Vocab words Flashcards

1
Q

Agonist

A

a drug that activates a receptor by binding to that receptor

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2
Q

Antagonist

A

a drug that binds to the receptor without activating the receptor; gets in the way

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3
Q

Competitive antagonism

A

present when increasing concentrations of the antagonist progressively inhibit the response to the agonist

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4
Q

Non-competitive antagonism

A

present when after administration of an antagonist; even in high concentrations of agonist cannot completely overcome the antagonism (covalent/allosteric)

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5
Q

partial agonists

A

drug that binds to a receptor where it activates the receptor but not as much as a full agonist; can not cause full effect

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6
Q

inverse agonists

A

bind at same site as the agonist but produce opposite effect of agonist. Turn off constitutive activity of receptor; decreases number of receptors

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7
Q

tolerance

A

decreased response to the same dose; develops slowly;. Up or down regulation of receptors, increased metabolism or adaptation in cellular pathways

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8
Q

pharmacokinetics

A

the quantitative study of the absorption, distribution, metabolism, and excretion of injected and inhaled drugs and their metabolites. What the body does to the drug.

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9
Q

central volume

A

volume that intravenously injected drug initially mixes into. Composed of those elements of the body that dilute the drug within the first minute after injection

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10
Q

vessel rich group

A

tissues that receive the bulk of arterial blood flow-brain, heart, kidneys, and liver

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11
Q

zero order processes

A

consumption of oxygen and production of carbon dioxide are processes that happen at a constant rate. Rate of change is constant.

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12
Q

first order processes

A

rate is proportional to the amount

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13
Q

elimination half time

A

amount of time it takes for the concentration of a drug to decrease by half after it has peaked

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14
Q

context sensitive half time

A

the time for the plasma concentration to decrease by 50% from an infusion that maintains a constant concentration

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15
Q

clearance

A

amount of blood completely cleared of drug per unit time

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16
Q

pharmacodynamics

A

study of the intrinsic sensitivity or responsiveness of tehe body to a drug and the mechanisms by which these effects occur. What the drug does to the body.

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17
Q

stereochemistry

A

the study of how molecules are structured in three dimensions

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18
Q

chirality

A

unique subset of stereochemistry. Chiral is used to designate a molecule that has a center of three-dimensional asymmetry

19
Q

enantiomerism

A

a pair of molecules existing in two forms that are mirror images of one another but cannot be superimposed; chemically identical

20
Q

racemic

A

two enantiomers present in equal proportions

21
Q

pharmacogenetics

A

genetically determined disease states that are initially revealed by altered responses to specific drugs

22
Q

amnesia

A

loss of memory, which can involve inability to remember past events (retrograde amnesia), difficulty forming new memories (anterograde amnesia) or both.

23
Q

recall

A

the process of retrieving or bringing information stored in the brain back into conscious awareness

24
Q

sedation (3 depths)

A
  1. Minimal sedation (anxiolysis): awake, able to respond normally to verbal commands (benzos)
  2. Moderate sedation (conscious sedation): patient is drowsy, remains conscious and responsive to verbal commands or light stimulation (low dose propofol)
  3. Deep sedation: on edge of unconsciousness and only responds to painful stimulation (high dose propofol/ketamine)
25
General anesthesia
process requiring a state of unconsciousness of the brain (produced by volatile or injected anesthetics) plus immobility in response to a noxious stimulus (surgical skin incision) that is mediated by the action of volatile anesthetics on the spinal cord administered at concentrations equivalent to MAC for that drug.
26
analgesia
absence or reduction of pain perception without a loss of consciousness
27
allodynia
perception of pain sensations in response to normally non-painful stimuli
28
Hyperalgesia
increased pain sensation to normally painful stimuli
29
sensitization
increased responsiveness to heat, cold, mechanical, or chemical stimulation; gives rise to primary hyperalgesia to these stimuli
30
neuropathic pain
characterized by a reduced nociceptive threshold, persists in the absence of a stimulus and is refractory to traditional analgesics
31
somatic pain
easily localized and characterized by distinct sensations
32
visceral pain
diffuse and poorly localized, usually associated with stronger emotional and autonomic reactions. Ex: muscle/skin pain
33
neuralgia
sharp, shooting, or burning pain that occurs along the path of a nerve
34
tachyphylaxis
decreased response to the same dose of medication after short period of time; due to receptor desensitization
35
additive
combined effect of two drugs that is equal to the sum of their individual effects; effects add up without enhancing or diminishing each other
36
synergistic
combined effect of two drugs that is greater than the sum of their individual effects; enhance each other. Often seen when drugs act on different pathways
37
efficacy
measure of the intrinsic ability of a drug to produce a given physiologic or clinical effect
38
potency
refers to the relative dose of two drugs; concentration versus response relationship. Left shift equals higher potency.
39
median effective dose (ED50)
dose of a drug required to produce a specific desired effect in 50% of individuals
40
Median Lethal Doses (LD50)
dose of a drug required to produce death in 50% of individuals
41
therapeutic index
ratio between LD50 and ED50 (LD50/ED50). The larger the TI, the safer the drug
42
acute pain
short-term pain, does not persist after initial injury has healed
43
chronic pain
persistent pain beyond the expected period of healing; pain receptors continue to fire even in the absence of tissue damage
44
Elimination half life
time it takes for the concentration of a drug to decrease by half during elimination phase