Tutorial 2- Somatosensation Flashcards
In the skin, sensation of touch is mediated by
cutaneous mechanoreceptors
maintained skin stretch is mediated by
ruffini endings
continuous pressure is sensed by
merkel disk receptors
vibration is sensed by
pacinian corpuscles
the nerve fibres that transmit touch info are mainly
A beta fibres
are there different thermoreceptors for each level of temperature?
yes
painful stimuli are mediated by
nociceptors
temperature and painful stimuli are transmitted by axons of
A delta and C fibres
pain is not a stimulus, rather
ex extreme cold is a stimulus
c fibres can respond to many simuli, such as
chemicals, temperature (warmth and cooling) and itch - it is therefore polymodal
sensory nerves respond to increasing stimulus intensity by
increasing firing frequency proportionately with strength of stimulus
nerves that are stimulated by inflammation/mechanical damage:
nociceptors
A alpha receptors are not involved in cutaneous touch, rather in
deep joint proprioception- therefore only present in DRGs involved in deep joint proprioception
are c fibres myelinated or unmyelinated?
unmyelinated
diameter, speed and detectable stimuli for c fibres:
0.2-1.5 microm, 0.5-2 m/s, pain+temp.+itch
diameter, speed and detectable stimuli for A delta fibres:
1-5 microm, 5-35 m/s, pain+temp.
diameter, speed and detectable stimuli for A beta fibres:
6-12 microm, 35-75 m/s, touch
diameter, speed and detectable stimuli for A alpha fibres:
13-20 microm, 8-120 m/s, proprioception
which NT do C, A delta and A beta fibres use?
glutamate
in addition to glutamate, which other NTs can C fibres use?
peptidergic transmitters such as substance P and CGRP
what do the differences in NT of c fibres do?
create 2 classes of c fibre, one which only uses glutamate and the other that uses both glutamate and peptidergic transmitters
the touch pathway can also be referred to as the
medial lemniscal, dorsal column pathway
where does the touch pathway cross the midline?
at the dorsal column nuclei in the medulla
the nociceptive pathway is also referred to as the
spinothalamic/ anterolateral tract
the nociceptive pathway crosses the midline
at the level of the spinal cord that it enters via a projection neuron, then doesn’t synapse again until the thalamus
the touch and nociceptive pathways travel from the thalamus to the cerebral cortex via the
internal capsule
does the brain receive both touch and nociceptive signals from the opposite side of the body?
yes
do the touch, temp. and nociceptive pathways from body have equivalent pathways subserving the head and neck/
yes
what are the names of the 3 pathways subserving the head and neck?
- Spinothalamic
- Trigeminal nerve
- Dorsal column/medial lemniscus—> divided into fasciculus gracilus and fasiculus cuneatus
what does the spinothalamic transmit?
body pain
what does the trigeminal nerve transmit?
face and neck pain
where are the cell bodies of trigeminal nerve?
the trigeminal ganglion, which is analogous to the DRG
how many branches are in the DRG?
2, 1 to organ and one to spinal cord
which DRG is the fasciculus gracilus from?
the lumbar DRG
which DRG is the fasciculus cuneatus from?
the cervical DRG
which DRG does the trigeminal go via?
the rostral DRG
which stimuli does the trigeminal nerve transmit?
all senses, so both nociception and touch
what are local anaesthetics and how do they work/
membrane stabilising drugs, work by blocking sodium channels so no influx of sodium so no pain
how do opioid painkillers work?
by acting on opioid receptors: delta, kappa and most importantly mew.
what are the 3 main side effects of opioids?
constipation, decreased respiration, addiction
how do NSAIDs work as painkillers?
they inhibit COX enzymes, which would normally produce prostaglandins which sensitize nociceptors
TENS can be used to control certain chronic pain states by:
inhibiting interneurons and therefore utilising the gate theory, although mechanism is debatable
what is the main theory of why electrodes permanently implanted into the PAG work? (ex in parkinsonian pain)
PAG is the pain centre, so this would stimulate descending pathways and signal to projection neurons in the spine, therefore “dumping” he NTs serotonin and NA onto the projection neurons which act as inhibitors and stop pain signals from c fibres reaching the brain.