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Neurogenesis: Factors

Neurogenesis: Factors. Poling. 4 essential features of a drug evaluation? DV Meds given according to protocol Design Data analysis must be adequate. Poling. Prescribing drugs to special populations in need of protection should involve safeguards.

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Neurogenesis: Factors

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  1. Neurogenesis: Factors

  2. Poling • 4 essential features of a drug evaluation? • DV • Meds given according to protocol • Design • Data analysis must be adequate

  3. Poling • Prescribing drugs to special populations in need of protection should involve safeguards. • Goals are clear with specific targets and in P interests • Tx decisions made on basis of drug effects • Flexible and integrated with beh Tx.

  4. Poling • 3 design factors • Single vs repeated observations • Pre-post testing vs daily recording • Between subject vs within subject • Between – either Tx or P • Within – each subject gets all conditions • Stats vs visual • T tests, F tests vs visual inspection

  5. 10 mg 15 mg 5 mg 5 mg

  6. McKim: Cannabis

  7. McKim: Cannabis • Source- plants • Active ingredient - THC • Hashish - dried resin from top • Hash oil? • Boil hash in alcohol, filter out residue, allow alcohol to evaporate (cannabinoids are soluble in alcohol) • Thai sticks: buds bound with string onto short sections of bamboo or stems • Spread by Scythians in 200 BC • Also known in China 6000 years ago

  8. McKim: Cannabis Scythians: “There is nothing new or strange in what we do. We follow our mode of life in peaceful times. We have neither towns nor cultivated lands in these parts which might induce us, through fear of their being ravaged, to be in any hurry to fight you. But if you must needs come to blows with us speedily, look about you, and behold our fathers' tombs. Attempt to meddle with them and you shall see whether or not we will fight with you."

  9. McKim: Cannabis

  10. McKim • Kinetics • Administration/Absorption: • Slow absorption orally • Fast if inhaled • Distribution • Lipid soluble so goes everywhere • Collects in liver, lungs, intestines • Metabolism • Liver • Many metabolites: some are active • Excretion • T ½ - biphasic: 30 min then 20-30 hours

  11. McKim • Neuropharmacology • CB1 found in CNS • CB2 found in spleen and immune system • Endogenous cannibinoids – THC is stronger • Potentiate NE, DA, SE, ACH, endogenous opiates • Effects on body – • dilation of eye vessels, hunger, dry mouth, increase in HR • Medicinal uses • decrease in intraocular pressure, anti-emetic, movement disorder, spasticity, analgesia

  12. McKim • Other effects • Sleep – will increase, but can disrupt on high doses • Perceptual effects – can disrupt time discrimination, decrease pain • Many things appear funny, dreamy state • Memory problems – disrupts short term memory • Attention – disrupts attention • Driving – problems with attention • Aggression decrease • Immune system – may depress

  13. McKim • Tolerance • Non-humans – yes • Humans –sensitization? some tolerance • W/D syndrome • Increase in anxiety, restlessness, irritability; AO for food

  14. McKim • Health risks • Will not produce psychosis. But, will increase intensity of schiz symp or paranoia • Effects on brain or “intellectual” functioning? • Humans – no. But might be problems in memory and attention. • Amotivational syndrome? • Humans – none.

  15. McKim • Gateway drug? • No. • Lung cancer? • There are 50-70% more carcinogenic material. • Decrease in testosterone • It may potentiate cigarette smoke • Weakens immune system

  16. Poling Review • Source of cannibis • Marijuana plant • Receptors • CB1 & CB2 • Effects • Dilation of capillaries in eyes • EO for food • Dry mouth • Increase HR

  17. McKim: Hallucinagens • LSD: • Hallucinogen class – similar to serotonin • Source – synthetic drug, but similar chemicals exist in ergot fungus that infects grains • SE agonist/antagonist • Kinetics • Oral administration; absorbed in stomach • Metabolized? – Liver • T ½ - 2 hours • Typical dose – 300 mics or less • Effects – dilation of pupils, hallucinations, early sweating, nausea, jaw grinding • Not lethal

  18. McKim • Psilocybin • Hallucinogen class – similar to serotonin • Source – mushrooms • Duration of action – 4-6 hours • Dose – 4-8 mg • Mechanism – SE agonist/antagonist • Not lethal

  19. McKim • Mescaline • Hallucinogen class – similar to NE • Source – cactus called peyote • Ceremonies by Native American Church • Usual dose – 200 mg • Effects – nausea, dilation, hallucinations • Not lethal

  20. McKim • MDMA/MDA (ecstasy) • Hallucinogen class – similar to NE • Usual dose – 100 mg • Effects – euphoria, state of well being, talkative, EO for everything • High dose may deplete serotonin • Sleep problems, anxiety, hostility, impulsiveness, selective impairment of memory/attention, depression, heat regulation • Typical use – rave drug • Mechanism – causes release and blocks re-uptake of SE, NE, DA • heart, liver damage, hyponatremia (low blood NA from drinking excessive water)

  21. McKim • PCP • Source – synthesized; “angel dust” • Use – originally an anesthetic and analgesic • Effects -trancelike state, disorientation, fear/anxiety, some psychosis • PCP has its own receptor on the NMDA receptor • Lethality problem: TI of 10 • Long term psychosis

  22. McKim Review • Classes of hallucinogens • SE – LSD/psilocybin • NE – Mescaline/Ecstasy • Effects of LSD • Hallucinations • Pupil dilation • Sources • LSD – synthetic • Mescaline – peyote • Psilocybin - mushroom

  23. McKim Review • Health risks • Ecstasy • Serotonin depletion • Dehydration • Heart trouble • PCP • Psychosis • Lethal

  24. SIB – Naltrexone effects

  25. SIB – Naltrexone effects

  26. SIB – Naltrexone effects

  27. SIB – Naltrexone review • Criteria for inclusion • Primary focus was the effect of naltrexone • Ss were diagnosed with ID • SIB was measured • Peer refereed English language journal • Results were in a quantitative format • Short-term or acute trials

  28. SIB – Naltrexone effects

  29. SIB – Naltrexone effects

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