PharmacoDYNAMICS Flashcards

1
Q

Define: THERAPUTIC EFFECT

A

What we want to see/happen

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2
Q

Define: SIDE EFFECT

A

Effect that is secondary to the intended effect… that may be good OR bad

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3
Q

Define: ADVERSE EFFECT

A

Effect that is UNINTENDED and UNWANTED. This includes not producing a desired clinical effect.

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4
Q

The study and monitoring of adverse effects is called

A

PHARMACOVIGILANCE

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5
Q

Define: TOXIC EFFECT

A

Responses to a RX that are harmful to the health or life of the animal

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6
Q

Drug action can be divided into these 2 categories:

A

PHYSICAL INTERACTIONS

BIOLOGICAL INTERACTIONS

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7
Q

Osmotic Diuretics, Antacids (direct neutralizes), and Radioactive Iodine are in what drug action category?

A

PHYSICAL

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8
Q

these molecules move through the body dragging water with them by osmosis until they are excreted.

A

OSMOTIC DIURETICS

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9
Q

Given orally they directly interact with acid in the GI tract, a form of physiologic antagonism.

A

ANTACIDS (direct neutralizes)

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10
Q

The iodine is actively concentrated in the thyroid (as all iodine is) and the radiation will destroy all tissue within 2-3mm causing focal, controlled destruction

A

Radioactive Iodine

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11
Q

What are Biological Interactions?

A

Receptors (signal-transduction) – specific recognition sites for a ligand

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12
Q

Ionotropic receptors

A

Open when ligand binds, RX binding can open the receptor OR antagonize (keeping it closed), Fast transmission– Nicotinic Ach

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13
Q

Metabotropic receptors

A

G-Protein coupled receptor/7TM

  • Receptor on outside that RX binds to > G-proteins on inside then talk to GTP > GTP tells them what to do depending on signal muscarinic Act/PNS
  • Slow secreting
  • Smooth Muscle
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14
Q

Kinase-coupled receptor

A

Talks to the outside
-Signal talks directly to enzyme
-NO G PROTEIN
(insulin and other hormones)

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15
Q

Nuclear receptors / Transcription factor receptors

A
  • Found in cytoplasm

- Bind to ligand > go into nucleus > effect DNA > Initiate transcription

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16
Q

__________: is an increase in the number of receptors resulting in an increase in the effect of the drug

A

UP-REGULATION

17
Q

__________: a reduction in effect. Can occur as part of developing tolerance. More common normal metabolic effect from body

A

DOWN-REGULATION

18
Q

Agonist

A

-Mimics the effect of the endogenous ligand

19
Q

_______: binds to the receptor to elicit a maximal response

A

FULL AGONIST

20
Q

_______: cannot reach strongest effect. Prevents anything else from binding to receptor while its “docked” there. Lower efficacy.

A

PARTIAL AGONST

21
Q

The “Ceiling Effect” is…

A

Can’t reach max effect aka partial agonist

22
Q

will bind to the receptor and cause the opposite effect as the endogenous ligand would (note that this is different from an antagonist

A

REVERSE AGONST

23
Q

Antagonist (or ‘neutral agonist’)

A

Binds to the receptor but does nothing on its own, however it sits there and prevents anything else (like an agonist) from binding and thus blocks the receptor.

24
Q

What is Competitive antagonism?

A

RX binds to where something should be… blocking receptor.

Whatever is higher in concentration will win and bind to receptor

25
Q

What is Non-Competitive Antagonism?

A

Changes receptor that blocks it ability to bind to the normal ligand. Doesn’t matter who is in higher concentration

26
Q

Non-Receptor Antagonism:

A
  • Chemical
  • Physical
  • ADME
27
Q

_________: Acts as an agonist in one type of receptors and as an antagonist on other types of receptors

A

Mixed agonist-antagonist

28
Q

Efficacy

A

Max effect a RX can have

29
Q

Potency

A

2 RX’s can have the same efficacy, but comparison of two drugs need to induce the same maximal effect

30
Q

Onset of action

A

Time between admin of RX and its effect

AKA latent period

31
Q

Duration of action

A

Time between effect and termination of effect

32
Q

Define PharmacoDYNAMICS….

A

What the DRUG DOES to the animal