Chapter 4 - Neural Comm 2/Properties Of Drugs Flashcards

1
Q

• Absorption:

A

passage of a drug from the site of administration to the bloodstream

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2
Q

• Liberation:

A

process of drug molecules separation from the pill or solution in which it was delivered

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3
Q

• Distribution:

A

the passage of a drug from the bloodstream to sites in the body

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4
Q

• Bioavailability:

A

ability of a drug to reach a site of action

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5
Q

• Blood-brain barrier (BBB):

A

barrier that surrounds the blood capillaries and vessels in the brain and prevents substances in blood from entering the brain

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6
Q

• Passive diffusion through the blood-brain barrier:

A

BBB penetration by lipid-soluble, uncharged, small substances

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7
Q

• Active transport through the BBB:

A

mechanisms consisting of channels or other types proteins that transport chemicals through endothelial cell membranes

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8
Q

• Nonspecific binding:

A

binding of a drug to sites that are not the intended target for a drug’s effects

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9
Q

• Biotransformation

A
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10
Q

• Metabolite:

A

product resulting from enzymatic transformation of a drug

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11
Q

• Phase I biotransformation:

A

first biotransformation phase for a drug that normally involves P450 enzymes and produces a water-soluble metabolite

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12
Q

• Phase II biotransformation:

A

second biotransformation phase occurring through conjugation of a drug’s metabolites, making them resistance to passive diffusion

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13
Q

• Personalized medicine:

A

method of prescribing treatments most appropriate for a patient’s unique biological makeup

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14
Q

• First-pass metabolism:

A

drug metabolism that occurs prior to absorption into the bloodstream

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15
Q

• Active metabolite:

A

a drug’s metabolite that has physiological effects

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16
Q

• Prodrugs:

A

a physiologically weak or inactive compound metabolized in the body to produce an active drug

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17
Q

• Elimination:

A

process for how a drug leaves the body

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18
Q

• Elimination rate:

A

amount of drug eliminated from the body over time

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19
Q

• Half-life:

A

duration necessary for the body to eliminate half of a drug

20
Q

• First-order kinetics:

A

the elimination of a drug in half-lives

21
Q

• Zero-order kinetics:

A

the elimination of a drug in non-half-lives

22
Q

• Pharmacodynamics:

A

mechanisms of action for a drug

23
Q

• Binding affinity:

A

drug’s strength of binding to a receptor

24
Q

• Receptor affinity:

A

drug’s ability to alter the activity of a receptor

25
• Agonist:
drug that activates a neurotransmitter receptor
26
• Antagonist:
drug that fails to activate a receptor
27
• Partial agonist:
drug that possesses a weaker efficacy for activating receptors than a full agonist
28
• Competitive antagonist:
drug that binds to the same site as a neurotransmitter, preventing a neurotransmitter from binding to the receptor
29
• Non-competitive antagonist:
drug that does not prevent a neurotransmitter from binding to the receptor, but does prevent the neurotransmitter from activating the receptor
30
• Allosteric regulator:
a substance that binds to site on a protein and causes a conformational change in the protein, but neither activates nor prevents activation in the protein
31
• Positive modulator:
a chemical substance that binds to an allosteric site on a receptor and increases the ability of a neurotransmitter to bind to and/or activate the receptor
32
• Negative modulator:
a chemical substance that binds to an allosteric site on a receptor and decreases the ability of a neurotransmitter to bind to and/or activate the receptor
33
• Neurotoxins:
substances that damage or destroy parts of the nervous system
34
• Environmental neurotoxicology:
a field devoted to the study of neurotoxins in the environment
35
• Tolerance:
occurs when a user must take greater doses of a drug to achieve the desired effects
36
• Pharmacokinetic tolerance
[drug dispositional tolerance]: pharmacokinetic action that reduce the amount of drug reaching its site of action increased rate of drug conversion to metabolites
37
• Pharmacodynamic tolerance:
reduced responsiveness to a drug at the drug’s site of action
38
• Behavioural tolerance:
decreased behavioural responsiveness to a drug’s effects
39
• Conditioned
[contingent tolerance]: occurs as a physiological response to stimuli associated with substance use that serves to counteract a drug’s physiological actions
40
• Cross tolerance:
tolerance for other drugs with similar biological actions
41
• Sensitization:
increased responsiveness to a drug’s effects
42
• Dependence:
needing a drug to be able to function normally
43
• Withdrawal syndrome:
the collection of withdrawal symptoms for a drug
44
• Physical dependence:
presence of physical withdrawal symptoms when a drug is not taken
45
• Psychological dependence:
presence of psychological withdrawal symptoms when a drug is not taken