Clinical Pharmacology Flashcards

1
Q

what is pharmacodynamics?

A

what the drug does tothe body
i.e. The action of a drug:
What does it target?
What is the response?

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2
Q

what is pharmacokinetics?

A

what the body does to the drug
i.e. Movement of drug within the body:
Where does the drug go?
Therapeutic plasma concentration

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3
Q

what is clinical pharmacology?

A

the study of clinical effects of a drug on patients

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4
Q

what interacting consideration do you need to take into account when using theraputics?

A
  1. underlying disease factors Importance of diagnosis leads to specific therapeutics goals
    But there can be a case for symptomatic therapy
  2. drug data
    efficacy and safety, licensed, off-lable, formulation
  3. owner needs
    financial, physical ability
  4. paitent factors
    can it be administered, special situations (pregnancy, laction, elderly)
  5. practice
    corporate practices, drug buying power,shelfstock and turnover
  6. compliance
    training and eductaion, theraputic option (long-term)
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5
Q

what are the 6 molecules that drugs target?

A
  • receptors
  • ion channels
  • structural proteins
  • enzymes
  • carrier molecules
  • DNA
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6
Q

describe the agonist does response curve

A
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7
Q

explain what a partial agonist is?

A

will only elicit a partial response,

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8
Q

what is potency?

A

the amount of drug required to produce 50% of its maximal effects (ED50).
used to compare drugs within a chemical class

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9
Q

what is efficacy?

A

the maximun theraputic response that a drug can produce (eg morphine vs buprenorphine)

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10
Q

what is drug specificity?

A

the capacity of a druf to cuase a particular action on a popultaion

Example: a drug with absolute specificity of action might decrease or increase the specific function of a given target. It must do either, but not both.

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11
Q

what is drug selectivity?

A

relates to a drugs ability to target only a selective population ie cell/tissue/signally pathway, protein ect in preference to others

Example: Atenolol is a B1-selective adrenoreceptor antagonist, while propranolol is a non-selective B-antagonist

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12
Q

how do you calculate the therapeutic index of a drug?

A
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13
Q

how do competative antagonists work?

A

Competitive antagonists compete with agonists for the receptor binding site
Antagonist binds to receptor in such a way as to prevent agonist binding

Competitive antagonism is surmountable – additional agonist can overcome the receptor blockade.

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14
Q

how do non-competative antagonsits work?

A

Either bind to a different receptor site or block “post” binding chain of events (i.e. act “downstream” of the receptor)

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15
Q

what dose a competative antagonist do to the agonist dose response curve?

A

shifts the agonist dose responce curve to the right in parallel

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16
Q

in what 4 ways can drugs act on enzymes?

A
  • competative inhibitor binds to catalytic (active) site - normal reation inhibited
  • non-competative inhibitor - binds to enzyme not at the catalytic site and the shape of the catalytic site changes preventing substrate binding
  • false substrate - will bind to catalytic site and will produce an abnormal metabolite
  • prodrug - bide to catalytic site, are converted and the active drug is produced
17
Q

what is tachyphylaxis?

A

loss of target sensitivity
the effect of a drug is decreased when given continuously or repreadedly (normally agonists)

18
Q

why does tachyphylaxis occur?

A
  • Change in receptors (become resistant to drug stimulation/conformational changes)
  • Loss of receptor number
  • Exhaustion of mediators
  • Increased metabolic degradation of the drug
  • Physiological adaptation (crosstalk between body systems, one takes over)
  • Drug transporters (active extrusion of the drug)