Deck 3: How Drugs Work in the Body and on the Mind

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Question
Elimination of drugs can be done via sweat and saliva.
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Question
Orally administered drugs are ingested at higher-than-needed doses because some of the drug will not make it through the bloodstream.
Question
The psychoactive effects of intravenous injections are faster than those of inhalation.
Question
The intravenous injection is the fastest type of injection to deliver a drug into the bloodstream.
Question
Fat-soluble drugs are eliminated faster than water-soluble drugs.
Question
The smaller the quantity of the drug, the faster the body tries to get rid of it.
Question
The elimination half-life of a drug will be faster if the drug is fat-soluble than if it is not.
Question
The half-life of nicotine is a few days.
Question
Older people eliminate drugs at a slower pace than younger people do.
Question
Regardless of which route of administration is used, the goal is for the drug to be absorbed into the bloodstream.
Question
A major disadvantage of drug inhalation is that the linings leading from the throat to the lungs become irritated over time.
Question
An overdose from an orally administered drug is easier to handle on an emergency basis than an overdose of a drug administered through an intravenous injection.
Question
Paint thinners, gasoline, and cleaning fluid are examples of abused products that are typically administered by absorption through the skin or membranes.
Question
The half-life of cocaine is only a few hours.
Question
Inhalation of smoked drugs such as crack does not present the same hazards to the respiratory system as do tobacco-based cigarettes.
Question
Intramuscular injections are often referred to as skin-popping.
Question
Mild electric currents can be used to help absorb drugs through the skin or membranes.
Question
Tetanus shots, flu shots, and most inoculations are administered by intramuscular injections.
Question
High-alkaline drugs (i.e., cocaine, morphine) are absorbed better in the stomach than weakly acidic drugs (i.e., aspirin).
Question
"First-pass metabolism" is an important function of the esophagus.
Question
The nervous system is made up of two parts known as the central nervous system and the peripheral nervous system.
Question
It is possible to develop a tolerance to a drug you have never taken before.
Question
An example of an antagonistic effect would be if Drug A had an effect of 5 and Drug B had an effect of 3, but the combination of the two drugs together resulted in an effect of 15.
Question
The danger of potentiation is that since the drug seems to have no effect, the combined effect may be so powerful that it can become lethal.
Question
An increased heart rate and a decreased rate of digestion are two signs of sympathetic activation.
Question
A man and a woman each weigh 79 kg (175 pounds). If they both take the same dose of a drug, the same effects can be expected.
Question
Two examples of hyperadditive combinations are synergism and potentiation.
Question
Administering the drug in a time-release form helps eliminate the undesirable side effects of excessive concentrations of a drug in the blood.
Question
Cross-dependence can be useful when trying to avoid the withdrawal symptoms of an unavailable drug.
Question
Analogy: Breathing is to somatic as lifting your arm is to autonomic.
Question
If Drug A has an effect of 3 and Drug B has an effect of 6, a purely additive combination effect would be equivalent to 18.
Question
Potentiation involves one drug having no effect at all unless taken with another.
Question
The length of the latency period is related to the absorption time of the drug.
Question
Potentiation is a special form of antagonistic drug interaction.
Question
According to the text, North Americans of African descent smoke fewer cigarettes per day than Caucasians because those of African descent may be retaining more nicotine per cigarette than Caucasians.
Question
Individual differences such as weight and gender can affect how one person reacts to a drug compared to another.
Question
The central nervous system consists of the brain and the spinal cord.
Question
If we can relieve the withdrawal symptoms of one drug by administering another, than the two drugs show cross-tolerance.
Question
The sympathetic and parasympathetic systems together form the peripheral nervous system.
Question
All drugs have similar elimination half-lives.
Question
Sensory nerves enter the CNS at the level of the brain but not the spinal cord.
Question
Ionotropic receptors are always linked to G proteins.
Question
The part of the brain that determines when we sleep and when we wake up is located in the pons.
Question
The receptor to which a neurotransmitter binds determines whether that neurotransmitter has an excitatory or inhibitory effect.
Question
The most recently evolved region of the human brain is the prefrontal cortex.
Question
The risk of asphyxiation from a certain dosage level of a drug most likely means that the drug is capable of stimulating the cerebral cortex.
Question
The processing of pain information occurs in the hindbrain.
Question
The myelin sheath on some neurons increases the speed of action potentials.
Question
There are approximately 100 billion neurons in the brain.
Question
Dendrites are to transmitting information as axon is to receiving information.
Question
The three categories of brain tissue are the medulla, the hypothalamus, and the cerebellum.
Question
The two ions that play the largest role in the generation of an action potential are Ca2+ and K+.
Question
Communication between neurons is accomplished through the actions of chemical substances called neurotransmitters.
Question
Most theories about the physiological basis for psychological dependence focus on the limbic system.
Question
The processing of reflex responses does not involve the brain at all.
Question
Psychoactive drugs can produce bodily effects that are oriented toward parasympathetic rather than sympathetic activation.
Question
Damage to the prefrontal cortex may be associated with loss of personal control with respect to the abuse of alcohol and other drugs.
Question
Reuptake is the process whereby a neurotransmitter returns from the receptor site back to the presynaptic terminal.
Question
The limbic system and hypothalamus are two structures of the brain that "overhang" the cerebral cortex.
Question
Brain tissue is classified in sections: the hindbrain, the midbrain, and the forebrain.
Question
Agonists facilitate synaptic transmission while antagonists decrease synaptic transmission.
Question
Drugs that relieve mania and depression act upon serotonin-releasing neurons.
Question
The blood-brain barrier cannot be crossed by a drug that is fat soluble.
Question
When multiple drugs activate the same type of receptor sites, the effects of each drug on the brain are equivalent.
Question
Alzheimer's disease has been linked to deficiencies in nicotinic receptors.
Question
Tolerance that is a result of changes in the drug's chemical breakdown in the liver is referred to as cellular (pharmacodynamic) tolerance.
Question
Dopamine is more fat-soluble than L-Dopa.
Question
Norepinephrine is to the hypothalamus as serotonin is to the pons.
Question
Glutamate is the most common inhibitory neurotransmitter.
Question
A major drug for the treatment of Parkinson's disease has been L-Dopa.
Question
Metabolic tolerance occurs when receptors become less sensitive due to being stimulated repeatedly by a drug over time.
Question
Acetylcholine is involved with the sympathetic autonomic nervous system, while norepinephrine is involved with the parasympathetic autonomic system.
Question
Involvement with the nucleus accumbens has been linked to compulsive gambling.
Question
The rewarding effects of certain psychoactive drugs are related to their effects upon the nucleus accumbens in the brain.
Question
GABA deficiencies are associated with a decreased tendency toward epileptic seizures.
Question
The key factor that determines whether a drug passes through the blood-brain barrier is water solubility.
Question
Antianxiety medications stimulate GABA-releasing neurons, providing a reduction in feelings of stress and fear.
Question
Barbiturates and caffeine easily pass through the blood-brain barrier.
Question
Set is defined as the immediate environment within which drug-taking behaviour occurs.
Question
The neurotransmitter responsible for regulating our mood states is acetylcholine.
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Deck 3: How Drugs Work in the Body and on the Mind
1
Elimination of drugs can be done via sweat and saliva.
True
2
Orally administered drugs are ingested at higher-than-needed doses because some of the drug will not make it through the bloodstream.
True
3
The psychoactive effects of intravenous injections are faster than those of inhalation.
False
4
The intravenous injection is the fastest type of injection to deliver a drug into the bloodstream.
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5
Fat-soluble drugs are eliminated faster than water-soluble drugs.
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6
The smaller the quantity of the drug, the faster the body tries to get rid of it.
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7
The elimination half-life of a drug will be faster if the drug is fat-soluble than if it is not.
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8
The half-life of nicotine is a few days.
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9
Older people eliminate drugs at a slower pace than younger people do.
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10
Regardless of which route of administration is used, the goal is for the drug to be absorbed into the bloodstream.
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11
A major disadvantage of drug inhalation is that the linings leading from the throat to the lungs become irritated over time.
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12
An overdose from an orally administered drug is easier to handle on an emergency basis than an overdose of a drug administered through an intravenous injection.
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13
Paint thinners, gasoline, and cleaning fluid are examples of abused products that are typically administered by absorption through the skin or membranes.
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14
The half-life of cocaine is only a few hours.
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15
Inhalation of smoked drugs such as crack does not present the same hazards to the respiratory system as do tobacco-based cigarettes.
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16
Intramuscular injections are often referred to as skin-popping.
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17
Mild electric currents can be used to help absorb drugs through the skin or membranes.
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18
Tetanus shots, flu shots, and most inoculations are administered by intramuscular injections.
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19
High-alkaline drugs (i.e., cocaine, morphine) are absorbed better in the stomach than weakly acidic drugs (i.e., aspirin).
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20
"First-pass metabolism" is an important function of the esophagus.
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21
The nervous system is made up of two parts known as the central nervous system and the peripheral nervous system.
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22
It is possible to develop a tolerance to a drug you have never taken before.
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23
An example of an antagonistic effect would be if Drug A had an effect of 5 and Drug B had an effect of 3, but the combination of the two drugs together resulted in an effect of 15.
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24
The danger of potentiation is that since the drug seems to have no effect, the combined effect may be so powerful that it can become lethal.
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25
An increased heart rate and a decreased rate of digestion are two signs of sympathetic activation.
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26
A man and a woman each weigh 79 kg (175 pounds). If they both take the same dose of a drug, the same effects can be expected.
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27
Two examples of hyperadditive combinations are synergism and potentiation.
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28
Administering the drug in a time-release form helps eliminate the undesirable side effects of excessive concentrations of a drug in the blood.
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29
Cross-dependence can be useful when trying to avoid the withdrawal symptoms of an unavailable drug.
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30
Analogy: Breathing is to somatic as lifting your arm is to autonomic.
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31
If Drug A has an effect of 3 and Drug B has an effect of 6, a purely additive combination effect would be equivalent to 18.
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32
Potentiation involves one drug having no effect at all unless taken with another.
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33
The length of the latency period is related to the absorption time of the drug.
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34
Potentiation is a special form of antagonistic drug interaction.
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35
According to the text, North Americans of African descent smoke fewer cigarettes per day than Caucasians because those of African descent may be retaining more nicotine per cigarette than Caucasians.
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36
Individual differences such as weight and gender can affect how one person reacts to a drug compared to another.
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37
The central nervous system consists of the brain and the spinal cord.
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38
If we can relieve the withdrawal symptoms of one drug by administering another, than the two drugs show cross-tolerance.
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39
The sympathetic and parasympathetic systems together form the peripheral nervous system.
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40
All drugs have similar elimination half-lives.
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41
Sensory nerves enter the CNS at the level of the brain but not the spinal cord.
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42
Ionotropic receptors are always linked to G proteins.
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43
The part of the brain that determines when we sleep and when we wake up is located in the pons.
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44
The receptor to which a neurotransmitter binds determines whether that neurotransmitter has an excitatory or inhibitory effect.
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45
The most recently evolved region of the human brain is the prefrontal cortex.
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46
The risk of asphyxiation from a certain dosage level of a drug most likely means that the drug is capable of stimulating the cerebral cortex.
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47
The processing of pain information occurs in the hindbrain.
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48
The myelin sheath on some neurons increases the speed of action potentials.
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49
There are approximately 100 billion neurons in the brain.
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50
Dendrites are to transmitting information as axon is to receiving information.
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51
The three categories of brain tissue are the medulla, the hypothalamus, and the cerebellum.
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52
The two ions that play the largest role in the generation of an action potential are Ca2+ and K+.
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53
Communication between neurons is accomplished through the actions of chemical substances called neurotransmitters.
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54
Most theories about the physiological basis for psychological dependence focus on the limbic system.
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55
The processing of reflex responses does not involve the brain at all.
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56
Psychoactive drugs can produce bodily effects that are oriented toward parasympathetic rather than sympathetic activation.
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57
Damage to the prefrontal cortex may be associated with loss of personal control with respect to the abuse of alcohol and other drugs.
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58
Reuptake is the process whereby a neurotransmitter returns from the receptor site back to the presynaptic terminal.
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59
The limbic system and hypothalamus are two structures of the brain that "overhang" the cerebral cortex.
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60
Brain tissue is classified in sections: the hindbrain, the midbrain, and the forebrain.
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61
Agonists facilitate synaptic transmission while antagonists decrease synaptic transmission.
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62
Drugs that relieve mania and depression act upon serotonin-releasing neurons.
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63
The blood-brain barrier cannot be crossed by a drug that is fat soluble.
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64
When multiple drugs activate the same type of receptor sites, the effects of each drug on the brain are equivalent.
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65
Alzheimer's disease has been linked to deficiencies in nicotinic receptors.
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66
Tolerance that is a result of changes in the drug's chemical breakdown in the liver is referred to as cellular (pharmacodynamic) tolerance.
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67
Dopamine is more fat-soluble than L-Dopa.
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68
Norepinephrine is to the hypothalamus as serotonin is to the pons.
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69
Glutamate is the most common inhibitory neurotransmitter.
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70
A major drug for the treatment of Parkinson's disease has been L-Dopa.
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71
Metabolic tolerance occurs when receptors become less sensitive due to being stimulated repeatedly by a drug over time.
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72
Acetylcholine is involved with the sympathetic autonomic nervous system, while norepinephrine is involved with the parasympathetic autonomic system.
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73
Involvement with the nucleus accumbens has been linked to compulsive gambling.
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74
The rewarding effects of certain psychoactive drugs are related to their effects upon the nucleus accumbens in the brain.
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k this deck
75
GABA deficiencies are associated with a decreased tendency toward epileptic seizures.
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76
The key factor that determines whether a drug passes through the blood-brain barrier is water solubility.
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77
Antianxiety medications stimulate GABA-releasing neurons, providing a reduction in feelings of stress and fear.
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78
Barbiturates and caffeine easily pass through the blood-brain barrier.
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79
Set is defined as the immediate environment within which drug-taking behaviour occurs.
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80
The neurotransmitter responsible for regulating our mood states is acetylcholine.
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