Deck 3: Pharmacodynamics: How Drugs Act

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Question
Barbiturates,like benzodiazepines,_____ the effect of GABA on the _____ channel within the GABA receptor.

A) decrease; potassium
B) decrease; chloride
C) increase; sodium
D) increase; chloride
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Question
Based on the concept of homeostatic control,you might expect drugs that block the action of carrier proteins to _____ the number of postsynaptic receptors for the endogenous neurotransmitter; further,you might expect drugs that facilitate the action of carrier proteins to _____ the number of postsynaptic receptors for the endogenous neurotransmitter.

A) decrease; decrease
B) increase; increase
C) increase; decrease
D) decrease; increase
Question
Drugs that block the action of presynaptic carrier proteins would be expected to ______ the level of neurotransmitter in the synapse ; drugs that facilitate the action of presynaptic carrier proteins would be expected to _____ the level of neurotransmitter in the synapse _____.

A) decrease; decrease
B) increase; increase
C) increase; decrease
D) decrease; increase
Question
G protein-coupled receptors respond to binding of a neurotransmitter by altering:

A) the external domain of the ion channel.
B) enzymes in the postsynaptic cell.
C) DNA replication.
D) chloride influx into the cell.
Question
The study of how a drug interacts with a receptor is termed:

A) pharmacology.
B) pharmacokinetics.
C) pharmacodynamics.
D) molecular physiology.
Question
All of the following are considered primary intracellular pathways for modulation of synaptic transmission,EXCEPT:

A) cyclic guanosine monophosphate (cGMP).
B) inositol triphosphate (IP3).
C) diacylglycerol (DG).
D) cyclic adenosine monophosphate (cAMP).
Question
Ionotropic receptors consist of _____ subunits.

A) three
B) four
C) five
D) six
Question
New advances in pharmacology enable,for the first time,the development of drugs that bind to:

A) more than one receptor.
B) one receptor only.
C) more than one neurotransmitter.
D) one neurotransmitter only.
Question
Transport proteins are thought to exist in all of the following ionic states,EXCEPT:

A) open to cytoplasm of the presynaptic cell.
B) open to the synapse.
C) open to the calcium channels of the presynaptic neuron.
D) blocked,but with the transmitter "trapped" inside.
Question
The primary advantage of G protein-coupled receptors over ionotropic receptors is that they:

A) amplify cellular signal by stimulating many second messenger molecules to be produced.
B) work more rapidly.
C) enhance cellular metabolism.
D) inhibit the formation of second messengers.
Question
A _____ can usually bind to many _____.

A) receptor; neurotransmitters
B) neurotransmitter; receptor subtypes
C) ligand; neurotransmitters
D) neurotransmitter; ligands
Question
A _____ usually binds to only one _____.

A) receptor; neurotransmitter
B) neurotransmitter; receptor
C) ligand; neurotransmitter
D) neurotransmitter; ligand
Question
The anxiolytic (anxiety-reducing)effect of benzodiazepines such as diazepam occurs through _____ receptor.

A) antagonist action at the serotonin
B) agonist action at the serotonin
C) antagonist action at the GABA
D) agonist action at the GABA
Question
Membrane-spanning receptor proteins include:

A) G-protein-coupled receptors,but not carrier/transport proteins.
B) carrier/transport proteins,but not G-protein-coupled receptors.
C) both G-protein-coupled receptors and carrier/transport proteins.
D) neither G-protein-coupled receptors nor carrier/transport proteins.
Question
The benzodiazepines (such as diazepam)bind at _____ site on the receptor as the endogenous neurotransmitter _____ of the neurotransmitter.

A) the same; and mimic the action
B) the same; and block the action
C) a different; to facilitate the action
D) a different; to inhibit the action
Question
Exposure to a drug that inhibits the breakdown of a neurotransmitter (NT)increases the level of NT by inhibiting breakdown:

A) in the synapse; an example of such a drug is acetylcholine esterase.
B) mainly in the presynaptic terminal; an example of such a drug is monoamine oxidase.
C) in the synapse; an example of such a drug is an acetylcholine esterase inhibitor.
D) in the presynaptic terminal; an example of such a drug is an acetylcholine esterase inhibitor.
Question
In metabotropic receptors:

A) G proteins activate the extracellular recognition site.
B) the associated ion channel activates the G protein.
C) the associated ion channel activates the receptor recognition site.
D) the activated extracellular receptor in turn activates the G protein.
Question
Some drugs are more selective than the endogenous:

A) receptors.
B) ligands.
C) neurotransmitters.
D) antagonists.
Question
Benzodiazepines are _____ agonists that _____ the conductance of chloride ions into the neuron.

A) allosteric; inhibit
B) allosteric; increase
C) inverse; facilitate
D) inverse; enhance
Question
The naturally occurring compounds that bind to receptors are termed:

A) neurotransmitters.
B) drugs.
C) pharmaceuticals.
D) second messengers.
Question
The placebo response appears to be related to:

A) the genetic make-up of individuals.
B) supersensitivity to experimental instructions.
C) situational factors related to a drug trial.
D) unknown variables.
Question
The variability and slope of the dose-response curve refer to:

A) the number of molecules of drug required to elicit a response.
B) the maximum effect obtainable with the drug.
C) whether the drug acts on presynaptic or postsynaptic receptors.
D) individual differences in response to the drug.
Question
Acetylcholine esterase and monoamine oxidase are examples of:

A) G-protein-coupled receptors.
B) carrier/transport proteins.
C) directly gated ion channels.
D) enzyme receptor proteins.
Question
The therapeutic index refers to the:

A) absolute number of molecules of drug required to elicit a response.
B) maximum effect obtainable.
C) individual differences in drug response.
D) relative safety of the drug.
Question
Bill has been taking Prozac (fluoxetine),a selective serotonin reuptake inhibitor,for his depression for some time now.However,he has found that the drug has become less effective over time.This effect may be due to receptor:

A) up regulation.
B) sensitization.
C) adaptation.
D) desensitization.
Question
A drug that blocks the effect of,and occupies the same receptor site as,the naturally occurring compound is termed a(n):

A) mimicker.
B) antagonist.
C) agonist.
D) facilitator.
Question
In the context of a dose-response curve,the relationship between a drug dosage and the effect observed is referred to as:

A) efficacy.
B) slope.
C) potency.
D) variability.
Question
A drug that exerts an effect similar to,and occupies the same receptor site as,the naturally occurring compound is termed a(n):

A) mimicker.
B) an antagonist.
C) agonist.
D) facilitator.
Question
A new nerve gas,Agousin,has been developed that acts on the cholinergic system; this gas would likely work as a(n)_____ inhibitor._____

A) reversible acetylcholine esterase
B) reversible monoamine oxidase
C) irreversible monoamine oxidase
D) irreversible acetylcholine esterase
Question
In a given population,the dose-response curve for the dose of drug that produces the desired effect may overlap with the dose response curve for the lethal dose of the drug.For this reason,a more useful index of the margin of safety for a drug is the ratio of the:

A) LD50 to ED50.
B) ED50 to LD50.
C) ED99 to LD1.
D) LD1 to ED99.
Question
A drug that is more potent than another drug has a:

A) larger maximal effect.
B) larger ED50.
C) larger LD50.
D) smaller ED50.
Question
The fact that caffeine cannot exert as much central nervous system stimulation as amphetamine indicates that caffeine:

A) is less potent than amphetamine.
B) is less efficacious than amphetamine.
C) has a lower therapeutic index than amphetamine.
D) has a steeper slope than amphetamine on a dose-response curve.
Question
The location of the dose-response curve along the horizontal axis reflects:

A) the therapeutic index of a drug.
B) the efficacy of a drug.
C) individual differences in drug response.
D) the potency of a drug.
Question
"Isomers" represent forms of a molecule that are:

A) identical in all respects.
B) identical save for a handful of different atoms.
C) charged versus uncharged.
D) mirror images of one another.
Question
Potency refers to the:

A) absolute number of molecules of drug required to elicit a response.
B) maximum effect obtainable.
C) individual differences in drug response.
D) relative safety of the drug.
Question
A drug that is more efficacious than another drug has a:

A) larger maximum effect.
B) larger ED50.
C) larger TI.
D) smaller LD50.
Question
The dose of drug that produces the effect desired in half of the subjects is called the drug's:

A) half-life.
B) therapeutic index.
C) ED50.
D) LD50.
Question
The therapeutic index is defined as the ratio of:

A) efficacy to potency.
B) potency to efficacy.
C) ED50 to LD50.
D) LD50 to ED50.
Question
The peak of the dose-response curve indicates:

A) the therapeutic index of a drug.
B) the efficacy of a drug.
C) individual differences in drug response.
D) the potency of a drug.
Question
Side effects of a drug include those related to:

A) the primary mechanism of the drug such as blocking 5-HT receptors.
B) the secondary mechanism of the drug such as blocking cholinergic receptors.
C) both primary and secondary mechanisms of the drug.
D) neither of these mechanisms-side effects are unrelated to drug action.
Question
Affinity refers to the strength of binding between a neurotransmitter and a receptor.
Question
A given receptor is usually capable of binding to more than one neurotransmitter.
Question
Drug A is more efficacious than Drug B.
Question
Drug B is 10 times more potent than Drug A.
Question
With rare exception,the binding of a drug to a receptor is irreversible.
Question
Drug A is 10 times more potent than Drug B.
Question
Fundamentally,drugs produce novel effects in the brain that would not be seen under normal circumstances.
Question
The G protein can directly,as well as indirectly,activate an ion channel.
Question
Two enantiomers of a given drug are almost always roughly equal to each other in biological activity.
Question
Ionotropic and metabotropic receptors mediate the effect of the steroid hormones.
Question
An antagonist binds to the same receptor site as the endogenous compound but produces an effect opposite to the endogenous compound.
Question
Metabotropic receptors form a membrane-spanning pore through which ions pass.
Question
Drug B is five times more efficacious than Drug A.
Question
Drug A and Drug B are equally efficacious.
Question
Drug A and Drug B each have a different ED50.
Question
Possible mechanisms for the placebo effect include:

A) biological action of the active ingredient in the placebo.
B) a clearly defined set of traits in the patient.
C) side effects of the placebo.
D) genetics of the patient.
Question
A given neurotransmitter is usually capable of binding to more than one receptor.
Question
Drug A is five times more potent than Drug B.
Question
Drug A is 10 times more efficacious than Drug B.
Question
Drug B is more potent that Drug A.
Question
Receptors that consist of an attachment site and a pore that allows specific ions to enter the cell are referred to as _____ receptors.

A) metabotropic
B) trophic
C) G-protein-coupled
D) ionotropic
Question
The binding of drugs to receptors involves _____ bonds that are ______.

A) weak; irreversible
B) ionic; irreversible
C) ionic; reversible
D) covalent; reversible
Question
Molecular isomers of drugs are _____ similar but are not _____active.

A) chemically; biologically
B) chemically; behaviorally
C) biologically; chemically
D) biologically; behaviorally
Question
In the context of polypharmacy,doses may be selected that are ineffective due to side effects- a phenomenon referred to as:

A) pharmacodynamic redundancy .
B) pharmacokinetic dosing.
C) inadequate dosing.
D) clinical dosing.
Question
Normal side effects to a drug may take all of the following forms EXCEPT:

A) fatal shock.
B) constipation.
C) dry mouth.
D) sleepiness.
Question
Pharmacodynamics is about:

A) what the body does to a drug.
B) how cells bind to drugs.
C) where drugs bind to cells in the body.
D) what a drug does to the body.
Question
Janette has been prescribed an antidepressant; over time,she may have to increase her dose due to receptor:

A) upregulation.
B) supersensitivity.
C) desensitization.
D) over production.
Question
Richard is participating in a research study involving a new pain medication.However,he is not actually receiving the biologically active medication.Research suggests that he:

A) is most likely to fall into the group of participants that sometimes respond to placebo.
B) is likely to always respond to placebo.
C) will not respond at all to the placebo.
D) he is more likely to respond to placebo because he is male.
Question
G-protein-coupled receptors are considered to be _____ while ionotropic are _____ receptors.

A) slow; fast
B) fast; direct
C) direct; fast
D) indirect; slow
Question
Ionotropic receptors consist of _____ coils embedded in the membrane with an attachment site(s)_____ the membrane.

A) spring; outside
B) spring; inside and outside
C) helical; outside
D) helical; beside
Question
The relative safety of a drug can be determined from the ratio of the LD50 to the ED50.
Question
Within the context of the dose-response curve,the _____ of the curve describes the association between the dose of the drug and its overall effect.

A) variability
B) height
C) slope
D) potency
Question
The double-blind randomized clinical trial without placebo is currently the gold standard for studying the effectiveness and safety of drugs in humans.
Question
An antagonist binds to the same receptor site as the endogenous compound but prevents the endogenous compound from acting.
Question
All of the following are types of receptors EXCEPT:

A) carrier proteins.
B) enzymes.
C) ion channel receptors.
D) cyclic AMP.
Question
If simultaneous administration of an agonist and antagonist cause a downward shift in the maximal effect of an agonist's response,the antagonist would be considered:

A) allosteric.
B) competitive.
C) noncompetitive.
D) reversible.
Question
The amount of drug that must be given to produce a given effect is called the drug:

A) efficacy.
B) potency.
C) intensity.
D) affinity.
Question
A drug that binds to a receptor site that elicits an opposite effect to that observed when an endogenous neurotransmitter binds is referred to as a(n):

A) partial antagonist.
B) allosteric agonist.
C) competitive antagonist.
D) inverse agonist.
Question
The _____ of a drug refers to how strongly it attaches to the receptor.

A) fit
B) affinity
C) binding
D) ionic nature
Question
G-protein-coupled receptors:

A) are sometimes referred to as ionotropic receptors.
B) possess a pore that opens allowing ions to enter the cell.
C) typically are made up of five helical,membrane-spanning coils.
D) involve the release of an attached intracellular protein after a drug binds.
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Deck 3: Pharmacodynamics: How Drugs Act
1
Barbiturates,like benzodiazepines,_____ the effect of GABA on the _____ channel within the GABA receptor.

A) decrease; potassium
B) decrease; chloride
C) increase; sodium
D) increase; chloride
D
2
Based on the concept of homeostatic control,you might expect drugs that block the action of carrier proteins to _____ the number of postsynaptic receptors for the endogenous neurotransmitter; further,you might expect drugs that facilitate the action of carrier proteins to _____ the number of postsynaptic receptors for the endogenous neurotransmitter.

A) decrease; decrease
B) increase; increase
C) increase; decrease
D) decrease; increase
D
3
Drugs that block the action of presynaptic carrier proteins would be expected to ______ the level of neurotransmitter in the synapse ; drugs that facilitate the action of presynaptic carrier proteins would be expected to _____ the level of neurotransmitter in the synapse _____.

A) decrease; decrease
B) increase; increase
C) increase; decrease
D) decrease; increase
C
4
G protein-coupled receptors respond to binding of a neurotransmitter by altering:

A) the external domain of the ion channel.
B) enzymes in the postsynaptic cell.
C) DNA replication.
D) chloride influx into the cell.
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Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
5
The study of how a drug interacts with a receptor is termed:

A) pharmacology.
B) pharmacokinetics.
C) pharmacodynamics.
D) molecular physiology.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
6
All of the following are considered primary intracellular pathways for modulation of synaptic transmission,EXCEPT:

A) cyclic guanosine monophosphate (cGMP).
B) inositol triphosphate (IP3).
C) diacylglycerol (DG).
D) cyclic adenosine monophosphate (cAMP).
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
7
Ionotropic receptors consist of _____ subunits.

A) three
B) four
C) five
D) six
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
8
New advances in pharmacology enable,for the first time,the development of drugs that bind to:

A) more than one receptor.
B) one receptor only.
C) more than one neurotransmitter.
D) one neurotransmitter only.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
9
Transport proteins are thought to exist in all of the following ionic states,EXCEPT:

A) open to cytoplasm of the presynaptic cell.
B) open to the synapse.
C) open to the calcium channels of the presynaptic neuron.
D) blocked,but with the transmitter "trapped" inside.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
10
The primary advantage of G protein-coupled receptors over ionotropic receptors is that they:

A) amplify cellular signal by stimulating many second messenger molecules to be produced.
B) work more rapidly.
C) enhance cellular metabolism.
D) inhibit the formation of second messengers.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
11
A _____ can usually bind to many _____.

A) receptor; neurotransmitters
B) neurotransmitter; receptor subtypes
C) ligand; neurotransmitters
D) neurotransmitter; ligands
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Unlock Deck
k this deck
12
A _____ usually binds to only one _____.

A) receptor; neurotransmitter
B) neurotransmitter; receptor
C) ligand; neurotransmitter
D) neurotransmitter; ligand
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Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
13
The anxiolytic (anxiety-reducing)effect of benzodiazepines such as diazepam occurs through _____ receptor.

A) antagonist action at the serotonin
B) agonist action at the serotonin
C) antagonist action at the GABA
D) agonist action at the GABA
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
14
Membrane-spanning receptor proteins include:

A) G-protein-coupled receptors,but not carrier/transport proteins.
B) carrier/transport proteins,but not G-protein-coupled receptors.
C) both G-protein-coupled receptors and carrier/transport proteins.
D) neither G-protein-coupled receptors nor carrier/transport proteins.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
15
The benzodiazepines (such as diazepam)bind at _____ site on the receptor as the endogenous neurotransmitter _____ of the neurotransmitter.

A) the same; and mimic the action
B) the same; and block the action
C) a different; to facilitate the action
D) a different; to inhibit the action
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
16
Exposure to a drug that inhibits the breakdown of a neurotransmitter (NT)increases the level of NT by inhibiting breakdown:

A) in the synapse; an example of such a drug is acetylcholine esterase.
B) mainly in the presynaptic terminal; an example of such a drug is monoamine oxidase.
C) in the synapse; an example of such a drug is an acetylcholine esterase inhibitor.
D) in the presynaptic terminal; an example of such a drug is an acetylcholine esterase inhibitor.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
17
In metabotropic receptors:

A) G proteins activate the extracellular recognition site.
B) the associated ion channel activates the G protein.
C) the associated ion channel activates the receptor recognition site.
D) the activated extracellular receptor in turn activates the G protein.
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Unlock Deck
k this deck
18
Some drugs are more selective than the endogenous:

A) receptors.
B) ligands.
C) neurotransmitters.
D) antagonists.
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Unlock Deck
k this deck
19
Benzodiazepines are _____ agonists that _____ the conductance of chloride ions into the neuron.

A) allosteric; inhibit
B) allosteric; increase
C) inverse; facilitate
D) inverse; enhance
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Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
20
The naturally occurring compounds that bind to receptors are termed:

A) neurotransmitters.
B) drugs.
C) pharmaceuticals.
D) second messengers.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
21
The placebo response appears to be related to:

A) the genetic make-up of individuals.
B) supersensitivity to experimental instructions.
C) situational factors related to a drug trial.
D) unknown variables.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
22
The variability and slope of the dose-response curve refer to:

A) the number of molecules of drug required to elicit a response.
B) the maximum effect obtainable with the drug.
C) whether the drug acts on presynaptic or postsynaptic receptors.
D) individual differences in response to the drug.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
23
Acetylcholine esterase and monoamine oxidase are examples of:

A) G-protein-coupled receptors.
B) carrier/transport proteins.
C) directly gated ion channels.
D) enzyme receptor proteins.
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Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
24
The therapeutic index refers to the:

A) absolute number of molecules of drug required to elicit a response.
B) maximum effect obtainable.
C) individual differences in drug response.
D) relative safety of the drug.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
25
Bill has been taking Prozac (fluoxetine),a selective serotonin reuptake inhibitor,for his depression for some time now.However,he has found that the drug has become less effective over time.This effect may be due to receptor:

A) up regulation.
B) sensitization.
C) adaptation.
D) desensitization.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
26
A drug that blocks the effect of,and occupies the same receptor site as,the naturally occurring compound is termed a(n):

A) mimicker.
B) antagonist.
C) agonist.
D) facilitator.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
27
In the context of a dose-response curve,the relationship between a drug dosage and the effect observed is referred to as:

A) efficacy.
B) slope.
C) potency.
D) variability.
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Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
28
A drug that exerts an effect similar to,and occupies the same receptor site as,the naturally occurring compound is termed a(n):

A) mimicker.
B) an antagonist.
C) agonist.
D) facilitator.
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Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
29
A new nerve gas,Agousin,has been developed that acts on the cholinergic system; this gas would likely work as a(n)_____ inhibitor._____

A) reversible acetylcholine esterase
B) reversible monoamine oxidase
C) irreversible monoamine oxidase
D) irreversible acetylcholine esterase
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
30
In a given population,the dose-response curve for the dose of drug that produces the desired effect may overlap with the dose response curve for the lethal dose of the drug.For this reason,a more useful index of the margin of safety for a drug is the ratio of the:

A) LD50 to ED50.
B) ED50 to LD50.
C) ED99 to LD1.
D) LD1 to ED99.
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Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
31
A drug that is more potent than another drug has a:

A) larger maximal effect.
B) larger ED50.
C) larger LD50.
D) smaller ED50.
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Unlock Deck
k this deck
32
The fact that caffeine cannot exert as much central nervous system stimulation as amphetamine indicates that caffeine:

A) is less potent than amphetamine.
B) is less efficacious than amphetamine.
C) has a lower therapeutic index than amphetamine.
D) has a steeper slope than amphetamine on a dose-response curve.
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Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
33
The location of the dose-response curve along the horizontal axis reflects:

A) the therapeutic index of a drug.
B) the efficacy of a drug.
C) individual differences in drug response.
D) the potency of a drug.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
34
"Isomers" represent forms of a molecule that are:

A) identical in all respects.
B) identical save for a handful of different atoms.
C) charged versus uncharged.
D) mirror images of one another.
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Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
35
Potency refers to the:

A) absolute number of molecules of drug required to elicit a response.
B) maximum effect obtainable.
C) individual differences in drug response.
D) relative safety of the drug.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
36
A drug that is more efficacious than another drug has a:

A) larger maximum effect.
B) larger ED50.
C) larger TI.
D) smaller LD50.
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Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
37
The dose of drug that produces the effect desired in half of the subjects is called the drug's:

A) half-life.
B) therapeutic index.
C) ED50.
D) LD50.
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Unlock Deck
k this deck
38
The therapeutic index is defined as the ratio of:

A) efficacy to potency.
B) potency to efficacy.
C) ED50 to LD50.
D) LD50 to ED50.
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Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
39
The peak of the dose-response curve indicates:

A) the therapeutic index of a drug.
B) the efficacy of a drug.
C) individual differences in drug response.
D) the potency of a drug.
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Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
40
Side effects of a drug include those related to:

A) the primary mechanism of the drug such as blocking 5-HT receptors.
B) the secondary mechanism of the drug such as blocking cholinergic receptors.
C) both primary and secondary mechanisms of the drug.
D) neither of these mechanisms-side effects are unrelated to drug action.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
41
Affinity refers to the strength of binding between a neurotransmitter and a receptor.
Unlock Deck
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Unlock Deck
k this deck
42
A given receptor is usually capable of binding to more than one neurotransmitter.
Unlock Deck
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Unlock Deck
k this deck
43
Drug A is more efficacious than Drug B.
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44
Drug B is 10 times more potent than Drug A.
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45
With rare exception,the binding of a drug to a receptor is irreversible.
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46
Drug A is 10 times more potent than Drug B.
Unlock Deck
Unlock for access to all 83 flashcards in this deck.
Unlock Deck
k this deck
47
Fundamentally,drugs produce novel effects in the brain that would not be seen under normal circumstances.
Unlock Deck
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48
The G protein can directly,as well as indirectly,activate an ion channel.
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49
Two enantiomers of a given drug are almost always roughly equal to each other in biological activity.
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50
Ionotropic and metabotropic receptors mediate the effect of the steroid hormones.
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51
An antagonist binds to the same receptor site as the endogenous compound but produces an effect opposite to the endogenous compound.
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52
Metabotropic receptors form a membrane-spanning pore through which ions pass.
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53
Drug B is five times more efficacious than Drug A.
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54
Drug A and Drug B are equally efficacious.
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55
Drug A and Drug B each have a different ED50.
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56
Possible mechanisms for the placebo effect include:

A) biological action of the active ingredient in the placebo.
B) a clearly defined set of traits in the patient.
C) side effects of the placebo.
D) genetics of the patient.
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57
A given neurotransmitter is usually capable of binding to more than one receptor.
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58
Drug A is five times more potent than Drug B.
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59
Drug A is 10 times more efficacious than Drug B.
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60
Drug B is more potent that Drug A.
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61
Receptors that consist of an attachment site and a pore that allows specific ions to enter the cell are referred to as _____ receptors.

A) metabotropic
B) trophic
C) G-protein-coupled
D) ionotropic
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62
The binding of drugs to receptors involves _____ bonds that are ______.

A) weak; irreversible
B) ionic; irreversible
C) ionic; reversible
D) covalent; reversible
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63
Molecular isomers of drugs are _____ similar but are not _____active.

A) chemically; biologically
B) chemically; behaviorally
C) biologically; chemically
D) biologically; behaviorally
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64
In the context of polypharmacy,doses may be selected that are ineffective due to side effects- a phenomenon referred to as:

A) pharmacodynamic redundancy .
B) pharmacokinetic dosing.
C) inadequate dosing.
D) clinical dosing.
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65
Normal side effects to a drug may take all of the following forms EXCEPT:

A) fatal shock.
B) constipation.
C) dry mouth.
D) sleepiness.
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66
Pharmacodynamics is about:

A) what the body does to a drug.
B) how cells bind to drugs.
C) where drugs bind to cells in the body.
D) what a drug does to the body.
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67
Janette has been prescribed an antidepressant; over time,she may have to increase her dose due to receptor:

A) upregulation.
B) supersensitivity.
C) desensitization.
D) over production.
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68
Richard is participating in a research study involving a new pain medication.However,he is not actually receiving the biologically active medication.Research suggests that he:

A) is most likely to fall into the group of participants that sometimes respond to placebo.
B) is likely to always respond to placebo.
C) will not respond at all to the placebo.
D) he is more likely to respond to placebo because he is male.
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69
G-protein-coupled receptors are considered to be _____ while ionotropic are _____ receptors.

A) slow; fast
B) fast; direct
C) direct; fast
D) indirect; slow
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70
Ionotropic receptors consist of _____ coils embedded in the membrane with an attachment site(s)_____ the membrane.

A) spring; outside
B) spring; inside and outside
C) helical; outside
D) helical; beside
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71
The relative safety of a drug can be determined from the ratio of the LD50 to the ED50.
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72
Within the context of the dose-response curve,the _____ of the curve describes the association between the dose of the drug and its overall effect.

A) variability
B) height
C) slope
D) potency
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73
The double-blind randomized clinical trial without placebo is currently the gold standard for studying the effectiveness and safety of drugs in humans.
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74
An antagonist binds to the same receptor site as the endogenous compound but prevents the endogenous compound from acting.
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75
All of the following are types of receptors EXCEPT:

A) carrier proteins.
B) enzymes.
C) ion channel receptors.
D) cyclic AMP.
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76
If simultaneous administration of an agonist and antagonist cause a downward shift in the maximal effect of an agonist's response,the antagonist would be considered:

A) allosteric.
B) competitive.
C) noncompetitive.
D) reversible.
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77
The amount of drug that must be given to produce a given effect is called the drug:

A) efficacy.
B) potency.
C) intensity.
D) affinity.
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78
A drug that binds to a receptor site that elicits an opposite effect to that observed when an endogenous neurotransmitter binds is referred to as a(n):

A) partial antagonist.
B) allosteric agonist.
C) competitive antagonist.
D) inverse agonist.
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79
The _____ of a drug refers to how strongly it attaches to the receptor.

A) fit
B) affinity
C) binding
D) ionic nature
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80
G-protein-coupled receptors:

A) are sometimes referred to as ionotropic receptors.
B) possess a pore that opens allowing ions to enter the cell.
C) typically are made up of five helical,membrane-spanning coils.
D) involve the release of an attached intracellular protein after a drug binds.
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