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Taste (gustation)
Detection of hydrophilic chemicals whether for distinguishing poison and food, types of food, and control of feeding`
Tastant
A chemical that stimulates the sense of taste
Saltiness
NaCl, receptor is the Na+ channel and passes through ion channels
Sourness
H+, receptor is the OTOP1 (H+ channel) and PKD2L1 (K+ channel), passes through ion channels
Sweetness
Sucrose, receptor is T1R2 + T1R3 and activates through GPCRs
Bitterness
Caffiene, T2R (~25 types), activates through GCPRs
Umami
Glutamate, T1R1 + T1R3, activates through GPCRs
How many taste buds are there on your tongue?
About 2000-5000
TRCs Taste Receptor Cells
50-150 within a taste bud, respond to stimuli (tastants), depolarize and release transmitters
Receptor potential
Stimulus induced change in membrane potential of a sensory receptor cell
TRCs preferences
Can respond to more than one basic taste but tend to have preferences for how much the cell will polarize/depolarize
TRC transmitters
Have excitatory effects on downstream neurons
Detection of saltiness
Will activate Na+ selective channels and cause depolarization (more positive membrane potential), also releases serotonin to activate gustatory afferent axons)
Detection of sourness
Through proton (H+) sensitive channels, also blocks K+ selective channels, causes depolarization and also releases serotonin to activate gustatory axons (there are multiple ways to detect sourness)
Detection of bitterness, sweetness and umami
Through GPCRs, transduction process is activating GPCRs, triggering PLC → IP3 → Ca2+ signaling cascade, causes depolarization and also releases ATP to activate gustatory afferent axons
Central taste pathway
Taste receptor cells → Gustatory nucleus → VPM of thalamus → Gustatory cortex
Smell (olfaction)
Detection of airborne chemicals, warns of incoming harm, combines with taste for identification of food, serves as mode for communication
Organ of smell
Olfactory epithelium
ORNs olfactory receptor neurons
Activated by odorants, chemical stimulants of smell
Mechanism of olfactory transduction
Uses Cl- in an intracellular manner, as Cl- allows Cl- to leave cell via Ca2+ activated Cl- channels, leading to depolarization
Pathway of olfactory transduction
Odorants bind to GPCRs → activates G-protein and adenylyl cyclase → Increase cAMP level → Open cAMP-gated cation channel (Na+ and Ca+ influx) → Open Ca2+-activates channel (Cl- flow out of cell) → become depolarized and fire action potential
Simplified central olfactory pathway
Olfactory receptor cells → Glomeruli → 2nd order olfactory neurons → Olfactory cortex
Population coding
A combination of responses from a large number of broadly tuned neurons specify the identity of a particular stimulus
Glomerulus
Bulb in olfactory bulb, each one is connected to many ORNs and are the first to receive olfactory information
Sensory map
An orderly arrangement of neurons that correlates with features of the environment, created by the mapping of glomeruli and ORNS
Olfactory map
When specific spatial representation of olfactory information at the olfactory bulb occur, creating a “map”
VGCC
Voltage-gated calcium channel
Pathway for calcium and neuron activity
Neuron activation → VGCCs open → Ca2+ rise → release neurotransmitter
GCaMPs
A class of genetically coded Ca2+ indicators
Temporal coding
The representation of information encoded through the timing of action potentials rather than by their rate
Audible Range for humans
20 Hz to 20,000 Hz
Outer Ear parts
Pinna, auditory canal
Middle Ear
Ossicles
Inner Ear
Cochlea
Five stages of auditory pathway
Sound wave → Tympanic membrane → Ossicles → Oval window → Fluid in cochlea → Auditory sensory neurons (hair cells)
Ossicles
Handle sound force amplification that is then transmitted to cochlea
Organ of Corti
Contains auditory receptor cells (hair cells)
Number of chambers in cochlea
Three
Endolymphj
A liquid with 150 mM K+ and 1mM Na+
Perilymph
A liquid with 7mM K+ and 140mM Na+
Vibration pathway in ear
Vibrations travel in cochlear fluid → then lead to the vibration of the basilar membrane
Stereocilia
Part of hair cells, have a hair like structure in the apical surface
Have both inner and outer hair cells, IHC and OHC
By bending stereocilia, sounds can cause receptor potential in hair cells
Sensory transduction to depolarize hair cells
As stereocilia bends and tip link is stretched, the mechanically gated K+ channels open and K+ ions enter the cell. Then there is a depolarization and an ensuing calcium influx through VGCC, which then causes the release of the transmitter glutamate
Ratio of IHC to OHC and synaptic output to SGCs
3:1 of OHC to IHC, 1 IHC feeds about 10 spiral ganglion cells (95% of output)
Prestin
Motor protein that can be compressed to result in depolarization of OHC
OHC function for basilar membrane
OHCs amplify basilar membrane deflections, causing further stretching
Cochlear amplifier
Loop mechanism in which the hearing sensitivity is boosted by causing IHC to bend more through the OHC amplifying basilar membrane deflections
Characteristic frequency
The given intensity frequency at which a neuron is most responsive, auditory nerves will still experience a number of spikes per second but have a peak for which they are specially tuned for
Properties of basilar membrane BASE
Stiffer and more narrow, tends to have higher frequency for maximum amplitude
Properties of basilar membrane at apex
More flexible, wider, tends to have have lower frequency for maximum amplitude
Tonotopy
Displays high frequency at the base, low frequency at the apex
The systemic organization within an auditory structure based on the sound frequency, a sensory map
Phase locking
The consistent firing of a neuron at the same phase of a sound wave, which helps encoding for low frequency sound
When does phase locking occur
With sound waves up to 5000 Hz, high frequency sound cannot elicit phase-locked response in neurons
Mechanism at 20-200Hz frequency
Phase locking
Mechanism for 200-5000Hz
Tonotopy and phase locking
Mechanism for 5000 to 20000
Tonotopy alone
Localization of sound in horizontal plane
Requires Interaural Time Delay and Interaural Intensity Difference, also depends on sound frequency
ITD Interaural Time Delay
Difference in time for the same sound to reach each ear, works for frequency range of 20-2000Hz
Interaural Intensity Difference
Difference in intensity of the same sound at each ear, works for frequency range of 2,000 to 20,000 Hz
Superior olive sensitivity
Has neurons sensitive to interaural time delay, as such biaural neurons (from both left and right cochlear nuclei)
Localization of sound in vertical plane
Is based on reflections from the pinna (outer ear), delays between direct path and reflected path changes as the sound source moves vertically
What makes somatic sensory system unique
Broadly distributed, responds to many kinds of stimuli, has many different kinds of sensory neurons
Somatic sensory system enables:
Ability to sense pressure, pain, and temperature, as well as proprioception and interoception
Proprioception
Ability to sense position/movement of body parts
Interoception
Sense of internal organ function
Skin
Beginning of somatosensory system, the largest sensory organ
Touch stimuli
Pressure on the skin
Mechanoreceptors
Used to detect touch
Within Epidermis (upper layer)
Merkel’s disks
Within Dermis (inner)
Pacinian corpuscles, Ruffini’s endings, Meissner’s corpuscles
Receptive field
The region of a sensory surface which, when stimulated, changes the membrane potential of a neuron
Small receptive field size
Meissner’s corpuscle and Merkel’s disk
Large receptive size
Pacinian corpuscle and Ruffini’s ending
Slow adaption
Merkel’s disk and Ruffini’s ending
Rapid adaption
Meissner’s corpuscle and Pacinian corpuscle
Small field size and rapid adaption
Meissner’s corpuscle
Large field size and rapid adaption
Pacinian corpuscle
Small receptive field size and slow adaption
Merkel’s disk
Large receptive field size and slow adaption
Ruffini’s ending
Reasoning behind Pacinian corpuscle’s unique response profile
Due to special ending (corpuscle), as it only fires when the probe makes and breaks contact
How do mechanosensitive ion channels open
Due to the force from the lipid membrane as depolarization occurs, or due to force on extracellular structures like proteins, or from internal forces like cytoskeletal protein
Piezo1 and Piezo2
Mechanosensitive gates, non-selective cation channels that are important for touch sensation, unfurl with force
Gene knockout: Cre
A site specific recombinase that knocks out a gene, cuts out the DNA section between two LoxP sites in the same orientation
Gene knockout: LoxP
A short sequence from bacteriophage P1, which is recognized by Cre
Types of primary afferent axons for somatic sensory system
A alpha, A beta, A S and C, in decreasing order of thickness and insulation
Divisions of spinal gray matter
Dorsal horn, intermediate zone, ventral horn
Abeta axon goes to brain in spinal chord, contains the mechanoreceptors of skin
Segmental organization of spinal cord
Divided in 30 segments between four divisions
Dermatomes
The area of the skin innervated by the right and left dorsal roots of a single spinal segment
Somatotopy
The topographic organization of somatic sensory pathway in which neighboring receptors in the skin feed information to neighboring cells in the target brain structure
A sensory map for touch sensation
The mapping of the body surface on the primary somatosensory cortex
Aα fibers
For proprioceptors of a skeletal muscle
Aβ fibers
Mechanoreceptors of skin
Aδ fibers
Pain and temperature (first pain)
C fibers
Pain temperature and itch (second pain)
Nociceptors
Pain receptor neurons
Types of nociceptors
Mechanical thermal and chemical
Methods of opening ion channels in nociceptors
Strong mechanical stimulation, temperature extremes, oxygen deprivation and chemicals, as well as substances released by damaged cells (proteases, ATP, K+ ions, histamine)
Capsaicin
Spicy, activates TRPV1
TRPV1
Ion channel that responds to both heat and capsaicin
TRP family
Are cation channels activated by various external stimuli