Hallucinogens and Club Drugs Notes PDF
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These notes cover various hallucinogens and club drugs, providing information on their pharmacology, effects, and use in both humans and animals. The document also discusses tolerance, withdrawal symptoms, and harmful effects.
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‘dancing with Molly’…..‘something ‘bout Mary she gone off that Molly’….‘a gnashing of teeth’…..‘as we moonshine and molly’…. HALLUCINOGENS, PHANTASTICANTS, AND CLUB DRUGS PSY3142 AGENDA - SAMPLING FORM THIS BROAD CATEGORY Monoamine-like drugs • E.g. LSD, psilocybin, Mescaline Synthetic mescaline...
‘dancing with Molly’…..‘something ‘bout Mary she gone off that Molly’….‘a gnashing of teeth’…..‘as we moonshine and molly’…. HALLUCINOGENS, PHANTASTICANTS, AND CLUB DRUGS PSY3142 AGENDA - SAMPLING FORM THIS BROAD CATEGORY Monoamine-like drugs • E.g. LSD, psilocybin, Mescaline Synthetic mescaline-like drugs • E.g. MDMA/MDA Salvia – unique mechanism among hallucinogens Dissociative anesthetics • E.g. Phencyclidine(PCP) Ketamine, Nitrous oxide 2 Dextromethorphan USE 3 USE 4 5 GLOBAL USE MDMA 6 LSD 7 LSD AND THE MONOAMINE-LIKE DRUGS • Indoleamine (serotonin)-like drugs • • • • • • LSD is similar to serotonin Psilocybin (magic mushrooms) Lysergic acid amide (morning glory seeds) DMT (Ayahuasca - tree bark/vine in South and Central America) Bufotenine (plants and venom from backs of toads) Harmine and harmaline (tropical vine in South America) • Catecholamine (dopamine & norepinephrine)-like drugs • Mescaline is similar to catecholamines dopamine and norepinephrine • Peyote DOSES AND SOURCES • LSD: Hits • 1970s: 100 micrograms • Gel tab, Microdots (candies, sm pills) • Mescaline: dried peyote cactus • Pharmacology • Usually taken orally • Effects begin between 30-90 min. after ingestion • Half-life: 3-5 hours in humans • Metabolized in the liver EFFECTS ON THE BODY • LSD: dilation of the pupils most common (also sometimes nausea, increased heart rate and body temp) • Neurophysiology • Effects on the nervous system are still not clear • effects on 5-HT2A receptors • Locus coeruleus • Cortex • Raphe nuclei SUBJECTIVE EFFECTS • Hallucinogenic Effects • Verbal reports • Largely visual: many consistent elements, similar to those produced in other nondrug hallucinations, similar across cultures Phantasticant and Perpetual Effects • Great emotional significance • Used in religion Entactogenic and Empathogenic Effects • Insight into one’s past and one’s own mind PERCEPTION, BEHAVIOR AND PERFORMANCE • Perception • Keener perceptions • Sight and sound become more acute • Slowing down of time • Behavior and Performance • • • • • Motivation issues Impairs reaction time Performance on a pursuit rotor task may be improved by LSD Functioning on intellectual tasks impaired Impairment of problem-solving and cognitive functions TOLERANCE & WITHDRAWAL • Tolerance develops rapidly • mediated by downregulation of serotonin 5-HT2A receptor • If LSD is take repeatedly, its effects disappear within 2 or 3 days. • No amount of the drug will be effective • Tolerance dissipates quickly, sensitivity returning in a week • Cross tolerance with other hallucinogens • No withdrawal symptoms SELF ADMINISTRATION • Generally not self-administered by nonhumans • Lab animals will work to avoid LSD infusions =Aversive effects • Never continuously consumed in humans HARMFUL EFFECTS • No recorded death from overdose • Acute psychotic reaction • Trailing phenomena • Flashbacks? MDMA 16 ECSTASY AND SYNTHETIC MESCALINE-LIKE DRUGS “Have you seen Molly?” Ecstasy (MDMA) • X, Adam, MDM, M & M, xtc, e, and beanies • White or colored tablets (100 mg) • *often not actually containing MDMA • Originally synthesized by the Merck drug company • Patented in 1914 • No use until the 1960s • Given to patients to enhance intimacy and communication with therapist • Reclassified in 1985; banned due to neurotoxic effects PHARMACOKINETICS • Orally • Peak level in 2 hrs • Metabolized to MDA • Half-life: about 8 hrs • Used more commonly by teens at raves • Associated with increase in sex, wakefulness, endurance, energy, euphoria, sharpened sensory perception, extroversion, sense of closeness to others NEUROPHYSIOLOGY • Increase transmission at synapses that use serotonin, norepinephrine, and dopamine • Causes the release of the neurotransmitter and blocking transmitter reuptake • Affects release of oxytocin BEHAVIOUR AND PERFORMANCE A dose of 75 to 100 mg induces a state similar to that caused by marijuana or low doses of PCP without hallucinations • Enhanced awareness of emotions and sensations • Increased muscular tension = jaw clenching & grinding teeth • Increase in body temperature, headache, nausea, blurred vision, and insomnia, difficulty in concentration, fatigue, and depression SELF-ADMINISTRATION Nonhumans • Readily self-administered by primates • Most reinforcing at moderate doses Human Epidemiology • Increase in the number of users throughout the 1990s • Increase in number of emergency room admissions between 1994 and 1999 • Use has begun to drop due to perceived risk* WITHDRAWAL AND HARMFUL EFFECTS • Withdrawal not seen • Harmful Effects of Ecstasy: depletion in serotonin • Sleep disorders, depression, persistent anxiety, impulsiveness, hostility, and selective impairment of memory and attention • Effects dissipate after about 6 months once drug is stopped for all but anxiety and hostility which can persist much longer • Most common causes of ecstasy-related deaths: • Heat regulation: increase in body temperature may lead to heatstroke, muscle tissue damage, kidney failure, liver damage, • Electrolyte imbalance: cause the brain to swell resulting in epileptic-like seizures OTHER LETHAL EFFECTS • Causes of death: heart and circulatory problems, liver damage, suicide, and accident • Quality control = impure • Contain drugs such as amphetamine, ephedrine, and PMA (potent with TI = 2.5) • Consumption of alcohol and other drugs increases risk of death SALVIA 24 SALVIA • Salvia • Plant based • visions and dissociative effects • Neurophysiology • kappa ()-opioid receptor agonist & partial D2 DA receptor agonist • Pharmacokinetics • effective only for a short time. from 5 to 30 minutes • Behavioral Effects • intense hallucinations , laughter, loss of motor cordination, perceptional changes, emotional swings, synaesthesia • Tolerance and Withdrawal • No tolerance/possible sensitization, no withdrawal DISSOCIATIVE ANESTHETICS 26 DISSOCIATEIVE ANESTHETICS: PHENCYCLIDINE AND KETAMINE • Phencyclidine (PCP) • Synthetic, dissociative anesthetic • Withdrawn from the marked due to delirium, disorientation, agitation (emergence delirium) • Crystal, angel dust, hob • Ketamine • Veterinary use • Liquid is colorless and tasteless • Swallowed or injected • Converted to powder, snorted • K, Special K, kitkat PHARMACOKINETICS AND DOSE • Weak, lipid soluble bases • Effective orally, inhaled, injected • Ketamine can be snorted, injected, or taken orally. • Oral administration is slowly absorbed. • Typically used intranasally • Effects last from 35 to 40 minutes • Typical oral dose is 175 mg; intranasal dose is 50 mg • PCP peaks in about 10 to 90 minutes • Effects last 4 to 8 hours • Typical does is 5 to 10 mg NEUROPHYSIOLOGY AND EFFECTS Neurophysiology • Block NMDA receptors • Act as reinforcers Behavior and Performance • • • • • Amnesia, schizophrenic behavior, coma Relaxation, warmth, numbness Euphoric feeling, distortions in body image, floating in space Mild depression (24 hrs to a week) Mood changes PROPERTIES, TOLERANCE, WITHDRAWAL • Stimulus Properties • Animals trained to discriminate PCP and ketamine do not generalize this response to any other class of drugs (only those that block NMDA like dextromethorphan) • Tolerance • When used everyday, tolerance develops • Dependence and withdrawal symptoms • Withdrawal • Vocalizations, grinding of the teeth, diarrhea, difficulty staying awake, anxiety, confusion, tremors • No systematic studies of PCP withdrawal in humans have been done SELF-ADMINISTRATION • Self-administered by nonhuman animals • • Has reinforcing effects Self-administration in humans = fairly low rates • Patterns of PCP are similar to LSD. • But, unlike LSD, some occasional users may become chronic users • Popular in metropolitan areas • Not very popular elsewhere • Ketamine seems to be more prevalent among high school students and in club scene HARMFUL EFFECTS • Large doses can cause: disorientation, agitation, hyperactivity and potentially longlasting psychotic behaviour (schizophrenic symptoms) • Not teratogenic • Slows growth of the fetus, precipitates labor, and causes fetal disease • Lethal Effects • A lethal dose of ketamine is 25 X the effective dose for intranasal administration. • Coma, convulsions, respiratory arrest, brain hemorrhage, kidney failure • Possibly lethal if mixed with alcohol or barbiturates due to potentiated lethal effects in combination with such depressants 33 DISSOCIATIVE ANESTHETICS DEXTROMETHORPHAN • Synthetic, opiate-like drug • Robitussin • Dextrophan • Neurophysiology • Bind with low affinity to the NMDA receptor complex • Pharmacological properties similar to the dissociative anesthetics and alcohol EFFECTS Nonhumans • Decrease in locomotor activity, memory impairment (dextromethorphan) • Effects resemble sedatives • Dextrophan caused an increase in motor activity. • Effects resemble PCP Humans • Cough suppressant at low doses with no other effects • High doses, effects are similar to PCP and ketamine • Ataxia, dizziness, euphoria, tactile and visual hallucinations AGENDA • Reviewed various categories & use in general • Individual examples withing many categories: • Pharmacology • Effects 36