Somatosensory 2 Flashcards
Anterolateral Pathway:
~ Poorly discrete localization from signal source.
~ No need for discrimination of fine degradations of intensity.
~ Pain, Heat, Cold, Crude, Tactile, Tickle, Itch, and Sexual Sensations.
Anteriolateral fibers of the spinal cord originate in the:
Dorsal horn laminae 1, 4, 5 and 6
Anteriolateral fibers cross ________ (decussate) in the anterior commissure of the cord to the opposite anterior & lateral white columns
Immediately
Anterolateral Pathway: Fibers progress cephalic (toward the head) via what two tracts?
The anterior spinothalamic tract and the lateral spinothalamic tract
What 4 places do the anterior spinothalamic tract and the lateral spinothalamic tracts terminate
1: Ventrobasl Complex (VPL) of the Thalamus (mostly tactile signals)
2: Reticular nuclei of the brainstem (think reticular activating system, sleep, consciousness)
3: Midbrain - Periaqueductal Gray & Locus Coeruleus (analgesia Modulation)
4: Hypothalamus
From these places the signals can be transmitted to the somatosensory Cortex along with the DCML signals
Velocity of the ALP is how fast compared to the DCML?
1/3rd the speed
In comparison to the DCML the Anterolateral Pathway is:
1/3rd the speed.
Spatial localization is poor.
Gradation intensities are much less accurate.
Poor ability to transmit rapidly changing or repetitive signals.
THINK CRUDE!
Does the Thalamus have the ability to discriminate tactical sensations?
The the somatosensory Cortex is destroyed a slight degree of crude sensation remains, indicating that although we tend to talk about the thalamus as a relay center, it also has a slight ability to discriminate tactile sensations
The somatosensory cortex is destroyed what effect does it have on pain sensation and perception and thermo perception?
When the somatosensory cortex is destroyed, it has little effect on pain sensation and perception and only a moderate effect on thermo perception.
What 3 areas of the brain play a primary role in discrimination of pain and thermo perception?
Brain stem
Thalamus
other basal regions
What are Cortiofugal signals?
Backward movement to control sensitivity and intensity of sensory input (lateral inhibition; controls range of sensitivity)
What is the function of Cortiofugal signals?
these fibers are INHIBITORY and act to suppress sensory input. they decrease the spread of a signal and sharpen degree of contrast and adjust the sensitivity of the system
What does Cortiofugal mean?
“Originating and running from the Cerebral Cortex”
C4:
Cape
C8:
Pinky Finger
T4:
Nipples
T10:
Belly Button
S2, S3, S4:
Keeps the poop off the floor
Opioid (mu) receptors exist in Rexed’s laminae/Tracts of Lissauer
~ Rexed Laminae: Substantia gelatinosa nucleus (a.l.a. gelatinous substance of posterior horn)
correlates to:
~ Tracts of Lissauer: 2 and 3
The spinal cord areas are defined by what two systems?
either by Rexed Laminae or Tracts of Lissauer
What are the 3 dimensions of pain?
Sensory - discriminative
Affective - motivational
Cognitive - evaluative
What type of pain is: felt within 0.1 seconds after pain is applied?
Fast pain
What type of pain is: Sharp, acute, pricking, electric?
Fast pain
What type of pain is: not felt in most deeper tissues?
Fast pain
What type of pain is: Caused by mechanical & thermal pain stimuli?
Fast pain
What type of pain is: Felt within 1 second after pain is applied & slowly increases over time?
Slow pain
What type of pain is: burning, throbbing, aching, chronic?
Slow pain
What type of pain is: Associated with tissue destruction?
Slow pain
What type of pain is: Caused by mechanical, thermal, and chemical stimuli?
Slow pain
What type of nerves are - widespread superficially in layers of skin, arteries, periosteum, joint surfaces, flax, and tentorium?
Free Nerve Endings
In deep tissues, free nerve endings are only sparsely disrupted but when tissue damage is profound enough what type of pain develops?
Slow-chronic aching
What Chemical Stimuli excite pain?
Bradykinin, Serotonin, Histamine, Potassium ions, acids, ACh, & proteolytic ensymes
What enhances sensitivity of pain endings but does not directly excite them
Prostaglandins and substance P
Do pain receptors adapt?
Very little (this is good because it allows pain to keep a person aware of tissue damage that is occurring)