Drug Receptors and Pharmacodynamics Flashcards

1
Q

Define receptor

A
  • Proteins (usually) on a cell membrane, transmembrane receptors
  • Bind ligands
  • Involved in signal transduction
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2
Q

Ligand

A

a molecule that is a drug, hormone, neurotransmitter that bind to a receptor

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3
Q

Drug-receptor complex

A

the receptor and ligand together, initiate changes in the activity of the cell via signal transduction

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4
Q

Signal transduction/cascades

A

conversion of external signal into internal signal

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5
Q

Ligand-gated channels

A

i. Regulate the flow of ions through plasma membranes
ii. Activated by a ligand
iii. Binding of ligand causes conformational change in receptor, allows ions to travel through channel

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6
Q

Enzyme linked receptors

A

i. Linked to enzyme in cell
ii. Made up of subunits
iii. When ligand binds, subunits fuse in conformational change
iv. Activated receptor phosphorylates tyrosine kinase → downstream signal
v. Ex insulin

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7
Q

G-protein linked receptor

A

i. Largest group
ii. Large, folded, transmembrane polypeptide
iii. Contains a G protein in plasma membrane near receptor which interacts w/ GDP and GTP
v. When ligand binds, activates g protein and GTP binds alpha subunit – activated G protein can lead to cascade of reactions:
1. Secretion of substances from cell
2. Ion channels open
3. Transcription

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8
Q

Intracellular receptors

A

i. Ligand is lipid soluble, passes through cell membrane
Ex. Corticosteroids
iii. Bind intracellular receptors in cytosol
iv. Ligand-receptor complex into nuclear membrane where binds with DNA to produce mRNA which produces proteins
vi. Actions:
1. Transactivate: increase rate of gene expression
2. Transrepress: one protein represses the activity of another protein

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9
Q

Agonist

A

drug that activates a receptor, elicits a response

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10
Q

Partial agonist

A

produces lower response when it occupies the receptor

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11
Q

Antagonist

A

drug binds to receptor and prevents activation of receptor. Reduce the effects of agonists (another drug or endogenous substance) that usually activate that receptor

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12
Q

Competitive antagonist

A

drug binds to same receptor as agonist; Reversible, weak, short duration

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13
Q

Noncompetitive antagonist

A

Drug binds receptor at site different from the agonist binding site:
• Usually (nearly) irreversible
• Effects cannot be overcome by adding more agonist
• Effect is long-lasting, dependent on turnover rate of receptor molecule

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14
Q

Chemical antagonist

A

drug directly binds an agonist, deactivating it; Ex: antacids neutralize gastric acid

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15
Q

Physiologic antagonist

A

drug has opposite effect through diff physiologic pathway; Ex: . Insulin and glucagon. Overcome insulin’s effects by adding glucagon

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16
Q

Down regulation

A

Type of desensitization; Ligand binding accelerates endocytosis of receptors. Then degraded and rebuilt. When process occurs faster than receptor synthesis, run out of receptors and cell can’t bind ligands

17
Q

Desensitization (aka tolerance)

A

o Common with agonists
o Attenuation of drug’s effects over time even in continued presence of agonist.
o Often rapidly reversible, second agonist response after termination of first exposure will result in similar response as initial

18
Q

Potency

A

o Concentration of drug needed to produce 50% of drug’s max effect
o Used to differentiate between agonists that have variable affinity for a receptor.
• More potent if produces effect at a lower concentration

19
Q

Dose response curve

A

o X axis: concentration of drug
o Y axis: response
o Might have 2 curves on one graph to represent desired effect vs. toxic effect at higher dose

20
Q

Efficacy

A

greatest response at a dose. How well it works

21
Q

Therapeutic index

A

ratio that compares blood concentration at which drug is toxic vs. effective
o Large TI, safer the drug.

22
Q

Therapeutic window

A

dosage range between minimal therapeutic dose and max toxic dose

23
Q

Tolerance

A

same as desensitization

24
Q

Tachyphylaxis

A

sudden onset of drug tolerance that is not dose dependent