Module Eight: Behavioural Pharmacology, Psychopharmacology & Neuropharmacology Flashcards

1
Q

What is behavioural pharmacology?

A

Assesses the effects of unknown drugs on behaviours with known neural substrates and psychopharmacological properties
Primarily for novel drug development
Determine potential therapeutic effects of novel drugs

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2
Q

What is psychopharmacology?

A

Uses drugs with known properties to determine the neural substrates of behaviour and understand the mechanisms for CNS disturbances

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3
Q

What is neuropharmacology?

A

Attempts to understand the molecular basis of the neural actions of the drugs

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4
Q

Why have animal models in psychiatric illness?

A

Objective: to determine possible neural causes of illness; to screen for new drugs that may improve the pharmacotherapy of the illness; to increase our understanding of the neural substrates of behaviour

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5
Q

What are the three types of validity in Animal models.

A
  1. Predictive validity
  2. Face validity
  3. Construct validity
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6
Q

What determines predictive ability?

A

True negatives, false negatives: known treatments are predicted to be ineffective

True positives and False positives: known ineffective drugs are predicted to be affective

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7
Q

What does sensitivity refer to?

A

How easily an animal model detects true positives

P HIT/ (p HIT + MISS)

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8
Q

What does specificity refer to?

A

How well a test avoids making false positives

1- p false alarm

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9
Q

What is face validity?

A

Model that has validity based on analogy rather than homology

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10
Q

What is construct validity?

A

The model has sound theoretical rationale

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11
Q

Define: phenomenology

A

The study of structures of consciousness as experienced from the first person point of view

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12
Q

What was the first antipsychotic

A

Chlorpromazine

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13
Q

Tolerance

A

The effect of drug declining with repeated treatment due to a shift to the right in the DCR

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14
Q

Sensitisation

A

Effects of a constant dose may increase with repeated treatment- left shift of DCR

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15
Q

Pharmacokinetic factors altering drug repsponse

A

Induction of metabolising enzymes
Age related changes in mets losing enzymes
Circadian rhythms
Progressive hepatotoxicty/ renal toxicity
Saturation of non specific or lipid / protein binding compartments

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16
Q

Pharmacodynamic factors: post synaptic

A

Receptor density changes
Receptor affinity changes
Efficacy changes

17
Q

Pharmacodynamic factors: presynaptic

A

Changes in release rates of endogenous neurotransmitter

18
Q

What is pharmacodynamic increase of response called?

A

Fast and short term: Reverse tachyphylaxis

Slow and long lasting: sensitisation, supersensitivity, up regulation

19
Q

Pharmacodynamic decrease in response is called:

A

Fast and short term: Desensitisation, auto inhibition, tachyphylaxis

Slow and long lasting: tolerance, down regulation, subsensitivity

20
Q

Receptor density changes

A

Reduction in density with agonists

Increase in density with antagonists

21
Q

Subsensitivity

A

Resultant from a chronic agonist use resulting in a reduction in receptor density

22
Q

Supersensitivity

A

Antagonist chronic use causing increase in receptor density

23
Q

The affinity effects are due to

A

Phosphorylation of sites on the receptor or conformational shifts of the receptor due to occupancy by drug or neurotransmitter