1 / 17

Psychology 317 Chapter 12

Psychology 317 Chapter 12. Hallucinogens. Hallucinogens. Hallucinogens are a class of drugs that alter perceptual, cognitive and emotional states. These drugs have been called hallucinogens, phantasticants, psychotomimetics, and psychedelics.

ledell
Download Presentation

Psychology 317 Chapter 12

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Psychology 317 Chapter 12 Hallucinogens

  2. Hallucinogens • Hallucinogens are a class of drugs that alter perceptual, cognitive and emotional states. • These drugs have been called hallucinogens, phantasticants, psychotomimetics, and psychedelics. • These drugs produce hallucinations and exert profound effects on mood, thinking processes, and psychological processes. • More than 90 plant species and many synthetic agents can produce these effects. • These drugs are divided into 4 groups based on their effects and mechanism of action • Serotonergic hallucinogens, methylated amphetamines, anticholinergic hallucinogens & dissociative anesthetics.

  3. Serotonergic Hallucinogens • These include lysergic acid diethylamide (LSD), the prototype hallucinogen in this group. • It was synthesized in1938 by Albert Hoffman. • Drugs with effects similar to LSD were used for centuries, before the synthesis of LSD, by Central and South American Indians (psilocybin, mescaline). • One, ibogaine was discovered and used by Africans. • Spanish conquistadors who explored and colonized Mexico observed natives(Aztecs) use of hallucinogenic plants in religious ceremonies. • In 1577 Spanish Royal Physician, Fernando Hernandez, studied and wrote about peyote cactus (peyotl) psilocybe mushrooms (teonanacatl) and morning glory seeds (ololuiqui).

  4. Serotonergic Hallucinogens continued • Each plant contained a different drug but all produced vivid visual hallucinations. • South American natives( Western Amazon of Brazil, Columbia, Peru, Equador, Bolivia) used two other hallucinogens harmine and harmaline from the bark and vines of Banisteropsis caapi and B. inebrians. • The local names of drinks made from the bark of vines are yage, pinde and dapa.

  5. Serotonergic Hallucinogens continued • The plants are used in healing ceremonies, initiation rites, or other rituals. • Other hallucinogens use by the same S. American, Amazon natives include various species of the Virola tree • (Virola calophylla, V. calophylloidea, V. theiodora) • The tree bark, powered and sniffed (as snuff) contains the hallucinogens dimethyltryptamine (DMT). • DMT has shorter duration and was used at funeral ritual where powdered bones of deceased was consumed along with the snuff.

  6. Recent History • European and American mainstream cultures knew little about hallucinogens until 1960s. • Albert Hoffman Swiss chemist at Sandoz Labs discovered LSD while studying derivatives of ergot, a fungus that infests grain. • The fungus occasionally caused outbreaks of disease in Medieval Europe when infected bread was eaten. • LSD was used in several animal studies, but showed no commercial use and was shelved. • Hoffman reexamined it in 1943; some spilled on his hand, got absorbed and Hoffman was the first person to experience the effects of LSD.

  7. Recent History continued • Hoffman had a bizarre experience and decided to test an hypothesis that his experience was caused by LSD- He took LSD and had similar experiences again. • Sandoz distributed LSD to psychologists and psychiatrists for use as an adjunct to psychotherapy. • By 1960s LSD was tried by many and its popularity and publicity grew. • Timothy Leary on east coast and Ken Kesey on west coast advocated use and legalization of LSD. • By the 1960s 2 mil. reported trying LSD in US • LSD also became most controversial drug in the world.

  8. Recent History continued • Negative publicity included: chromosomal damage, mutant children, insanity, suicide, violence, homicidal behavior. • LSD use declined in 1970s and 1980s • LSD and other hallucinogen use increased again in the1990s and peaked in 1996 • NIDA survey showed that I 8.8% reported using LSD and 1.8% high school seniors (NIDA). • Hallucinogens became associated with “club” or “rave” scene.

  9. Recent History continued • MDMA (ecstasy) was also considered a prototypical club drug. • LSD and MDMA are both popular drugs but LSD more so • LSD use by 18 yr. olds was 48.6%, MDMA 32.3%. • LSD use by 18-32 yrs. 42.9%, MDMA 37.0%

  10. Mechanism of Action of LSD-Like Drugs • LSD and other drugs in the class affect serotonin neurons. They are sympathomimetic drugs. • These drugs produce diverse psychological effects which include: Visual hallucination, alterations of mood and thought, and dreamlike visions. • LSD like drugs have been associated with many adverse effects including psychotic reactions (bad trips), flashbacks, and long-term psychological deficits.

  11. Methylated Amphetamine • Methylated Amphetamine includes drugs such as MDA and MDMA (ecstasy), MDE • These drugs are sympathomimetics and they produce many LSD like effects but they do not produce visual hallucinations. • MDMA has become perhaps the most controversial illegal drug in the US today. • In 1996, 6.1% HS seniors reported having tried MDMA at least once. • By 2001 11.7% HS seniors reported having tried MDMA.

  12. Methylated Amphetamine continued • Since then use has declined to pre 1996 levels. • Reason given for decline: publicity of MDMA adverse effects, brain damage, and death. • MDE, MDA and MDMA are similar and grouped together as DOM. • They are similar to mescaline and LSD. • Usually taken orally but can be injected or absorbed intranasally (snorted). • Absorbed rapidly & duration of action 6-8 hours.

  13. Methylated Amphetamine continued • Have effects by releasing monoamines particularly serotonin & dopamine. • MDMA also blocks reuptake of 5-HT and DA to lesser extent. • They mimic sympathetic effect producing: increased heart rate, blood pressure, pupil dilation, muscle tension, teeth grinding, increased temperature, appetite suppression, and insomnia.

  14. Methylated Amphetamine continued • Psychological effects include: euphoria, emotional warmth, empathy, lowered defensiveness, increased verbal behavior. • Toxic effects include: dehydration, heatstroke, heat exhaustion, muscle breakdown, kidney failure, stroke, seizures, heart attacks.

  15. Anticholinergic Hallucinogens • Anticholinergic hallucinogens include atropine and scopolamine. • Found in plants such as belladonna (deadly nightshade) mandrake, henbane, jamison weed and datura. • These plants have been use before the birth of Christ, by ancient Greeks at the Oracle of Delphi, and by Middle Age witchcraft doctors. • They produce semisleep state marked by vivid visions and poor memory of drug experience later.

  16. Dissociative Anesthetic Hallucinogens • Phencyclidine (PCP, Angel Dust) and Ketamine are dissociative anesthetic hallucinogens. • They produce potent intoxication at moderate doses, complete surgical anesthesia at higher doses. • PCP was synthesized in 1956 as an anesthetic. • PCP and Ketamine produced hyperexcitability, delirium, and visual disturbance in humans and was abandoned for human use. • They are marketed as anesthetic and tranquilizers in veterinary medicine. • PCP emerged as street drugs in 1970s (Angel dust, hog, horse tranquilizer, lovely)

  17. Dissociative Anesthetic Hallucinogens continued • Used as sprinkled powder on cigarettes or marijuana joints. • Effects last 4-6 hrs- (“k-hole”) but variable • May produce seizures, prolonged coma, or death from respiration failure. • Produces bad trips in 56%-80% of users. • Produces toxic psychosis characterized by paranoia and sometimes violence that may last several days.

More Related