Week 12 - Pharmacology: Intro to Pharmacodynamics Flashcards

1
Q

What is a drug

A

A chemical substance of known structure, other than a nutrient or an essential dietary ingredient, which, when administered to a living organism, produces a biological effect

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2
Q

What are examples of drugs

A

Penicillin, Aspirin, Caffeine, St John’s wort, Flavonoids (green tea)

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3
Q

What is pharmacodynamics

A

the study of what the drugs does to the body

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4
Q

What are drug targets

A

Any binding site that interacts with a drug
Drug molecules have to interact with the target to have an effect

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5
Q

What do dose response curves show the relationship between

A

drug concentration and pharmacological response. (how much drug is required to produce the desired effect)

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6
Q

What is the threshold in a dose response curve

A

the concentration where effects start to occur

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7
Q

What is EC50 in a dose response curve

A

the concentration where half of the maximum effect occurs

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8
Q

What is the maximum effect on a dose response curve

A

the concentration where the full response occurs

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9
Q

What is efficacy

A
  • the maximum effect that can be produced once binding has occurred. The higher
  • The higher the maximum effect of the drug the higher the efficacy of the drug
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10
Q

What is potency

A
  • The amount of drug needed to provide clinical effect
  • If a small amount is required then the drug has a high potency (ideal)
  • If a large amount is required then the drug has low potency
  • Potency is influenced by both efficacy and affinity
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11
Q

What is affinity

A
  • The amount of binding to receptor the drug does
  • High affinity means that the drug is binding to more receptors at lower concentrations
  • Low affinity means that the drug is binding less and or dissociates more easily from receptors
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12
Q

What type of drugs are receptor binding

A
  • agonist
  • antagonist
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13
Q

What is an agonist

A

Agonist mimic the effect of the ligand (such as neurotransmitters, hormones or other signaling molecules) by binding to the same receptor and producing a similar effect.

It enhances the receptor effect

These can have high affinity and high efficacy

E.g. Type 2 diabetes drug (GLP-1) which mimics insulin receptor to lower blood sugar levels

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14
Q

What are the 2 types of agonist drugs

A
  • full agonist
  • partial
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15
Q

What is a full agonist

A

agonist drug which can achieve maximal response (high efficacy)

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16
Q

What is a partial agonist

A

agonist drug which produces a submaximal response even with high concentration, low efficacy (will never achieve maximum effect)

17
Q

What is an antagonist

A

Antagonist bind to specific receptors in the body without activating them, thereby blocking or inhibiting the action of the substrate that would normally activate the receptor.

e.g. Naloxone

18
Q

What is a reversible antagonist

A

Doesn’t strongly bond to the receptor and can be overridden by a high concentration of agonist

19
Q

What is a irreversible antagonist

A

Forms strong bond to the receptor and cannot be disrupted by an agonist

20
Q

What type of drugs are enzyme binding

A

inhibitors

21
Q

What type of drug are carrier proteins/molecules

A

Drugs which are carrier proteins/molecules act in a similar manner to enzymes and acts as an inhibitor.
E.g. GLUT-4 which lets glucose be taken up by cells or NA+/K+ pump which helps resets the charge of a cell in the production of active potential

22
Q

What is selectivity

A

The ability of a drug to interact preferentially with one type of receptor or target over others. A drug can be specific and only bind to certain or singular receptors, or a drug can be non-specific and bind to several types of receptors.

23
Q

What is specificity

A

Refers tot he degree to which a drug interacts only with its intended target and does not interact with other targets in the body.

A specific drug will interact exclusively with its target without binding to unrelated receptor or molecules.

24
Q

Explain how beta blockers showcase side effects of drugs

A

The B-adrenergic receptor increases the heart rate and has 2 subunits - B1 and B2

Some selective drugs only interact to subunit B1 e.g. dobutamine

Other non-selective drugs interact to both B1 and B2 subunits e.g. propranolol

The issue is that B2 receptors can also be found in other locations other than the hear such as the lungs, blood vessels, GI tract, bladder, uterus , liver. Hence in non-selective drugs effects can be seen on these organs, resulting in side effects such as breathing problems, constipation nausea, dizziness.

25
Q

What are common local anesthetics

A

lidocaine and antiacne

26
Q

What type of drug is local anesthetic

A

antagonic

27
Q

How does local anesthetics work

A
  • Local anesthetic works by blocking the generation and propagation of action potentials in neurons, by blocking the flow of Na+
  • They bind to ion channels and block the flow of Na+
  • By blocking sodium channels it prevents the transmission of nerve impulses along sensory nerves, and hence the sensation of pain is temporarily abolished
  • They are unionized molecules
28
Q

Local anesthetics targets what

A

voltage gated sodium channels - antagonist

29
Q

Does local anesthetics work intracellularly or extracellularly

A

Intracellular