Term
An unpleasant state of tension, apprehension, or uneasiness best describes: |
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Definition
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Term
_____ is generally a constant, unwarranted, or from unknown sources; it may be debilitating or harmful in some fashion. |
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Definition
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Term
This is a disorder that causes patients to suddenly panic. |
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Definition
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Term
This is a constantly present fear of something. |
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Definition
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Term
Events that cause extreme stress and problems after the event describe: |
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Definition
Post-traumatic Stress Disorder |
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Term
Anxiety may cause these diseases: |
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Definition
Insomnia, cardiac problems, etc. |
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Term
This neurochemical theory of anxiety theorizes that there is a heightened stimulation in the brain by Epi, NE, DA. |
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Definition
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Term
This neurochemical theory for anxiety states that heightened stimulation results from inhibited inhibitory mechanisms. |
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Definition
GABA receptor model OR Serotonin model |
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Term
This neurochemical theory of anxiety states that reduced action of the serotonin neuronal receptor system allows excitation. |
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Definition
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Term
This class of drugs reduces anxiety and exerts a calming effect. |
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Definition
Sedatives (anxiolytic drugs |
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Term
This class of drug produces drowsiness and promotes onset and maintenance of sleep. |
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Definition
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Term
Recall that GABAa receptors (benzodiazepine receptors are inhibitory. GABAa receptors act through (depolarization/hyperpolarization)? |
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Definition
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Term
Hyperpolarization of a cell ________. |
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Definition
Inhibits action potential |
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Term
These drugs bind to chloride channels, enhancing the opening of the channels in the presence of endogenous ligands. |
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Definition
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Term
Benzodiazepines bind to these receptors: |
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Definition
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Term
In the presence of GABA, benzodiazepines will cause ________. |
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Definition
The Cl- channel to open and stay open longer. |
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Term
Benzodiazepines bind to an allosteric site on GABAa receptors. What is an allosteric site? |
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Definition
Site that is not the same site that binds the endogenous ligand |
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Term
The generic name for Valium is |
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Definition
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Term
The generic name for Xanax is: |
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Definition
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Term
This benzodiazepine is often used before surgery to reduce pre-op anxiety: |
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Definition
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Term
Diazepam is used to clinically: |
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Definition
To treat anxiety, as a sedative, and as an anticonvulsant |
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Term
Alprazolam is used to treat: |
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Definition
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Term
Flurazepam has a _______ duration of action. |
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Definition
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Term
Diazepam has a _______ duration of action. |
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Definition
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Term
Temazepam has an ____________ duration of action. |
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Definition
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Term
Triazolam has a ______ duration of action. |
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Definition
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Term
Temazepam and midolazam are sometimes used for: |
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Definition
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Term
Clonazepam is clinically used for: |
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Definition
Anticonvulsant (anti-seizure) |
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Term
The rate of benzodiazepine absorption depends on the drug's _____. |
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Definition
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Term
Benzodiazepines (are/are not) distributed into the placenta and breast milk. |
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Definition
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Term
Benzodiazepines are metabolized by: |
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Definition
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Term
Benzodiazepines are excreted in the: |
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Definition
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Term
What are some of the adverse effects of benzodiazepines? |
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Definition
Dependence, tolerance, drowsiness and confusion, withdrawal, acute closed-angle glaucoma, depresses CNS |
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Term
This barbiturate is sometimes used in surgeries as an anesthetic. |
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Definition
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Term
Thiopental has a ___ duration of action. |
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Definition
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Term
Pentobarbital has a _________ duration of action. |
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Definition
Intermediate (Duration of hours) |
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Term
Phenobarbital has a _______ duration of action. |
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Definition
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Term
Thiopental is often nicknamed "_____". |
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Definition
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Term
The primary adverse effect of barbiturates is: |
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Definition
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Term
Adverse effects of barbiturates include: |
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Definition
Respiratory depression, enzyme induction, reduce cognition, drowsiness, addiction/dependence, tolerance, and poisoning. |
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Term
Selective Serotonin Reuptake Inhibitors act by: |
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Definition
Preventing the reuptake of serotonin in the synaptic cleft |
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Term
Escitalopram and paroxetine are examples of: |
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Definition
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Term
This drug acts as an SSRI and can act as a NE reuptake inhibitor. |
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Definition
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Term
Buspirone is described as a 5-HT1a _________. |
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Definition
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Term
This drug is a long-term anxiolytic that acts as a partial agonist on 5-HT1a receptors. |
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Definition
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Term
This 5-HT1a partial agonist has much less adverse effects than benzodiazepines. |
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Definition
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Term
This hypnotic is used for short-term insomnia, and is notorious for causing hallucinations and sleep walking. |
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Definition
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Term
Zolpidem binds to the __________ receptor, much like benzodiazepines. |
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Definition
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Term
Zolpidem is metabolized by CYP ______. |
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Definition
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Term
Adverse effects of zolpidem include: |
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Definition
Day time drowsiness, anterograde amnesia, increased sedation with anti-depressants, and hallucinations |
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Term
Eszopiclone is (slowly/rapidly) absorbed. |
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Definition
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Term
Eszopiclone binds to the ______ receptor. |
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Definition
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Term
Ezzopiclone is effective for up to _____. |
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Definition
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Term
This drug is a highly selective, potent MT1 and MT2 melatonin receptor agonist. |
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Definition
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Term
Ramelteon, unlike zolpidem and eszopiclone, is not a: |
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Definition
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Term
The MT (melatonin) receptor controls your ________. |
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Definition
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Term
MT receptors are GPCRs that couple to ___. |
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Definition
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Term
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Definition
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Term
MT2 receptors are thought to help the body: |
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Definition
Shift between day and night |
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Term
Adverse effects of ramelteon include: |
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Definition
Drowsiness, fatigue, headache, hyperprolactinemia, and adrenal insufficiency |
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Term
Ramelteon is contraindicated in patients with: |
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Definition
Severe hepatic disease, COPD, alcohol use, and endocrine disease |
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Term
Hydroxyzine is an _____ that crosses the BBB and acts on __________. |
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Definition
Antihistamine; H1 receptors |
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Term
Hydroxyzine is an anxiolytic given to patients with: |
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Definition
Past history of addiction |
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Term
Chloral hydrate is an anxiolytic, and its mechanism is: |
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Definition
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