Motorneuornes, Weakness, Paralysis Flashcards
Upper motor neurones
Cell bodies in primary motor cortex of the brain, synapse onto lower motor neurones or on interneuones in the spinal cord (or in brainstem motor nuclei)
Lower motor neurones
Cell bodies into grey matter of spinal cord (or in brain stem motor nuclei) axons in travel in peripheral nerves and synapse onto
What is looked for in a clinical motor assessment
-co ordination, balance, perception
-observation
-muscle power
-muscle tone
-deep superficial reflexes
-eyes
-mouth
-facial expression
What determines the strength of muscle contraction
1)number of active motor units in a muscle- recruitment
More motor unit (lower motor unit, connected muscle tissue) recruited = more muscle strength
2)frequency of action potentials is received by muscle fibres in active motor units> firing units
Monoaminergic input
Arousal activity from brain stem onto LMN circuits- if you are excited, you can work harder
Spinal reflexes
-knee jerk reaction (but can be activated from any accessible tendon)
-simple, fast, spinal, monosynaptic, reflex
-can be modulated by higher centres
-can be normL, absent, hyper or hypo reacitve
Clinical testing of withdraw reflex
-flexor plantar reflex
-sharp instrument stroked on the side of the foot
-big toe flexion> sole of foot curves into stop contact with painful stimulus (normal, negative babinksi)
-big toe extension> abnormal positive babinksi suggests a problem with descending tracts
UMN lesions
-sites of damage (axons in descending tracts of the spinal cord, cell bodies in motor cortex)
Clinical findings:
Increased muscle tone
Muscle paralysis or weakness
Hyper reflexive
Positive Babinski
LMN lesions
-sites of damage: muscle fibres, nmj, mn axon
Clinical findings:
Muscle wasting
Muscle weakness
Fasiculation
Decreased muscle tone
Decreased reflexes
Examples of LMN disease
• motorneurone disease- progressive death of UMN’s and LMN’s
• Infection/ inflammation of nerves- Bell’s palsy
• Accidental section/ compression of peripheral nerves or spinal roots- sciatica
• Failure of NMJ transmission - myasthenia gravis
• Muscle fibre disease-myopathy, muscular dystrophy