Bio Test 2 (ch4)

25 July 2022
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A(n) ________ is a drug that blocks or inhibits postsynaptic receptor effects.
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antagonist
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Drugs that facilitate the postsynaptic receptor effects are termed
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agonists
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Administering a molecule that is a precursor for the synthesis of a synaptic neurotransmitter would be expected to
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increase the rate of synthesis and release of that neurotransmitter.
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We would classify a drug as a(n) ________ if that drug acted to block the capacity of vesicles to be filled with neurotransmitter molecules.
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antagonist
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A drug that binds with a postsynaptic receptor, but does not open ion channels would be termed a(n)
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direct antagonist.
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A drug that binds at a postsynaptic site different from that of the neurotransmitter and facilitates the opening of ion channels would be termed a(n)
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indirect agonist.
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A(n) ________ is defined as drug that binds at a postsynaptic site different from that of the neurotransmitter and that prevents the opening of ion channels by the neurotransmitter.
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indirect antagonist
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A drug that activates a presynaptic autoreceptor will usually
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reduce the release of the neurotransmitter from the axon terminal.
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Activation of dendritic autoreceptors produce ________; a drug that is an agonist at these autoreceptors would be classified as an ________ for the synapse.
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hyperpolarizations; antagonist
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A drug that blocks a presynaptic autoreceptor most likely
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increases the release of the neurotransmitter from the axon terminal.
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A synapse that contains a presynaptic heteroreceptor would be classified as a(n) ________ synapse.
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axoaxonic
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Activation of a presynaptic autoreceptor on dendrites can produce a hyperpolarization that
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reduces transmitter release by reducing the axon firing rate.
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Inactivation of a transporter in the presynaptic membrane would be expected to
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increase the levels of the transmitter in the synapse.
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Termination of the postsynaptic potential would be expected from a drug or process that acts to
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enzymatically degrade the neurotransmitter molecule.
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The two most commonly used synaptic neurotransmitters in the brain are
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glutamate; GABA
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Which of the following is an incorrect match between a neurotransmitter and its effects?
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acetylcholine; subject to reuptake by the axon terminals
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Which pair of transmitters are the primary excitatory and inhibitory (respectively) transmitters in the brain?
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glutamate; GABA
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________ is the primary neurotransmitter secreted by motor axons of the CNS.
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Acetylcholine
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Which transmitter below induces muscle movement and is the primary transmitter secreted by efferent axons of the central nervous system?
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acetylcholine
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Match up the transmitter substance below with the appropriate behavioral role or action of that transmitter:
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acetylcholine; facilitation of perceptual learning
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Cholinergic neurons within the ________ are thought to ________.
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dorsolateral pons; elicit most of the aspects of REM sleep
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Match up the cholinergic fiber system with the correct role of that system in the control of behavior:
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Cholinergic neurons in the medial septum are involved in the control of the electrical rhythms of the hippocampus.
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Damage to the ________ cholinergic system would be expected to impair learning.
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basal forebrain
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Acetylcholine is produced when ________ accepts an acetate ion from coenzyme A and transfers it to a choline molecule.
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choline acetyltransferase
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Activation of the ________ has been related to the control of REM sleep.
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dorsolateral pons ACh system
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Which pair of drugs below is known to facilitate and inhibit (respectively) the release of acetylcholine?
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botulinum toxin; black widow spider venom
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In the anecdote on cholinergic toxicity, Mr. F. contracted botulism by
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tasting the liquid from a spoiled jar of asparagus.
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An ionotropic cholinergic receptor produces a postsynaptic potential that is
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rapid and short in duration.
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The disease process of myasthenia gravis produces muscle weakness by
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reducing the number of ACh receptors on muscles.
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A drug that blocks acetylcholinesterase in brain would be expected to
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increase the synaptic levels of acetylcholine.
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The postsynaptic action of acetylcholine is terminated by
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enzymatic destruction via acetylcholinesterase.
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Which of the following is true of the cholinergic systems?
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Muscarinic receptors are more numerous than nicotinic receptors in the brain.
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Nicotinic receptors are found in ________ in the periphery and in ________ in the brain.
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muscle fibers; axoaxonic synapses
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Which pair below represents the receptor subtypes for acetylcholine?
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nicotinic; muscarinic
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Which pair of drugs below are antagonists for the muscarinic and nicotinic (respectively) receptors?
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atropine; curare
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Curare is used in medical clinics to
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induce relaxation in muscles that are to be cut during a surgical procedure.
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The drug ________ causes pupil dilation by blocking ________ receptors.
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atropine; muscarinic
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The amino acid ________ is the synthesis precursor for dopamine and norepinephrine.
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tyrosine
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Which of the following is classified as an indolamine?
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serotonin
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Tyrosine is the precursor for the synthesis of
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dopamine.
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Degeneration of neurons within the ________ dopamine system leads to Parkinson's disease.
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nigrostriatal
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Damage to the ________ dopaminergic system would be expected to impair movement.
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nigrostriatal
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The neostriatum consists of the
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caudate nucleus and the putamen.
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The ________ dopamine system plays a key role in the control of ________.
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mesocortical; planning and problem solving
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Low doses of the drug apomorphine
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inhibit the synthesis and release of dopamine.
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The drug reserpine
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blocks the storage of monoamines in vesicles.
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Which of the following is true of dopamine receptors?
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Dopamine receptors are metabotropic.
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A drug that causes the transporters for dopamine to run in reverse would
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spill dopamine into the synaptic cleft.
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Drugs that inactivate monoamine oxidase B would be expected to
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increase the release of dopamine in response to the arrival of an action potential at the terminal buttons.
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Abnormal brain levels of dopamine are associated with
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schizophrenia and Parkinson's disease.
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A person who eats cheese while taking a(n) ________ may suffer a fatal increase in blood pressure.
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monoamine oxidase inhibitor drug
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The final synthesis step for norepinephrine occurs in the ________ and requires the presence of ________.
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vesicle; dopamine and DBH
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Which of the pairs below are synonymous?
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epinephrine and adrenaline
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The unique aspect of norepinephrine (NE) release is that
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axonal varicosities release NE.
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Drugs that block MAO-A are ________ agonists, whereas MAO-B blockers are ________.
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norepinephrine; dopamine agonists
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Activation of 1- and 2-adrenoceptors in brain produce ________ and ________, respectively.
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slow depolarization; slow hyperpolarization
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Serotonin is synthesized from
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tryptophan
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Drugs that block the reuptake of serotonin or that cause the release of serotonin are used therapeutically to treat
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depression.
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The ________ serotonin receptor subtype is classified as an ionotropic receptor.
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5-HT3
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Cell bodies of serotonin neurons are located within the
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raphe nuclei
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Drugs that block histamine receptors produce
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drowsiness
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Which of the following is a reason that is it is difficult to prove that amino acids can function as neurotransmitters?
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Amino acids play a role in protein synthesis for all nerve cells.
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Glutamate, GABA, and glycine are important because these are
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the most common neurotransmitters in the CNS.
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Which of the following is a true of NMDA receptors?
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Activation of the NMDA receptor allows sodium and calcium ions to flow into the nerve cell.
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Alcohol withdrawal can lead to seizures because of the effect of alcohol on
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blocking NMDA receptors.
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The hallucinatory drug PCP (phencyclidine)
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is an antagonist of the NMDA receptor.
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Gamma-aminobutyric acid (GABA) is produced from
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glutamic acid.
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Which of the following is true of GABA in the brain?
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The inhibitory effects of GABA act to stabilize the electrical activity of the brain.
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The GABAA receptor is ________ and controls a ________ channel.
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ionotropic; chloride
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Which of the following is a correct match between a drug and its effect on GABA function?
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picrotoxin; indirect antagonist of the GABAA receptor
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The GABAA antagonist ________ can induce motor convulsions.
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picrotoxin
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Which of the following is characteristic of glycine?
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The glycine receptor is ionotropic.
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Inactivation of glycine receptors would be expected to result in
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convulsions
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Neuropeptides are distinctive in that these transmitters
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are secreted from all parts of a terminal button.
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The term "opioid" refers to ________, while the term "opiates" refers to ________.
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endogenous chemicals; exogenous drugs
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Which of the following is true of opioid effects in brain?
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Opioids can induce euphoria and reward.
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Drugs such as morphine and heroin are classified as
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opiate drugs
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Activation of cannabinoid receptors by THC
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occurs when a person smokes marijuana.
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Which of the following is true of CB1 receptors?
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Memory impairment results from the effects of THC on hippocampal CB1 receptors.
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The excitatory effects of caffeine result from
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blockade of adenosine receptors.
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Nitric oxide
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dilates blood vessels in metabolically active brain regions.
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A drug that mimics the effects of a neurotransmitter would be labeled as a direct ______.
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agonist
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Activation of ________ autoreceptors inhibits the rate of firing of the nerve cell.
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dendritic
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________ is the primary inhibitory neurotransmitter in the spinal cord.
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Glycine
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Acetylcholine is inactivated within the synapse by the action of the enzyme ________.
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acetylcholinerase or ache
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________ is the precursor for the synthesis of dopamine.
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Tyrosine
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________ is synthesized from tryptophan.
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Serotonin
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Hallucinogenic drugs such as LSD are ______ for the 5HT2A receptor.
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agonists
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Secretion of histamine increases ________.
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wakefulness
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The hallucinatory drug PCP (phencyclidine) is an antagonist of the ________ receptor.
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NMDA
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Memory impairment results from the effects of THC on CB1 receptors located in the ________.
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hippocampus
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________ induces behavioral activation by blocking adenosine receptors.
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Caffeine