Showing papers on "Thalamus published in 1981"

Neocortical cholinergic innervation: a description of extrinsic and intrinsic components in the rat.

Abstract: Electrothermic lesion of the peri-pallidal region of the rat caused a marked reduction in the activity of choline acetyltransferase in the ipsilateral fronto-parietal cortex without affecting the activity of glutamate decarboxylase Only lesions that involved the ventral globus pallidus significantly reduced cortical choline acetyltransferase activity; and lesions limited to the thalamus, internal capsule, pyriform cortex or zone incerta were ineffective Excito-toxin lesions of the ventral globus pallidus caused 45-5% reductions in all presynaptic markers for cholinergic neurons but did not significantly decrease presynaptic markers for noradrenergic, serotonergic or histaminergic neurons in the cortex The maximal reductions in cortical choline acetyltransferase activity achieved with the pallidal lesion was 70%; and enzyme activity reached its nadir by four days after placement of the lesion The pallidal lesion, which ablated the large isodendritic acetylcholinesterase positive neuronal perikarya, resulted in a profound loss in histochemically stained acetylcholinesterase-reactive fibers in the fronto-parietal cortex but not in the cingulate, pyriform and occipital cortex or hippocampal formation; analysis of the subregions in choline acetyltransferase activity The kainate lesion of the parietal cortex to ablate intrinsic neurons did not reduce the activity of tyrosine hydroxylase, a marker for noradrenergic terminals, but depressed glutamate decarboxylase by 68%; in contrast choline acetyltransferase activity fell only 29% The results indicate that approximately 70% of the cholinergic innervation in the fronto-parietal cortex is derived from acetylcholinesterase positive neurons in the peripallidal nucleus basalis, whereas the remainder appears to be localized in cortical intrinsic neurons

The visual claustrum of the cat. I. Structure and connections

Abstract: The cat's dorsocaudal claustrum was studied in Golgi preparations, by electron microscopy, and by anterograde and retrograde tracer techniques. It receives a convergent retinotopic projection from several visual cortical ares, including areas 17, 18, 19, 21a and PMLS (posteromedial lateral suprasylvian area). The projection arises from spiny dendrite cells (pyramidal and fusiform) in the middle of cortical layer VI. As shown by a double label experiment, they form a separate population from those projecting to the lateral geniculate nucleus. There are also inputs from the lateral hypothalamus, from the nucleus centralis thalami, and probably from the locus coeruleus, but not from the sensory nuclei of the thalamus. Non-visual cortical areas do not project to the visual claustrum, but many of them are connected to other parts of the nucleus. For example, the splenial (cingulate) gyrus projects to a claustral zone just ventral to the visual area, and regions anterior to the visual area are connected with somatosensory and auditory cortex. The commonest cell type in the claustrum is a large spiny dendrite neuron whose axon leaves the nucleus after giving off local collaterals. Small spine-free cells, with beaded dendrites and a locally arborizing axon, are found also. Electron microscopy of the claustrum after ablation of the visual cortex showed degenerating type 1 axon terminals synapsing on spines and beaded dendrites, suggesting a direct cortical input to both cell types. The visual claustrum projects back to the visual cortex, to the same areas from which it receives an input. The return projection is predominantly ipsilateral, but there is, in addition, a small crossed projection. The claustrocortical axons terminate in all cortical layers but most heavily in layers IV and VI. The majority of the cells in the visual claustrum project to the cortex, and retinotopy is maintained throughout the entire corticoclaustral loop. No subcortical projections from the claustrum could be identified.

Thalamic Neglect: Possible Role of the Medial Thalamus and Nucleus Reticularis in Behavior

Abstract: • A patient had an ischemic infarction of the right medial thalamus, with a resultant contralateral neglect syndrome. We propose that the medial thalamic nuclei, particularly centromedian and parafascicularis (CMPF), are normally involved in the arousal-activation process by which an organism can be aroused by and respond to novel or important stimuli. Specifically, we propose that (1) the mesencephalic reticular formation subserves tonic arousal to novel or painful stimuli by inhibiting the nucleus reticularis thalami (NR) and (2) that selective attention is mediated by cortical input to NR. The CMPF is closely associated with motor systems (basal ganglia, ventrolateral nucleus of the thalamus [VL], and frontal lobes). A pathway involving CMPF, the frontal cortex, and the portion of NR associated with VL may be important in preparing the tonically aroused organism for action. Unilateral lesions of CMPF therefore induce an asymmetric hypokinesia, and bilateral lesions may induce akinetic mutism.

Brain-stem auditory-evoked potentials recorded directly from human brain-stem and thalamus

Abstract: Brain-stem auditory-evoked potentials were recorded in neurosurgical patients from surface electrodes applied to the VIIIth nerve, medulla, pons, midbrain and cortex; from depth electrodes in the thalamus; and from a movable electrode in the IVth, IIIrd, and lateral ventricles. The potentials recordable over the scalp within 10 ms after click stimulation are characterized by a slow positive wave (peaking at 5 to 6 ms) and a negative wave (8 to 10 ms) with 7 small positive wavelets superimposed upon them. The sources of these components have been identified by observing their increased amplitude in depth recordings, and by tracing the potentials from their intracranial maxima to the scalp. Wave I is generated within the most distal portion of the VIII nerve; Wave V in the midbrain (inferior colliculus); and Wave VI the medial geniculate body. Both low positive and negative components have their origins in the inferior colliculus. Intracranially-recorded brain-stem auditory-evoked potential showed very rapid changes in amplitude within the brain-stem but only slight changes in the more rostral regions, although their amplitude gradients varied in the different components. They also demonstrated minor but systematic shifts in latency with distance from the potential sources, reflecting a significant overlap of separate potentials. This effect must be taken into account in the interpretation of a 'concurrent' intracranial potential as the source of a far-field surface-recorded potential.

Aspartate and glutamate as possible neurotransmitters in the visual cortex.

Abstract: To identify possible neurotransmitters in the visual cortex, high pressure liquid chromatography was used to measure the release of endogenous compounds from a tissue slice preparation of the visual cortex of the rat. When synaptic release was induced, either by raising the K+ concentration in the medium or by adding veratridine, of the compounds measured, marked increases (6- to 35- fold) in release rate were observed for aspartate, glutamate, and gamma-aminobutyric acid (GABA). This increased release was blocked either with a low Ca2+/high Mg2+ or a tetrodotoxin-containing medium. To label possible aspartate or glutamate pathways, D-[3H]aspartate and D-[3H]glutamate were injected in the lateral geniculate nucleus (LGN), superior colliculus, and visual cortex. Following injections in the LGN, labeling was observed in the pyramidal cells in cortical layer 6 and in a diffuse band in layer 4, whereas no cortical cells were labeled after injections in the superior colliculus. When D-[3H]aspartate was injected in the cortex, the uptake again was concentrated in the layer 6 cells, but not labeled cell bodies were seen in the LGN, confirming the specificity of the uptake and retrograde filling process. Diffuse labeling was present in the LGN, however, presumably produced by anterograde filling process. Diffuse labeling was present in the LGN, however, presumably produced by anterograde transport from the layer 6 cells. These results suggest that layer 6 cells in the cortex, which are the source of the recurrent projection to the thalamus, may use aspartate or glutamate as their transmitter. Analysis of the function of the corticothalamic pathway may be facilitated by these findings.

Thalamic connections with limbic cortex. I. Thalamocortical projections.

Abstract: The thalamocortical projections to limbic cortex in the cat have been studied with retrograde and anterograde axonal transport techniques. Five limbic cortical areas were identified on the basis of cytoarchitecture. The five areas are the anterior limbic area, the cingular area, the dorsal and ventral retrosplenial areas, and the presubiculum. Each of these cortical areas received small injections of horseradish peroxidase, and the afferent thalamic nuclei were identified by retrograde labelling of cells. The cortical projection of each of the anterior thalamic nuclei and the lateral dorsal nucleus was determined autoradiographically. Each of the anterior thalamic nuclei and the lateral dorsal nucleus projects to limbic cortex by two pathways. One group of fibers leaves the rostral thalamus by the fornix, pierces the corpus callosum, joins the cingulate fasciculus to reach limbic cortex. The other group travels through the lateral thalamic peduncle and internal capsule. The anterior ventral nucleus projects primarily to the dorsal retrosplenial area, particularly to layer I, the deep portion of layer II, and superficial portion of layer III. Sparse projections also exist to the ventral retrosplenial area, the cingular area, and the presubiculum. Very sparse projections to the anterior limbic area are seen. The anterior dorsal nucleus projects primarily to the ventral retrosplenial area, particularly layers I, the deep portion of layer II, and superficial layer III. sparse projections exist to the dorsal retrosplenial area and presubiculum, but apparently no projections exist to the cingular or anterior limbic area. The anterior medial nucleus projects primarily to layers I and superficial III of the ventral retrosplenial area. sparse projections exist to each of the other limbic cortical areas. The lateral dorsal nucleus projects extensively onto limbic cortex. Prominent projections occur to layer I, the external granular layer and lamina dessicans of the presubiculum, layers I and III-IV of the dorsal retrosplenial area, and layers I, III, and IV of the cingular area. Sparse projections occur to the ventral retrosplenial area and the anterior limbic areas. Thalamocortical projections also originate in the midline and intralaminar nuclei including the central medial, reuniens, rhomboid, paracentral, central lateral, and central dorsal nuclei. These data indicate that the anterior thalamic nuclei project upon limbic cortex in a complex manner. Further, the projections to limbic cortex from the anterior nuclei overlap with projections from the lateral dorsal nucleus. This overlap of thalamic projections onto limbic cortex suggests a convergence of information from nonprimary sensory systems with information from the classical limbic system.

Organization of extrinsic tectal connections in goldfish (Carassius auratus)

Abstract: Nonretinal sources of tectal afferents, the laminar and regional organization of the inputs, and the relation of the tectum with primary and secondary visual and motor centers in goldfish were studied following HRP injections in the optic tectum, orbit of the eye, cerebellum, pretectal area, and dorsolateral mesencephalic tegmentum. Ipsilateral tectal afferents include the area dorsalis centralis of the forebrain, the nucleus dorsalis lateralis of the thalamus, the area pretectalis, the nucleus pretectalis, a nucleus in the rostral mesencephalic tegmentum, the torus longitudinales, the torus semicircularis, a dorsolateral tegmental nucleus, the nucleus isthmi, and a rostral cell group of the nucleus motorius tegmenti. Comparison of results in a series of tectal HRP injections which differed in depth, tangential extent, and location indicated that projections from the area pretectalis, nucleus pretectalis, and nucleus isthmi terminate in the stratum fibrosum et griseum superficiale of the tectum. Terminals of the forebrain and nucleus dorsolateralis and contralateral tectum are sparse and widely branching. Projections from the area and nucleus pretectalis tend to terminate in the rostral tectum, and those from the contralateral tectum, torus semicircularis, dorsolateral tegmental nucleus, and nucleus motorius tegmenti terminate preferentially in the caudal tectum. Cells of origin of extrinsic tectal efferents were also identified following HRP injections in the pretectal area and mesencephalic tegmentum. Proximal dendrites and axons of these cells were labeled sufficiently to allow comparison with morphological types characterized in Golgi studies. HRP injections in the cerebellum labeled cells bodies in the area pretectalis, nucleus pretectalis, and the nucleus of the posterior commissure. Double label experiments with intraocular injection of tritiated proline demonstrated direct retinal input to these three areas. No indications of direct connections between the tectum and cerebellum were found following tectal or cerebellar HRP injections.

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

Abstract: 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 conjuctivum, 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.

Thalamic connections with limbic cortex. II. Corticothalamic projections

Abstract: The corticothalamic projections from the cat limbic cortex have been investigated with anterograde and retrograde axonal transport techniques. Five limbic cortical areas—the anterior limbic area, the cingular area, the granular and dysgranular retrosplenial areas, and the presubiculum—were identified on the basis of their cytoarchitecture. Emphasis was placed on determining the laminar distribution of the cells of origin of the efferent projections, the projection pathways, and the sites of termination within the thalamus. Projections to the thalamus originate in layers V and VI of limbic cortex. In the cingular region the cells of origin are predominantly in layer V and to a lesser extent in layer VI, while the majority of cells projecting from the more caudal retrosplenial areas and presubiculum are in layer VI. There are two fiber pathways from each cortical area to the thalamus. One system of fibers passes through the internal capsule and lateral thalamic peduncle, and a second system travels in the cingulate fasciculus before piercing the corpus callosum to join the postcommissural fornix. The lateral dorsal nucleus and the anterior nuclear group, including the anterior dorsal, anterior ventral, and anterior medial nuclei, are the major thalamic recipients of projections from limbic cortex. Corticothalamic projections also terminate sparsely in the midline and intralaminar nuclear complex, including the central lateral, central dorsal, paracentral, central medial, rhomboid, and reuniens nuclei. Projections from the anterior limbic area project predominantly to the anterior medial, centrall lateral, and paracentral nuclei. The anterior ventral nucleus, anterior medial nucleus, and lateral dorsal nucleus are the major thalamic recipients of projections from the cingular area, the granular and dysgranular retro-splenial areas, and the presubiculum. It appears that the anterior dorsal nucleus receives afferents only from the dysgranular retrosplenial area. Bilateral corticothalamic projections were found in the anterior medial, dorsal medial, central lateral, central medial, paracentral, and reuniens nuclei.

Orderly anomalous retinal projections to the medial geniculate, ventrobasal, and lateral posterior nuclei of the hamster

Abstract: Experiments were performed to determine (1) under what conditions early brain surgery can cause sensory afferents to the thalamus to form connections at abnormal thalamic sites and (2) the extent to which such ectopic projections are receptotopically organized. In newborn Syrian hamsters, two of the retina's principal synaptic targets, the superior colliculus and dorsal lateral geniculate nucleus, were destroyed, respectively, by a direct lesion and by retrograde degeneration following a lesion of the occipital cortex. In the same brains, alternative terminal space for the retinofugal axons was made available in auditory (medial geniculate) or somatosensory (ventrobasal) thalamic nuclei by lesions of ascending auditory or somatosensory pathways, respectively; additional terminal space was made in the lateral posterior nucleus by degeneration of afferents from the superior colliculus. The projections of the contralateral retina were traced in neonatally operated adults by making one or two small peripheral retinal lesions and intraocular injections of 3H-proline 5 days and 1 day, respectively, prior to sacrifice. The neonatal surgery reliably produced anomalous crossed retinal projections to the partially deafferented structures. These projections terminate preferentially at the nuclear surfaces. Computer reconstructions from serial sections demonstrated several signs of spatial order suggestive of receptotopic organization in the anomalous retinothalamic projections. In order of increasing stringency, these signs (which are not mutually exclusive) are: (1) In each nucleus, a restricted retinal sector gives rise to a limited part of the abnormal projection. (2) In each nucleus, different parts of the retina give rise to different parts of the anomalous projection. (3) In each nucleus, there is a more or less consistent polarity of the anomalous connection. Each small retinal sector appears to be represented along a “line of projection” in each of its abnormal thalamic targets, as it normally is in the dorsal and ventral lateral geniculate nuclei and in the superior colliculus. In some brains, some of the abnormal projections produce only a partial representation of the retina. However, in a single animal, a retinal sector not represented in the anomalous projections to one nucleus can contribute to the abnormal connections with another nucleus. In additional experiments, an attempt was made to direct developing auditory and somatosensory fibers normally terminating in the medial geniculate and ventrobasal nuclei, respectively, to anomalous thalamic targets. The axons were deprived of some of their normal thalamic sites of termination and alternative terminal space was made available in another thalamic sensory nucleus. These experiments failed to produce reliable evidence of ectopic auditory or somatosensory thalamic projections. The anomalous retinal projections to nuclei that normally recieve little (lateral posterior) or no (medial geniculate, ventrobasal) optic tract input, show that the preference of retinal axons for their normal targets is relative, not absolute. The orderliness of the ectopic projections opposes the hypothesis that the formation of retinotopic connections depends upon the matching of a set of signals distributed among the retinofugal fibers and a corresponding set of cues unique to the normal terminal fields of optic axons. The results are consistent with the formation of receptotopic connections by interactions among developing axons and suggest the action of additional factors that determine the terminal sites and organization of central neuronal connections.

The distribution of neurons projecting from the retina and visual cortex to the thalamus and tectum opticum of the barn owl, Tyto alba, and the burrowing owl, Speotyto cunicularia.

Abstract: Using the HRP retrograde transport technique in two different genera of owls (Speotyto and Tyto), we have studied the distribution of neurons projecting to the optic tectum and the visual thalamus. Small injections of HRP were made into these structures from the pial surface after they had been visualized directly by dissection of the overlying bone. In contrast to the findings in mammals, retinal ganglion cells were labeled only in the eye contralateral to the injection site, whether this was in the thalamus or tectum, and the labeled ganglion cells were found on both nasal and temporal sides of the vertical retinal meridian through the fovea. After thalamic injection, labeling was prominent in temporal retina representing the binocular field, temporal to the optic nerve head. Retinothalamic ganglion cells formed roughly concentric lines of isodensity centered on the fovea (Speotyto) or area centralis (Tyto); labeling form thalamic injections involved both large and medium-sized neurons, but did not involve the smallest nor a conspicuous class of very large neurons. Tectal injections led to prominent labeling along the horizontal streak region, with horizontally elongated isodensity contours in both Tyto and Speotyto; retinotectal ganglion cells were heterogeneous and included a group of very large neurons and another group of small neurons, neither of which was labeled from the thalamus. In the visual Wulst, labeled neurons were confined to the supragranular layers after both tectal and thalamic injections. Corticotectal neurons were found in both ipsilateral and contralateral visual Wulst. They were characterized by large cell bodies and prominent dendrites. Corticotectal neurons were distributed throughout the mediolateal extent of the ipsilateral Wulst and therefore involved both the monocular and binocular representations of the visual field. Corticothalamic neurons, found only in the ipsilateral Wulst, were characterized by smaller cell bodies and fine dendrites. They were confined to the monocular crescent on the extreme medial edge of the Wulst.

Development of the pyramidal tract in the hamster. I. A light microscopic study

Abstract: The development of the pyramidal tract and other projections from the sensorimotor cortex was studied in the postnatal hamster with both (3H) proline and horseradish peroxidase (HRP) as anterograde tracers. In the 1-day-old animal labeled axons extend as far as the pons. Other corticofugal fibers have penetrated into the corpus striatum and the thalamus. By 2 days postnatally, the pyramidal tract has grown to midmedullary levels and there is substantial retrograde (HRP) and anterograde labeling in the thalamus. The pyramidal decussation is formed at 3 days of age and by 4 days the pyramidal tract has descended in the dorsal funiculus as far as midcervical spinal cord. Corticofugal fibers invade the pontine nuclei at 4 days and both the dorsal column nuclei and the superior colliculus at 6 days of age. At 6 days the pyramidal tract can be traced to midthoracic levels of the spinal cord, by 8 days the tract reaches lumbar levels, and by 14 days it has completed its caudal growth to the coccygeal spinal cord. Fibers first penetrate the gray matter of a given spinal cord level approximately 2 days after the tract has grown past that level in the dorsal funiculus. Pyramidal fibers continue their lateral growth into the dorsal horn at all levels of the cord throughout the third postnatal week such that by 21 days of age the pyramidal tract appears similar to that of the adult. The projections from sensorimotor cortex to the pontine nuclei, the superior colliculus, and the dorsal column nuclei appear to have a pattern similar to that of the adult soon after the fibers grow into these structures. There is a consistent delay of 2 to 3 days between the arrival of the pyramidal tract axons in the white matter adjacent to target structures and their innervation of a given terminal field. The pyramidal tract grows more quickly through the dorsal funiculus of the spinal cord than it does along the ventral surface of the medulla. Extensive elongation of pyramidal tract axons is achieved long before the growth and differentiation of the sensorimotor cortical neurons from which they originate. Finally, the pyramidal tract appears to grow as a compact bundle and not by the addition of temporally staggered groups of fibers. The relatively protracted period of innervation of the spinal cord by the pyramidal tract coupled with the immaturity of the cortical neurons at birth may be factors contributing to the significant regrowth of pyramidal tract axons severed early in development.

Neonatal Frontal Lesions in the rat: sparing of learned but not species-typical behavior in the presence of reduced brain weight and cortical thickness.

Abstract: Rats with complete removal of the cortex anterior to bregma in adulthood (frontal cortex) were compared behaviorally and neuroanatomically with rats with similar removals at 7 or 25 days of age. Excision of the frontal cortex in adult rats produced transient aphagia, chronic motor abnormalities in feeding, a chronic drop in body weight, increased activity in running wheels, impaired performance at a spatial reversal learning task, and chronic abnormalities in a variety of species-typical behaviors, including swimming, food hoarding, and defensive burying. In contrast, similar lesions in infant rats failed to produce aphagia, a chronic drop in body weight, increased activity, or impaired learning of a spatial reversal task. Infant lesions did not allow sparing of complex species-typical behaviors, however, such as those involved in feeding, swimming, hoarding, or defensive burying. Furthermore, when the brains of neonatally operated rats were compared with those of control rats or rats operated on in adulthood, there were striking differences. The cerebral hemispheres of the neonatal operates were smaller both in surface dimensions and weight, the thalamus was smaller, and the cerebral cortex was thinner. These data imply that there may be substantially less sparing of function following frontal cortex lesions in infancy than previously believed and that neonatal frontal lesions in rats have significant effects on brain development in regions far removed from the actual site of surgical excision.

Low Energy Levels in Thiamine-Deficient Encephalopathy

Abstract: Pyrithiamine-induced acute thiamine-deficient encephalopathy was produced in adult male Wistar rats. Twenty-four hours before the onset of neurological signs the brain showed no morphological abnormalities. Encephalopathic rats had symmetrical lesions of edematous necrosis localized in the thalamus, mammillary body, and pontine tegmentum. Biochemically, encephalopathic rats had brain thiamine levels less than 20% of controls. For the assay of the concentrations of adenosine triphosphate (ATP) and phosphocreatine, the brains were fixed using 5 KW microwave irradiation and were divided into four parts: cerebral cortex, diencephalon, lower brainstem, and cerebellum. In the lower brainstem of the encephalopathic rats ATP concentrations were 89.5% of normal controls. Phosphocreatine levels were lowered to 70% of controls in the diencephalon and to 75% in the lower brainstem. Total high energy phosphate levels were decreased to 89% of controls in the diencephalon and 91% in the lower brainstem before the onset of neurological signs and to 76% and 79%, respectively, after the onset. In the cerebral cortex and cerebellum high energy phosphates were not significantly reduced. Lower high energy phosphate levels and the distribution of edematous lesions were coincident in the brain. These findings suggest that a low energy state is closely related to the formation of edematous lesions in thiamine-deficient encephalopathy.

Organization of spinothalamic tract axons within the rat spinal cord.

Abstract: Two techniques have been used to examine the organization of spinothalamic tract axons within the spinal cord of the rat In the initial experiments, the thalamus was filled on one side with horseradish peroxidase (HRP) using a series of small injections The injections were preceded by lesions of various areas of the ventral quadrant These studies indicated that the cells of origin of STT axons ascending within the ventral funiculus (VF) are located primarily in the ventral-most areas of the dorsal horn and the intermediate gray zone The cells of origin of STT axons projecting within the ventrolateral funiculus (VLF) are located not only deep within the gray matter but in addition within the dorsal-most two thirds of the dorsal horn, the area of the spinal cord gray matter shown in previous studies to contain the vast majority of cells with cutaneous tactile and nociceptive input To examine these projections directly, rats received either a series of HRP injections that filled the thalamus on one side or a small injection into either medial or lateral thalamus Examination of the labeled axons in horizontal sections through the cervical cord indicated that STT axons ascending to lateral thalamus do so in the VLF In contrast, axons terminating in medial thalamus ascend in the VF Additional experiments have shown that axons ascending to the lateral thalamus are distributed throughout the VLF at lumbar levels Within the thoracic cord, lateral projecting SST axons are distributed throughout much of the VLF but are not found in close proximity to the ventral horn At cervical levels all lateral-projecting STT axons have assumed a position on the lateral rim of the VLF These and previously published data have demonstrated that the rat spinothalamic tract is composed of two components that differ in the distribution of their cells of origin, the area of the cord in which they ascend, and the thalamic nuclei in which they terminate

Efferent systems of the rabbit visual cortex: Laminar distribution of the cells of origin, axonal conduction velocities, and identification of axonal branches

Abstract: Several efferent systems of visual area I in Dutch rabbits were studied with anatomical (horseradish peroxidase) and physiological (antidromic) methods. Anatomical studies provided information regarding the laminar origin of the projections to the contralateral hemisphere, visual area II, the dorsal lateral geniculate nucleus, and the superior colliculus. Physiological studies provided information regarding conduction velocities and multiple destinations of efferent axons. Both the callosal projection and the projection to V-II were shown to originate primarily in layer II-III. However, approximately 10-20% of the callosal projection and 20–40% of the projection to V-II originated in layers IV and V. In contrast, the projection to the dorsal lateral geniculate nucleus originated nearly exclusively in layer VI, while corticotectal neurons occurred primarily in layer V. A significant number of corticotectal neurons were, however, found in layer IV. Thus, the above efferent systems were found to differ in their principal laminar origin and in the diffuseness of that origin. The origins of corticocortical projections were considerably more diffuse than those of corticofugal projections. In addition to differences in laminar origin, efferent systems also differed significantly in the conduction velocities of their axons. The projection to visual area II and to the lateral geniculate nucleus consisted primarily of very slowly conducting axons, while the projection to the superior colliculus was fast conducting. The callosal projection consisted of both slow and fast conducting axons. Finally, the question of branching of V-I efferent axons was addressed. Although the laminar origin of the projections to the contralateral hemisphere and to visual area II overlapped considerably, none of these corticocortical axons could be shown to project to both locations or to a subcortical destination. In contrast, approximately one-third of corticotectal axons were shown to project a collateral into the thalamus. Although the destination of this collateral is unclear, it is medial to the lateral geniculate nucleus and may be the pulvinar.

Connections of the ventroposterior nucleus of the thalamus with the body surface representations in cortical areas 3b and 1 of the cynomolgus macaque, (Macaca fascicularis)

Abstract: The somatotopic pattern of the connections of the ventroposterior nucleus of the thalamus with the representations of the body surface in somatic cortical Areas 3b and 1 were investigated in macaque monkeys using the anatomical tracers horseradish peroxidase (HRP), and 3H-proline. These tracers, in combination or separately, were injected into one or more cortical sites, after the skin surface capable of activating neurons at each site had been defined with microelectrode mapping methods. These injection sites were later related to the overall organizations of the two cutaneous representations as determined in more extensive mapping experiments (Nelson et al, '80). Finally, zones of anterograde and retrograde label in the thalamus were located with reference to architectonically defined subnuclei in the ventroposterior nucleus (VP). The results led to the following conclusions. (1) Zones of cells in VP projecting to a given location in either Area 3b or 1 also receive reciprocal projections from the cortical target. (2) A given cortical location typically relates to a disc-shaped or lamellar region in VP with the disc extending rostrocaudally and dorsoventrally, being most narrow in the mediolateral dimension. (3) The representations of the same body surface in Area 1 and Area 3b relate to the same region of VP. However, since fewer cells were generally labeled after Area 1 injections, less dense terminations are suggested from VP to Area 1 than to Area 3b. (4) VP is the major or exclusive relay of somatosensory information to the two cutaneous representations from the thalamus. Labeled neurons or zones of terminations were found outside VP in other parts of the somatosensory thalamus only when injection sites extended into cortex outside Areas 3b and 1. (5) The face, hand, limbs, and foot are represented in a mediolateral sequence of subnuclei within VP. A dorsal capping subnucleus is apparently largely devoted to the axial trunk and perhaps other hairy skin surfaces such as some parts of the proximal surfaces of the limbs. (6) While anterior and posterior surfaces of the hind limb are widely separated by the glabrous foot in the cortical representations, they appear to be represented in adjacent zones in the thalamus.

The effects of transient functional depression of the thalamus on spindles and on bilateral synchronous epileptic discharges of feline generalized penicillin epilepsy

Abstract: A transient functional depression of thalamic activity (TFDTA) was induced in acute experiments in cats by the microinjection of 25% KCl into the thalamus. Spontaneous and evoked thalamic electrical activity was markedly depressed at the site of KCl microinjection. Spread of this depression to other thalamic areas often occurred, mainly when KCl was injected into the midline thalamus. In normal cats both spontaneous and evoked cortical spindle bursts as well as other evoked thalamocortical responses were reduced or abolished during the KCl-induced TFDTA. The generalized spike-and-wave discharges of feline generalized epilepsy were also suppressed for the duration of TFDTA, while incidental focal cortical interictal and ictal epileptic discharges, as well as generalized tonic-clonic seizure discharge, remained unaffected. The same effects were observed in animals with lesions of the mesencephalic reticular formation, indicating that the suppression of spindles and spike-and-wave discharges cannot be attributed to a release of the activity of the reticular formation by the TFDTA. An unexplained occurrence of generalized tonic-clonic EEG seizure was observed in most cases late after thalamic KCl microinjection, usually after the spike-and-wave discharges had recovered. These data are consistent with the hypothesis that the spontaneous bilaterally synchronous epileptic bursts of feline generalized penicillin epilepsy are not only closely related to spindles but are crucially dependent on thalamic inputs to the cerebral cortex.

The Effects of Transient Functional Depression of the Thalamus on Spindles and on Bilateral Synchronous Epileptic Discharges of Feline Generalized Penicillin Epilepsy

Abstract: A transient functional depression of thalamic activity (TFDTA) was induced in acute experiments in cats by the microinjection of 25% KCl into the thalamus. Spontaneous and evoked thalamic electrical activity was markedly depressed at the site of KCl microinjection. Spread of this depression to other thalamic areas often occurred, mainly when KCl was injected into the midline thalamus. In normal cats both spontaneous and evoked cortical spindle bursts as well as other evoked thalamocortical responses were reduced or abolished during the KCl-induced TFDTA. The generalized spike-and-wave discharges of feline generalized epilepsy were also suppressed for the duration of TFDTA, while incidental focal cortical interictal and ictal epileptic discharges, as well as generalized tonic-clonic seizure discharge, remained unaffected. The same effects were observed in animals with lesions of the mesencephalic reticular formation, indicating that the suppression of spindles and spike-and-wave discharges cannot be attributed to a release of the activity of the reticular formation by the TFDTA. An unexplained occurrence of generalized tonic-clonic EEG seizure was observed in most cases late after thalamic KCl microinjection, usually after the spike-and-wave discharges had recovered. These data are consistent with the hypothesis that the spontaneous bilaterally synchronous epileptic bursts of feline generalized penicillin epilepsy are not only closely related to spindles but are crucially dependent on thalamic inputs to the cerebral cortex.

Divergent collaterals from deep cerebellar neurons to thalamus and tectum, and to medulla oblongata and spinal cord: retrograde fluorescent and electrophysiological studies.

Abstract: In cat the existence of collaterals from deep cerebellar neurons, which project to mesencephalon and thalamus has been investigated anatomically by means of the multiple retrograde fluorescent tracer technique as well as electrophysiologically by means of conventional antidromic techniques. Both sets of data indicate that several neurons in the medial nucleus, which project to mesencephalon and thalamus, also distribute collaterals to medulla oblongata and spinal cord. These branching neurons were principally located in the caudal and intermediate portions of the medial nucleus. The electrophysiological data in addition indicate that the branching point of the neurons in the medial nucleus is located relatively close to the cell soma. The anatomical findings show a further group of branching neurons in the lateral nucleus at the border with the interpositus nuclei. The majority of these latter neurons distribute collaterals to medulla oblongata but some distribute collaterals to spinal cord. However, it could not be decided as yet whether the collaterals to the medulla oblongata terminate either in medullary medial reticular formation or in inferior olive or in both.

Two visual pathways to the telencephalon in the nurse shark (Ginglymostoma cirratum) : I. Retinal projections

Abstract: The central projections of the retina in the nurse shark were studied by anterograde transport of horseradish peroxidase and tritiated proline. With regard to efferent retinal fibers, both techniques gave completely identical results. Projections were found to pretectal area, dorsal thalamus, basal optic nucleus, and optic tectum, all at the contralateral side. The retinal target cells in the dorsal thalamus are restricted to the ventrolateral optic nucleus and the posterior optic nucleus. No evidence was found for an earlier-reported projection to the lateral geniculate nucleus. The present findings show that the ventrolateral optic nucleus exhibits homological features of the dorsal lateral geniculate nucleus in other vertebrate groups, whereas the lateral geniculate nucleus of the nurse shark is much more comparable to the nucleus rotundus of teleosts and birds and would be more appropriately so named. The application of the HRP technique also allowed us to study afferents to the retina by retrograde transport of tracer. Retrogradely labeled cells were observed in the contralateral optic tectum and are apparently similar to those reported for teleosts and birds.