Olfactory system- Johening Flashcards

1
Q

it is important to study the olfactory system because…

a. in many neurodegenerative diseases and especially Alzheimer’s disease, olfactory symptoms ofter occur prior to onset
b. to understand perception of food and consumption of food
c. brain circuitry underlying flavour perception is altered in obese people
d. all of the above

A

d

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2
Q

what is the difference between orthonasal and retronasal smell?

A

Orthonasal smell: direct nasal inhalation of air particles from the environment (we breath in air and sniff food and environment).

Retronasal smell: food consumed by the mouth is chewed–> releases volatile molecules which enter the nasopharynx and travels up to the olfactory epithelium and from there to the olfactory bulb and cortex.

  • retronasal smell is much more important for humans because of food perception
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3
Q

why does hot coffee taste better than cold coffee?

A

volatile layer of HOT coffee molecules travel to the nose much faster and in larger amounts because the high temperature increases broconian motion and diffusion of molecules

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4
Q

what is the advantage of using miniature head microscopes combined with GRIN-lense? what is the procedure?

A

Obesity is a universal problem which is affecting many people all over the world and our understanding of the neuronal mechanisms underlying overeating and obesity is limited.
–> this method allows to look at the cell assemblies that are active while the mouse is eating, and the activity is connected to the sensor at the feeder so number of licks consumed is recorded too.

Procedure:

  • the method images the mouse’s brain while its moving freely, by putting a huge glass prism in the cortex until the puriform cortex is reached.
  • behavioural paradigm: sensory specific satiety - mouse drinks a lot of milkshake in the first trial and consumption decreases in the next bouts, because cells adapt to the smell of milkshake after the first trial –> signals satiation
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5
Q

describe the physiological reaction to smell (steps)

A
  1. odourant molecules go through the nose and bind to 7-TM-G-protein
  2. conformational change of G-protein
  3. ß-gamma and G-protein components are dissociated
  4. G-protein binds to adenylate cyclase
  5. cAMP channel opens
  6. Na+ and Ca2+ flow in and depolarise the cell
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6
Q

which of the following statements about olfactory receptor neurons (ORN) is/are correct?

a. ORNs can express various types of olfactory receptors
b. ORN are specific to smell types like ‘coffee’ or ‘chocolate’
c. ORN are not specific to single molecules but rather they react to chemical groups
d. odourants activate different ORNs in the same intensities

A

c

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7
Q

which of the following statements is WRONG?

a. odour coding starts already at the level of nasal mucus
b. subtle structural changes result in fundamentally different smells
c. different odourants activate different receptors at changing intensities
d. odour coding starts in the olfactory cortex

A

d

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8
Q

olfactory projection…(which of the following statements is/are correct?)

a. ORN are everywhere but they converge and project to 2 specific glomeruli in the olfactory bulb
b. this convergence is acquired during childhood (exposure)
c. odours are deconstructed to their components in the olfactory bulb, and then reconstructed and mixed in the cortex
d. single glomerulus project to a single neuron in the olfactory cortex
e. neurons in the olfactory cortex respond to groups of glomeruli.

A

a, c, e

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9
Q

what is the population code?

A

population code is a term that describes odour processing of olfactory signals in the cortex.

  • -> odours are deconstructed to their chemical components in the olfactory bulb, but when the info is projected to the cortex the signals are mixed.
  • -> large neuronal cell assemblies in the olfactory bulb respond to groups of glomeruli–> population code
  • -> distinction between odour components is lost
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10
Q

how can you empirically test if it is possible to distinct between components of smell? (study + results)

A
  • 2 test groups: wine experts and naive subjects
  • test: subjects exposed to a number of smells with increasing complexity–> asked to identify the smell and components
  • results: very small difference between the groups as complexity of the smell goes beyond 3-4 components.; but experts perform better in deconstructing simple smells.
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11
Q

how are cell assemblies formed in the olfactory cortex, and what are the benefits of assembly formation?

A
  1. external stimulus
    - -> 2. activation of neuronal population by stimulus
    - ->3. activity continues after stimulus is gone (creation of engram)
    - -> 4. Hebbian modification strengthens reciprocal connections between neurons in the same assembly
    - -> 5. strengthened connections contain the engram for the stimulus

–>When partial stimulus comes–> partial activation of the assembly lead to activation of the entire assembly (representation of the ‘full’ stimulus

Advantages:

  • even parts of the olfactory stimulus can activate the assembly and generate a behaviour
  • good for dangerous smells or smells that trigger memories - we can recognise the dangerous smell even when it is partial or low intensity and still react to it.
  • pattern completion- reconstruction of engrams
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12
Q

what are sister cells?

A

sister cells are group of mitral cells that send apical dendrites to the same glomerulus

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13
Q

what are the advantages of the convergence of cells in the olfactory bulb?

A
  • olfactory neurons keep rebuilding (consistent, 2 week turnover) and by converging into the same glomerulus, centrally, they increase the stability of the system, as they wire up and the same smells can be identified easily.
  • optimisation of the detection of smells at low concentrations
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14
Q

which of the following statements is/are correct?

a. glomeruli have a Ih pacemaker current (H-channel) that activate upon hyperpolarisation
b. H-channel resets the neuron to a different potential - hyperpolarisatio and direct depolarisation after (Sag current)
c. H-channel is activated upon depolarisation
d. H-channel decreases response at the dendrite and increases input at the soma
e. cells from different glomeruli the H-current varies dramatically in comparison to sister cells.

A

a, b, e

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15
Q

which of the following statements about information coding of smell is/are correct?

a. number of generated APs decreases with increasing odour concentration
b. changes in firing rate occurs in the bulb, and it is the strongest during adaptation to smell.
c. information coding depends on spatial population dynamics but not on temporal population patterns.
d. information coding contributes to generation of oscillations by the olfactory bulb.
e. all of the above

A

b, d

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16
Q

the olfactory bulb transforms linear output from ORN into oscillations. Which frequencies correspond to which function of information processing (initiation, discrimination, memorisation)

A
  1. Initiation- Theta (slow wave), associated with respiration
  2. odour discrimination- low gamma (40-60 Hz) and high gamma (60-100 Hz)
  3. memorising odours- ß (20 Hz)
17
Q

which of the following statements about oscillations is/are correct?

a. oscillations can occur together (in parallel to each other)
b. Oscillations decrease with more exposure/inhalation of the same smell
c. studies have shown that oscillations differ in type and intensity according to behavioural state of the subject (hungry/satiated)
d. oscillations contribute to functional connectivity in the olfactory bulb
e. oscillations have spatial advantage

A

c

18
Q

Mitral cells…

a. integrate primary and secondary dendritic shafts and connect glomerular and mitral cell input
b. generate unidirectional APs
c. the dendrites of mitral cells can be described as passive cables
d. when AP fire in mitral cells there is depolarisation of the cell
e. all of the above

A

a

19
Q

how could we prove the active conductance in dendrites of mitral cells?

A
  • addition of TTX (blocks Na+ channel) decreases dendritic response.
20
Q

describe the reciprocal feedback/recurrent inhibition in the olfactory bulb

A
  1. mitral cell (MC) fires
  2. AP travels via dendrite to granule cell (GC-inhibitory)
  3. AP releases Glu from MC to GC
  4. GC is depolarised –> EPSP in GC increases Ca2+ in dendritic spine of GC
  5. Ca2+ triggers SV release of GABA from GC to MC
  6. hyperpolarisation of MC
21
Q

how does the reciprocal feedback inhibition affect the release probability of mitral cells?

A
  • Glu released from MC activates both fast AMPA and slow NMDA receptors
  • -> fast AMPAR increase Ca2+ release
  • -> slow NMDAR require coincident depolarisation to relieve the Mg2+ block (modulatory function)
  • -> the more depolarisation by AMPAR the more Mg2+ block is relieved from NMDAR–> CA2+ increase through NMDAR increases release probability
  • -> increased Ca2+ concentration triggers GABA release from GC –> hyperpolarisation –> decreased release probability of MC
22
Q

what are cortico-bulbar loops?

A

cortico-bulbar loops are connections between the olfactory cortex and the olfacory bulb.

  • cortical inputs can be modulated via glutamatergic inputs
  • these mechanisms are governing the connections between hunger and olfaction
  • connections in the piriform cortex can work together to modulate food intake
23
Q

which of the following statements about endocannabinoids is/are correct?

a. the endocannabinoid system is activated upon hunger
b. THC in cannabis decreases endocannabinoid release
c. the endocannabinoid system controls food intake via the olfactory system
d. THC increases odour sensitivity and thus increases threshold for food intake
e. THC increases Glu release from mitral cells

A

a, c, d

24
Q

how did they prove causality between THC and hunger?

A

to investigate the interaction between portico-bulbar fibres and cannabinoids and prove the causality between hunger and THC they conducted a 3 part experiment:

  1. behaviour: food exploration task
    - 4 groups: control- A. WT B. WT+ THC, C. KO of THC receptor (w/o THC administration), D. KO of THC receptor (w. THC administration)
    - results:
    A. WT only start exploring after increasing odour concentration to 0.1%;
    B. WT+THC-receptor response increases massively
    C. & D. KO THCR (w. and w/o THC) behave like WT (A)
    –> correlation but no causation
  2. physiology: optogenetics
    - activation of piriform cortex with light
    - -> one can see the field potential and activation of GC
    - -> record synaptic input from GC and spiking of MC
    - -> injection of WIN (agonist for CB1R): decrease in EPSP amplitude –> cannabinoid decrease signalling
    - -> still no causality
  3. A. loxP-cre to create local KO CB1- decreases food intake (because activity of GC is not down regulated)
    when portico-bulbar fibres are taken out- effect is gone!
    B. stop-codon of CB1 is removed (over expression)–> food intake increases.

–> THC reduces GABA input so there is no inhibition and subject eat more!