Week 11 : sense of touch Flashcards

1
Q

Sense(s) of touch…

A
  • different sensations that arise from the skin are extremely broad
  • object features are often combined with tactile sensations that arise internally (vestibular & proprioceptive) to gain full understanding of objects & how to interact them
  • cues incredibly useful when other sensory info isn’t available (searching for object in purse e.g.)
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2
Q

Haptic exploration…

A
  • the use of our hands to define an object by its features
  • powerful way to explore environment & form predictions about behaviour & use of novel object
  • can give us… texture (lateral motion), weight (unsupported holding), hardness (pressure), shape & volume (contour following & enclosure), temperature (static contact) & contour following
  • integrates info from mechanoreceptors, proprioceptors, thermoreceptors & maybe nociceptors
  • key in reading braille
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3
Q

Skin

A
  • 9 pounds
  • sense organ of touch
  • touch receptors exist everywhere on the surface of the skin, not necessarily in a uniform way tho (more on fingers & lips, less upper back & legs/arms)
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4
Q

Sensory cells within the skin… (2)

A
  1. epidermis = outer layer, consists mainly of dead cells that function to protect the underlying tissue… avascular (gets oxygen from air instead of blood stream)… keep out pathogens & keep in fluids
  2. dermis = contains oil & sweat glands, vasculature, hair cells a variety of sensory cell subtypes
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5
Q

mechanoreceptors

A
  • sensory receptors in the skin that transduce physical movement on the skin into neural signals
  • touch perception
  • stimulation of skin activates one or more of the 4 types of mechanoreceptors (SAI, SAII, FAI, FAII)
  • these mechanorlecpeors induce a neural signal sent to the spinal column then the brain
  • by combining the outputs our skin can encode texture, patterns of stimulation, amount of pressure & when the touch occurred, etc.
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6
Q

SAI

A
  • Merkel cells = have sustained response to continued pressure, giving max response to steady pressure
  • slow adapting
  • small receptive field
  • high spatial resolution
  • respond best to vibrations at low frequencies
  • important for perception of pattern and texture in touch
  • upper dermis
  • produce steady stream of neural response when skin is deformed
  • responsible for 2-point threshold
  • important when we need fine manual control, esp without visual feedback
  • highest density on fingertips & lips
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7
Q

FAI

A
  • Meissner corpuscle endings
  • fast adapting
  • small receptive field
  • high spatial resolution
  • respond well to low-frequency vibrations
  • upper dermis
  • respond vigorously when the skin is first touched, then again when the stimulus ends
  • esp good at detecting ‘slip’
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8
Q

SAII

A
  • Ruffini endings = have a sustained response t continued pressure, so maximum response to steady pressure
  • slow adapting
  • good at stretching from side to side (crucial for object grasping)
  • larger receptive fields
  • more vital for detecting presence of light touch than pinpointing where it occurs (low spatial resolution)
  • in lower dermis
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9
Q

FAII

A
  • Pacinian corpuscle endings
  • fast adapting
  • large receptive field
  • low spatial resolution
  • respond well to high-frequency vibrations
  • lower dermis
  • respond vigorously when the skin is first touched, then again when the stimulus ends(onset & offset)
  • used when we use fine motor control (fine texture)
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10
Q

Two-touch threshold response

A
  • distribution of the receptor subtypes are highly variable by body area… so our sensitively to different tactile sensations is also highly variable
  • two-touch threshold demonstrates this
  • The smallest separation between the two points that can be distinguished reliably as two separate points of pressure is taken as the threshold for that area of the body
  • these thresholds vary across the body and even in one part (e.g. finger tip way more sensitive than palm)
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11
Q

Thermoreception

A
  • to survive we must keep our internal temperature fairly constant
  • the ability to sense changes in temperature on the skin is called thermoreception
  • passive = cold air against face / active = touch someones face to see fi they have fever
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12
Q

Thermoreceptors

A
  • sensory receptors in the skin that signal info about the temperature as measured on the skin
  • free nerve endings in the upper dermis
  • respond to a range of skin temperatures from 17c-43c and take action to move to wamer/cooler environment if our internal temperature is threatened
  • our skin maintains a surface temperature between 30c-36c (here our thermoreceptors are mostly inactive)
  • can also asses temperature of objects placed against skin
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13
Q

Cold fibres vs warm fibres

A
  • they respond preferentially to temperatures that are colder/warmer than resting body temp
  • at regular body temp, both maintain some level of output
  • temperatures below body temp result in increased output from cold fibres & decreased from warm fibres (vice versa)
  • more interested in changes in temp & the output is reduced with prolonged exposure to other temp
  • warm fibres have secondary peak when exposed to very low temps (paradox heat experience) super cold temp = burning pain
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14
Q

Pain…

A
  • the perception & unpleasant experience of actual/threatened tissue damage
  • result of activation of receptors in our skin & elsewhere, as well as unpleasant subjective feeling associated w it
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15
Q

Nociceptive pain…

A
  • the pain that develops from tissue damage that causes nociceptors in the skin to fire
  • occurs from direct trauma to the skin
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16
Q

Nociceptors…

A
  • free nerve endings in skin (receptors) that cause us to feel pain when activated
  • found in dermis & epidermis
  • 2 main types…
    1. a-delta fibers = myelinated / conduct signal rapidly / respond to both heat and pressure / stinging feeling of pain & experience when first injured
    2. c-fibers = nonmyelinated / much slower / respond to pressure, extreme degree & toxic chemicals / chronic experience of throbbing pain & a bit delayed
17
Q

pain reflex

A
  • signal generated by pain-sensitive receptors travel via ascending neural pathways to cortex…
  • but also secondary pathway that bypasses brain to reflex away from bad stimuli…
  • touch hot object… signal from pain receptors travels via afferent projection to spinal cord… targets interneuron… interneuron targets efferent motor neuron that innervates a muscle in the area of sensation… this contract muscle to pull affected area away from hot object
  • all within a fraction of a second
18
Q

Gate theory of pain control

A
  • Nociceptors In the skin detect damage/trauma at the skin and transmit that information up the spinothalamic pathway
  • there is also a downward pathway… that can inhibit the flow of info upward from the pain receptors… then the experience of pain is reduced/inhibited
  • pathway… message from pain receptors in skin stimulates neurons & relay to brain… brain responds to this pain signal by releasing endorphins that send inhibitory input back down to the neurons… this reduce the signals generated by those neurons & pain to brain
19
Q

why is gate theory of pain control important to us?

A
  • the ability to down regulate pain is useful in managing situations in which pain is experienced but where there Is no real threat to survival (e.g. working out/dentist trip)
  • BUT not being able to perceive pain has crazy bad circumstances (ppl with mutation to the gene SCN9A)
20
Q

closed loop…

A

somatosensory & motor systems are often illustrated in and conceived of as 2 halves of a closed loop… info travels via ascending or afferent pathways to the brain, where it is interpreted by the somatosensory cortex & used to generate appropriate commands in the motor cortex …. them send back down via descending/efferent pathways to generate muscle activity… we will focus on ascending path

21
Q

neural pathways outside the brain…

A
  • nerve endings send axon into a nerve bundle where its joined by many other axons from adjacent nerve fibres
  • this enters the spinal cord in the dorsal root ganglion… cells enter the spinal cord in the dorsal root
  • once in spinal column, sensory info divided into 2 distinct pathways, which travel up the spinal column to the brain
22
Q

Dorsal column-medial leminiscal pathway

A
  • carries info from tactile (mechanoreceptors) and from the proprioceptors (muscle position)
  • travels on dorsal side (back) of spinal column
  • makes a synapse in the medulla of the brain, where it crosses over to the contralateral side (in the brain stem it crosses)
  • then, ascends into the brain as the medial lemniscus fibre bundle to the ventral posterior nucleus of the thalamus
  • last to somatosensory cortex
23
Q

Spinothalamic pathway

A
  • carries info from the pain (nociceptors) and thermoreceptors (temp)
  • cross over to contralateral side within spinal column (spinal synapse allows for reflexes before brain)
  • then, pass through medulla on way to ventral posterior nucleus of the thalamus via spinothalamic tract
  • last to somatosensory cortex & insular cortices
24
Q

the differences and consequences of the paths

A
  • the spinothalamic pathway crosses the body at the spinal cord and the dorsal column medial laminisco pathway doesn’t until the brain stem
  • this causes weird things if we have spinal cord damage
  • we would loose tactile + proprioceptive sensation from the side of the body on which the damage occurs, and loss of pain and temp sensation on opposite side
25
Q

somatosensory cortex

A
  • located in parietal lobe of cerebral cortex
  • all of the sensory info from the cell subtypes project to the primary somatosensory cortex (S1 located posterior to central sulcus) from the ventral posterior nucleus of the thalamus
  • maintains a somatotopic map of the body
  • can be subdivided into 4 functionally separate subregions…
  • at the bottom of S1 is S2 (secondary) & this area responds to variety of sensations that arise from both sides of body (ventral ‘what’)
26
Q

somatosensory cortex 4 regions

A
  1. area 1 = mechanoreceptors
  2. area 2 = proprioceptors
  3. area 3A = nociceptors
  4. area 3B = nociceptors & mechanoreceptors
    1/3B = skin / 2/3A = deep bone & muscle sensation
27
Q

temperature info takes a slightly different pathway…

A
  • Thermoreceptors send axons up the spinothalamic pathway that travel to the ventral posterior nucleus of the thalamus
  • From there to S1
  • Then goes to areas of the frontal lobe, including the insular cortex and the anterior cingulate cortex
28
Q

Somatosensory homunculus

A
  • Wilder Penfield 70 years ago
  • illustration of important concepts (somatotopic map)
  • it has an orderly organization & neighbouring areas of the body are represented by neighbouring areas of cortex
  • the size of the region of cortex that represents a given body part is not related to the size of the body part, but the importance of input from that region (majority hand & face)
29
Q

Modern homunculus

A
  • mapping mainly held up over time
  • but developments have allowed it to be even more detailed (down to individual finger)
  • thumb has largest representation & lots of overlap with pinky+ring finger which makes sense
  • when index finger removed, area of brain normally responding to that digit became sensitized to stimulation of the tomb & middle finger
  • this plasticity also demonstrated by enhanced foot/hand representations in soccer players & musicians
30
Q

Perception of itch…

A
  • pruriceptors
  • respond mostly to chemical irritants on skin instead of tissue damage
  • send axons up spinothalamic tract & synapse in the somatosensory cortex
  • function of itching… (1) scratch to remove irritant (2) itching causes us to scratch, which then induces actual, minor, tissue damage & induces an autoimmune response
31
Q

Proprioception

A
  • gives us our awareness of how our bodies are positioned
  • perception of the movements & position of our limbs
  • afferent fibers carry this info to the brain (somatosensory cortex)
  • all consumption affects this system
32
Q

3 different kinds of sensory receptors in proprioceptive system give us info…

A
  1. muscle spindles = muscle cells that have receptors connected to them that sense info about muscle length (flexed/extended/) & therefore muscle action
  2. joint receptors = receptors found in each joint that sense info about the angle of the joint from the pressure applied to the bones in the joint
  3. Golgi tendon receptors = receptors in the tendons that measure the force of a muscle’s contraction
33
Q

proprioception & reflexes…

A
  • proprioceptive receptors are important part of reflex circuitry that allows us to quickly correct limb position to maintain balance/correct unexpected deviations
  • like the kicking motion of a reflex test
  • like pain receptors, synapse in spinal cord on innerneurons & motor neurons to correct
34
Q

Vestibular system

A
  • responsible for spatial orientation & acceleration of the head (motion)
  • info from here is used by brain to generate motor commands that allow us to maintain balance, stabilize head & body during movement & maintain posture
  • located in semicircular canals (rotations) & otolith organs (acceleration) adjacent to the inner ear
  • same nerve that carries auditory info to brain carries vestibular info also
35
Q

semicircular canals

A
  • 3 tubes aligned perpendicular (right angled) & each encode movement of head in one direction
  • each canal is filled with liquid called endolymph
  • when head moves in any direction, endolymph lags behind cuz gravity & inertia cause relative movement in opposite direction
  • this relative motion bends cilia on the hair cells & triggers neural response
  • By comparing the movement in each canal, the brain can make inferences about rotations to the left or right (yaw), front or behind (roll) and up or down (pitch)
  • At the bottom of each canal is a chamber called the ampulla, which contains a structure called the crista
  • Inside the crista are the hair cells with stereocilia, the receptors
36
Q

otolith 2 organs…

A
  1. urticle = encode horizontal movement (like walking along a sidewalk)
  2. saccule = encode vertical movement (bouncing on tramp)
    - in both cases… movement causes a shift of small crystals called otoliths which lie atop a gelatinous material into which the hair cells & their stereocilia are embedded
    - these shifts displace the gelatinous which applies a force to the hair cells which depolarize to signal movement
37
Q

vestibular brain

A
  • nerve fibers from the semicircular canals & otolith come together in vestibular nerve then synapses in brain stem area called the vestibular complex
  • vestibular complex projects to several areas, including the parietal insular vestibular cortex, located in the parietal lobe
  • This area of the brain is thought to maintain a representation of head angle, critical for maintaining balance
38
Q

Vertigo

A
  • caused by disruption to the arrangement of otoliths within the urticle & saccule
  • such that the vestibular organ signals head movement when the eyes say a person is not moving
  • this gives a chronic feeling of sea sickness
39
Q

Tactile agnosia…

A
  • inability to identify objects by touch (like haptic perception)
  • Neurological condition caused by damage to the somatosensory areas of the parietal lobe
  • problem of identification, not perception
  • usually only one hand effected