1 / 36

Stimulant Drugs Part 3

Stimulant Drugs Part 3. Kim Edward Light, Ph.D. Professor, College of Pharmacy University of Arkansas for Medical Sciences. Objectives part 3. Discuss prescription amphetamine products and uses. Discuss other prescription stimulant drugs and their uses and problems.

oshin
Télécharger la présentation

Stimulant Drugs Part 3

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. Stimulant DrugsPart 3 Kim Edward Light, Ph.D. Professor, College of Pharmacy University of Arkansas for Medical Sciences

  2. Objectives part 3 • Discuss prescription amphetamine products and uses. • Discuss other prescription stimulant drugs and their uses and problems. • Discuss use and abuse of cocaine. • Identify the differences between cocaine abuse and methamphetamine abuse. • Discuss other illicit stimulants such as khat and arecoline (betel).

  3. Amphetamine Products • Adderall® • Adderall-XR® • Benzedrine® • Biphetamine® • Dexedrine® • Dexedrine Spansule®

  4. Amphetamine - Uses • Treatment • Attention Deficit Hyperactivity Disorder (ADHD) • Narcolepsy • Obesity • Extended or sustained release to reduce dosing frequency.

  5. Amphetamine - Side Effects • Similar to methamphetamines but more cardiovascular • Abuse often leads to abuse of methamphetamine • Escalating use among college students as “study drug”

  6. Other Stimulant Drugs • Treatment of ADHD • Methylphenidate - Ritalin® • Atomoxetine - Strattera® • Treatment of Obesity • Phenmetrazine – Preludin® • Phentermine – Fastin® • Fenfluramine - Pondimin® • Treatment of Narcolepsy • Modafinil - Provigil® • Methylphenidate - Ritalin®

  7. Methylphenidate Ritalin® • Treatment of narcolepsy and ADHD • Onset of action within one hour • Duration of action is less than 4 hours. • Sustained or extended release preparations. • Used as a “study drug” • Side effects similar to methamphetamine and amphetamine • May lead to abuse of methamphetamine

  8. Phenmetrazine Preludin® • Anorexiant drug for treatment of obesity • Sustained release preparation once daily - AM. • Tolerance development (within a few weeks). • Actions, mechanisms, and adverse consequences are similar to those of amphetamines and methylphenidate. • Less availability - less evident abuse • Popular among medical professionals due to their increased access

  9. PhentermineFastin® • Anorexiant drug in treatment of obesity • Sustained release preparation once daily - AM. • Actions and adverse consequences are similar • Dosage escalation is a common feature • Less availability - less evident abuse • Also popular among medical professionals due to increased access

  10. FenfluraminePondimin® • Anorexiant drug in treatment of obesity • Generally administered three times daily before meals • Duration generally 4-6 hours • Mechanism of action includes CNS serotonin systems • Combined with phentermine → Phen-fen. • Cardiovascular problems - palpitations, hypertension and valvular heart disease led to discontinuation. • Development of pulmonary hypertension • Tolerance, dependence, and addiction

  11. AtomoxetineStrattera® • Treatment of ADHD • Administered once or twice daily • Must take for several weeks before onset of acceptable effect • Classified as non-stimulant in 2004 but must carry warning label for possible liver toxicity. • Not stimulatory like amphetamines, although increases in • blood pressure • heart rate • weight loss

  12. Modafinil Provigil® • Approved in 1999; Schedule IV drug, • Once daily dosing • Treatment of narcolepsy, obstructive sleep apnea and excessive daytime sleepiness. • Adverse effects may include hypertension, headache, dizziness, agitation, and insomnia. • Mechanism of action and effects are markedly different from amphetamines, may enhance glutamate neurotransmission.

  13. Cocaine - History • From the leaves of the plant Erytrhroxylon coca; grows in the Andes Mountains 1000-3000 m above sea level • Used by natives for suppression of appetite, thirst, and tiredness especially on long hunting trips • Inca civilizations used coca in religious rituals

  14. Cocaine - History • Sigmund Freud and Carl Koller introduced cocaine into clinical practice • Koller (an ophthalmologist) was intrigued by its activity as a local anesthetic • Freud, working as a neurologist (~1884), was more interested in the stimulant effects

  15. Cocaine - History • Late 1800’s -- early 1900’s • ingredient in many products as an elixir, balm or other medicinal • Early 1900’s, awareness of problems resulted in a decrease in its availability • Passage of the Narcotics Tax Acts in 1914 further decreased its availability

  16. Cocaine - Mechanism • Blocks reuptake of neurotransmitters - dopamine, norepinephrine, epinephrine, and serotonin.

  17. Cocaine - Pharmacokinetics • Duration of action is minutes. • Rapidly metabolized • esterase enzymes - in blood & tissues. • Rapid metabolism results in • rapid decrease in euphoria • intense craving or drug “hunger” results

  18. Cocaine - Routes of Administration

  19. Cocaine • Powder • Crack or Freebase

  20. Caudate VTA NcA Cocaine – Binding Sites

  21. Cocaine - Adverse Effects • Tolerance & Sensitization • Restlessness, irritability, anxiety, aggressiveness, hypersexuality, and paranoia • Acute toxicity and death • seizures or stroke in the brain • arrhythmias or infarctions in the heart • Vasoconstriction may lead to necrosis and tissue death in the sinuses or injection sites.

  22. Cocaine – Use Patterns • Binge • Combination • Marijuana • Benzodiazepines • Heroin (“Speedball”) • Alcohol • Cocaine + Ethanol ®Cocaethylene

  23. Cocathethylene • Equipotent with cocaine atDA sites • Less potent at serotonin sites. • More euphorigenic and addictive. • More toxic to the liver & heart.

  24. Methamphetamine vs Cocaine • Origins • Methamphetamine is man-made • Cocaine is plant-derived • Common Methods of Use • Smoked, injected intravenously, or snorted. • Methamphetamine also is commonly ingested orally.

  25. Methamphetamine vs Cocaine • Euphoria • Intense pleasurable rush or high • Duration of the high is major difference • Methamphetamine - 8 to 24 hours • Cocaine - 20 to 30 minutes.

  26. Methamphetamine vs Cocaine • Chronic Use • Methamphetamine may result in more violent behavior • Methamphetamine withdrawal • drug hunger • anhedonia.

  27. Methamphetamine vs Cocaine • Methamphetamine • Damage to the neurons that produce dopamine and serotonin. • Cocaine • No demonstrated damage to dopamine or serotonin neurons.

  28. Transmissionof HIV/AIDS • Intravenous injection of both contributes to transmission of HIV/AIDS • High-risk sexual behaviors and in exchange of drugs for sex

  29. Other Stimulant Plants Khat derived from Catha Edulis, a small tree/shrub that grows in East Africa and Arabian Peninsula Arecoline derived from Betel nuts of the palm tree Arecacatechu prevalent throughout southeast Asia

  30. Khat - History • Cultivated in East Africa since the early 1300s. • Predates the use of coffee in the region • 20th century - some countries in region officially banned its use - seldom enforced. • Increased publicity a result of the U.S. efforts in Somalia during 1993.

  31. Khat Cathine Cathinone Methcathinone • Contains cathinone and cathine, • Methcathinone is semisynthetic from cathinone • Cathine much less potent than cathinone or methcathinone. • Cathine is a Schedule IV drug; cathinone and methcathinone are Schedule I drugs.

  32. Khat - Use • Leaves and shoots are chewed, • like tobacco, for the stimulation and appetite suppression effects. • Cathinone only present in fresh leaves since it degrades within about 48 hours. • Often refrigerated immediately upon harvesting for transport.

  33. Khat - Effects • Similar to amphetamines. • mild euphoria and excitement • reduced appetite • increased HR & BP • Withdrawal symptoms • lethargy • depression • nightmares and tremors.

  34. Arecoline - History • Widely used in India, Thailand, Indonesia and other Asian countries. • Used by more people in the world than any other single plant. • Traditionally used for intestinal worms and as an antihelminthic in veterinary medicine. • Crushed betel nuts wrapped in pieces or leaves from the Piper betel vine along with lime and sometimes other flavorings including tobacco.

  35. Arecoline - Mechanisms • Acts by stimulation of cholinergic neurotransmission in both CNS and ANS • May also act on other neurotransmitter systems (i.e. GABA) • Produces mild stimulation and euphoric not unlike tobacco • Increased risk of throat & mouth cancers.

  36. Summary (part 3) • Amphetamine in therapeutics • Methylphenidate, Phenmetrazine • Phentermine, Fenfluramine • Atomoxetine, Modafinil • Cocaine • Methamphetamine vs Cocaine • Khat – cathine, cathinone • Methcathinone • Arecoline – Betel nut

More Related