Lecture 16 Flashcards
Basal ganglia functions
Predicts the effects of various actions
Makes and executes action plans
Parts of basal ganglia located in cerebrum
Caudate, Putamen and Globus pallidus
Parts of basal ganglia located in diencephalon
Subthalamic nucleus
Parts of basal ganglia located in midbrain
Substantia nigra
Neurotransmitter Cortical motor areas produce excitation of the striatum
Glutamate
Neurotransmitter produced by Substantia nigra
dopamine
Output of the basal ganglia motor circuit regulates
Muscle contraction Muscle force Multi-joint movements Sequence of movements and most importantly, the size of movement
Stimulation of the pedunculopontine nucleus (PPN) regulates contraction of
postural and girdle muscles via the lateral reticulospinal neurons
Stimulation of the midbrain locomotor region elicits rhythm
lower limb movements similar to walking or running
Globus pallidus INTERNUS main functions
Inhibits the motor thalamus
Inhibits the pedunculopontine nucleus (PPN)
Inhibits the midbrain locomotor region
Overall action to reduce size of motor output
Head of the caudate function in loops
executive functions like decision making, goal directed, planning and learning
Body of the caudate function in loops
A part of the oculomotor loop
Makes decision about eye movements and spatial attention
Ventral striatum functions in loops
limbic functions
Head of caudate and substantia nigra functions in loops
behavior control
Putamen and globus pallidus functions in loops
motor control
Neurotransmitter for the pedunculopontine nucleus (PPN)
Acetylcholine
Parkinson’s disease symptoms
Tremor, rigidity, bradykinesia/akinesia, “mask-like” facial expressions
Death of acetylcholine-producing cells in Pedunculopontine tegmental nucleus what happens?
Leads to increased postural muscle movements due to disinhibition of the reticulospinal tracts
Death of dopamine-producing cells in the substantia nigra compacta. What happens?
decreased voluntary movements due to loss of dopamine to putamen
Clinical Features of Parkinson’s Disease
Shuffling gait Autonomic dysfunction Sleep disorders Psychiatric symptoms, depression in 50% Dementia at end stage 20-30%
Unpredictable speed of progression
Akinesia
loss of automatic movements
blinking, swallowing, protective reflexes
Huntington’s disease
Autosomal dominant disorder
Excessive motor output from cerebral cortex
Caused by mHTT protein is responsible for cell loss and gliosis of the striatum (basal ganglia) and thalamus resulting in severe atrophy and loss of the inhibitory pathway.
Look back at indirect pathway