Modulations of input-output properties of corticospinal tract neurons by repetitive dynamic index finger abductions

2004 ◽  
Vol 161 (2) ◽  
pp. 255-264 ◽  
Author(s):  
Susumu Yahagi ◽  
Yusaku Takeda ◽  
Zhen Ni ◽  
Makoto Takahashi ◽  
Toshio Tsuji ◽  
...  
1995 ◽  
Vol 73 (6) ◽  
pp. 2584-2590 ◽  
Author(s):  
G. Cadoret ◽  
A. M. Smith

1. Neurons with proprioceptive or cutaneous receptive fields associated with the hand were identified in the ventral bank of the cingulate sulcus in the monkey. Cells with proprioceptive fields outnumbered cells receiving cutaneous afferents by more than three to one. No cells were encountered that received convergent proprioceptive and cutaneous input. The high concentration of these neurons in the lateral depth of the cingulate sulcus establishes that a distinct hand representation exists within the rostral part of area 23c. 2. Hand-related neurons in area 23c exhibited strong activity modulations during grasping, lifting, and holding an object with the contralateral thumb and index finger. Force pulse perturbations applied to the object elicited excitatory responses at latencies of approximately 45 ms. The modulation of the cellular activity and the input-output properties of these cingulate neurons suggest that, like neurons of primary motor and sensory cortex, these cingulate neurons are also involved in the sensorimotor control of finger movements.


2011 ◽  
Vol 106 (1) ◽  
pp. 122-126 ◽  
Author(s):  
B. Alstermark ◽  
L. G. Pettersson ◽  
Y. Nishimura ◽  
K. Yoshino-Saito ◽  
F. Tsuboi ◽  
...  

In motor control, the general view is still that spinal interneurons mainly contribute to reflexes and automatic movements. The question raised here is whether spinal interneurons can mediate the cortical command for independent finger movements, like a precision grip between the thumb and index finger in the macaque monkey, or if this function depends exclusively on a direct corticomotoneuronal pathway. This study is a followup of a previous report (Sasaki et al. J Neurophysiol 92: 3142–3147, 2004) in which we trained macaque monkeys to pick a small piece of sweet potato from a cylinder by a precision grip between the index finger and thumb. We have now isolated one spinal interneuronal system, the C3-C4 propriospinal interneurons with projection to hand and arm motoneurons. In the previous study, the lateral corticospinal tract (CST) was interrupted in C4/C5 (input intact to the C3-C4 propriospinal interneurons), and in this study, the CST was interrupted in C2 (input abolished). The precision grip could be performed within the first 15 days after a CST lesion in C4/C5 but not in C2. We conclude that C3–C4 propriospinal interneurons also can carry the command for precision grip.


1992 ◽  
Vol 88 (3) ◽  
Author(s):  
I. Hashimoto ◽  
T. Gatayama ◽  
K. Yoshikawa ◽  
M. Sasaki ◽  
M. Nomura

2018 ◽  
Vol 77 ◽  
pp. 206-210 ◽  
Author(s):  
Alexander J. Barry ◽  
Wendy M. Murray ◽  
Derek G. Kamper
Keyword(s):  

Stroke ◽  
2001 ◽  
Vol 32 (suppl_1) ◽  
pp. 334-334
Author(s):  
Steven C Cramer ◽  
Keith C Stegbauer ◽  
Angela Mark ◽  
Robert Price ◽  
Kristin Barquist ◽  
...  

100 Little is known about the function of surviving motor cortex after hemiparetic stroke. Though the corticospinal tract may be damaged, function may persist via intact intracortical connections. We probed motor cortex function using paradigms unrelated to genesis of paretic limb movement. Seven patients with chronic post-stroke hemiparesis, including total hand plegia, were studied with functional MRI (fMRI). Brain activation was achieved by alternating between rest and one of several stimuli. For the plegic hand, stimuli were passive index finger movement, or viewing active movements; for the non-plegic hand, active or passive index finger movement. Brain activation maps (p<.001) were generated, after which anatomical landmarks were used to identify regions of interest within non-infarcted tissue. Tasks were rehearsed before fMRI, during which surface EMG leads were placed on 5 muscles in each arm. Patients were median 5 months post-stroke, median age 66 years. Median NIH stroke scale score was 9; Rankin, 3; and arm motor Fugl-Meyer score, 18 (normal=66); Motor Activity Log confirmed no plegic hand use. Studies with excess head movement were excluded, including all plegic hand tasks for 1 patient. Plegic hand tasks (10 studies across 6 patients) activated the stroke hemisphere in all patients, including primary motor cortex (5 patients), primary sensory cortex (5 patients), premotor cortex (4 patients), and supplementary motor area (3 patients). Non-stroke hemisphere was also activated, particularly primary motor cortex (5 patients). In a few instances, EMG disclosed paretic arm muscle activity, but this had no relationship to fMRI activation. Non-plegic hand tasks (9 studies across 7 patients) activated the stroke hemisphere ipsilaterally, including supplementary motor area in all 7 patients, and primary motor cortex in 6 patients. In patients with post-stroke hemiparesis, passive stimulation activates surviving motor cortex regions within the stroke-affected hemisphere. After corticospinal tract damage, motor cortex can still be activated during tasks unrelated to paretic limb movement. The results may suggest therapeutic avenues for improving motor function after stroke.


2014 ◽  
Vol 111 (7) ◽  
pp. 1479-1486 ◽  
Author(s):  
Pablo Arias ◽  
Verónica Robles-García ◽  
Nelson Espinosa ◽  
Yoanna Corral-Bergantiños ◽  
Laura Mordillo-Mateos ◽  
...  

The corticospinal tract excitability is modulated when preparing movements. Earlier to movement execution, the excitability of the spinal cord increases waiting for supraspinal commands to release the movement. Movement execution and movement observation share processes within the motor system, although movement observation research has focused on processes later to movement onset. We used single and paired pulse transcranial magnetic stimulation on M1 ( n = 12), and electrical cervicomedullary stimulation ( n = 7), to understand the modulation of the corticospinal system during the “preparation” to observe a third person's movement. Subjects passively observed a hand that would remain still or make an index finger extension. The observer's corticospinal excitability rose when “expecting to see a movement” vs. when “expecting to see a still hand.” The modulation took origin at a spinal level and not at the corticocortical networks explored. We conclude that expectancy of seeing movements increases the excitability of the spinal cord.


1970 ◽  
Vol 15 (2) ◽  
pp. 115, 118
Author(s):  
WILLIAM E. COLEMAN

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