lecture 13- modern qs in learning and memory Flashcards

1
Q

what is classical conditioning

A

associating 2 stimuli with eachother
conditional stimulus should precede/ coincide with the unconditional stimulus

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2
Q

describe the T maze test for flies

A

flies exposed to odour A with either sugar treat or shock
after training the flies can choose between A and B (normal odour)
record percentage spent with each odour

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3
Q

describe the Computer method for flies

A

1fly in each chamber
pump in different odours and track movements

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4
Q

describe the olfactory circitory pathway in flies

A

odour -> olfactory receptor neurons -> projection neurons -> kenyon cells

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5
Q

where are kenyon cells located, describe their firing

A

mushroom bodies
they require multiple simultaneous inputs to fire so they fire selectively
sample small regions of 3D space of axon projections

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6
Q

how does dopamine work with kenyon cells to elicit a response

A

dopamineric neurons modify the outputs of kenyon cells

coactivation of kenyon cells and dopamine leads to either reward/punishment response

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7
Q

what is the GAL4/ UAS system used for

A

artificial expression of arbitrary transgenes in specific cells

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8
Q

describe how the GAL4 / UAS system works

A
  • GAL4 gene is placed under control of specific promotor/enhancer
  • GAL4 protein is a TF that binds to UAS
  • the choice of the promotor determines when and where this binds
  • UAS is placed upstream of gene of interest
  • Alone they dont work but when you cross a GAL4 fly with a UAS fly, the offsping inherit both so it activates transcription of the target gene
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9
Q

describe split GAL4 and what this can be used for

A

provides greater specificity in gene expression
GAL4 is split into two separate domains:
DNA-Binding Domain (DBD) – Binds to the UAS but cannot activate transcription alone.
Activation Domain (AD) – Activates transcription but cannot bind DNA alone.

Gene expression occurs only in cells where both DBD and AD are present, allowing precise targeting of specific cell populations.

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10
Q

which 2 structures can divide kenyon cells into certain compartments

A

mushroom body output neurons (MBONs)
dopainergic neurons (DANs)

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11
Q

describe synaptic depression between kenyon cells and their outputs

A

1) DANs in MB release dopamine in response to electric shock

2) DANs activate specific compartments of KC -> MBON synpases

3) dopamine triggers synaptic depression at KC -> MBON synpases which decreases MBON activation in response to conditional odour

4) the next time the fly encounters the same odour, the MBON is weaker so it avoids

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12
Q

How was synaptic depression in kenyon cells proved

A

split GAL4 system

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13
Q

are KC-MBON synapses depressed pre or post synaptically

A

pre

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14
Q

what is paired pulse stimulation

A

stimulate pre-synaptic neuron x2 in quick sucession and record excitatory postsynaptic currents (EPSCs) in the post synaptic neuron

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15
Q

describe paired pulse depression

A

2nd pulse is smaller than first as pre synaptic neuron used lots of vesicles on the first pulse

this means higher release probability (each vesicle has a higher change of being released)

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16
Q

describe paired pulse facilitation

A

2nd pulse bigger than first as leftover Ca2+ in presynaptic terminal from first pulse

this mean low release probability

17
Q

what is the result of a paired pulse test for dopamine ->MBONs and what does this tell us

A

the original paired pulse depression turns into paired pulse facilitation

means presynaptic effect

18
Q

describe learning in insect mushroom bodies

A

training reduces the ‘wrong’ behaviour

19
Q

describe learning in the cerebellum

A

motor learning tries to correct the ‘wrong’ behaviour

20
Q

describe learning in fish

A

they have electroreceptors that receive inputs from electric organ and external electric fields
this allows them to learn to ignore ‘wrong’ electric signals generated by their own electric organ