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Sensory systems
Vision, somatic sensory/touch, gustatory/taste, olfaction/smell, auditory/hearing, balance/movement, and proprioception.
Proprioception
The ability to know where different body parts are in relation to other things.
Why do we need sensory reception?
Maintain homeostasis, detect and react to changes in the environment, and protect the body from noxious stimuli
Stimulus
A change in the environment that triggers a response.
Sensory receptor
Specialized cells that detect and respond to specific stimuli.
Afferent neuron
carries information from the sensory receptor to the CNS
Efferent neuron
Neuron that carries motor commands from the CNS to the effector organ (muscle or gland).
Effector organ
Muscle or gland that carries out the response to a stimulus.
What are sensory receptors required for?
sight, hearing, taste, smell, pain, temperature, pressure and touch
Cutaneous receptors
Receptors that respond to chemical pain, thermal pain, mechanical pain, and touch.
proprioceptors
receptors which detect body position
C fibers
Unmyelinated fibers that transmit slow pain signals.
A-delta fibers
Myelinated fibres which transmit fast, sharp pain signals
Pain receptors
Activated by the release of ATP and prostaglandins from damaged or stressed cells.
Prostaglandins
Chemical messengers that bind to prostaglandin receptors and contribute to pain signaling.
specialised Schwann cells in the skin (2019)
detect mechanical pain and transmit signals to C fibers.
TRPM8
Receptor activated by extreme cold (<15 degrees) and menthol
TRPV1
Receptor activated by extreme heat (>45 degrees) and capsaicin (chillies).
Pacinian corpuscles
specialised receptors in the skin sensitive to pressure and vibration.
Pacinian corpuscle structure
nerve ending surrounded by layers of highly specialised connective tissue. The nerve ending contains specialised stretch mediated sodium ion channels.
Merkel's discs, Messner's corpuscles, and Ruffini's endings
Other sensory receptors in the skin sensitive to various types of touch.
Merkel cells and innocuous mechanical itch
protect against itch via stretch-activated Piezo2 channels.
slowly adapting receptors
allow continual awareness and response eg receptors for pain, temperature and body position
Why are some mechanoreceptors rapidly adapting?
so ‘unimportant’ information can be ignored
Dorsal column system
Sensory pathway which responds to fine touch, pressure and proprioception
Spinothalamic system
Responds to pain, temperature and coarse touch
Decussation
Crossing of sensory pathways to the opposite side of the brain.
Post-central gyrus
Area of the brain where sensory information is processed and consciously experienced
Nociceptors
Receptors for pain, temperature, and body position. A-delta and C fibres
polymodal nociceptors
activated by high intensity mechanical, chemical and thermal stimuli and the fibres are C fibres
Referred pain
Perception of pain in a different part of the body from where the pain signals are generated.
Enkephalins
Neurotransmitters released by interneurons to modulate pain signals
Gate control theory of pain modulation
spinal cord contains a neuronal ‘gate’ which blocks/allows pain signals → brain. Action potentials along A-beta fibres (dorsal columns) may depolarise inhibitor interneurons
Why is sharp pain harder to treat?
A-delta fibres synapse in a different area of the spinal cord to C fibres and there are no interneurons that release enkephalins. Also no opiate receptors
different perceptions of pain
Everybody perceives pain differently due to prior experience, expectation of pain, mood eg anxiety/depression, genetics etc.
Non-steroidal anti-inflammatory drugs (NSAIDs)
block inflammation and can treat pain eg aspirin and ibuprofen block COX-1 and COX-2
Local anaesthetics
block voltage-gated sodium ion channels and block action potentials eg lidocaine
Opioids (eg morphine)
activate descending inhibition and inhibit transmitter release
Acute pain
Beneficial pain that helps keep us safe.
Chronic pain
Non-beneficial pain that persists over a long period of time.
Neuropathic pain
occurs as a result of changes in nociceptor pathways and neuronal death