Test One Flashcards

0
Q

Pharmacology

A

Study of properties and effects of drugs on living systems

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1
Q

Drug names

A

Chemical, generic, trade

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2
Q

Main sites of drug action

A

Ligand-gated channel G-protein coupled receptors Kinase-linked receptors Nuclear receptors

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3
Q

Ligand-gated ion channel receptors

A
  • Transmembrane proteins arranged around a central aqueous pore
  • Channel opens in response to a ligand or voltage change
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4
Q

G Protein-coupled receptors

A
  • Transmembrane receptor coupled to intracellular system
  • Subunits alpha, beta, and gamma
  • GTP binds, alpha is released, starts second messenger system
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5
Q

Kinase-linked receptors

A
  • Transmembrane protein
  • Intracellular tail has enzyme activity
  • Binding causes phosphorylation, possibly a cascade
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6
Q

Nuclear Receptors

A
  • DNA-coupled receptors stimulate gene transcription
  • Ligand must be lipophilic - normally steroids
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7
Q

Mechanism of Action

A

Specific cellular changes mediated by a drug that cause a clinically evident response

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8
Q

Receptor Occupancy

A

The number of receptors bound to the drug

Intensity is related to concentration and affinity

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9
Q

Intrinsic activity

A

How much effect does the drug have on receptor action?

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10
Q

Efficacy vs Potency

A
  • Efficacy - the magnitude of a drug response
  • Potency - how much drug is required to reach desired effect
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11
Q

Competitive vs Noncompetitive Antagonist

A
  • Competitive - reduces potency but not maximum effect. Normally competes for receptors
  • Noncompetitive - reduces the efficacy but not potency. Different binding site
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12
Q

Margin of Safety

A

TD50 / ED50

  • The larger the margin, the safer the drug
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13
Q

Hyper-reactivity

A

Response at low dose

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14
Q

Hypo-reactivity

A

No response until a high dose administered

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15
Q

Tolerance

A

Hyporeactivity that results from repeated drug administration

16
Q

Tachyphylaxis

A

Rapid onset of tolerance

17
Q

Idiosyncrasy

A

Unexpected deviation from normal or expected drug response

18
Q

Bioavailability

A
  • Fraction of unchanged drug reaching the systemic circulation
  • IV has 100% bioavailabiltiy
19
Q

Absorption

A
  • Drug entry into systemic circulation from site of administration
  • Depends on route of administration and physiochemical properties of drug
  1. Simple diffusion
  2. Facilitated diffusion
  3. Active transport
  • Compatibility depends on size and charge (ionization)
20
Q

Drug ionization and absorption

A
  • Drugs that are weak acids are non-ionized in an acid solution
  • Vice versa
21
Q
A