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Understanding the Spinal Cord and Reflexes
Feb 16, 2025
Lecture Notes: The Spinal Cord
Overview
Second lecture of the third unit focusing on the spinal cord.
Previously covered nervous tissue.
Upcoming focus on the anatomy and physiology of the spinal cord.
Emphasis on spinal reflexes and reflex arcs.
Anatomy of the Spinal Cord
Dimensions
:
About 18 inches long.
Ends around vertebrae L1 or L2.
Diameter ~ 0.5 inches.
Bilateral symmetry with posterior median sulcus and anterior median fissure.
Regions and Structures
:
Starts at the medulla oblongata.
Ends at the conus medullaris, tapering into the cauda equina.
Enlargements: Cervical (shoulders), Lumbar (pelvis, lower limbs).
31 spinal cord segments aligned with vertebrae.
Dorsal and ventral roots combine to form spinal nerves.
Gray and White Matter
:
Gray matter: Neuron cell bodies.
White matter: Columns of nerve fibers.
Meninges of the Spinal Cord
Three-layer structure
:
Dura Mater
: Outer tough layer, epidural space contains adipose tissue.
Arachnoid Mater
: Middle layer, subarachnoid space contains cerebrospinal fluid (CSF).
Pia Mater
: Innermost layer, collagen and elastic fibers.
Clinical Relevance
:
Meningitis: Infection of the meninges.
Epidural anesthesia and spinal taps involve these spaces.
Physiology: Reflexes
Definition
: Automatic responses to stimuli.
Components of Reflex Arc
:
Arrival of stimulus.
Activation of sensory neuron.
Information processing.
Activation of motor neuron.
Response of effector (e.g., muscle contraction).
Types of Reflexes
:
Development
: Innate vs. acquired.
Response
: Somatic (skeletal muscle) vs. visceral (organ systems).
Complexity
: Monosynaptic (simple) vs. polysynaptic (complex).
Site of Processing
: Cranial vs. spinal.
Monosynaptic and Polysynaptic Reflexes
Monosynaptic Reflexes
:
Example: Stretch reflex (knee-jerk).
Direct connection between a sensory neuron and a motor neuron.
Polysynaptic Reflexes
:
Example: Withdrawal reflex.
Involves interneurons, more than one synapse.
Reciprocal inhibition allows the flexor reflex to function.
Clinical Focus: Amyotrophic Lateral Sclerosis (ALS)
Characteristics
: Degeneration of motor neurons, leads to muscle atrophy.
Causes
:
90% sporadic cases, 10% familial.
2% linked to mutations in SOD1 gene.
Symptoms
: Weakness, muscle atrophy, difficulty breathing.
Treatment
: Limited; Riluzole provides modest survival extension.
Conclusion
Next focus will shift to the brain.
Final lecture for this unit will cover the brain anatomy and function.
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