Pharmacology and Agonists Flashcards

1
Q

AGONIST

A

Activates the (β-2) like adrenaline

Mimic the key in the lock and key model

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2
Q

Antagonist

A

Block the (β-1); decreases heart rate

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3
Q

Adrenaline

A

Activates a and b adrenoceptors

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4
Q

Dopamine

A

Binds to dopamine receptors

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5
Q

Receptor, as molecular switch;

A

Receptor receives the drug > and then binds which activates it > response

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6
Q

Salbutamol (anti-asthma) - AGONIST

A

acts on same site where adrenaline binds to the B-2 receptor and gives a SIMILAR physiological response

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7
Q

Propanolol (Anti-hypertensive) - ANTAGONIST

A

Block B-2; decreases heart rate

it binds to the receptor where Receptor, as molecular switch
is meant to go = BLOCKS adrenaline

can’t occupy the receptor
will not be ay response for the adrenaline

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8
Q

ability of drug to bind to receptor is

A

affinity

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9
Q

Agonists have both ‘a_____’ and ‘e_____’

A

affinity
efficacy

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10
Q

ability of drug to have a pharmacological response on receptor (activate the receptor)

A

efficacy

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11
Q

Antagonists have only ‘affinity’ (no efficacy)

A

therefore does NOT activate the receptor - blocks receptor to chemicals

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12
Q

Free drug and sub-drug will reach _____ .
Ratio will be equal.

A

equilibrium

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13
Q

Drug action measures? Binding (association & dissociation)

A

D + R <> DR
Law of mass action
forward and backward reaction will be equal

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14
Q

k

A

rate constant

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15
Q

equation to measure drug action

A

[D] [R]/ [DR]= k reverse rate / k forward rate = kD

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16
Q

kD

A

Equilibrium Dissociation Constant

17
Q

Drug action measures?
What is the equation for; Receptor occupancy?

A

X = DR
1-X = R

D + R <> DR

kD = [D][R] / [DR] = [D] (1-X) / X

kD = [D] (1-X) / X

X = [D] / [D] + kD

18
Q

What would be the receptor occupancy?

A

x = kD / kD = kD = 0.5

19
Q

kD ALSO defined as the conc of drug required to occupy __% of receptors: MEASURE OF DRUG AFFINITY

A

50

20
Q

the lower the conc the receptor the _____ the % measure of drug affinity

A

higher

21
Q

lower kD value; what kind of affinity

A

drug is well bound to receptor - better affinity

22
Q

parabolic curve

A

when arch is very steep and line goes straight at end

23
Q

how to easily figure out the 50% occupancy?

A

sigmoid curve

put drug conc in Log (M) - curve will be easier to identify when 50% is occupied

24
Q

1000 micromolar = millimolar

A

1 millimolar

25
Q

Rmax is the

A

maximum occupancy (saturated)

26
Q

Agonist Potency:

A

EC50 - Effective Concentration of agonist for 50% response

27
Q

Potency (EC50) is often lower than Affinity (kD)???
1. drug effect
2. drug binding

A

drug effect comes before (lower) drug binding

28
Q

receptor > response

A

amplification of signals

29
Q

Spare receptors/ receptor reserves

A

if there are antagonist (going to use them up)

agonist CANNOT bond to receptors

30
Q

if occupation is at 50% what will the percentage of response be?

A

100%

31
Q

if agonist produces less than 100% max response with maximal receptor occupation - the response:

A

40% (lower)

32
Q

partial agonist good or bad drug?

A

appears to be an effective and possibly a superior treatment option for patients with schizophrenia

33
Q

What is the best agonist - related to graphs

A

one showing a maximal response (steep line)

34
Q

Which drug is least potent?

A

calculate both on graph potency and compared

what is the drug conc when the response is at 50%?