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.

Projections of digit afferents to the cuneate nucleus in the raccoon before and after partial deafferentation.

Abstract: Within the cuneate nucleus of the raccoon, the representations of individual forepaw digits are anatomically separated by densely myelinated laminae. This unique arrangement was utilized to determine whether the terminations of cutaneous afferents from individual digits are precisely restricted to the appropriate region of the cuneate nucleus or overlap with afferents from adjacent digits. By using the transganglionic transport of horseradish peroxidase (HRP), it was found that, for each digit, the terminal labeling was restricted to the appropriate 150-250-micron-wide column that extended rostrocaudally throughout the nucleus. The topographical arrangement of digit input corresponded to the known electrophysiology, with the terminal column for the fifth digit located most medially within the nucleus and those for digits 4 to 1 successively more laterally. Within a column, the density of labeling was greater over cell clusters than between clusters. These results indicate that afferents from adjacent digits do not overlap in the cuneate nucleus. In six animals, the fifth digit was amputated, and 2-4 months later, HRP was injected into the nerves of the fourth digit to determine whether its afferents had sprouted into the denervated fifth-digit column. The projection pattern from the fourth digit in each of these animals was the same as in normal animals and the same as in the intact contralateral side. These results indicate that the reorganization seen in the cerebral cortex following peripheral deafferentation cannot be attributed to changes in the afferent fiber projections to the cuneate nucleus.

Patterns of firing in cuneate neurones and some effects of flaxedil

Abstract: In cats under pentobarbitone anaesthesia, single cuneate cells excited directly by microiontophoresis of glutamate (or ATP) reproduce the temporal patterns of firing seen during spontaneous activity or during activity evoked by peripheral stimulation. In particular, the glutamate-evoked discharges of hair or touch cells show their characteristic tendency to fire in high-frequency pairs or bursts of impulses. Since glutamate acts mainly on the post-synaptic cell, the explanation for the multiple discharges must lie in special, repetitive properties of the hair and touch cells. Cuneate neurones are strongly excited by microiontophoretic applications of Flaxedil. The most prominent effect is the appearance of prolonged bursts of spikes at a high frequency. Even systemic Flaxedil can alter the discharge of cuneate hair cells; short intervals occur more frequently, and, in some cases, there is an acceleration in spontaneous firing.

Corticospinal neurons with branching axons to the dorsal column nuclei in the monkey

Abstract: Previous work in cats has shown that cells of origin of the corticospinal tract give rise to collateral branches to the dorsal column nuclei (DCN). The present experiments were performed in monkeys (Macaca fascicularis) in which 2% fast blue and 2% diamidino yellow were delivered to infiltrate the dorsolateral funiculus at levels between C2 and C6 and the cuneate nucleus on the same side. Retrograde labelling in the cortex allows simultaneous visualizaion of three classes of neurons: corticospinal tract (CST) neurons, corticocuneate tract (CCT) neurons, and double-labelled neurons. The morphological features and distribution of CST and CCT neurons are similar to those previously reported from investigations based mainly upon the retrograde transport of horseradish peroxidase (HRP). CST neurons occur in layer V in the pre- and postcentral gyri, except for the lateral part (face representation), in the supplementary motor and sensory cortex, and in SII. CCT neurons are present in layer V largely in the postcentral gyrus and in SII. Double-labelled neurons are present wherever CST and CCT neurons are found. Reconstruction and quantitative data from the pericentral corted show that up to 60% of CCT neurons are double-labelled and are found predominantly in areas 1 and 2, and that their perikarya are in the size range of the larger CCT neurons. Comparison of these results with those obtained previously in cats by using HRP and tritiated, enzymatically inactive HRP (3H-apo-HRP, Rustioniand Hayes: Exp. Brain Res. 43:237–245, 1981) suggests that CST neurons with branching axons to the DCN are considerably more numerous in monkeys than in cats. To determine whether this difference is caused by the different tracers used in the two species. 2% fast blue and 2% diamidino yellow were delivered in cats to infiltrate the dorsolateral funiculus at C2-C3 and the nucleus on the same side. The results in these cats are remarkably similar to those obtained in the previous study, which used HRP and 3H-apo-HRP: double-labelled neurons occur predominantly in area 3a and constitute 14–16% of the CCT neurons in the pericruciate area. The results bear upon mechanisms of descending control and tuning of performances that characterize the dorsal column-medial lemniscal system, e.g., discrimination of discrete spatiotemporal cues. The species differences may be related to the higher degree of tactile resolution and synchronous control of sensory inflow at the DCN and spinal cord in monkeys relative to cats.