Chapter 6: How do Drugs and Hormones influence the Brain and Behavior? Flashcards
MULTIPLE-CHOICE QUESTIONS
- Various forms of ______ have been used as study pills by students. A) barbiturates B) opioids C) amphetamines D) antipsychotics
C) amphetamines
______ is the study of how drugs affect the nervous system and behavior. A) Neuroscience B) Biopsychology C) Neuropsychology D) Psychopharmacology
D) Psychopharmacology
Drugs that are used to manage neuropsychological illness are called: A) prophylactic drugs. B) psychoactive drugs. C) mood drugs. D) psychodepressant drugs.
B) psychoactive drugs.
Which of the following is the least efficient method of drug administration? A) injection into the bloodstream B) injection into the brain C) oral consumption D) inhaling the drug
C) oral consumption
If a person is dying and needs lifesaving medication to be administered as quickly as possible, what is the best method of administration? A) oral consumption B) injection into muscle C) injection into the bloodstream D) a patch on the skin
C) injection into the bloodstream
The correct order from least efficient to most efficient method of drug administration is: A) oral consumption, inhalation, injection into the bloodstream B) skin patch, oral consumption, injection into muscle C) injection into muscle, injection into bloodstream, oral consumption D) inhalation, oral consumption, injection into the brain
A) oral consumption, inhalation, injection into the bloodstream
Approximately how many liters of blood are in the circulatory system at any one time? A) 3 B) 6 C) 9 D) 12
B) 6
Which of the following are most effective in passing through the blood–brain barrier easily? A) weak-base drugs B) drugs bound to proteins C) hydrophilic drugs D) water-soluble drugs
D) water-soluble drugs
One thousand micrograms of amphetamine taken orally is equivalent to: A) 100 micrograms injected into the cerebrospinal fluid. B) 10 micrograms injected into the cerebrospinal fluid. C) 5 micrograms injected into the cerebrospinal fluid. D) 1 microgram injected into the cerebrospinal fluid.
B) 10 micrograms injected into the cerebrospinal fluid.
Endothelial cells are: A) surrounded by the end feet of astrocyte glial cells. B) associated with veins. C) organized in the same fashion throughout the body. D) None of the answers is correct
A) surrounded by the end feet of astrocyte glial cells.
Tight junctions are associated with: A) astrocyte glial cells. B) endothelial cells. C) synaptic clefts. D) drugs bound to proteins.
B) endothelial cells.
The pituitary gland is to the area postrema of the lower brainstem as: A) toxins are to hormones. B) hormones are to toxins. C) vomiting is to shivering. D) shivering is to vomiting.
B) hormones are to toxins
The ______ does not have a blood–brain barrier. A) amygdala B) pineal gland C) thalamus D) All structures in the brain have a blood–brain barrier
B) pineal gland
Drugs that influence hormones primarily do so by acting on the: A) hypothalamus. B) pituitary gland. C) area postrema. D) pineal gland.
B) pituitary gland.
Which of the following substances can pass through the endothelial membrane in the blood–brain barrier unassisted (i.e., without active transport)? A) glucose B) carbon dioxide C) amino acids D) All of the answers are correct.
B) carbon dioxide
An active-transport system transports: A) glucose and other food items. B) glucose and amino acids. C) amino acids and other food items. D) only one specific substance
D) only one specific substance
The blood–brain barrier does not allow ______ to pass through. A) glucose B) amino acids C) neurochemicals D) oxygen
C) neurochemicals
Which of the following does not cross the blood–brain barrier? A) oxygen B) glucose C) amino acids D) carbon
D) carbon
Approximately ______ of drugs that can influence brain function cannot pass through the blood– brain barrier. A) 50 percent B) 78 percent C) 90 percent D) 98 percent
D) 98 percent
The breakdown of drugs by the body is referred to as: A) reuptake. B) metabolization. C) catabolization. D) deactivation.
C) catabolization.
The ______ is especially important for catabolizing drugs in the body. A) liver B) pancreas C) kidneys D) gallbladder
A) liver
______ cannot be easily broken down by the body and can cause severe neurological side effects. A) Mercury B) Magnesium C) Aluminum D) Potassium
A) Mercury
Psychoactive drugs have most of their effects at the: A) cell body. B) axon. C) synapse. D) dendrite
C) synapse.
A drug that prevents the breakdown of acetylcholine at synapses is an example of an: A) antagonist. B) accelerant. C) blocker. D) agonist.
D) agonist.
Agonist is to antagonist as: A) receptor is to terminal button. B) drug is to neurotransmitter. C) accelerate is to brake. D) slow is to fast.
C) accelerate is to brake.
- Botulin toxin (botulism) causes paralysis and slowed breathing and is therefore: A) an acetylcholine agonist. B) an acetylcholine antagonist. C) a dopamine agonist. D) a dopamine antagonist.
B) an acetylcholine antagonist.
Botulin toxin is used pharmacologically to: A) reduce muscle spasms. B) reduce skin wrinkling. C) reduce both muscle spasms and skin wrinkling. D) treat Parkinson’s disease.
C) reduce both muscle spasms and skin wrinkling.
Black widow spider venom: A) promotes the release of acetylcholine. B) blocks receptors. C) stimulates receptors. D) inhibits the release of acetylcholine.
A) promotes the release of acetylcholine.
drug that blocks the release of acetylcholine is called a(n): A) antagonist. B) agonist. C) desynthesizer. D) contragonist.
A) antagonist
Black widow spider venom affects its victim by: A) promoting the release of acetylcholine. B) inhibiting the release of acetylcholine. C) blocking the postsynaptic acetylcholine receptors. D) activating the postsynaptic acetylcholine receptors.
A) promoting the release of acetylcholine.
Botulin toxin is found in: A) bee and wasp stings. B) the crocus plant. C) tainted food. D) plant berries.
C) tainted food.
Nicotine acts as a(n): A) acetylcholine agonist. B) serotonin agonist. C) acetylcholine antagonist. D) dopamine antagonist.
A) acetylcholine agonist.
Curare: A) promotes the release of acetylcholine. B) blocks receptors. C) stimulates receptors. D) inhibits the release of acetylcholine.
B) blocks receptors.
______, an ______, was used to make poison arrowheads by South American natives. A) Curare; acetylcholine agonist B) Physostigmine; acetylcholine antagonist C) Physostigmine; acetylcholine agonist D) Curare; acetylcholine antagonist
Curare; acetylcholine antagonist
Nicotine, a chemical found in tobacco smoke, has its effect by: A) promoting the release of acetylcholine. B) inhibiting the release of acetylcholine. C) blocking the GABA receptors. D) activating the GABA receptors.
A) promoting the release of acetylcholine.
______ has been used to treat some memory disorders. A) Curare B) Botulin toxin C) Physostigmine D) None of the answers is correct.
C) Physostigmine
An example of an organophosphate is: A) curare. B) physostigmine. C) insecticide. D) botulinum toxin
C) insecticide.
______ is a decreased response to a drug over time. A) Addiction B) Tolerance C) Dependence D) Sensitization
B) Tolerance
When the number of enzymes needed to break down a drug in the liver increases, it is called: A) cellular tolerance. B) metabolic tolerance. C) sensitization. D) habituation.
B) metabolic tolerance
The development of ______ can explain why a person may appear to be unintoxicated despite having a high blood alcohol level. A) metabolic tolerance B) addiction C) sensitization D) cellular tolerance
D) cellular tolerance
______ is likely to increase with ______ drug use. A) Tolerance; occasional B) Sensitization; repeated C) Sensitization; occasional D) None of the answers is correct.
C) Sensitization; occasional