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level: Level 2

Questions and Answers List

Psychoactivate substances. Pharmacology of the reward system.

level questions: Level 2

QuestionAnswer
Binding affinity (affinity)the propensity of molecules of a drug or other ligand, to bind to receptors.
Efficacy (intrinsic activity)the extent to which a drug activates a response when it binds to a receptor.
Partial agonista drug that, when bound to a receptor, has less effect than the endogeneous ligand would.
Dose-response curve (DRC)a formal plot of a drug's effects on the y-axis vs the dose given on the x-axis.
Pharmacodynamicscollective name for the factors that affect the relationships between a drug and its target receptors, such as affinity and efficacy.
Tolerancea condition in which, with repeated exposure to a drug, an individual becomes less responsive to a constant dose.
Metabolic tolerancethe form of drug tolerance that arises when repeated exposure to the drug causes the metabolic machinery of the body to become more efficient at clearing the drug.
Functional tolerancedecreased responding to a drug after repeated exposures, generally as a consequence of up- or down-regulation of receptors.
Down-regulationa compensatory reduction in receptor availability at the synapses of a neuron.
Up-regulationa compensatory increase in receptor availability at the synapses of a neuron.
Cross-tolerancea condition in which the development of tolerance for one drug causes an individual to develop tolerance for another drug.
Withdrawal symptoman uncomfortable symptom that arises when a person stops taking a drug that he or she has used frequently, especially at high doses.
Sensitizationa process in which the body shows an enhanced response to a given drug after repeated doses.
Bioavailablereferring to a substance, usually a drug, that is present in the body in a form that is able to interact with physiological mechanisms.
Biotransformationthe process in which enzymes convert a drug into a metabolite that is itself active, possibly in ways that are substantially different from the actions of the original substance.
Pharmacokineticscollective name for all the factors that affect the movement of a drug into, through, and out of the body.
Blood-brain barrierthe mechanisms that make the movement of substances from blood vessels into brain cells more difficult than exchanges in other body organs, thus affording the brain greater protection from exposure to some substances found in the blood.
Local anesthetica drug, such as procaine or lidocaine, that blocks sodium channels to stop neural transmission in pain fibers.
Autoreceptora receptor for a synaptic transmitter that is located in the presynaptic membrane, telling the axon terminal howmuch transmitter has been released.
Caffeinea stimulant compound found in coffee, caco and other plants.
Adenosinein the context of neural transmission, a neuromodulator that alters synaptic activity.
Transmitter reuptakethe reabsorption of synaptic transmitter by the axon terminal from which it was released.
Transporterspecialized receptors in the presynaptic membrane that recognize neurotransmitter molecules and return to the presynaptic neuron for reuse.
Degradationthe chemical breakdown of a neurotransmitter into inactive metabolites.
Antipsychoticsa class of drugs that alleviate the symptoms of schizophrenia.
Typical antipsychoticsa class of antischizophrenic drugs whose principal mode of action is antagonism of dopamine D2 receptors.
Atypical antipsychotics (atypical neuroleptics)a class of antischizophrenic drugs that have actions other than or in addition to the dopamine D2 receptor antagonism that characterizes the typical antipsychotics.
Antidepressantsa class of drugs that relieve the symptoms of depression.
Tricyclic antidepressantsa class of drugs that act by increasing the synaptic accumulation of serotonin and norepinephrine.
Selective serotonin reuptake inhibitor (SSRI)a drug that blocks the reuptake of transmitter at serotonergic synapses.
Serotonin-norepinephrine reuptake inhibitor (SNRI)a drug that block the reuptake of transmitter at both serotonergic and noradrenergic synapses.
Anxiolyticsa class of substances that are used to combat anxiety.
Depressantsa class of drugs that act to reduce neural activity.
Barbiuratea powerful sedative anxiolytic derived from barbituric acid, with dangerous addiction and overdose potential.
Benzodiazepine agonistsa class of antianxiety drugs that bind to sites on GABAA receptors.
Orphan receptorany receptor for which no endogenous ligands has yet been discovered.
Allopregnanolonea naturally occurring steroid that modulates GABA receptor activity in much the same way that benzodiazepine anxiolytics do.
Neurosteroidssteroids produced in the brain.
Opium (papaver somniferum)a heterogeneous extract of the seedpod juice of the opium poppy.
Morphinean opiate compound derived from the poppy flower.
Analgesicreferring to painkilling properties.
Heroindiacetylmorphine, an artificially modified, very potent form of morphine.
Opioid receptora receptor that responds to endogenous and or exogenous opiates.
Periaqueductal graythe neuronal body-rich region of the midbrain surrounding the cerebral aqueduct that connects the third and fourth ventricles, involved in pain perception.
Endogenous opioidsa family of peptide transmitters that have been called the body's own narcotics. The three kinds are nekephalins, endorphins and dynorphins.
Enkephalinsone of three kinds of endogenous opioids.
Endorphinsone of three kinds of endogenous opioids.
Dynorphinsone of three kinds of endogenous opioids.
Marijuanaa dried preparation of the Cannabis sativa plant, typically smoked to obtain THC.
Δ9-tetrahydrocannabinol (THC)the major active ingredient in marijuana.
Endocannabinoidan endogenous ligand of cannabinoid receptors, thus, and analog of marijana that is produced by the brain.
Anandamidean endogenous substance that binds the cannabinoid receptor molecule.
Khat (qat)an african shrub that, when chewed, acts as a stimulant.
Nicotinea compound found in plants, including tobacco, that acts as an agonist on a large class of cholinergic receptors.
Cocainea drug of abuse, derived from the coca plant, that acts by potentiating catecholamine stimulation.
Dual dependencedependence for emergent drug effects that occur only when two drugs are taken simultaneously.
Amphetaminea molecule that resembles the structure of the catecholamine transmitters and enhances their activity.
Fetal alcohol syndromea disorder, including intellectual disability and characteristic facial anomalies, that affects children exposed to too much alcohol (through maternal ingestion) during fetal development.
Hallucinogensa class of drugs that alter sensory perception and produce peculiar experiences.
LSD (acid)lysergic acid diethylamide, a hallucinogenic drug.
Ketaminea dissociative anesthetic drug that acts as an NMDA receptor antagonist.
Dissociative druga type of drug that produces a dreamlike state in which consciousness is partly separated from sensory inputs.
MDMA (ecstasy)a drug of abuse, 3,4-methylenedioxymethamphetamine.
Dysphoriaunpleasant feelings, the opposite of euphoria.
Nucleus accumbensa region of the forebrain that receives dopaminergic innervation from the ventral tegmental area.
Insulaa region of cortex lying below the surface, within the lateral sulcus, of the frontal, temporal and parietal lobes.
Cue-induced drug usean increased likelihood to use a drug (especially an addictive drug) because of the presence of environmental stimuli that were present during previous use of the same drug.
Vaccinationinjection of a foreign substance, such as deactivated viruses or conjugated molecules of drugs of abuse like cocaine, in order to provoke the production of antibodies against the foreign substance.