NURS 260 Pathophysiology Study Notes
Components of the Neuromuscular System
Neuromuscular unit containing motoneurons
Myoneural junction
Muscle fibers
Spinal cord
Descending pathways from the brain stem circuits
The Motor Control System
The final common pathway transmits all central nervous system (CNS) commands to the skeletal muscles.
This path is influenced by sensory input from the muscle spindles and tendon organs as well as descending signals from the cerebral cortex and brain stem.
The cerebellum and basal ganglia influence motor function indirectly via the brain stem.
Motor Homunculus
Representation of the areas of the brain responsible for motor control of different body parts:
Little
Ring
Middle
Index
Thumb
Neck
Eyebrow
Eyelid and eyeball
Face
Lips
Jaw
Tongue
Swallowing
Hand
Wrist
Elbow
Trunk
Shoulder
Hip
Knee
Ankle
Toes
Motor Systems
Pyramidal Motor System
Originates in the motor cortex.
Provides control of delicate muscle movements.
Extrapyramidal System
Originates in the basal ganglia.
Provides background for more crude, supportive movement patterns.
Disorders of Motor Function
Upper Motoneuron Lesions
Can affect the motor cortex, internal capsule, or brain structures through which the corticospinal or corticobulbar tracts descend, or the spinal cord.
Lower Motoneuron Lesions
Disrupt communication between the muscle and all neural input from spinal cord reflexes, including the stretch reflex, which maintains muscle tone.
Disorders of Skeletal Muscle Groups
Muscular Atrophy
If a normally innervated muscle is not used for long periods, the muscle cells shrink in diameter, lose contractile protein, and weaken.
Muscular Dystrophy
Genetic disorders that result in progressive deterioration of skeletal muscles due to mixed muscle cell hypertrophy, atrophy, and necrosis.
Muscular Dystrophy
Characteristics:
Normal fibers
Overcontracted fibers
Endomysial collagen
Regenerating fibers
Macrophages in degenerated fiber (myophagocytosis)
Alterations of Neuromuscular Function
Drugs and agents can alter neuromuscular function by changing the release, inactivation, or receptor binding of acetylcholine.
Curare
Acts on the postjunctional membrane of the motor end plate to prevent the depolarizing effect of the neurotransmitter.
Commonly used during various surgical procedures.
Myasthenia Gravis
Definition
A disorder of transmission at the neuromuscular junction affecting communication between the motoneuron and the innervated muscle cell.
Cause
An autoimmune disease causing antibody-mediated loss of acetylcholine receptors at the neuromuscular junction.
Components of the Peripheral Nervous System
Motor and sensory branches of the cranial and spinal nerves.
The peripheral parts of the autonomic nervous system.
Peripheral ganglia.
Peripheral Neuropathies
Mononeuropathies
Caused by localized conditions such as trauma, compression, or infections affecting a single spinal nerve, plexus, or peripheral nerve trunk.
Examples:
Fractured bones may lacerate or compress nerves.
Excessively tight tourniquets may directly injure nerves or produce severe effects.
Polyneuropathies
Involves demyelination or axonal degeneration of multiple peripheral nerves, leading to symmetric sensory, motor, or mixed sensorimotor deficits.
Typically, the longest axons are involved first, with symptoms beginning in the distal parts of the extremities.
Carpal Tunnel Syndrome
Caused by compression of the median nerve due to repetitive use of the wrist.
Characterized by areas of numbness in the carpal tunnel regions (depicted in shaded green).
Guillain-Barre Syndrome
Characteristics
Acute, immune-mediated condition.
Often preceded by an acute influenza-like illness prior to the onset of symptoms.
Nerve Root Injuries
A common cause of back pain due to trauma, aging, or degenerative processes affecting nerve roots at L4, L5, S1 levels.
Disorders of the Cerebellum
The cerebellum is responsible for:
Coordination of motor movement.
Cerebellum-associated movement disorders
Causes: congenital defects, vascular accidents, or tumors.
Types of disorders include:
Vestibulocerebellar ataxia
Decomposition of movement
Basal Ganglia
A group of deep, interrelated subcortical nuclei that play an essential role in movement control.
Receive:
Indirect input from the cerebellum and all sensory systems (including vision).
Direct input from the motor cortex.
Function in organizing inherited and learned automatic movement programs.
Key pathways include:
A dopamine pathway from the substantia nigra to the striatum.
A γ-aminobutyric acid (GABA) pathway from the striatum to the globus pallidus and substantia nigra.
Acetylcholine-secreting neurons involved in network functions within the neostriatum.
Several pathways from the brain stem secreting norepinephrine and serotonin.
Characteristics of Basal Ganglia-Associated Movement Disorders
Movement Disorder Characteristics:
Tremor: Involuntary, oscillating contractions of opposing muscle groups around a joint.
Hypokinetic disorders: Slowness in initiating movement and reduced range and force (bradykinesia).
Chorea: Irregular wriggling and writhing movements, accentuated by movement and environmental stimuli.
Athetosis: Continuous wormlike, twisting, and turning motions of a limb or body.
Ballismus: Violent, sweeping, flinging motions of one side of the body (hemiballismus).
Dystonia: Abnormal maintenance of a posture due to simultaneous contraction of antagonist and agonist muscles.
Dyskinesias: Bizarre wriggling and writhing movements often affecting facial regions.
Definition of Parkinson's Disease
A degenerative disorder of basal ganglia function characterized by tremor, rigidity, and bradykinesia.
Characteristics:
Progressive destruction of the nigrostriatal pathway, leading to reduced striatal dopamine concentrations.
Amyotrophic Lateral Sclerosis (ALS)
A devastating neurologic disorder affecting motor function, typically following a progressive course with a mean survival period of 2 to 5 years from the onset of symptoms.
Motor Neurons affected:
Anterior horn cells of the spinal cord.
Motor nuclei of the brain stem, particularly hyoglossal nuclei.
UMNs of the cerebral cortex.
Death of LMNs leads to denervation, resulting in musculature shrinkage and muscle fiber atrophy.
Multiple Sclerosis (MS)
A demyelinating disease of the CNS, it is the most common nontraumatic cause of neurologic disability among young and middle-aged adults.
Characterized by exacerbations and remissions over many years, affecting multiple sites in the CNS.
Initially, individuals may have normal or near-normal neurologic function between exacerbations.
As the disease progresses, there is less improvement between exacerbations.
Spinal Cord Injury (SCI)
Definition: Damage to the neural elements of the spinal cord.
Causes: Motor vehicle crashes, falls, violence, and sporting activities.
Involvement: Most SCIs involve damage to the vertebral column and/or supporting ligaments in addition to the spinal cord.
Commonly affect:
Sensory and motor functions, spinal reflexes, the autonomic nervous system, temperature regulation, sensorimotor function, skin integrity, pain reception, bladder and bowel function, and sexual functions.