Final Exam Flashcards
type of plant that contains THC in all of its parts
Cannabis
marijuana refers to the dried leaves and flowers of this plant
Cannabis
hashish refers to the dried resin from the top of the female version of this plant
Cannabis
plant that for centuries was grown in Western Europe chiefly for its fiber, from which rope was made, without widespread recognition of its intoxicating properties
cannabis
is the abbreviation for tetrahydrocannabinol
THC
is the primary psychoactive ingredient in cannabis
THC
the most psychoactive and common cannabinoid
THC
ingredient in cannabis that has increased in seized samples of marijuana from 1.5% in the 1960s to over 10% in 2008
THC
class of chemical compounds that is naturally found exclusively in the cannabis plant and contributes to the behavioral effects of cannabis
Cannabinoid
class of chemical compounds that includes 85 different types that have been identified in cannabis
Cannabinoid
class of chemical compound that includes cannabinol and cannabidiol
cannabinoid
class of drug that originated in central Asia and was spread to other parts of the world during the second century BCE by a Middle Eastern tribe known as the Scythians
cannabinoid
the intoxicating effects of this class of drug remained unnoticed by Europeans until the publication of Le Club des Hachichins by the French writer Theophile Gautier in 1846
cannabinoid
class of drug that spread slowly through the United States in the early twentieth century by racial minorities and jazz musicians, which did much to shape the perceptions of white legislators and to motivate opponents
cannabinoid
class of drug that was made illegal by the Marijuana Tax Act passed by the U.S. government in 1937
cannabinoid
class of drug that, in 1970 by the U.S. government, was declared in the Controlled Substances Act as having no potential medical use and as having a high potential for abuse, despite considerable medical evidence to the contrary
cannabinoid
class of drug that is currently the most common illicit drug
cannabinoid
class of drug that, although having analgesic and psychomotor-depressant properties, has little effect on the breathing reflex
cannabinoid
for this class of drug, bloodshot eyes is its most common physiological effect
cannabinoid
for this class of drug, heavy use can be detected because the user looks stoned: an appearance marked by a slight droop in the eyelids
cannabinoid
class of drug that causes an intense feeling of hunger, known as the “munchies”, typically 3 hours after smoking it and when other effects have declined
cannabinoid
class of drug that produces an experience typically characterized by swings of mood from euphoric gaiety with hilarious laughter to placid dreaminess
cannabinoid
class of drug that has as one of its most reliable behavioral effects an increase in subjective time rate: experiencing time as passing more quickly
cannabinoid
class of drug has been claimed to cause an amotivational syndrome: apathy, loss of effectiveness, and a diminished capacity or willingness to carry out plans
cannabinoid
for this class of drug, a tolerance to its impairing effect on operant behavior develops within a few days and lasts for more than a month, but shows no tolerance at all to its anorexic effects or to its subjective effects
cannabinoid
for this class of drug, its tolerance is associated with a downregulation/desensitization of cannabinoid receptors in the brain
cannabinoid
for this class of drug, there is little or no evidence to support many myths about it, such as that it directly causes violence, aggression, permanent intellectual impairment, or irreversible brain damage
cannabinoid
for the cannabinoid receptor, is the endogenous ligand: a substance that occurs naturally in the body and activates this type of receptor
anandamide
endogenous neurotransmitter that is released postsynaptically and causes the presynaptic neuron to shut down both excitatory and inhibitory transmission
anandamide
a neurotransmitter that contributes to functions involved in stress recovery
anandamide
class of drug that is primarily characterized by its ability to cause hallucinations, although they are often not taken in high enough doses to do so and other effects seem to be important to the user
hallucinogen
class of drug that typically has the following pharmacokinetics: is taken orally, is effective between 30 to 90 minutes after ingestion, has a half-life of 175 to 300 minutes, and has a duration of 8 to 12 hours for its hallucinating effects
hallucinogen
is the abbreviation for lysergic acid diethylamide
LSD
hallucinogenic drug that has a chemical structure that is indoleamine-like
LSD
hallucinogenic drug that is chemically similar to ergot: a fungus that grows on rye and other grains, and that causes hallucinations in the disease known as St. Anthony’s fire
LSD
hallucinogenic drug that is a derivative of lysergic acid, which was first synthesized by the Swiss researcher Albert Hofmann in 1938 and tested on himself in 1943
LSD
hallucinogenic drug that is sold as hits given in blotting paper, gel tabs, or tiny pills called microdots
LSD
is one of the most potent synthetic hallucinogenic drugs, with a minimum dose of only 200 micrograms to produce a full psychedelic experience with visual hallucinations
LSD
is a natural hallucinogenic drug that has a chemical structure that is catecholamine-like
mescaline
is the main psychoactive ingredient in the peyote cactus, which is native to the deserts of Mexico and southwestern United States
mescaline
hallucinogenic drug that is acquired from the dried heads of the peyote cactus and can be consumed orally or soaked in water to create an intoxicating drink
mescaline
refers to MDMA (3,4-methylenedioxymethamphetamine)
ecstacy
hallucinogenic drug that has chemical and behavioral properties similar to mescaline and amphetamines
ecstacy
hallucinogenic drug that, prior to its legal reclassification in 1985, was given to patients by psychiatrists in order to enhance intimacy and communication between the patient and the therapist
ecstacy
hallucinogenic drug that increases monoamine transmission by increasing the release and blocking the reuptake of monoamines
ecstacy
hallucinogenic drug that is known to affect oxytocin, a hormone involved in bonding, which may be the cause of the drug’s empathogenic properites
ecstacy
hallucinogenic drug that has as its most dangerous effect the loss of heat regulation, since this can lead to hyperthermia and hyponatraemia (electrolyte disturbance)
ecstacy
hallucinogenic drug that has stimulus properties that do not generalize to cocaine or mescaline, despite being chemically similar to them, but instead generalizes to serotonin agonists
ecstacy
is a natural hallucinogenic drug from the plant Salvia divinorum, which is native to Oaxaca, Mexico and has a long history of use in tribal ceremonies
salvia
hallucinogenic drug that does not chemically resemble other typical hallucinogenic drugs, since it is not an alkaloid (meaning it does not contain a basic nitrogen)
ecstacy
hallucinogenic drug that differs from other hallucinogenic drugs in that it has no action at 5-HT2A receptors but instead is a highly selective kappa-opioid receptor agonist
ecstacy
hallucinogenic drug that is not only very potent (requiring a minimum dose of only 200 micrograms) but also short-lasting (with effects lasting anywhere from 5 to 30 minutes) and shows no tolerance
salvia
class of drug that generally acts as a selective 5-HT2A receptor agonist in the central nervous system, although it triggers a particular intracellular signaling cascade that is distinct from other 5-HT2A receptor agonists
hallucinogen
class of drug that suppresses the release of norepinephrine from the locus coeruleus and serotonin from the raphe system
hallucinogen
class of drug that enhances the response of the locus coeruleus to novelty, which may be the cause of it making people feel like they are seeing things for the first time
hallucinogen
class of drug that increases activity within the medial prefrontal cortex, such as by stimulation of 5-HT2A receptors there
hallucinogen
class of drug that (in the case of MDMA) has been shown at doses slightly higher than normal effective doses to cause depletion of serotonin in the brain for 1 week after a single administration
hallucinogen
class of drug that produces images which are initially of geometric quality but in a later stage take the form of meaningful pictures of people, animals, and places
hallucinogen
class of drug that causes the perception of time to be distorted but not in any consistent direction
hallucinogen
class of drug that has as a common side effect acute psychosis or psychedelic crisis when the user is having an unpleasant experience or bad trip
hallucinogen
class of drug that can unpredictably produce its main effect long after the drug has worn off, which is commonly known as flashbacks
hallucinogen
class of drug that in animals has aversive effects, and in humans is self-administered only episodically and typically in smaller doses now than was used in the 1960s since using a high dose is not always a pleasurable experience
hallucinogens
characteristic of hallucinogens that refers to the enhancement of enjoyment or appreciation of music and social situations
phantasticant
characteristic of hallucinogens that refers to the user feeling closer to God or the universe
phantasticant
characteristic of hallucinogens that refers to having experiences of great emotional or worldly significance, often of a spiritual nature
phantasticant
characteristic of hallucinogens that has made them widely used in traditional religious ceremonies
phantasticant
characteristic of hallucinogens that refers to an enhancement of pleasure that can be derived from viewing art and listening to music
phantastican
characteristic of hallucinogens that means literally “mind manifester”
psychedelic
characteristic of hallucinogens that refers to accessing and developing unused potentials of the human mind
psychedelic
characteristic of hallucinogens that means literally “touching within”
entactogen
characteristic of hallucinogens that refers to the user feeling in touch with their inner self
entactogen
characteristic of hallucinogens that refers to the production of personal insights into one’s past and into one’s own mind
entactogen
characteristic of hallucinogens that refers to the revealing of repressed thoughts and unrecognized feelings
entactogen
characteristic of hallucinogens that refers to the gaining of insights similar to those that psychoanalysis attempts to achieve through psychotherapy
entactogen
characteristic of hallucinogens that suggested that they might be useful tools in psychotherapy
entactogen
characteristic of hallucinogens that refers to an enhanced awareness of emotions and sensations
entactogen
characteristic of hallucinogens that means literally “empathy enhancer”
empathogen
characteristic of hallucinogens that refers to the users feeling in touch with others around them
empathogen
What characteristic of hallucinogens made psychiatrists in the 1960s administer them to people undergoing couples therapy?
empathogen
for this class of drug, tolerance develops within 2 or 3 days when taken repeatedly and sensitivity returns within a week
hallucinogen
class of drug that shows cross-tolerance only to drugs of the same class (e.g., LSD, psilocybin, and mescaline) and not to other drugs such as amphetamine or THC
hallucinogen
for this class of drug, its tolerance is associated with a downregulation of serotonin 5-HT2A receptors in the brain
hallucinogen
class of drug that does not cause a loss of consciousness but rather produces a trance-like state that separates people from sensory experience
dissociative anesthetic
class of anesthetic that produces emergence delirium: experiencing delirium, disorientation, and agitation while recovering from the drug
dissociative anesthetic
class of drug that includes phencyclidine (PCP) and ketamine
dissociative anesthetic
class of drug that primarily acts as an antagonist of NMDA receptors through a specific (PCP) binding site on that glutamate receptor
dissociative anesthetic
class of drug that induces significant negative psychotic symptoms and a thought disorder very similar to that seen in schizophrenic patients
dissociative anesthetic
class of drug that produces euphoric feelings, distortions in body image, and a feeling of floating in space
dissociative anesthetic
class of drug that has stimulus properties that generalize only to other drugs known to block NMDA receptors (e.g., dextromethorphan) and not to any other class of drug
dissociative anesthetic
class of drug that is used to treat the psychoses
antipsychotic
class of drug that is used to diminish the symptoms of psychosis that appear in schizophrenia
antipsychotic
class of drug that is also referred to by the term major tranquillizer or neuroleptic
antipsychotic
class of drug that can produce side-effects that result from a deficiency of dopamine along the nigrostriatal pathway
antipsychotic
class of drug that, when given to healthy subjects, causes slower thinking, tiredness, dejection, anxiety, and irritability
antipsychotic
class of drug that is found in animals and humans to have aversive properties that develop slowly with repeated doses
antipsychotic
class of drug that is useful in treating Huntington’s chorea, Tourette’s syndrome, and tardive dyskinesia through its dopamine blocking effects
antipsychotic
state that is characterized by a loss of touch with reality, and may be briefly brought on by drugs or be a life-long battle in the case of disorders, such as schizophrenia
psychosis
in this state people grossly misunderstand and misinterpret events going on around them
psychosis
in this state people respond to events inappropriately in both an intellectual and emotional sense
psychosis
in this state people may experience bizarre hallucinations and have their behavior be guided by delusions
psychosis
is the most well-known of the psychotic disorders
schizophrenia
the name of this psychotic disorder literally means “to split the mind”, which refers to not split-personality but rather a separation of thought, emotion, and behavior
schizophrenia
psychotic disorder that is characterized by delusions, hallucinations, disorganized speech, disorganized or catatonic behavior, and negative symptoms
schizophrenia
type of symptoms that are traits that are abnormally present in psychosis
positive symptoms
type of schizophrenic symptoms that hallucinations, delusions, incoherent thought & speech, excessive motor activity, or odd mannequin-like postures would be considered
positive symptoms
type of schizophrenic symptoms that typically develop later in schizophrenia, emerging gradually over years after the onset of other symptoms
positive symptoms
type of symptoms that are traits that are abnormally absent in psychosis
negative symptoms
type of schizophrenic symptoms that affective flattening, anhedonia, alogia, avolition, or social withdrawal would be considered
negative symptoms
type of schizophrenic symptoms that are typically the first to develop in schizophrenia
negative symptoms
side-effect of antipsychotic medication that resembles Parkinson’s disease: tremors, slowed motor functions, stiff limbs, and trouble maintaining balance
pyramidal system = motor cortex , when you want to voluntarily move a body part
basal ganglia (extrapyramidal)
side effects of blocking dopamine in the basal ganglia
extrapyramidal signs and symptoms (EPS)
theory that has been the dominant theory of the neurological basis of schizophrenia from the 1960s to this day
dopamine hypothesis
theory that has NOT been confirmed by evidence that dopaminergic circuits progressively deteriorate along with other neurotransmitter circuits in schizophrenia
dopamine hypothesis
theory that posits that schizophrenia and other psychoses result from excessive dopamine activity in the brain
dopamine hypothesis
theory that is supported by the strong correlation between the therapeutic dose of a typical antipsychotic and the drug’s affinity for the dopamine D2 receptor
dopamine hypothesis
theory that is supported by two main observations: (1) drugs which increase dopamine function can produce psychoses & (2) typical antipsychotics are all dopamine antagonists
dopamine hypothesis
theory that is supported by the fact that typical antipsychotic medications also produce severe EPS
dopamine hypothesis
theory that has NOT been confirmed by evidence of differences in D2 receptor densities between individuals with versus without schizophrenia
dopamine hypothesis
theory that is contradicted by the fact that the therapeutic effect of antipsychotic drugs may be delayed for several weeks despite blocking dopamine activity immediately
dopamine hypothesis
theory that is contradicted by the fact that negative and cognitive symptoms of schizophrenia do not improve with D2 receptor blockade
dopamine hypothesis
theory that is supported by the fact that phencyclidine (PCP) and ketamine both produce symptoms similar to the positive, negative, & cognitive symptoms of schizophrenia
glutamate hypothesis
theory that is supported by a correlation between a drug’s ability to produce schizophrenia-like symptoms and its affinity to the NMDA receptor’s PCP binding site
glutamate hypothesis
theory that posits that schizophrenia results from glutamate hypoactivity, specifically at the NMDA receptor
glutamate hypothesis
theory that has NOT been confirmed by evidence of differences in cerebrospinal fluid glutamate levels between individuals with versus without schizophrenia
glutamate hypothesis
theory that is contradicted by the fact that doses of NMDA receptor antagonists that produce schizophrenia-like symptoms increase glutamate release in the prefrontal cortex
glutamate hypothesis
type of antipsychotic medication that is also known as a first-generation antipsychotic
typical antipsychotic
type of antipsychotic medication that primarily blocks D2 receptors
typical antipsychotic
type of antipsychotic medication that was developed first, before 1975
typical antipsychotic
type of antipsychotic medication that is most effective in treating the positive symptoms of schizophrenia, rather than the negative or cognitive symptoms
typical antipsychotic
with this type of antipsychotic medication adverse EPS side-effects commonly occur
typical antipsychotic
type of antipsychotic medication that is more likely to cause tardive dyskinesia
typical antipsychotic
type of antipsychotic medication that is also known as a second-generation antipsychotic
atypical antipsychotic
type of antipsychotic medication that was developed more recently
atypical antipsychotic
type of antipsychotic medication that has only a weak affinity for D2 receptors and has a high affinity for D3 & D4 receptors
atypical antipsychotic
type of antipsychotic medication that alleviates the positive, negative, and cognitive symptoms of schizophrenia
atypical antipsychotic
with this type of antipsychotic medication adverse EPS side-effects do NOT commonly occur
atypical antipsychotic
type of antipsychotic medication that has a greater ability to block 5-HT2A receptors ((serotonin))
atypical antipsychotic
side-effect of antipsychotic medication that is characterized by uncontrolled restlessness, constant compulsive movement, and sometimes a protruding tongue and facial grimacing
Akathisia
without sit
aka = without
thisia = sit
side-effect of antipsychotic medication that is characterized by involuntary, tic-like, repetitive movements of the face, such as muscle twitching, smacking of the lips, or flicking of the tongue
tardive dyskinesia
for this side-effect of antipsychotic medication the symptoms can be permanent and not go away even after the drug is stopped
tardive dyskenisia
mood disorder that is characterized by depressed mood, loss of appetite, anhedonia, lack of energy, problems sleeping, feelings of worthlessness & guilt, and thoughts of death & suicide
major depressive disorder
mood disorder that can occur in people who do not feel depressed but show anhedonia, weight loss, insomnia, psychomotor retardation, loss of energy, and inability to concentrate
major depressive disorder
disorder that has been called the “common cold of mental illness” because large segments of the population experience it at some time in their lives
major depressive disorder
disorder that is currently, in Western cultures, the second leading cause of premature mortality and disability leading to loss of productive life
major depressive disorder
with this disorder women are more likely to have feelings of sadness, worthlessness, and guilt, whereas men are more likely to be tired & irritable, anhedonic, and have insomnia
major depressive disorder
with this disorder the probability of suicide is estimated to be five times greater
major depressive disorder
Based on the results of conditioning studies with animals, if Annie wants to improve her motivation to work and also decrease her performance anxiety, what class of drug would you recommend to her?
antidepressant
class of drug that is used to treat depression
antidepressant
for this class of therapeutic drug the placebo effect accounts for up to 75% of the improvement in depressive symptoms seen with the drug
antidepressant
class of drug that is more effective than stimulants at increasing operant response rates, and also decrease avoidance behavior at doses that have no effect on escape behavior
antidepressant
theory that is contradicted by the fact that the therapeutic effect of antidepressant drugs may be delayed for several weeks despite increasing synaptic monoamine transmitter levels immediately
monoamine theory
theory that is contradicted by the fact that tryptophan depletion has no effect on the mood of individuals with no personal or family history of depression
monoamine theory
theory that is supported by the fact that depressed individuals have low cerebrospinal-fluid levels of 5-HT, its amino acid precursor tryptophan, and its major metabolite 5-H1AA
monoamine theory
theory that posits that depression results from reduced levels of monoaminergic activity, especially serotonin (5-HT) activity
monoamine theory
theory that is supported by the fact that drugs which increase monoamine activity levels enhance mood
monoamine theory
theory that is supported by the fact that drugs (e.g., reserpine) that deplete monoamines, or tryptophan-free diets that deplete serotonin, can produce depression
monoamine theory
theory that is contradicted by a lack of antidepressant effect of CRH antagonists in some clinical trials with depressed individuals
glucocorticoid theory
theory that posits that depression results from hyperactivity of the hypothalamic-pituitary-adrenal (HPA) axis
glucocorticoid theory
theory that is supported by the fact that stress is the most influential environmental factor that predisposes an individual to depression
glucocorticoid theory
theory that is supported by the fact that depressed individuals show overactivity of the hypothalamic-pituitary-adrenal (HPA) axis, as indicated by high levels of CRH & cortisol
glucocorticoid theory
type of antidepressant drug that works by blocking the activity of monoamine oxidase so that monoamines in the cytoplasm are not destroyed and can be available for release
monoamine oxidase inhibitors (MAOIS)
taking this type of antidepressant drug before ingesting tyramine-rich food can result in the cheese effect: sympathetic nervous system activation that can potentially result in death
monoamine oxidase inhibitors (MAOIS)
what is a monoamine?
serotonin, dopamine, epinephrine, norepinephrine
what antidepressant involves enzymes?
monoamine oxidase inhibitors (MAOIS)
type of antidepressant drug that, although classified as a first-generation antidepressant, is actually more similar in function to the second-generation antidepressants
tricyclic antidepressants (TCAS)
type of antidepressant drug that works by blocking reuptake of the monoamines into presynaptic neurons and so prolongs postsynaptic receptor stimulation
tricyclic antidepressants (TCAS)
What class of antidepressant drug can have dangerous cardiovascular effects due to its effects upon adrenergic activity through a mechanism that does not involve enzymes**?
tricyclic antidepressants (TCAS)
type of antidepressant drug that is fluoxetine (Prozac) and is included in the designation known as second-generation antidepressants
selective serotonin reuptake inhibitors (SSRIS)
type of antidepressant drug that is safer than the other types of antidepressant drugs, with fewer of their bothersome side effects
selective serotonin reuptake inhibitors (SSRIS)
type of antidepressant drug that works by blocking reuptake of just serotonin into presynaptic neurons and so prolongs postsynaptic receptor stimulation by serotonin
selective serotonin reuptake inhibitors (SSRIS)
potentially lethal condition associated with antidepressant drug use that is caused by an acute increase in serotonergic transmission
serotonin syndrome
potentially lethal condition that often results from an interaction between an antidepressant drug and a tryptophan-containing food or other drugs that increase serotonin levels
serotonin syndrome
Neurologic vs. Psychiatric disorders
neurological = usually can measure something that is wrong in brain
Psychiatric = subjective
type of opioid drug that is derived by taking the sap that exudes from the seed pods of the opium poppy and then compressing it into cakes that are dried
opium
type of opioid drug that has been cultivated in the western Mediterranean region since 7000 BCE and was described in writing by the Sumerians in 4000 BCE as a “joy plant”
opium
type of opioid drug whose smoking was first invented by the Chinese when tobacco smoking was banned by a Chinese emperor in 1644
opium
type of opioid drug that was popularly sold in nineteenth century Britain in a form that was dissolved in alcohol, called laudanum
opium
type of opioid drug that naturally contains the following three psychoactive ingredients: morphine, codeine, and thebaine
opium
type of opioid drug whose injection by means of the hypodermic syringe became popular in late nineteenth century America due to the widespread use of its injections to treat wounded soldiers during the Civil War
morphine
is both a type of opioid drug and the major psychoactive ingredient in opium, which accounts for 10% of the weight of opium
morphine
metabolite that heroin and codeine must be converted into within the brain in order to have a direct action on receptors
morphine
is the lesser of the two main psychoactive ingredients in opium, and accounts for only 0.5% of the weight of opium
codeine
minor psychoactive ingredient in opium that is also known as paramorphine
thebaine
minor psychoactive ingredient in opium that is the source of many semisynthetic opioid drugs including oxycodone
thebaine
minor psychoactive ingredient in opium that is the source of the semisynthetic opioid drug found in many prescription analgesics, such as Percocet, Percodan, and OxyContin
thebaine
type of opioid drug that was invented in 1898 by Heinrich Dreser working for the Bayer Company of Germany and originally advertised as having the valuable analgesic effects of morphine without the undesirable side effects of respiratory depression and addiction
heroin
is a semisynthetic opioid drug made by adding two acetyl groups to the morphine molecule
heroin
type of opioid drug that is more powerful than morphine due to its being 10 times more lipid soluble and, therefore, able to get to the brain faster and in higher concentrations
heroin