reeler mouse. This suggests that extrinsic factors are the principal determinants of the mature form which granule neurons assume in vivo. On the other hand, the dissociated granule cells are able to express certain other aspects of their in vivo phenotype including the synthesis and transport of an antigen which is characteristically found in mossy fibers. Certain neuropeptide-containing non-granule neurons found in these cultures are also capable of maintaining aspects of their in vivo phenotype.

Animals↗

PubMed1987

Organization of radial glial cells during the development of the rat dentate gyrus.

The temporal and spatial patterns of development of radial glial processes in the rat dentate gyrus have been studied in immunohistochemical preparations stained for the presence of either the glial fibrillary acidic protein (GFAP) or the vimentin-associated antigen R4. Additional electron microscopic (EM) observations were made from material prepared either immunohistochemically or by the Golgi method. R4 immunoreactive radial fibers were observed in the incipient dentate gyrus as early as E13 and by E14 the density of stained fibers was clearly higher in the anlage of the dentate gyrus than in the adjacent hippocampus. By E15 it was possible to identify in the EM the endfeet of radial glial cells that contained numerous glycogen particles. GFAP-positive radial processes were first observed on E17; these processes tended to be of larger diameter than those stained with the R4 antibody, suggesting that they were among the more mature processes. The orientation of both the R4- and GFAP-positive glial processes changed throughout the last week of embryonic life and by the end of the first postnatal week they formed a complex meshwork of intertwined processes. The distribution of their cell bodies also changed with time; initially their perikarya were located in the neuroepithelium at the lateral margin of the hippocampal primordium; later they were found mainly beneath the granule cell layer. Dividing cells that contained GFAP were observed along the trajectory of the migrating granule cell precursors and in the hilus of the dentate gyrus; at later stages some GFAP-positive mitotic figures were seen within and immediately below the granule cell layer. On the basis of these observations, we have attempted to reconstruct the role that radial glial processes play in the morphogenesis of the dentate gyrus. First, radial processes extend from the neuroepithelium to the pial surface prior to the migration of neurons that will form the dentate gyrus. These early generated glia appear to form the boundaries of the developing dentate gyrus and provide an internal lattice that may guide the initial wave of migrating progenitor cells. As the dentate gyrus enlarges, these early formed processes maintain their contacts along the hippocampal fissure and along the pial surface of the dentate anlage. Thus, with time they become increasingly distorted and are ultimately compressed into two bundles; one lies deep to the hippocampal fissure parallel to the granule cell layer and the other is located at the fimbriodentate juncture.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

PubMed1987

The entorhinal cortex of the monkey: I. Cytoarchitectonic organization.

As an essential preliminary to a series of experimental studies of the afferent and efferent connections of the monkey entorhinal cortex, we have carried out a detailed analysis of its cytoarchitectonic organization. Primarily on the basis of features observed in Nissl- and fiber-stained preparations, supplemented with Golgi-stained material and preparations stained for heavy metals by Timm's method and histochemically for acetylcholinesterase, the entorhinal cortex has been divided into seven fields that are named according to their rostrocaudal and mediolateral positions except for one rostrally located field that is named for the prominent input that it receives from the olfactory bulb. At rostral levels, the entorhinal cortex is marked by a number of morphological inhomogeneities. The neurons tend to be organized in patches that are surrounded by large, thick, radially oriented bundles of fibers. At caudal levels, the entorhinal cortex has a more distinctly laminated appearance, reminiscent of that in the neocortex, and most of the neurons and fiber fascicles are arranged in discrete radial columns. The cortical region adjoining the entorhinal cortex laterally, which is commonly known as the "perirhinal cortex," is in fact composed of two separate fields corresponding to areas 35 and 36 of Brodmann. Area 35 occupies the fundus and part of the lateral aspect of the rhinal sulcus. Area 36 extends from the lateral bank of the rhinal sulcus into the inferior temporal gyrus, where it borders fields TA and TE rostrally, and field TF of the parahippocampal gyrus caudally. The surface extents of each of the entorhinal fields have been determined by making "unfolded" two-dimensional maps of the region and measuring the areas with a computerized digitizing system.

Acetylcholinesterase↗

PubMed1987

The entorhinal cortex of the monkey: II. Cortical afferents.

The entorhinal cortex of the monkey is commonly viewed as the major link between the cerebral cortex and the other fields of the hippocampal formation. Until recently, however, little was known about the origins of the cortical projections to the entorhinal cortex, and most of the available information is still based on degeneration studies. We have carried out a systematic analysis of these connections by placing small injections of the retrograde tracer wheat germ agglutinin conjugated to horseradish peroxidase into each of the fields of the entorhinal cortex of the Macaca fascicularis monkey. Retrogradely labeled cells were observed in several areas of the frontal and temporal lobes, the insula, and the cingulate cortex. In the frontal lobe, the greatest number of labeled cells were observed in the orbital region and specifically in areas 13 and 13a: labeled cells were also seen in areas 14, 11, and 12. In the dorsolateral frontal cortex, labeled cells were observed mainly in the rostral half of area 46; occasionally cells were also seen in areas 9, 8, and 6. In the cingulate cortex, labeled cells were observed in area 25, area 32, and rostral levels of area 24; fewer cells were observed at caudal levels of area 24 or in area 23. The retrosplenial region (areas 30 and 29), including its caudal extension along the rostral calcarine sulcus and its ventral extension into the temporal lobe, contained numerous labeled cells. In the temporal lobe, retrogradely labeled cells were arranged in two rostrocaudally oriented bands. Rostral to the hippocampal formation, the first band encompassed the piriform and periamygdaloid cortices and areas 35 and 36; the labeling in area 36 was continuous to the temporal pole. At more caudal levels this band was located immediately lateral to the hippocampal formation and included areas 35 and 36 rostrally and areas TH and TF caudally. The second band was situated in the superior temporal gyrus where labeled cells were observed in several distinct cytoarchitectonic fields, including the parainsular cortex in the fundus of the inferior limiting sulcus. In the insula proper, retrogradely labeled cells were seen mainly in the rostral or agranular division; far fewer were observed in the dysgranular and granular insula. Whereas there is little available physiological information concerning many of the cortical regions that project to the entorhinal cortex, on anatomical grounds they may be generally characterized as polysensory associational regions.

Afferent Pathways↗

PubMed1987

The entorhinal cortex of the monkey: III. Subcortical afferents.

The subcortical afferent connections of the entorhinal cortex of the Macaca fascicularis monkey were investigated by the placement of small injections of the retrograde tracer wheat germ agglutinin conjugated to horseradish peroxidase into each of its subdivisions. Retrogradely labeled cells were observed in several subcortical regions including the amygdaloid complex, claustrum, basal forebrain, thalamus, hypothalamus, and brainstem. In the amygdala, labeled cells were observed principally in the lateral nucleus, the accessory basal nucleus, the deep or paralaminar portion of the basal nucleus, and the periamygdaloid cortex. Additional retrogradely labeled cells were found in the endopiriform nucleus, the anterior amygdaloid area, and the cortical nuclei. Retrogradely labeled cells were observed throughout much of the rostrocaudal extent of the claustrum and tended to be located in its ventral half. In the basal forebrain, retrogradely labeled cells were observed in the medial septal nucleus, the nucleus of the diagonal band, and to lesser extent within the substantia innominata. Several of the cells in the latter region were large and located within the densely packed neuronal clusters of the basal nucleus of Meynert. Most of the labeled cells in the thalamus were located in the midline nuclei. Many were found in nucleus reuniens, but even greater numbers were located in the centralis complex. Additional labeled cells were located in the paraventricular and parataenial nuclei. In all cases, numerous retrogradely labeled cells were observed in the medial pulvinar. In the hypothalamus, most of the retrogradely labeled cells were located in the supramamillary area, though scattered cells were also observed in the perifornical region and in the lateral hypothalamic area. Caudal to the mamillary nuclei there were labeled cells in the ventral tegmental area. There were relatively few labeled cells in the brainstem and these were invariably located either in the raphe nuclei or locus coeruleus.

Amygdala↗

PubMed1987

On the numbers of neurons in fields CA1 and CA3 of the hippocampus of Sprague-Dawley and Wistar rats.

In a previous study it was found that there are significant differences in the numbers of granule cells in the dentate gyrus of adult Sprague-Dawley and Wistar rats and also that the continued postnatal addition of new cells to the dentate gyrus has quite different consequences in the two strains. We have now extended these observations to the two major cytoarchitectonic fields of the hippocampus (the regio superior or field CA1; and the regio inferior or field CA3). The mean number of pyramidal neurons in field CA1 of 1-month-old Sprague-Dawley rats is 420,000 (+/- 60,000 S.E.), while Wistar rats at the same age have 320,000 (+/- 20,000). The numbers of neurons in field CA3 in the two strains are: 330,000 (+/- 30,000) and 210,000 (+/- 20,000), respectively. Whether these strain differences reflect specific differences in the neural organization of the hippocampal formation in the two strains, or are related to more general differences in total body weight or brain weight, is unknown. Since during the first two days postnatally we estimate that there are between 358,000 and 491,000 cells in field CA1 of Sprague-Dawley rats, it would seem that there is no significant naturally-occurring neuronal death in this hippocampal field. This may be due to the extensive collateral projections of the hippocampal pyramidal neurons.

Animals↗

PubMed1986

A light and electron microscopic analysis of the mossy fibers of the rat dentate gyrus.

The axon collaterals of dentate granule cells have been analyzed with the aid of a computerized microscope, following intracellular injections of horseradish peroxidase in hippocampal slice preparations. The axon of each granule cell gives rise to approximately seven primary collaterals; these collaterals usually divide into secondary and tertiary branches, which form an extensive plexus within the hilar region of the dentate gyrus. Individual axon collaterals vary greatly in length, but most have been found to be between 100 and 300 microns long. On average, the summed lengths of the collaterals (exclusive of the parent mossy fiber) are approximately 2,300 microns. Except for an occasional collateral that is given off by a mossy fiber in the proximal part of field CA3 of the hippocampus, the collaterals of the granule cell axons are confined to the hilar region; they are rarely seen in the granule cell layer itself and have never been observed in the molecular layer. In the longitudinal dimension of the dentate gyrus, most of the collaterals are contained within a zone about 400 microns wide. The distribution of the collaterals within the hilar region is correlated with the location of the granule cell body. Those that arise from cells near the tip of the suprapyramidal blade tend to be confined to the region above field CA3; those from cells nearer the crest and from the infrapyramidal blade ramify widely throughout the hilus. Two types of varicosities are present on the collaterals. Numerous small (approximately 2 microns), round varicosities are distributed unevenly along the collaterals; in electron micrographs these varicosities can be seen to make asymmetric synaptic contacts with dendritic shafts. On average, each granule cell collateral plexus has about 160 of these varicosities. The second type of varicosity is irregular in shape and ranges from 2 to 4 microns in diameter; there is usually only one such varicosity per collateral. In all respects except size, these varicosities resemble the expansions found on the parent mossy fibers. Mossy fiber trajectories in the proximal part of field CA3 were studied after extracellular injections of HRP into localized regions of the granule cell layer. Granule cells at different locations around the blade send their mossy fibers to different depths within the pyramidal cell layer in the proximal part of field CA3. However, further distally, mossy fibers from all parts of the granule cell layer contribute to the suprapyramidal bundle that occupies the stratum lucidum.

Animals↗

PubMed1986

Evidence that late-generated granule cells do not simply replace earlier formed neurons in the rat dentate gyrus.

Ten-day-old Sprague-Dawley rats were injected intraperitoneally with 3H-thymidine (3H-TdR) and allowed to survive until postnatal day (P) 40, P120, P200, P300 or P450. Following the preparation of the tissue for autoradiography, the location of the labeled neurons within the granule cell layer of the dentate gyrus was determined at two different septo-temporal levels. At P40 the labeled cells in the suprapyramidal blade of the dentate gyrus were found only in the deep part of the granule cell layer, where it borders on the hilus, and more than four cell diameters from the molecular layer. The latter relationship remained constant at each of the five ages studied, but between P40 and P120 the average distance from the labeled granule cells to the hilus almost doubled. At the middle of the temporal portion of the dentate gyrus this trend continues with age, so that by P450 the labeled neurons, though no nearer to the molecular layer than at earlier stages, were found, on average, in the middle of the granule cell layer, more-or-less halfway between the hilus and the molecular layer. Near the middle of the septal half of the dentate gyrus a similar pattern was seen at P40 and P120 but thereafter the labeled cells within the granule cell layer remained at about the same distance from the hilus.(ABSTRACT TRUNCATED AT 250 WORDS)

Aging↗

PubMed1986

The effect of intraocular tetrodotoxin on the postnatal reduction in the numbers of optic nerve axons in the rat.

We have examined the effects of blocking retinal ganglion cell activity with the sodium channel blocker tetrodotoxin (TTX) on the postnatal reduction in the number of optic nerve axons (and, by interference, the degree of ganglion cell loss in the retina). TTX was injected every other day into the left eyes of a series of albino rats beginning on the day of birth, continuing through the 3rd, 7th, 12th or 14th days when the animals were killed and the optic nerves from both eyes were prepared for electron microscopy. The numbers of axons in the TTX treated and untreated optic nerves from the opposite side were determined from electron micrographs, and compared to the number seen in normal rats at the same ages. Both the magnitude and the time course of the reduction in the number of axons in the TTX-treated and untreated nerves were found to be similar to those seen in normal animals. However, there was a slight reduction in the loss of optic axons in the untreated nerves on the side opposite the TTX injections; this attenuation in axon loss could be mimicked by large systemic injections of TTX, and is probably attributable to a general systemic effect following repeated intraocular injections. These findings indicate that blocking ganglion cell activity with intraocular injections of TTX has little effect on the normal rate of axon loss from the optic nerve and on the numbers of ganglion cells that die during the first two weeks of postnatal life.

Animals↗

PubMed1986

Fibroblast growth factor promotes survival of dissociated hippocampal neurons and enhances neurite extension.

Basic fibroblast growth factor (FGF) has been found to increase neuronal survival and neurite extension in a highly purified population of fetal rat hippocampal neurons under well-defined serum-free cell culture conditions. In the presence of FGF, neuronal survival after 7 days in culture on a simple plastic substrate is increased 4-fold, to 54% of the initial population. Survival is increased 2-fold to 40% on polyornithine-laminin. When FGF was bound to plastic or heparin substrates, neurite outgrowth was significantly increased to lengths comparable to those seen with laminin; however, FGF produced no further increase in neurite outgrowth on laminin. Half-maximal survival was observed at FGF concentrations of about 15 pg/ml (1 pM); half-maximal process outgrowth occurred at about 375 pg/ml (20 pM). The responsive cells were identified as neurons by their labeling with tetanus toxin and by antibodies to neurofilaments and to the neuron-specific enolase. Astrocytes, identified by the presence of glial fibrillary acidic protein, constituted about 10% of cells present at 1 week both in the presence and in the absence of FGF. These results strongly suggest that, in addition to its known mitogenic effects on nonneuronal cells, FGF possesses neurotrophic activity for hippocampal neurons.

Animals↗

PubMed1986

Topographic targeting errors in the retinocollicular projection and their elimination by selective ganglion cell death.

In adult rats, as in other rodents, the retinocollicular projection is topographically organized in a very precise manner. Experiments involving the use of the retrogradely transported fluorescent dye fast blue as either a short- or long-term marker in neonatal rats indicate that the precision of this retinotopic projection does not arise ab initio, but rather is brought about by the preferential elimination of those ganglion cells whose axons project to topographically inappropriate regions of the colliculus. Such topographic targeting errors have been identified along both the rostrocaudal and mediolateral axes of the colliculus, and their elimination occurs during the period of naturally occurring ganglion cell death, which is completed by about postnatal day 10. When impulse activity in the retinal ganglion cell axons is blocked by repeated intraocular injections of the sodium channel-blocking agent tetrodotoxin (TTX) throughout the postnatal period of ganglion cell death, the preferential loss of the incorrectly projecting ganglion cells does not occur in the activity-blocked eye, although, as reported elsewhere, the overall loss of ganglion cells is comparable to that seen in normal animals. This supports the notion that the mechanism for selecting against incorrectly projecting ganglion cells is based on impulse activity among the competing ganglion cell axons. However, under activity-block conditions, the aberrantly projecting axons appear to retract from the caudal margin of the colliculus. The death of retinal ganglion cells during development thus seems to serve 2 purposes: It provides for the quantitative matching of the ganglion cell population to the needs of its central projection fields, and, at the same time, it serves to selectively eliminate those cells whose axons project to inappropriate targets or to inappropriate regions within the correct target fields.

Amidines↗

PubMed1985

The thalamic relations of the caudal inferior parietal lobule and the lateral prefrontal cortex in monkeys: divergent cortical projections from cell clusters in the medial pulvinar nucleus.

The thalamic relations of the caudal inferior parietal lobule and the dorsolateral prefrontal cortex in monkeys have been investigated with both anterograde and retrograde neuroanatomical tracing techniques. The results of these experiments indicate that the medial pulvinar nucleus (Pul.m.) is the principal thalamic relay to the gyral surface of the caudal inferior parietal lobule (area 7a). Within the Pul.m. there are two or three disklike aggregates of neurons which project to area 7a; these disklike neuronal aggregates are oriented from dorsomedial to ventrolateral and extend over most of the rostrocaudal extent of the nucleus. Within these disks there are rodlike clusters of neurons which are elongated in the rostrocaudal dimension of the thalamus, and which project in a topographically ordered manner to area 7a. Thus, the more rostrally located neurons within the Pul.m. disks project to more rostral parts of area 7a and, conversely, the more caudally located neurons project to the caudal part of this cortical field. Similarly, the medial part of each disk projects to the lateral part of area 7a while the laterally placed neurons project to the medial part of the cortical field. In addition to its input from the Pul.m., area 7a is also reciprocally connected with the magnocellular division of the nucleus ventralis anterior, with the nuclei which abut upon the medullary capsule of the laterodorsal nucleus, and with the suprageniculate nucleus and the nucleus limitans. The cortex on the lateral bank of the intraparietal sulcus (the so-called lateral intraparietal area, LIP) projects principally to the lateral pulvinar nucleus (Pul.l) of the thalamus rather than to Pul.m. Area LIP has been found to project to the pregeniculate nucleus, the zona incerta, the anterior pretectal nucleus, and the superior colliculus. Area 7a projects to none of these structures, but it does project to the posterior pretectal nucleus. The thalamic relations of the neighboring cortical regions, such as the prelunate gyrus and area 7b, are also distinct from those of area 7a. It thus seems that the prelunate gyrus is primarily interconnected with the Pul.l., and area 7b with the oral pulvinar nucleus. Taken together these different subcortical relationships provide further evidence for the view that the caudal inferior parietal lobule is not a homogeneous cortical area, but is composed of a number of subsidiary fields. The projection from the Pul.m. to the lateral prefrontal cortex arises from disklike aggregates of neurons, similar in their orientation to the neuronal disks that project to area 7a.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

PubMed1985

On the number of neurons in the dentate gyrus of the rat.

We have estimated the number of dentate granule cells in Sprague-Dawley and Wistar rats at 1, 4 and 12 months of age. In Sprague-Dawley rats the number of granule cells is relatively constant throughout this period at about 1 million. In Wistar rats, on the other hand, there is a progressive increase in the number from about 700,000 at 1 month to 1 million at 4 months; thereafter the number declines to about 800,000 at 1 year. Estimates of the numbers of cells in the polymorphic zone that can be stained immunohistochemically for somatostatin, cholecystokinin, vasoactive-intestinal peptide, and glutamic acid decarboxylase show no appreciable differences in the two strains.

Age Factors↗

PubMed1985

Postnatal development of the ipsilateral retinocollicular projection and the effects of unilateral enucleation in the golden hamster.

Anterograde transport of wheat germ agglutinin conjugated to horseradish peroxidase (WGA-HRP) was used to study the normal development of the ipsilateral retinocollicular projection in golden hamsters, and to examine the effect of enucleation of the other eye at birth. In neonatal animals there were retinal fibers and sparsely distributed granular labeling in the superficial layers of the ipsilateral superior colliculus over its entire areal extent. Differences in the uncrossed projections of normal and enucleated animals first became clear at day 5. In normal animals, retinal fibers withdrew from the superficial layers of the superior colliculus, and the projection became concentrated in the stratum opticum, where denser clumps of label in the rostral part of the superior colliculus were first seen at day 5. In enucleated animals, the retinal projection persisted in the most superficial layers, and the density of labeling was higher than in normals. The very sensitive WGA-HRP technique showed retinal fibers extending to the caudal pole of the superior colliculus at all ages: even in normal animals more than 2 weeks of age some fibers reached as far as the inferior colliculus. When the shrunken size of the superior colliculus in the enucleated animals was taken into account, the total areal distribution of the ipsilateral projection was similar in normal animals and enucleates. The major difference between the two groups was in the higher density of ipsilateral labeling, especially in the caudal part of the superior colliculus, and in its more superficial laminar distribution in the enucleated animals.

Aging↗

PubMed1985

Callosal and prefrontal associational projecting cell populations in area 7A of the macaque monkey: a study using retrogradely transported fluorescent dyes.

The spatial interrelationship of neurons in area 7a in the inferior parietal lobule that project through the corpus callosum to the corresponding field in the contralateral hemisphere or to the ipsilateral prefrontal cortex has been analyzed in macaque monkeys by using double-labeling procedures with retrogradely transported fluorescent dyes. The populations of callosal and associational projecting neurons have similar laminar distributions and are topographically intermingled. Less than 1% of the neurons were double-labeled, thus suggesting that the two populations are largely separate. Two-dimensional reconstructions of the distribution of labeled cells made on flattened reconstructions of the inferior parietal lobule revealed that the areal distribution of the two cortico-cortical output arrays is complex. Although each pattern of labeling showed some discontinuities in density, there was no obvious periodicity within or between the spatial distributions of the two projecting populations. It was consistently observed that the cortex of the lateral wall of the intraparietal sulcus, adjacent to area 7a, projects more heavily to the prefrontal cortex than does area 7a itself.

Animals↗