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Cuneate nucleus

About: Cuneate nucleus is a research topic. Over the lifetime, 614 publications have been published within this topic receiving 24859 citations. The topic is also known as: cuneate nucleus of spinal cord.


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Journal ArticleDOI
TL;DR: The results of the present anatomical study on macaque monkeys concern some aspects of the dorsal column nuclei, their projection to the thalamus and the cytoarchitecture and topography of the recipient areas in theThalamus for the somatosensory pathways.
Abstract: The results of the present anatomical study on macaque monkeys concern some aspects of the dorsal column nuclei, their projection to the thalamus and the cytoarchitecture and topography of the recipient areas in the thalamus for the somatosensory pathways. Some observations regarding the cytoarchitecture of the dorsal column nuclei are reported; the gracile nucleus differs cytoarchitectonically over the rostrocaudal dimension in a way similar to the feline nucleus; the cuneate nucleus has a distinct pars rotunda (Ferraro and Barrera, '35) which might be analogous to a similar structure in the raccoon shown to be activated by afferents from the volar side of the hand and digits (Johnson et al., '68). Cytoarchitectonic observations and other arguments suggesting the presence of the nucleus Z in the monkey are presented. In Nissl stained frontal sections, cut in the stereotaxic frontal plane as well as in sections cut perpendicular to the long axis of the brain stem the cytoarchitecture and topography of the posteromedial, ventroposterior and centrolateral thalamic nuclei of the macaque were analysed. The posteromedial nucleus (POm) has been found to include portions of Olszewski's ('52) magnocellular medial geniculate, suprageniculate and pulvinar nuclei. The nucleus ventralis posterolateralis (VPL) corresponds to the main portion of Olszewski's VPLc, whereas most of his VPLo corresponds to the nucleus ventralis intermedius of Hassler ('59) and Mehler ('71). Electrolytic lesions were used to study the projection from the gracile and cuneate nuclei to the thalamus. With postoperative survival periods of 6 to 14 days the resulting degeneration was studied in frontal sections stained according to the Wiitanen modification of the Fink-Heimer method. Both the gracile and cuneate nuclei project profusely to the contralateral nucleus ventralis posterolateralis and more sparsely to the contralateral posteromedial nucleus and the zona incerta. A distinct somatotopic organization exists in the projection to the ventroposterior nucleus, but not in that to the other target areas. The projection to the ventroposterior nucleus is very dense and evenly distributed except rostrally and dorsally, where it is more scattered. It is concluded that the posteromedial and the ventroposterior thalamic nuclei are very similar in monkeys and cats regarding cytoarchitecture, topography and afferent projections from the dorsal column nuclei.

98 citations

Journal ArticleDOI
TL;DR: It is shown that large-scale reorganization in area 3b following spinal cord injuries is due to changes at the level of the brainstem nuclei and not due to cortical mechanisms.
Abstract: Adult mammalian brains undergo reorganization following deafferentations due to peripheral nerve, cortical or spinal cord injuries. The largest extent of cortical reorganization is seen in area 3b of the somatosensory cortex of monkeys with chronic transection of the dorsal roots or dorsal columns of the spinal cord. These injuries cause expansion of intact face inputs into the deafferented hand cortex, resulting in a change of representational boundaries by more than 7 mm. Here we show that large-scale reorganization in area 3b following spinal cord injuries is due to changes at the level of the brainstem nuclei and not due to cortical mechanisms. Selective inactivation of the reorganized cuneate nucleus of the brainstem eliminates observed face expansion in area 3b. Thus, the substrate for the observed expanded face representation in area 3b lies in the cuneate nucleus.

98 citations

Journal ArticleDOI
TL;DR: Transganglionic transport of HRP has been used to trace the pathways and termination sites of cutaneous and muscle afferent axons entering from the C2 and C3 dorsal rami and found that the cutaneous spinal projection is abundant with extensive filling of axons in the tract of Lissauer and many termination sites in the lateral substantia gelatinosa.
Abstract: Transganglionic transport of HRP has been used to trace the pathways and termination sites of cutaneous and muscle afferent axons entering from the C2 and C3 dorsal rami. The muscle afferent projection in the spinal cord is restricted and (apart from the ventral horn) largely confined to the intermediate gray matter. There is a muscle afferent projection to the ventrolateral main cuneate nucleus and a complex pattern of projection through the extent of the external cuneate nucleus. In contrast, the cutaneous spinal projection is abundant with extensive filling of axons in the tract of Lissauer and many termination sites in the lateral substantia gelatinosa. Axons enter the lateral gray matter of the cervical spinal cord from the dorsal columns and the dorsolateral funiculus and terminate in the lateral one-third of the dorsal horn as far rostral as the spinomedullary junction. Axons of the tract of Lissauer form a complex web around the dorsal horn and many penetrate rostrally to the region of the spinomedullary junction, where they terminate among clusters of interstitial cells on and close to the dorsal medullary surface. Cutaneous afferent axons from the dorsal columns turn into the main cuneate nucleus and enter a dense mass of HRP-reaction product which occupies the most ventrolateral part of the nucleus for its entire length.

96 citations

Journal ArticleDOI
TL;DR: The retrograde transport of horseradish peroxidase (HRP) has been used for the present study and provides anatomical evidence of a DCN‐cerebellar pathway.
Abstract: The existence of a cerebellar projection from the dorsal column nuclei (gracile and cuneate nuclei, DCN) has been proposed on electrophysiological grounds but questioned when studied with neuroanatomical techniques. The retrograde transport of horseradish peroxidase (HRP) has been used for the present study and provides anatomical evidence of a DCN-cerebellar pathway. In adult cats, 1 to 6 μl of 30% HRP were injected in pars intermedia of the anterior lobe (lobules IV–V), in paramedial lobule and in vermis of the anterior (lobules IV–V) and of the posterior lobe (lobule VII). After survival of 24 to 48 hours, all animals were perfused with a double aldehyde mixture and serial 40 μ sections through the medulla oblongata were incubated for visualization of HRP. In all cases, medullary nuclei known to project to the injected cortical regions of the cerebellum contained HRP-positive neurons mainly ipsilateral to the injection (e.g., external cuneate nucleus) or mainly contralateral to it (e.g., inferior olivary complex). Following ipsilateral injections in either the paramedian lobule or the pars intermedia, HRP-positive neurons in the cuneate nucleus were concentrated in its rostral portion where multipolar cells with radiating dendrites predominate. In contrast, none of the cells of the clusters region, in the caudal part of the cuneate nucleus, displayed HRP-positive granules. In cases in which the anterior vermis was injected a few labelled cells were present in the rostral part of the gracile nucleus but not in the clusters region of this nucleus. No labelling of DCN neurons was evident after posterior vermis injection. To compare the distribution of cells contributing to the DCN-cerebellar pathway with that of thalamic relay cells in the DCN, 0.5 to 3 μl of 30% HRP were injected in the nucleus ventralis posterolateralis of the thalamus in another series of cats. Contralateral to the thalamic injection, labelled cells were concentrated in the clusters region of the gracile and cuneate but rostrally in these nuclei they were scattered among unlabelled neurons. The preferential location in the DCN of cells which project to the cerebellum and of cells which project to the thalamus stresses the heterogeneous organization of these nuclei along the rostrocaudal axis. Further, the results indicate that regions of the DCN which have been distinguished on the basis of cytoarchitectonics (Kuypers and Tuerk, '64) and of afferents (Rustioni, '73, '74) differ also in their efferent projections.

95 citations

Journal ArticleDOI
TL;DR: The central terminations of afferent nerve fibers from the extraocular muscles of the monkey were investigated by means of transganglionic transport of wheat germ agglutinin‐conjugated horseradish peroxidase and terminal labeling was apparent in the ipsilateral trigeminal sensory and cuneate nuclei.
Abstract: The central terminations of afferent nerve fibers from the extraocular muscles of the monkey were investigated by means of transganglionic transport of wheat germ agglutinin-conjugated horseradish peroxidase (WGA/ HRP). Following injections of selected extraocular muscles with WGA/HRP, terminal labeling was apparent in the ipsilateral trigeminal sensory and cuneate nuclei. The density of trigeminal projections varied markedly from one rostrocaudal level to the next, being heaviest within the ventrolateral portion of pars interpolaris of the spinal trigeminal nucleus. A second extraocular muscle afferent representation was noted in ventrolateral portions of the cuneate nucleus. This projection was restricted to rostral portions of pars triangularis of the cuneate nucleus, partially overlapping the afferent termination from dorsal neck muscles. It is likely that some of the problems encountered in formulating conclusions regarding the functional role of extraocular muscle proprioception are due to a lack of detailed information of the central termination pattern of muscle afferents. Taken together, the present findings should provide a basis for further anatomical and physiological studies designed to elucidate the role played by extraocular muscle proprioceptors in vision and oculomotor control.

94 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20234
20222
202115
20204
20195
20186