Search PubMed⌕ Search

PubMed · 12164724

Improving hand function in chronic stroke.

Abstract

BACKGROUND: Recovery of function following stroke plateaus in about 1 year, typically leaving upper arm function better than that in the hand. Since there is competition among body parts for territory in the sensorimotor cortex, even limited activity of the upper arm might prevent the hand from gaining more control, particularly when the territory is reduced in size because of the stroke. Deafferentation of a body part in a healthy brain enhances cortical representations of adjacent body parts, and this effect is markedly increased by voluntary activity of the adjacent part. OBJECTIVE: To explore whether deafferentation of the upper arm, produced by a new technique of regional anesthesia during hand motor practice, helps recovery of hand function in patients with long-term stable weakness of their hand following stroke. METHODS AND RESULTS: Deafferentation, produced by a new technique of regional anesthesia of the upper arm during hand motor practice, dramatically improved hand motor function including some activities of daily living. The improvement was associated with an increase in transcranial magnetic stimulation-evoked motor output to the practice hand muscles. CONCLUSION: This is a novel therapeutic strategy that may help improve hand function in patients with long-term weakness after stroke.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Wolf Muellbacher, Coletta Richards, Ulf Ziemann, George Wittenberg, Deborah Weltz, Babak Boroojerdi, Leonardo Cohen, Mark Hallett. 2002. Improving hand function in chronic stroke.. https://doi.org/10.1001/archneur.59.8.1278

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Projections from the paraventricular nucleus of the thalamus to the rat prefrontal cortex and nucleus accumbens shell: ultrastructural characteristics and spatial relationships with dopamine afferents.

The paraventricular nucleus of the thalamus (PVT) participates in the functional integration of limbic cortical and striatal circuitry. In the rat, the PVT projects to the deep layers of the medial prefrontal cortex (PFC) and to the shell of the nucleus accumbens (NAc). However, the synaptic organization of PVT afferents within these regions remains undescribed. Furthermore, although dopamine (DA) modulates excitatory glutamate transmission in both areas, possible anatomic substrates for specific DA modulation of PVT inputs have not yet been investigated. To address these issues, immunoperoxidase labeling for tyrosine hydroxylase (TH) in DA axons was combined with anterograde tract-tracing, either by biotinylated dextran amine (BDA) labeled with immunogold-silver or by degeneration after lesions of the PVT. In both regions, and with either tracing method, PVT terminals formed primarily asymmetric axospinous synapses; in the NAc, a proportion of PVT terminals also synapsed onto dendrites. PVT profiles in both regions were often seen in direct apposition to TH-immunoreactive axons; this association was more evident in the NAc where the DA innervation is denser. Within the PFC, PVT profiles and TH-labeled axons were occasionally apposed to the same dendrites, but synaptic specializations were not typically seen at these seeming points of convergence. Within the NAc, PVT profiles occasionally made synapses onto spines and distal dendrites that received convergent synapses from TH-immunoreactive varicosities. These findings represent the first demonstration of postsynaptic convergence between DA and thalamic afferents to a striatal region and are consistent with direct synaptic modulation of PVT transmission by DA in the NAc but not the PFC.

Afferent Pathways↗

Tactile sensory function in the forearm of the monotreme Tachyglossus aculeatus.

Peripheral tactile neural mechanisms in the forepaw of the echidna (Tachyglossus aculeatus, from the order Monotremata) were investigated to establish the extent of correspondence or divergence that has emerged over the widely different evolutionary paths taken by monotreme and placental mammals. Electrophysiological recordings were made in anesthetized echidnas from 29 single tactile sensory nerve fibers isolated in fine strands of the median or ulnar nerves of the forearm. Controlled tactile stimuli were applied to the forepaw glabrous skin to classify fibers, initially, into two broad divisions, according to their responses to static skin displacement. One displayed slowly adapting (SA) response properties, and the other showed a selective sensitivity to the dynamic components of the skin displacement. The SA class was made up of low-threshold SA fibers and other less sensitive SA fibers, and the purely dynamically sensitive tactile fibers could be subdivided according to vibrotactile sensitivity and receptive field characteristics into a rapidly adapting (RA) class, sensitive to low-frequency (< or =50-Hz) vibration, that resembled a corresponding RA class in placental species, and another class, sensitive to a broader range of vibrotactile frequencies (approximately 50-300 Hz), that may represent a monotreme equivalent of the Pacinian corpuscle (PC)-related fiber class of placental mammals. The differential tactile sensitivity of the three principal fiber classes and their individual coding characteristics, determined by quantitative stimulus-response analysis, indicate, first, that this triad of fiber classes can subserve high-acuity tactile signalling from the echidna footpad and, second, that peripheral tactile sensory mechanisms are highly conserved across evolutionarily divergent mammalian orders.

Afferent Pathways↗

Morphology and axonal arborization of rat spinal inner lamina II neurons hyperpolarized by mu-opioid-selective agonists.

The ventral or inner region of spinal substantia gelatinosa (SG; lamina II(i)) is a heterogeneous sublamina important for the generation and maintenance of hyperalgesia and neuropathic pain. To test whether II(i) neurons can be hyperpolarized by the mu-opioid agonist [D-Ala(2), N-Me-Phe(4), Gly(5)-ol]-enkephalin (DAMGO; 500 nM) and to address possible downstream consequences of mu-opioid-evoked inhibition of II(i) neurons, we combined in vitro whole-cell, tight-seal recording methods with fluorescent labeling of the intracellular tracer biocytin and confocal microscopy. Twenty-one of 23 neurons studied had identifiable axons. Nine possessed axons that projected ventrally into laminae III-V; six of these were hyperpolarized by DAMGO. Three of four neurons with identifiable axons that projected to lamina I were hyperpolarized by DAMGO. Most neurons could be classified as either islet cells or stalked cells. Five of nine labeled islet cells and only two of seven stalked cells were hyperpolarized by DAMGO. Three were stellate cells: one resembled a spiny cell and three could not be classified. DAMGO hyperpolarized each of the stellate cells, the spiny cell, and 1 of the unclassified cells. Our data support the hypothesis that part of the action of mu-opioid agonists involves the inhibition of interneurons that are part of a polysynaptic excitatory pathway from primary afferents to neurons in the deep and/or superficial dorsal horn.

Afferent Pathways↗