Vocabulary Flashcards

1
Q

drug that activates a receptor by binding to that receptor

A

Agonist

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2
Q
  • drug that binds to a receptor without activating that receptor
  • Block the action of agonists simply by getting in the way of the agonist, preventing the agonist from binding to the receptor and producing the drug effect
A

Antagonist

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3
Q

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

A

Competitive antagonism

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4
Q

present when, after administration of an antagonist, even high concentrations of agonist cannot completely overcome the antagonism. (either covalent bond or allosteric bound)

A

Non-competitive antagonism

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5
Q
  • drug that binds to a receptor but doesn’t cause full drug effect drug that binds to a receptor (usually at the agonist site) where it activates the receptor but not as much as a full agonist.
  • Even at supramaximal doses, this cannot cause the full drug effect.
  • May also have antagonist activity in which case they are also called agonist-antagonists.
  • When administered with a full agonist, it decreases the effect of the full agonist
A

Partial agonist

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6
Q
  • bind at the same site as the agonist (and likely compete with it), but they produce the opposite effect of the agonist.
  • “turn off ” the constitutive activity of the receptor
A

Inverse agonists

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7
Q

decreased response to the same dose of drug

A

Tolerance

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8
Q
  • the quantitative study of the absorption, distribution, metabolism, and excretion of injected and inhaled drugs and their metabolites
  • describes what the body does to a drug
A

Pharmacokinetics

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9
Q

the volume that intravenously injected drug initially mixes into.

A

Central volume

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10
Q

tissues receiving high arterial flow.

A

Vessel rich group

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11
Q

a constant amount of drug is eliminated per unit of time.

A

Zero-order processes

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12
Q
  • amount eliminated will be dependent on the maximum blood/plasma concentration and not of time
  • indicates that the rate of elimination is proportional to the concentration (ie, the higher the concentration, the greater the amount of drug eliminated per unit time.
A

First-order processes

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13
Q

the half-time for equilibration between plasma and the site of the drug effect

A

Elimination Half-time

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14
Q
  • the time required for a 50% decrease in x;
  • constant regardless of the amount of drug in the body.
  • The concentration of such a drug in the blood will decrease by 50% for every this
A

Elimination Half-life

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15
Q
  • the time for the plasma concentration to decrease by 50% from an infusion that maintains a constant concentration.
A

Context-sensitive half-time

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16
Q

the amount of blood completely cleared of drug per unit time

A

Clearance

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17
Q

describes what the drug does to the body

A

Pharmacodynamics

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18
Q

the study of how molecules are structured in three dimension

A

Stereochemistry

19
Q

a molecule with a center of 3 dimensional asymmetry

A

Chirality

20
Q

pairs of molecules that are mirror images

A

Enantiomerism

21
Q

enantiomers present in equal proportion

A

Racemic

22
Q
  • study of genetic factors determining drug response and the use of gene sequencing or expression profile data to tailor therapies specific to an individual patient
  • The response to many drugs varies greatly among patients
A

Pharmacogenetics

23
Q

temporary loss of recall

A

Amnesia

24
Q

conscious memory

A

Recall

25
Q

Dee

altered level of consciousness – Minimal, Moderate, and Deep

A

Sedation

26
Q

drug-induced loss of consciousness during which patients are not arousable, even by painful stimulation. The ability to independently maintain ventilatory function is often impaired. Patients often require assistance in maintaining a patent airway, and positive pressure ventilation may be required because of depressed spontaneous ventilation or drug-induced depression of neuromuscular function. Cardiovascular function may be impaired.

A

General Anesthesia

27
Q

inability to feel pain

A

Analgesia

28
Q

pain response from typically non-painful stimulation

A

Allodynia

29
Q

an abnormally increased sensitivity to pain

A

Hyperalgesia

30
Q

increased sensitivity to subsequent inoffensive stimuli; refers to the increased responsiveness of peripheral neurons responsible for pain transmission to heat, cold, mechanical, or chemical stimulation

A

Sensitization

31
Q

pain that persists after tissue injury has healed and is characterized by reduced sensory and nociceptive thresholds (allodynia and hyperalgesia); Injury of peripheral nerves by trauma, surgery, or diseases (diabetes) frequently results in the development of this

A

Neuropathic pain

32
Q

pain related to muscles, skeleton.

A

Somatic pain

33
Q
  • pain related to activation of nociceptors in the thorax, abdomen, pelvis.
  • Diffuse and poorly localized, typically referred to somatic sites (eg muscle and skin), and it is usually associated with stronger emotional and autonomic reactions
A

Visceral pain

34
Q

pain in the nerve pathway

A

Neuralgia

35
Q

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

A

Tachyphylaxis

36
Q

combination of 2 drugs with summative effects

A

Additive

37
Q

combination of 2 drugs with greater than summative effects

A

Synergistic

38
Q

*the ability to produce the intended result

*a measure of the intrinsic ability of a drug to produce a given physiologic or clinical effect.

A

Efficacy

39
Q

the relationship of the dose to the effect

A

Potency

40
Q

dose of a drug required to produce a specific desired effect in 50% of individuals receiving the drug.

A

Median effective dose (ED50):

41
Q

the dose of a drug required to produce death in 50% of patients (or more often animals)

A

Median lethal does (LD50):

42
Q

the ratio between the LD50 and the ED50 (LD50/ED50). The larger this is of a drug, the safer the drug is for clinical administration

A

Therapeutic index

43
Q
  • limited to the short-term, typically extending for days to weeks after injury.
  • provides an important protective mechanism, signaling the individual to protect the injured region from repeated injury, so that tissue healing can ensue.
  • Under most circumstances, as tissue heals, the acute sensitization in the region surrounding the injury gradually subsides, and sensory thresholds revert to normal.
  • Acute pain and the accompanying sensitization that accompany any injury do not typically persist after the initial injury has healed.
A

Acute pain

44
Q
  • is persistent pain that persists after all tissue healing appears to be complete and extends beyond the expected period of healing.
  • In individuals with chronic pain, pain receptors continue to fire, even in the absence of tissue damage.
  • There may no longer be a physically discernible tissue injury, yet the pain response persists.
A

Chronic pain