Animal Model 3 Flashcards

1
Q

What other disorders is OCD co-morbid with?

A

Tourette’s, depression, schizophrenia

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2
Q

What are the most common obsessions?

A

doubts, indecisions, contamination, need for symmetry

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3
Q

What are the most common compulsions?

A

checking, washing, counting, hoarding

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4
Q

What is OCD?

A

inability in achieving a sense of task completion

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5
Q

What is the name of the circuit involved in OCD?

A

Alexander Circuit

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6
Q

Which areas of the brain show increased activity in OCD?

A
  • orbitofrontal cortex
  • basal ganglia
  • thalamus
    (direct pathway)
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7
Q

Which drug is used to induce OCD? Class?

A

quinpirole (dopamine D2/D3/D4 agonist)

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8
Q

What type of rat was used in the quinpirole model?

A

long evans rats

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9
Q

What were the main findings of the quinpirole model?

A
  • increased frequency of visit to home base
  • increased rate of visit to home base
  • faster return time to home base
  • less visits to other zones on trips
  • rituals at home base
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10
Q

Does the quinpirole model fit the mckinney criteria?

A
  • similarity of inducing conditions: QNP = D2 agonist –> DA imbalance in humans ass. with social/emotional circumstances?
  • similarity of behavioural state induced: compulsive checking and rituals present –> YES
  • similarity of clinically effective treatments: clomipramine works –> YES
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11
Q

repeated exposure to the startle stimulus results in ___________.

A

habituation or less response

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12
Q

What is prepulse inhibition (PPI)?

A

mild stimulus given before startle stimulus will decrease the startle response

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13
Q

Patients with schizophrenia show ___________ PPI. (excess/deficient)

A

deficient

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14
Q

Which drug disrupts PPI? Class of drug?

A

apomorphine (non-selective DA agonist)

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15
Q

Which drug type can reverse disrupted PPI?

A

antipsychotics

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16
Q

What can a stroke be caused by?

A

middle cerebral artery occlusion (MCAO) –> restrict blood flow –> apoptosis

17
Q

What kind of drugs were developed in the stroke animal models to treat stroke?

A
  • NMDA antagonists
  • Edaravone, free radical scavengers
18
Q

What is multiple sclerosis (MS)?

A
  • CNS directed autoimmune disease
  • T cell mediated inflammation, demyelination, axonal injury
19
Q

What was the animal model for MS? Describe what occurred in this model.

A

experimental autoimmune encephalomyelitis (EAE)

  • immunize rodent with specific myelin peptide (antigen)
  • immune system mounts a response against the myelin antigen (found in brain and spinal cord)
  • weakness/paralysis scored
20
Q

What makes the Cre-Lox system different from other gene manipulation procedures?

A

knock-out/in a specific gene IN A DEFINED POPULATION OF CELLS

21
Q

How do you use the Cre-Lox system?

A

1) flank gene of interest by adding loxP sites on either side
2) Cre recombinase cuts loxP sites

22
Q

What are the advantages of the Cre-Lox system?

A
  • no off-target effects
  • turn on/off your gene manipulation at selected time point
23
Q

What is optogenetics? How does it work?

A

optogenetics: controlling neuronal activity with light

1) ion channel protein (from algae) only opens in response to BLUE light
2) insert protein’s DNA into specific neurons in brain
3) shining BLUE light on those neurons causes firing

24
Q

Which channel is activated by blue light? Is it excitatory or inhibitory?

A

channel rhodopsin (ChR2); excitatory

25
Q

Which channel is activated by yellow light? If it excitatory or inhibitory?

A

Halorhodopsin (NpHR); inhibitory