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Vocabulary flashcards for reviewing key terms and concepts from the lecture notes.
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Cocaine
Indirect agonist of monoamine; increases dopamine, serotonin, and norepinephrine; activates SNS.
Methamphetamine
Indirect agonist of monoamine (longer lasting); activates SNS.
MDMA (Ecstasy)
Serotonin agonist (high abuse potential); rapid tolerance; hyperthermia (cause coma, organ damage, and death).
patent medicines
U.S manufactures promoted small amounts of cocaine in their products for headaches, neuralgia, and depression
Harrison Narcotics Act
Made cocaine illegal in 1914.
Obesity (amphetamine medical use)
Decreases appetite and food intake; increases metabolic rate.
Narcolepsy (amphetamine medical use)
Increases wakefulness.
ADHD (amphetamine medical use)
Increases attention.
systematic racism on cocaine
African Americans were more likely to use crack than whites, who were more likely to use power cocaine (War on Drugs) resulting in harsher penalties and disproportionate incarceration rates.
stimulant routes of administration
Methods for delivering stimulants, including intravenous (injection into vein), intranasal (snorting), oral (ingestion), and inhalation(smoking).
effects of cocaine
Cocaine produces a short-term euphoria, increased energy, and heightened alertness, but can also lead to negative effects such as paranoia, anxiety, and potential addiction.
Conditioned Place Preference
A learned behavior where an animal develops a preference for a specific environment associated with a rewarding drug.
Progesterone
High levels reduce the positive response to stimulant drugs.
stimulant addiction risk
compulsive use starts to emerge in some users after only a few exposures; rapid progression
Methamphetamine Psychosis
Paranoid delusions (contributes to skin picking).
Stereotyped Behavior (chronic stimulant use)
Head movements, self-licking (non-human animals); sorting, cleaning, grooming, skin picking (humans).
Cognitive Impairment(chronic stimulant use)
Deficits in attention, memory, and executive function.
Neurotoxicity (chronic stimulant use)
Changes in neurotransmitter functions, glucose utilization, blood circulation.
stimulant use prevalance
12.3 million
stimulant use disorder prevalence
5 million
endogenous opiods
4 classes (Mu, delta, kappa, nociception); distributed in CNS; mu-receptions most important; involved in pain modulation and reward pathways.
U.S. opioid overdose deaths 1999-2019
500,000 people
U.S. opioid overdose deaths 2020 +
about 70,000 (~192 people a day)
Nociceptors
Specialized receptors activated by noxious insults in skin and deep tissues (dorsal horn of the spinal cord).
Mu Opioid Reception
Reduction of neural activity in the pain circuit. 70% on presynaptic neurons and 30% on post-synaptic neurons.
Full Opioid Agonists
Having strong effects at the opioid receptors similar to those of endogenous options.
Partial Opioid Agonists
Similar effects to opioids but lower level of activity in the receptors. (Buprenorphine)
Opioid Agonist Mechanism (Presynaptic)
Entry of calcium (Ca++) ions is decreased, stops neurotransmitter release.
Opioid Agonist Mechanism (Postsynaptic)
Opens potassium (K+) ion channels; efflux (out of cell); hyperpolarizes neuron.
Recreational Opioid Abuse
Driven by a desire to experience the drug effect (high), use in higher than prescribed doses, used in combination with other drugs.
Quasi-Therapeutic Opioid Misuse
Longer than prescribed, larger dose than prescribed, “doctor shopping” or illicit purchase.
prevalance of opioid use disorder
74% of 886,000 who reported using heroin or fentanyl in 2017
Methadone Effects
Reduces opioid withdrawal symptoms; full mu-opioid receptor agonist; thrice-weekly dosing.
Barbiturate
Short/intermediate-active barbiturates are usually prescribed as sedatives and sleeping pills.
Benzodiazepine
Prescribed for relief of acute anxiety in specific and time-limited situations (e.g., air travel).
Benzodiazepine Mechanism of Action
Binds to GABA(A) receptor in the Chloride channel
Barbiturate Mechanism of Action
Binding keeps the chloride (Cl-) ion channel open longer; can open channel without GABA binding; opens channel more frequently when GABA binds.
Active Metabolites of Benzodiazepines
Extends duration of drug (e.g., half-life); cytochrome p450 enzymes
Flunitrazepam (Rohypnol)
Produce sedation and anterograde amnesia (severe when paired with alcohol); roofies
GABAA Receptor Structure
5 subunits forming a conducting channel for chloride (Cl-) ions.
Z-Drugs
At appropriate doses, fast acting, have relatively brief duration, and little next day sedation. Ambien, Lunesta, Sonata
Minnesota Model
90% Residential treatment program (28 days) with key elements like professional staff, disease concept, family involvement, abstinence, and aftercare.
types of addiction treatments
AA, online mutual support groups, intensive outpatient
Benzos (valium)
withdrawal
Disulfiram (Antabuse)
Blocks eliminations of acetaldehyde
Naltrexone (revia, vivitrol)
Mu opioid receptor antagonist; reduces craving
Acamprosate (Campral)
Affects NMDA glutamate and GABA receptors
Recovery Capital
Sources of support and self-esteem that have survived the addiction; most likely to succeed in stopping drug use with sufficient recovery capital
Washingtonians (principles of AA)
Pledge of abstinence, mutual support
Oxford Group (principles of AA)
Quasi-religious, admit powerlessness over alch
Stages of Change
Precontemplation, contemplation, preparation, action, maintenance, relapse.
Motivational Interviewing
Structured interviews concerned with client’s perspective using open-ended questions to analyze cost and benefits of SU
Cognitive Behavioral Therapy
Problem focused and action oriented to change learned behaviors, thoughts cause feelings and behaviors
Brief Intervention
Simple structured advice, written or internet-based information, and motivational counseling.
Past year substance use disorder (%)
48.7 million (17.3%)
No past year SUD (%)
233.3 million (82.7%)
Alcohol use disorder
29.5 million
Cocaine, meth, and stimulant use disorder
5 million
Drug use disorder
27.2 million
In dorsal horn of spinal cord ____ of opioid receptors are u on presynaptic neurons
70%
Naloxone (u-opioid receptor antagonist)
added to buprenorphine to decrease the likelihood of diversion and misuse of the combination drug product