Chapter 5: Motor Systems: The Organisation of Action Flashcards
motor program
plan to produce a particular motor action, such as writing one’s name, that occurs independently of the effectors used to carry out the movement
lower motor neuron/ primary motor neuron
motor neuron that directly innervates muscle
interneuron/ local circuit neuron
neuron whose local connections contribute to processing circuitry
upper motor neuron
neuron that gives rise to a descending projection that controls the activity of lower motor neurons in the brainstem and spinal cord
primary motor cortex
major source of descending projections to motor neurons in the spinal cord and cranial nerve nuclei; located in the precentral gyrus (area 4) and essential for the voluntary control of movement
premotol cortical area
cortical areas, including the premotor cortex, supplementary motor cortex, and parts of the parietal cortex, that provide motor programming signals to the primary motor cortex
premotor cortex
part of the prefrontal cortex lying just anterior to the primary motor cortex; involved in planning movement
supplementary motor area/ SMA/ area 6
premotor area, lying anterior to the primary motor cortex on the medial surface of the cerebral hemisphere, that plays an important role in movement planning
medullary pyramids
longitudinal bulges on the ventral aspect of the medulla that signify the corticospinal tracts at this level of the nervous system
frontal eye fields
region of the prefrontal cortex in human and non-human primates, often associated with area 8a, that plays a key role in voluntary visual orienting movements
superior colliculus
paired structures that form part of the roof of the midbrain; important in orienting movements of the head and eyes
saccade
ballistic eye movement that changes the point of binocular visual fixation; normally occur at a rate of about three to four per second
readiness potential
electrical potential, recorded from the motor and premotor cortices with EEG electrodes, that signals the intention to initiate a voluntary movement well in advance of actual production of the movement
anosognosia
lack of awareness of one’s own disability
reward value
likelihood that a particular movement will yield a reward, multiplied by the amount of reward expected
optic ataxia
neurological condition associated with damage to the dorsal parietal cortex and characterized by deficits in visually guided reaching
basal ganglia
group of nuclei lying deep in the subcortical white matter of the frontal lobes that organize motor behavior. The caudate, putamen, and globus pallidus are major components of the basal ganglia; the subthalamic nucleus and substantia nigra are often included
gating
allowing/ permitting
the basal ganglia, for example, gate movement initiation. Channels through the neuronal membrane are often gated, allowing the access of certain ions under certain conditions
caudate
one of the three major nuclei that make up the basal ganglia in the cerebral hemispheres; together with the putamen, serves as the input structure for the globus pallidus. Damage to the caudate nucleus leads to hyperkinetic movement disorders such as Huntington’s disease
putamen
one of the three major nuclei that make up the basal ganglia
striatum
input nuclei of the basal ganglia, consisting of the caudate and the putamen. So called because of the striped appearance of these structures in brain sections
globus pallidus
one of the three major nuclei that make up the basal ganglia in the cerebral hemispheres; relays information from the caudate and putamen to the thalamus
substantia nigra pars reticulata/ SNr
component of the midbrain substantia nigra nucleus that plays a key role in the suppression and initiation of saccadic eye movements
Parkinson’s disease
neurodegenerative process affecting the substantia nigra that results in a characteristic tremor at rest and a general paucity of movement
Huntington’s disease
autosomal dominant genetic disorder in which a single gene mutation results in damage to the basal ganglia that causes personality changes, progressive loss of the control of voluntary movement, and eventually death
choreiform movement
uncontrollable, dancelike (“choreiform”) writhing or twisting associated with damage to the basal ganglia, as occurs in disorders such as Huntington’s disease
hemiballismus
neurological disorder resulting from unilateral damage to the basal ganglia; manifested by flinging movements of the limbs contralateral to the lesion
cerebellum
prominent hindbrain structure that is concerned with motor coordination, posture, balance, and some cognitive processes; composed of a three-layered cortex and deep nuclei, and attached to the brainstem by the cerebellar peduncles
intention tremor
tremor that occurs during performance of a voluntary motor act. Characteristic of cerebellar pathology