Cutaneous Senses Flashcards
sensory (afferent) neurons
- how we start an AP
- have specialized channels that are opened or closed in response to a stimulus
- most open or close in response to a mechanical stimulus such as deformation of the cell membrane will cause the Na channel to open and depolarization of the membrane
depolarization of sensory neurons
- produces a local response upon opening of the Na channels when the mechanical stimulus is initiated
- this depolarization in a sensory neuron is called “generator potential”
- if stimulus is strong enough or lasts long enough, the generator potentials will cause the afferent neuron to come to threshold and generate an AP
generator potential–touch/pressure
- Pacinian corpuscle is a receptor in the skin that responds to touch
- comprised of alternating layers of membrane with fluid b/w them surrounding the nerve ending
- when we touch something, all the layers of the membrane are deformed and this mechanical stimulus leads to the opening of the mechxnosensitive Na channels on the membrane and the influx of Na and an AP sent
adaptation
- if a stimulus is maintained, the AP gradually die as accommodation occurs
- the number of AP dies away even though the stimulus is still there b/c the fluid rearranges in the Pacinian corpuscle and then there is no more transmission of force to the neuron
- the force is still there and the outer layers still deformed by the inner layers rearrange so mechanical force no longer goes all the way to neuron and channels close
- the number of AP dies away even though the stimulus is still there b/c the fluid rearranges in the Pacinian corpuscle and then there is no more transmission of force to the neuron
- *much but not all of the adaptation that occurs is the result of changes in the periphery
afterdischarge
- sometimes when we remove the stimulus, this triggers APs as the ending reforms
- when we remove the force, the fluid that reformed now has to move again so this triggers an AP, so this helps us know when the stimulus ends and goes away
- property of the R itself but adaptation can be due to brain and receptor
sensory unit and receptive field
- sensory unit–sensory neuron and all its branches
- all the branches within the area of the skin
- receptive field–area from which stimulation produces activation of the neuron
- area on the skin, visual field, etc which will activate the same sensory neuron if activated
- fine touch wold have a small receptive area where as crude touch would be in an area with a large receptive area
coding sensory stimulus
- number of APs is one way of coding the intensity
- with greater intensity, we see more APs
- with further increases, we may see patterned discharges–doublets or triplets
- number of receptors firing also inc with increased intensity
- stimulus may only produce activation in one neuron if small stimulus so neighboring neurons get no signal
- if the stimulus is bigger, then we can get more than one neuron firing and at different rates b/c one neuron is impinging on the receptive field of another
quantification of the coding of the sensory stimulus
-we need to see about a 10% change in for conscious recognition of the change
perceived intensity vs. measured intensity
perceived intensity=K(measured intensity)^A
- K and A vary depending on the type of sensory R
- muscle senses–both are close to 1 so our perceived intensity matches our actual (measured) intensity very closely
- this is important so that we know exactly where our muscles are to make the motion that we want
- cutaneous senses–more variability so what we perceive may diverge from the actual rather substantially
- if inc actual intensity, then inc perceived, but don’t know how much or exact fine motions
- muscle senses–both are close to 1 so our perceived intensity matches our actual (measured) intensity very closely
multiple pathways of central processing of the senses in the brain
- dorsal columns–proprioceptive and discriminative (fine touch)
- spinothalamic tract–thermal, nociceptive, and coarse touch
- spinoreticulothalamic system–nociceptive
- spinocerebellar tract
pre-synaptic inhibition
- special case of inhibition that arises from an axo-axonal synapse and involves the post-synaptic cell which is a pre-synaptic terminal
- end result of pre-synaptic transmission: reduced NT release from the inhibited pre-synaptic terminal
- so, we start with a normal chemical synapse with NT release from neuron A to B
- then we have another neuron that synapses on the pre-synaptic terminal (neuron C)
- the third neuron when activated release GABA at the synapse b/w it and the first neuron which allows Cl to enter neuron A, so this hypoerpolarized neuron A, so when bring in Ca at the junction b/w A and B, it will not depolarize the membrane as much and won’t release as much NT and reducing the probability of APs from neuron B
where does presynaptic inhibition occur?
b/w neighboring receptors at the first synapse in the their pathway
-increases the brain’s ability to localize the signal
thalamus in transmitting central processing of senses
- often makes decision that the thalamus does not need certain sensory information
- this is important during sleep where large chunks of info do not get past the thalamus b/c it is so hyper polarized
- regardless of which pathway is used, every synapse along the way represents a chance to modify or respond to the stimulus
organization of the cortex
- sensory cortex is arranged somatotopically
- homunculus is what represents the sensory going to the parts of the body from the cortex–hand, face, and mouth get huge areas of cortex devoted to them
neocortex
- somatosensory cortex is neocortex so it has 6 layers and the neurons in the cortex are arranged in columns–each column deals with ONE sensory modality in ONE part of the body
- sensory information arrives at its respective column in layer IV–via the thalamus
- neighboring columns receive information from the same part of the body but a different sensory modality