week 5+6+7 (gustatory) Flashcards

(33 cards)

1
Q

question: which papillae are associated with which cranial nerves?

A
  • circumvallate = CN IX glossopharyngeal
    ⤷ back border of tongue
  • fungiforme = CN VII facial
    ⤷ tip of tongue
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2
Q

explain: taste bud (function, structure)

A
  • has the receptor cells to transduce chemicals signals after exposure to tastant
  • not a neuron
    ⤷ considered neural epithelial cells
  • regenerated by basal cells
  • has microvilli
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3
Q

name + explain: types of papillae (4)

A
  1. circumvallate
    - v shaped border
    - posterior part of tongue (back border)
    - least in #
  2. fungiform
    - mushroom shaped
    - around surface (scattered)
    - each have 1 - 8 taste buds
    - receptors for pressure and temp
  3. filiform
    - flame shaped
    - scattered across tongue
    - rough surface to manipulate food
    - no taste buds
    - most abundant
  4. foliate
    - leaf shaped
    - lateral (sides)
    - 1300 taste buds w/in the folds
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4
Q

name + explain: types of taste receptor cells (3)

A
  1. type I
    - glial-like functions (support)
    - no recep. for tastants
    - around 50% of the cells
  2. type II
    - resp. to sweet, bitter, and umami
    - 1/3 of the cells
    - G-prot. coupled receptors
    - no synapses with afferent fibres
    - releases ATP -> activates nearby neurons
  3. type III
    - 2 - 20% of the cells
    - has synapses with afferent fibres
    - can indirectly resp. to bitter, sweet, and umami bc reacts to the NT release by Type 2
    - used to detect sour
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5
Q

question: which receptor type mediates salty?

A
  • unsure
  • possibly a type 4
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6
Q

question: which receptor type mediates with tastes? what mechanisms do each use?

A
  • type 2 = sweet, bitter, umami
  • type 3 = sour
  • ion channels = salty, sour
  • GPCR = sweet, bitter
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7
Q

explain: ion channel mechanism for taste

A
  • for sour and salty
  • tastant enters cell
    ⤷ Na+ for salty, H+ for sour
  • proton binds to K+ channel
  • closes the K+ channel -> depolarization -> message to brain about tastant
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8
Q

explain: GPCR mechanism for taste

A

BITTER
- type 2 taste receptors (t2r)
- usually tastant = ligand containing alkaloid (ex. quinine)
- monomers or dimers

  • GPCR activated
  • depol. indirectly
    ⤷ activates phospholipase -> breaks down PIP2 into IP3 -> IP3 binds to channel to open and release Ca+
  • Ca+ open and Na+ and K+ activated
    ⤷ increased Ca+ intracellularly

SWEET
- type 1 taste receptors (t1r)
- tastant = sugars
- heterodimers

**Ca+ causes serotonin release
⤷ for type III

**bitter uses phospholipase, PIP, IP
**sweet uses gustudin, cAMP, protein kinase

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9
Q

question: which cranial nerves innervate taste receptors?

A
  • facial
  • glossopharyngeal
  • vagus
    ⤷ for throat
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10
Q

question: struc. of taste neurons?

A
  • pseudounipoloar
  • cell bodies in ganglia
  • peripherals endings in tongue + mouth
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11
Q

question: does different parts of the tongue taste different flavours?

A
  • no
  • not diff. receptors for each flavour
  • diff. thresholds for diff. areas -> diff. sensitivities in each area

**more sensitivite = lower threshold

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12
Q

question: labeled line coding vs cross fibre coding?

A
  • labeled line/parallel processing = diff. recept. are responsible for transmitting highly specific info
    ⤷ aka each receptor = specialized for a taste
  • cross fibre = diff. qualities of a sensory modality are distinguished by pattern of nerve discharges across a large pop. of fibres
    ⤷ aka receptors resp. to multiple tastes so the perception is from the pattern of activity
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13
Q

name: evidence that taste signals are combinatorial

A
  • some taste recep. are selectively sensitive to certain tastants
  • show resp. to multiple tastants vs only resp. to one tastant
    ⤷ generalists vs specialists
    ⤷ type III (sour) = generalist, type II (sweet, bitter, umami) = specialists
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14
Q

explain: the combinatorial model of taste

A
  • specialists and generalists converge onto afferent axons
  • axons less sensitive
  • get resp. from large # of broadly tuned neurons
    ⤷ so it takes the pattern of activation across the neurons (cross-fibre)
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15
Q

explain: order of gustatory processing in brain

A
  • taste transmitted to cranial nerves
  • nucleus of solitary tract
    ⤷ in medulla
  • project to a nucleus in the thalamus
    ⤷ VPMN (ventral posteromedial nucleus)
  • primary gustatory cortex
    ⤷ in frontal lobe in sylvian fissure (insula)
  • secondary taste cortex (for higher aspects)
    ⤷ sends to amygdala or hypothalamus
    ⤷ amyg = emotion, hypothal = motivation
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16
Q

question: how is label line coding supported by brain?

A
  • cells in insular cortex (primary gustatory cortex) = preferentially sensitive to diff. tastes
17
Q

define: basic taste

A
  • any of the 4 taste qualities used to describe human taste exp.
  • sweet, salty, sour, bitter
  • hardwired effect to be born liking or disliking them
    ⤷ innate
18
Q

explain: importance/purpose of each basic taste

A

SALT
- Na important to maintain nerve and muscle function

BITTER
- often indicate poison and toxicity

SOUR
- acids damage external and internal body tissues

SWEET
- sugar = principle energy source for humans

**taste provides info about what we should/should not ingest
⤷ nutrient = sodium and sugar
⤷ antinutrient = acid and poison

19
Q

question: what is umami and fat?

A

UMAMI
- savouriness
- claims that it signals protein

FAT
- fatty acids = attached to a support structure
- some broken down in mouth
⤷ most in gut

20
Q

question: what makes a basic taste? (how to decide/requirements?)

A
  • receptors found in mouth
  • activating the receptors leads to distinct sensations
  • hardwired affect (innate)
21
Q

name: support and against for umami and fatty being added to basic tastes

A

SUPPORT
- receptors in mouth can regulate palatability of prot. and fat

AGAINST
- proteins and fat = large molecules
⤷ mostly broken down by digestion
- have receptors for AA and fats that don’t relate to taste
- umami and fat don’t have hardwired like/dislike
- conscious sensations of fats are from somatosensory system

22
Q

question: how does miraculin work?

A
  • binds to sweet receptors
    ⤷ t1r2 and t1r3
  • does not activate the sweet receptors
  • exposure to lower pH makes miraculin activate the receptors -> sour tasting like sweet
  • neutral pH = blocking sweet recep.
  • acidic pH = activates sweet recep.

**acidity causes change in shape of miraculin from inhibitory to activator

23
Q

define: supertaster

A
  • indiv. whose perception of taste is themsot intense
  • dep. on density and number of fungiforme papillae and genetics
24
Q

question: specific hungers theory?

A
  • missing nutrients are craved
  • this theory got debunked
25
question: how do food preferences develop?
- olfactory = important when nutrients aren't labelled by taste - like/dislike foods based on the consequences of eating them ⤷ ex. nausea -> negative - innate preferences **preferences are learned
26
question: electrogustometry vs chemogustometry?
ELECTRO - deliver smaller elec. current through electrode to specific point on tongue - discrete (stim. specific points on tongue) - fast - can measure detection thresholds - good for locating lesions in taste pathways CHEMO - stim. = chemical solutions onto tongue - can be regional or whole mouth - more time consuming
27
name + explain: taste abnormalities (3)
1. **ageusia** - total loss of taste - injury to gustatory nerves 2. **hypogeusia** - reduction in taste sensitivity - from dry mouth, smoking, illnesses 3. **dysgeusia** - taste perceptions are distorted - ex. sweet things taste salty - ex. metallic taste for cancer patients
28
question: rank the basic tastes' thresholds
bitter < sour < salty < sweet **higher threshold for bitter, lower threshold for sweet **smaller amount of sweet needed to taste sweet
29
question: what are taste detection thresholds affected by?
- other tastants (masking) - temperature - location on tongue - age - stim. area - genes
30
explain: adaptation vs cross adaptation for taste
ADAPTATION - prior and ongoing stim. reduces perceived intensity to a tastant - time req. dep. on conc. of tastant CROSS ADAPTATION - perceived intensity of a compound decreases because adaptation to a diff. compound of the same taste quality - ex. lemonade tastes more sour after a dessert **basic tastes don't cross adapt (consisten w/ labeled line coding)
31
define: mixture suppression (masking)
- one taste quality suppresses another ⤷ ex. sugar in tonic water makes water taste less bitter
32
explain: PTC experiment (genes involved)
- PTC = phenylthiocarbamide - PROP = propylthiouracil - PTC and PROP taste bitter to some indiv. - PTC and PROP bind to bitter recep. encoded by **TAS2R38 gene** - taster = perceives PTC/PROP as bitter ⤷ has 1 - 2 dom. versions of TAS2R38 gene - non taste = unable to taste PTC/PROP ⤷ or needs higher conc. (to meet thres.) ⤷ has 2 recessive versions of TAS2R38
33
question: why don't artificial sweeteners work for dieters?
- only need small amounts to taste sweet - but metabolic benefits weren't matching the sweet taste so people ate more to compensate and get the calories to match