Test Bank
TEST BANK
,Drugs Behavior And Modern Society 8th Edition Levinthal Test Bank
CHAPTER 3
HOW DRUGS WORK IN THE BODY AND ON THE MIND
DISCUSSION QUESTIONS AND ASSIGNMENTS
1. Science-oriented news stories often are featured on a certain day each week in daily blogs, websites,
and on a number of medical websites. During the semester, assign students to watch for articles that
specifically bear upon one of the neurotransmitters described in the chapter. You might consider
having a regularly scheduled “Neurotransmitter of the Week” discussion in class, where information
about new findings regarding that neurotransmitter can be shared either as part of a lecture or as a
class discussion/presentation.
2. Have students make a list of circumstances under which they feel they would be strongly influenced by
the psychological effects of a placebo. Responses can be collected, transcribed (on an anonymous
basis to protect their privacy), and photocopied for the entire class to receive as a handout. A class
discussion could ensue regarding the reasons why a particular student might think that he or she
would have a similar reaction. Likewise, if there is disagreement among students, an interesting
discussion could follow regarding individual differences.
3. Bring a square cloth dinner napkin (approximately 18 inches by 18 inches) to class. Wrinkle it up into
an oval-shaped ball by folding it into itself like a fan. Try to make it appear as an approximation of the
convoluted cerebral cortex. Show it to the class then smooth the napkin out on a flat surface. This is
an approximation of the surface area of the cerebral cortex if it were possible to be “un-convoluted.”
The class could come up with at least two reasons why it would not have been good for humans to
have a larger brain that included a cerebral cortex without convolutions. One reason is that the skull
encasing the brain would have been too heavy for us to support at the neck and walk upright at the
same time. Another reason is that the larger head would have not been able to fit through the birth
canal during labor and delivery. Cortical convolutions have provided a greatly expanded cortical
organization for higher-order information processing without requiring a greatly enlarged brain volume.
NOTE: A useful source for information about prescription and over-the-counter drugs available in
the United States can be accessed through the following web site:
The National Library of Medicine/National Institutes of Health
http://www.nlm.nih.gov/
LECTURE OUTLINE FOR CHAPTER THREE
A. How Drugs Enter the Body
1. Oral administration involves ingesting a drug by mouth, digesting it, and absorbing it
into the bloodstream through the gastrointestinal tract. Orally administered drugs have a
relatively long absorption time and require specific pharmacological features and
circumstances for successful passage into the bloodstream. Enzymes in the liver break down
(metabolize) the structure of certain drugs, reducing the amount that eventually enters the
bloodstream. This function of the liver is referred to as first-pass metabolism.
2. Administration by injection allows a drug to be delivered directly into the bloodstream,
bypassing the digestive process. Examples of an injection administration include
Visit TestBankDeal.com to get complete for all chapters
, intravenous (into a vein), intramuscular (into a muscle), and subcutaneous (underneath the
skin) procedures. Of these possibilities, an intravenous injection is the fastest form of drug
administration. Heroin injected into the forearm, for example, arrives at the brain in less than
fifteen seconds.
3. Inhalation refers to the ingestion of a drug in a gaseous or vaporous state into the
lungs. It is an extremely rapid form of drug administration. One inhalation method, smoking—
burning a substance and breathing the smoke-borne particles in the air—has the
disadvantage of carrying toxic particles produced by the burning process into the throat and
lungs.
4. Absorption of drugs can be accomplished by dissolving the drug and allowing it to pass
through the skin or thin membranes. Intranasal and rectal administration involves thin
mucous membranes of the nose or rectum, respectively. Transdermal patches permit drugs to
be absorbed slowly through the skin. Alternative methods under development include small
silicon chips containing a grid of microscopic needles that painlessly pierce the skin and allow
the passage of large molecules into the bloodstream.
B. How Drugs Exit the Body
1. The body eliminates drugs through a series of biotransformation processes in which the drug is
chemically changed into forms called metabolites. A number of factors determine the rate of
biotransformation during the elimination process. These factors include the quantity of the
drug (alcohol is an exception, its elimination rate being independent of the quantity ingested),
the age of the individual, and the drug’s fat solubility. A fat-soluble drug will be eliminated
more slowly than a water-soluble drug, all other factors being equal.
2. The elimination half-life is the amount of time required for the drug to be reduced in the
bloodstream by 50 percent. Each additional interval of time reduces the quantity of the
drug by half until there is a negligible amount remaining.
C. Factors Determining the Behavioral Impact of Drugs
1. One factor that impacts on a drug’s behavioral effect is the time interval between two
successive administrations of the drug. Time-release forms of medicines allow for a continual
absorption over a longer period of time than would a single dose.
2. A second factor is the interacting effect of two different drugs administered at the same time.
Drug combinations can be additive, hyperadditive, or antagonistic. An additive effect
produces an end result that is the mathematical sum of the effects of the two drugs
separately. A hyperadditive effect produced by a combination of two or more drugs is
referred to as synergism. If two drugs are perfectly antagonistic, each one cancels out
the effect of the other.
3. Some drugs can interact with each other during chronic usage. Cross-tolerance between two
drugs is a phenomenon in which the tolerance that results from the chronic use of one
drug induces a tolerance effect with regard to a second drug that has not been used
before. Alcohol, barbiturates, and some antianxiety medications, for example, show cross-
tolerance. Cross-dependence is a phenomenon in which one drug can be used to
reduce the withdrawal symptoms following the discontinuance of another drug. Cross-
dependence provides the means for continuing an abused drug in the guise of a new one.
4. Features of the individual who is taking the drug can influence the effect of the drug. Such
features include weight, gender, ethnic background, and race.
D. Introducing the Nervous System
, 1. The nervous system is divided into the central nervous system (brain and spinal cord)
and the peripheral nervous system. The peripheral nervous system either brings
information in from the environment (sensory pathways) or out to the muscles (motor
pathways). Motor control is exerted either through somatic nerves leading to skeletal muscle
or autonomic nerves leading to cardiac or smooth muscle.
2. Autonomic nerves are divided into sympathetic and parasympathetic divisions. Increased
activity in sympathetic autonomic nerves produces body changes that are oriented
toward dealing with some kind of emergency or stress. Increased activity in
parasympathetic autonomic nerves produces body changes that are oriented toward
calm, rest, nurturance, and internal maintenance.
E. Understanding the Brain
1. The brain is divided into the hindbrain, midbrain, and forebrain. The hindbrain is
concerned with basic life-support functions and primitive functions (medulla, pons, reticular
formation, and cerebellum). The midbrain is a center for the control of important sensory and
motor reflexes, body movements, and the processing of pain information (substantia nigra).
The forebrain is concerned with motivational and emotional activity (hypothalamus and limbic
system) and complex information-processing (cerebral cortex).
2. Of all the areas within the cerebral cortex, the most recently evolved is a region closest to the
front of the brain called prefrontal cortex. Our higher-order, intellectual abilities (often referred
to as executive functioning) as well as our personality characteristics emerge from activity in
this region. It has been speculated that a dysfunction in the prefrontal cortex may be
associated with a loss of personal control with respect to the abuse of alcohol and other drugs.
F. Understanding the Neurochemistry of Psychoactive Drugs
1. Psychoactive drugs work by virtue of their effects on the functioning of specialized cells called
neurons. Neurons are cells that receive and transmit information. The principal
components of a neuron are the cell body, the dendrites, and the axon. There are an
estimated 100 billion neurons in the brain alone.
2. Communication between neurons is accomplished at the synapse. Synaptic communication
can be either excitatory (causing an increase in the activity of the receiving neuron) or
inhibitory (causing a decrease in the activity of the receiving neuron).
3. Synaptic communication comprises a sequence of three basic processes. Neurotransmitters
stored in the synaptic vesicles are stimulated by a nerve impulse causing (1) neurotransmitter
release from the synaptic knob, (2) binding to receptor sites on the surface of another neuron,
and (3) reuptake of neurotransmitter into the synaptic knob whence it came.
G. The Major Neurotransmitters in Brief: The Big Seven
1. Synaptic communication is achieved through the action of special molecules called
neurotransmitters. Seven major neurotransmitters in the brain are acetylcholine,
norepinephrine, dopamine, 5-hydroxytryptamine (serotonin), gamma aminobutyric acid
(GABA), glutamate, and a group of neurotransmitters referred to as endorphins. Whether a
neurotransmitter has an excitatory or inhibitory effect depends upon the nature of the receptor
at the synapse. Thus, excitation requires the activation of excitatory receptors and inhibition
requires the activation of inhibitory receptors.
2. Psychoactive drugs change the functioning of these and other neurotransmitters at the
synapse or alter the functioning of receptors that are sensitive to these molecules. As
TEST BANK
,Drugs Behavior And Modern Society 8th Edition Levinthal Test Bank
CHAPTER 3
HOW DRUGS WORK IN THE BODY AND ON THE MIND
DISCUSSION QUESTIONS AND ASSIGNMENTS
1. Science-oriented news stories often are featured on a certain day each week in daily blogs, websites,
and on a number of medical websites. During the semester, assign students to watch for articles that
specifically bear upon one of the neurotransmitters described in the chapter. You might consider
having a regularly scheduled “Neurotransmitter of the Week” discussion in class, where information
about new findings regarding that neurotransmitter can be shared either as part of a lecture or as a
class discussion/presentation.
2. Have students make a list of circumstances under which they feel they would be strongly influenced by
the psychological effects of a placebo. Responses can be collected, transcribed (on an anonymous
basis to protect their privacy), and photocopied for the entire class to receive as a handout. A class
discussion could ensue regarding the reasons why a particular student might think that he or she
would have a similar reaction. Likewise, if there is disagreement among students, an interesting
discussion could follow regarding individual differences.
3. Bring a square cloth dinner napkin (approximately 18 inches by 18 inches) to class. Wrinkle it up into
an oval-shaped ball by folding it into itself like a fan. Try to make it appear as an approximation of the
convoluted cerebral cortex. Show it to the class then smooth the napkin out on a flat surface. This is
an approximation of the surface area of the cerebral cortex if it were possible to be “un-convoluted.”
The class could come up with at least two reasons why it would not have been good for humans to
have a larger brain that included a cerebral cortex without convolutions. One reason is that the skull
encasing the brain would have been too heavy for us to support at the neck and walk upright at the
same time. Another reason is that the larger head would have not been able to fit through the birth
canal during labor and delivery. Cortical convolutions have provided a greatly expanded cortical
organization for higher-order information processing without requiring a greatly enlarged brain volume.
NOTE: A useful source for information about prescription and over-the-counter drugs available in
the United States can be accessed through the following web site:
The National Library of Medicine/National Institutes of Health
http://www.nlm.nih.gov/
LECTURE OUTLINE FOR CHAPTER THREE
A. How Drugs Enter the Body
1. Oral administration involves ingesting a drug by mouth, digesting it, and absorbing it
into the bloodstream through the gastrointestinal tract. Orally administered drugs have a
relatively long absorption time and require specific pharmacological features and
circumstances for successful passage into the bloodstream. Enzymes in the liver break down
(metabolize) the structure of certain drugs, reducing the amount that eventually enters the
bloodstream. This function of the liver is referred to as first-pass metabolism.
2. Administration by injection allows a drug to be delivered directly into the bloodstream,
bypassing the digestive process. Examples of an injection administration include
Visit TestBankDeal.com to get complete for all chapters
, intravenous (into a vein), intramuscular (into a muscle), and subcutaneous (underneath the
skin) procedures. Of these possibilities, an intravenous injection is the fastest form of drug
administration. Heroin injected into the forearm, for example, arrives at the brain in less than
fifteen seconds.
3. Inhalation refers to the ingestion of a drug in a gaseous or vaporous state into the
lungs. It is an extremely rapid form of drug administration. One inhalation method, smoking—
burning a substance and breathing the smoke-borne particles in the air—has the
disadvantage of carrying toxic particles produced by the burning process into the throat and
lungs.
4. Absorption of drugs can be accomplished by dissolving the drug and allowing it to pass
through the skin or thin membranes. Intranasal and rectal administration involves thin
mucous membranes of the nose or rectum, respectively. Transdermal patches permit drugs to
be absorbed slowly through the skin. Alternative methods under development include small
silicon chips containing a grid of microscopic needles that painlessly pierce the skin and allow
the passage of large molecules into the bloodstream.
B. How Drugs Exit the Body
1. The body eliminates drugs through a series of biotransformation processes in which the drug is
chemically changed into forms called metabolites. A number of factors determine the rate of
biotransformation during the elimination process. These factors include the quantity of the
drug (alcohol is an exception, its elimination rate being independent of the quantity ingested),
the age of the individual, and the drug’s fat solubility. A fat-soluble drug will be eliminated
more slowly than a water-soluble drug, all other factors being equal.
2. The elimination half-life is the amount of time required for the drug to be reduced in the
bloodstream by 50 percent. Each additional interval of time reduces the quantity of the
drug by half until there is a negligible amount remaining.
C. Factors Determining the Behavioral Impact of Drugs
1. One factor that impacts on a drug’s behavioral effect is the time interval between two
successive administrations of the drug. Time-release forms of medicines allow for a continual
absorption over a longer period of time than would a single dose.
2. A second factor is the interacting effect of two different drugs administered at the same time.
Drug combinations can be additive, hyperadditive, or antagonistic. An additive effect
produces an end result that is the mathematical sum of the effects of the two drugs
separately. A hyperadditive effect produced by a combination of two or more drugs is
referred to as synergism. If two drugs are perfectly antagonistic, each one cancels out
the effect of the other.
3. Some drugs can interact with each other during chronic usage. Cross-tolerance between two
drugs is a phenomenon in which the tolerance that results from the chronic use of one
drug induces a tolerance effect with regard to a second drug that has not been used
before. Alcohol, barbiturates, and some antianxiety medications, for example, show cross-
tolerance. Cross-dependence is a phenomenon in which one drug can be used to
reduce the withdrawal symptoms following the discontinuance of another drug. Cross-
dependence provides the means for continuing an abused drug in the guise of a new one.
4. Features of the individual who is taking the drug can influence the effect of the drug. Such
features include weight, gender, ethnic background, and race.
D. Introducing the Nervous System
, 1. The nervous system is divided into the central nervous system (brain and spinal cord)
and the peripheral nervous system. The peripheral nervous system either brings
information in from the environment (sensory pathways) or out to the muscles (motor
pathways). Motor control is exerted either through somatic nerves leading to skeletal muscle
or autonomic nerves leading to cardiac or smooth muscle.
2. Autonomic nerves are divided into sympathetic and parasympathetic divisions. Increased
activity in sympathetic autonomic nerves produces body changes that are oriented
toward dealing with some kind of emergency or stress. Increased activity in
parasympathetic autonomic nerves produces body changes that are oriented toward
calm, rest, nurturance, and internal maintenance.
E. Understanding the Brain
1. The brain is divided into the hindbrain, midbrain, and forebrain. The hindbrain is
concerned with basic life-support functions and primitive functions (medulla, pons, reticular
formation, and cerebellum). The midbrain is a center for the control of important sensory and
motor reflexes, body movements, and the processing of pain information (substantia nigra).
The forebrain is concerned with motivational and emotional activity (hypothalamus and limbic
system) and complex information-processing (cerebral cortex).
2. Of all the areas within the cerebral cortex, the most recently evolved is a region closest to the
front of the brain called prefrontal cortex. Our higher-order, intellectual abilities (often referred
to as executive functioning) as well as our personality characteristics emerge from activity in
this region. It has been speculated that a dysfunction in the prefrontal cortex may be
associated with a loss of personal control with respect to the abuse of alcohol and other drugs.
F. Understanding the Neurochemistry of Psychoactive Drugs
1. Psychoactive drugs work by virtue of their effects on the functioning of specialized cells called
neurons. Neurons are cells that receive and transmit information. The principal
components of a neuron are the cell body, the dendrites, and the axon. There are an
estimated 100 billion neurons in the brain alone.
2. Communication between neurons is accomplished at the synapse. Synaptic communication
can be either excitatory (causing an increase in the activity of the receiving neuron) or
inhibitory (causing a decrease in the activity of the receiving neuron).
3. Synaptic communication comprises a sequence of three basic processes. Neurotransmitters
stored in the synaptic vesicles are stimulated by a nerve impulse causing (1) neurotransmitter
release from the synaptic knob, (2) binding to receptor sites on the surface of another neuron,
and (3) reuptake of neurotransmitter into the synaptic knob whence it came.
G. The Major Neurotransmitters in Brief: The Big Seven
1. Synaptic communication is achieved through the action of special molecules called
neurotransmitters. Seven major neurotransmitters in the brain are acetylcholine,
norepinephrine, dopamine, 5-hydroxytryptamine (serotonin), gamma aminobutyric acid
(GABA), glutamate, and a group of neurotransmitters referred to as endorphins. Whether a
neurotransmitter has an excitatory or inhibitory effect depends upon the nature of the receptor
at the synapse. Thus, excitation requires the activation of excitatory receptors and inhibition
requires the activation of inhibitory receptors.
2. Psychoactive drugs change the functioning of these and other neurotransmitters at the
synapse or alter the functioning of receptors that are sensitive to these molecules. As
