6.9 Pharmacodynamics and Drug Receptor Mechanisms Flashcards

1
Q

What are common biologic targets for drugs?

A

1) Enzymes (activate/inhibit)
2) Receptors (G protein coupled; Tyrosine Kinase)
3) Ion channels
4) Transport proteins
5) DNA/RNA and ribosomes
6) Targets of monoclonal antibodies

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2
Q

What determines the magnitude of the response?

A

Depends on the number of receptors/drug interactions.

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3
Q

Describe receptor states

A

Receptors have active state and inactive states, most receptors work slightly even without ligand. The inverse agonist completely shuts this basal level off.

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4
Q

Which bond is the strongest?

A

Covalent bonds

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5
Q

What are other types of bonds?

A
  • Electrostatic-more common but not as strong as covalent.
    1) Ionic bonds
    2) Hydrogen bonds
    3) Dipole interaction
  • Hydrophobic bonds
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6
Q

Describe the effects of receptors on drug effectiveness.

A
  • Receptors are responsible for selectivity of drug action.
  • Receptors mediate the actions of pharmacological agents.
  • Receptors determine quantitative interaction between dose or concentration and pharmacological effects.
  • Components of a cell or organism that interacts with a drug and initiates activity that leads to observed effects.
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7
Q

What is a full agonist?

A

Stimulates maximum effect

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8
Q

What is a partial agonist?

A

Stimulates partial effect

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9
Q

What is an inverse agonist?

A

Binds to a receptor and causes an opposite effect of the agonist, turns off basal activity of receptors.

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10
Q

What is an antagonist?

A

Binds to the receptor compete with and prevent binding by other molecules.

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11
Q

What are the two types of antagonist?

A

Competitive and non-competitive

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12
Q

Describe a competitive antagonist

A
  • Binds to active site and prevents agonist from binding.

- reversible

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13
Q

Describe a non-competitive antatgonist

A
  • Can bind to an active site or allosteric site and blocks binding.
  • Irreversible
  • Binds active site with covalent bond or high affinity
  • At allosteric site prevents receptor activation by agonist.
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14
Q

What is a non-receptor antagonist?

A
  • Chemical- two drugs combine and neutralize activity. Example Protamine (basic) binds to heparin (acid)
  • Physical- Receptor is activated facilitates an effect that is opposite of the antagonist.
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15
Q

What does it mean if a molecule is chiral?

A
  • Chiral substances possess a unique architecture such that despite sharing identical molecular formulas, atom-to-atom linkages, and bonding distances, they cannot be superimposed.
  • Must have 4 unique side chains.
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16
Q

What handedness are most sugars?

A

D-sugars

17
Q

What handedness are all amino acids for life?

A

L-amino acids

18
Q

What direction is chiral L?

A

Counter-Clockwise

19
Q

What direction is chiral D?

A

Clockwise

20
Q

What is the most important amino acid?

A

Glutamate

21
Q

How are most drugs sold in relation to chirality?

A

Racemix 50/50

22
Q

What is tolerance?

A

Occurs when responsiveness decreases as a consequence of continued drug administration

23
Q

What is tachyphylaxis?

A

Rapid appearance of progressive decrease in response to a given dose after repetitive administration of a pharmacologically or physiologically active substance.

24
Q

What is desensitization?

A

When receptors and cell response diminishes by a drug or ligand, can have underlying tolerance but does not have to.

25
Q

What is homologous desensitization?

A

Decrease response at a single type of receptor

26
Q

What is heterologous desensitization?

A

Decreased response at two or more receptors

27
Q

What is refractoriness?

A

State when time is required to pass before receptor can be stimulated again. Example voltage gated sodium channels

28
Q

What is down-regulation?

A

Prolonged stimulation leads to endocytosis and sequestration of receptors.