Transcript Document
Neurophysiological Basis of Movement
World VI:
Motor Disorders
Lecture 30: Peripheral Muscular
and Neurological Disorders
Sites of Damage in Nerve and Muscle
Site
Disorder
Neuron cell body
Root
Axon
Demyelination
Neuromuscular synapse
Muscle
ALS (Lou Gehrig’s disease)
Cervical or lumbar radiculopathy
Axonal neuropathy
Guillain-Barré syndrome
Myasthenia gravis
Muscular dystrophy
Muscular Dystrophies
Genetic diseases: progressive weakness and
degeneration of skeletal muscles
Duchenne and Becker dystrophy—1 in 3,500 to
5,000 births
Mostly males are affected
Muscular Dystrophies:
Duchenne Dystrophy
Mutation of a gene responsible for dystrophin, a
protein involved in maintaining integrity of
muscle fibers
Clinical symptoms at 2 to 6 years; all muscles are
affected
Late to walk; waddling, unsteady gait
Respirator dependence by the age of 20
Muscular Dystrophies:
Becker Dystrophy
Similar to Duchenne dystrophy; mutation of a
gene responsible for dystrophin
Clinical symptoms appear at adolescence
Slower disease progression; longer life
expectancy
Muscular Dystrophies:
Myotonic Dystrophy
Most common adult form of muscular dystrophy
Myotonia: prolonged episode of muscle activity
after its voluntary contraction
Commonly in finger and facial muscles
High-stepping, floppy-footed gait
Long face; drooping eyelids
Myotonic Discharge
Stiff Person Syndrome
Excessive motoneuron excitation
Starts at 30 to 60 years of age
Leads to boardlike rigidity of trunk muscles
Stiff Person Syndrome
Continuous Muscle Fiber
Activity Syndromes
Tetanus (induced by tetanus toxin):
The toxin blocks postsynaptic inhibition
at the spinal level.
EMG bursts can be stopped by
neuromuscular or peripheral nerve block.
Discharges are attenuated during sleep
and under general or spinal anesthesia.
Continuous Muscle Fiber
Activity Syndromes
Stiff person syndrome:
Excessive motoneuron excitation
Coactivation of agonist–antagonist muscles
Proximal muscles are particularly involved
Neuromyotonia:
Continuous activity of single muscle fibers
Seen at rest and on the background of vol. activation
Defect probably in the motor axon terminals
Neuromyotonia
Small potentials on the background on voluntary
activation
Myasthenia Gravis
Disorder of transmission at the neuromuscular synapse
Clinical signs:
– fatigue, exhaustion, muscle atrophy
– any muscle(s) can be affected, but especially eye, face,
lip, tongue, throat, neck, and limb muscles
– ocular signs (eyelid droop; inability to open one eye)
– facial weakness (stiffness of the face; difficulties with
chewing, swallowing, laughing, and speech [dysarthria])
– may lead to ventilatory insufficiency and death
Myasthenia Gravis: Epidemiology
3 to 4 new cases per million annually
Prevalence: 60 cases per million
Can start at any age
Women are affected 2:1 over men
Death rate in the 1930s was 40%; death rate in the
1970s–1980s was 7%
Myasthenia Gravis: Physiology
Autoimmune process (the body produced
antibodies to ACh receptors)
Reduction of ACh receptors
Reduction of postsynaptic potentials
Myasthenia Gravis: Increased Duration
of Action Potentials in the Muscle
Myasthenia Gravis: Treatment
ACh-esterase inhibitors (neostigmine, distigmine)
Thymectomy to suppress autoimmune processes
Plasmapheresis to remove autoimmune antibodies
Side effects with any treatment
Peripheral Neuropathies:
Mononeuropathies
Slowed conduction in a single nerve
Reduced amplitude of motor and/or sensory potentials
Signs of denervation
Carpal tunnel syndrome: entrapment of the median nerve
at the wrist
Ulnar nerve can be entrapped near the elbow
Brachial plexus lesions: mostly seen in muscles innervated
by median and ulnar nerves
Peroneal: peroneal pressure palsy
Tibial: tarsal tunnel syndrome
Sciatic
Carpal Tunnel Syndrome
Peripheral Neuropathies:
Multiple Mononeuropathies
Diabetes mellitus
Polyarteritis nodosa (connective tissue
disorder, vasculitis)
Leprosy
Diabetes (Diabetes Mellitus):
Impaired Ability to Metabolize Glucose
Total number of cases in the U.S.: 16 million
Yearly increase: 650,000 new cases
Long-term complications:
– Peripheral sensory neuropathy
– Peripheral motor neuropathy
– Loss of autonomic nerve function
– Atrophy of peripheral tissues
Diabetes
Clinically apparent peripheral nerve damage occurs:
In 25% of patients after 10 years
In 50% of patients after 20 years
Consequences:
Loss of balance and coordination
Increased probability of falls, fractures,
bruises, etc.
Diabetes
Effects of muscle vibration on posture:
Lower during vibration of Achilles tendon
Higher during vibration of hamstrings
Reorganization of postural control: switch
to alternative sources of information
Consequence of Diabetes:
Atrophy of Peripheral Tissues
Is it a consequence of inadequate blood supply?
Is it a consequence of abnormal pressure
distribution with foci of high pressure?
Studies by the group of Peter Cavanagh
Diabetes
VIF
VIF
VIF
VIF
Peripheral Neuropathies:
Polyneuropathies
May be associated with demyelinating
neuropathies
Guillain-Barré syndrome: reduced recruitment;
conduction block; may result in permanent
axonal loss
Chronic inflammatory demyelinating
polyneuropathy: common recovery, but nerve
conduction velocity may remain slow
Peripheral Neuropathies:
Polyneuropathies
Axonal neuropathies (mostly of toxic origin)
Neuronal degenerations:
– Amyotrophic lateral sclerosis (Lou Gehrig’s
disease)
– Poliomyelitis (enterovirus destroying anterior
horn cells; EMGs show chronic denervation;
may lead to weakness and pain—a postpolyo
syndrome)
ALS
20,000 Americans have ALS (one in 15,000).
5,000 people in the United States are diagnosed with
ALS each year.
Men are affected more often than women.
ALS most commonly strikes people between 40 and
60 years of age.
About 5 to 10 percent of all ALS cases are inherited.
About 20 percent of all familial cases result from a
specific genetic defect: mutation of superoxide
dismutase 1 (SOD1).
ALS
The earliest symptoms may include twitching,
cramping, or stiffness of muscles; muscle weakness
affecting an arm or a leg; slurred and nasal speech;
or difficulty chewing or swallowing.
Patients have increasing problems with moving,
swallowing (dysphagia), and speaking or forming
words (dysarthria).
Patients have tight and stiff muscles (spasticity)
and exaggerated reflexes (hyperreflexia).