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EFFECTS OF DRUG ABUSE
CANNABIS & AMPHETAMINES
©Emmanuel M. Kingston
CANNABIS ABUSE
• Abuse- use of a chemical substance or a drug
for non-therapeutic purposes.
• The effects are caused by chemicals in
cannabis, including cannabinoids such as
tetrahydrocannabinol (THC).
• Cannabis has both psychological and
physiological effects on the human body.
Cannabinoid receptors
• G-protein coupled receptor.
• CB1 receptors bigger and extraordinarily abundant in the
brain: 10 times more plentiful than μ-opioid
receptor(morphine).
• CB2 receptors are structurally different (similarity 44%), are
found only on cells of the immune system, and seems to
function similarly to its CB1 counterpart.
• CB2 receptors are most commonly prevalent on B-cells, NK
cells, and monocytes, but can also be found on
polymorphonuclear neutrophil cells, CD 8, and CD 4 cells. In
the tonsils the CB2 receptors appear to be restricted to Blymphocyte-enriched areas.
• THC and endogenous anandamide additionally interact with
glycine receptors.
Prevalent brain locations:
• Basal ganglia, cerebellum, hippocampus,
cerebral cortex and nucleus accumbens
(“reward centre of the brain”).
• Others: hypothalamus, amygdala, spinal cord,
brainstem and nucleus of the solitary tract
(visceral sensations of N,V)
Preparations
Behavioral changes that may be symptoms of prolonged
marijuana use include:
• distorted perceptions
• impaired coordination
• difficulty in thinking and problem solving
• ongoing problems with learning and memory
Other signs of marijuana abuse are frequently visible in users:
• red, blurry, bloodshot eyes
• constant, mucus-filled cough
• rapid heartbeat
• Hunger & dry mouth
• anxiety, paranoia, or fear
• poor memory
• poor coordination and slow reaction time
• Addiction
•

Cancer of the lungs is also linked to marijuana use because unfiltered marijuana smoke has more
carcinogens than cigarettes.
• Blood-shot eye
AMPHETAMINE ABUSE
• CNS stimulants.
• Amphetamine is made up of two distinct
compounds (enantiomers): pure
dextroamphetamine and pure levoamphetamine.
• Dextroamphetamine is more potent than
levoamphetamine.
• Medications containing amphetamines are
prescribed for narcolepsy, obesity, and attention
deficit/hyperactivity disorder.
Methods of Use
• Dependence liability: Moderate
• Routes:
• Medical: Oral, nasal inhalation
Recreational: Oral, nasal inhalation, insufflations,
rectal, intravenous
• Pharmacokinetic data
• Bioavailability: Rectal 95–100%; Oral 75–100%
• Protein Binding: 15–40%
• Metabolism:
Hepatic: CYP2D6, BDH, and FMO(flavin monooxygenase)
• Half life: D-amph:9–11h; L-amph:11–14h
Disorders Medically Treated With
Amphetamines
•
•
•
•
•
•

Attention deficit hyperactivity disorder
Narcolepsy (uncontrolled episodes of sleep)
Obesity
Parkinson's disease
Nasal congestion
Causes release of dopamine and
norepinephrine in the brain and inhibits their
reuptake.
Short-Term Effects
•
•
•
•
•
•
•
•
•
•
•

High body temperature
Cardiovascular system failure
Hostility or paranoia
Irregular or increased heart
rate
Increased blood pressure
Increased activity
Euphoria
Decreased fatigue/drowsiness
Decreased appetite
Dry mouth
Dilated pupils

•
•
•
•
•
•
•

Increased respiration
Heightened alertness/energy
Nausea
Headache
Palpitations
Altered sexual behavior
Tremor/twitching of small
muscles
• Release of social inhibitions
Long-Term Effects
• Toxic psychosis
• Physiological and
behavioral disorders
• Dizziness
• Pounding heartbeat
• Cardiomyopathies
• Difficulty breathing
• Mood or mental changes
• Unusual fatigue
• Cardiac arrhythmias
• Repetitive motor activity

•
•
•
•
•
•
•

Ulcers
Malnutrition
Mental illness
Skin disorders
Vitamin deficiency
Flush or pale skin
Loss of coordination and
physical collapse
• Convulsions, coma, and
death
Das ENDE

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Effects of Drug abuse: Cannabis & Amphetamines

  • 1. EFFECTS OF DRUG ABUSE CANNABIS & AMPHETAMINES ©Emmanuel M. Kingston
  • 2. CANNABIS ABUSE • Abuse- use of a chemical substance or a drug for non-therapeutic purposes. • The effects are caused by chemicals in cannabis, including cannabinoids such as tetrahydrocannabinol (THC). • Cannabis has both psychological and physiological effects on the human body.
  • 3. Cannabinoid receptors • G-protein coupled receptor. • CB1 receptors bigger and extraordinarily abundant in the brain: 10 times more plentiful than μ-opioid receptor(morphine). • CB2 receptors are structurally different (similarity 44%), are found only on cells of the immune system, and seems to function similarly to its CB1 counterpart. • CB2 receptors are most commonly prevalent on B-cells, NK cells, and monocytes, but can also be found on polymorphonuclear neutrophil cells, CD 8, and CD 4 cells. In the tonsils the CB2 receptors appear to be restricted to Blymphocyte-enriched areas. • THC and endogenous anandamide additionally interact with glycine receptors.
  • 4. Prevalent brain locations: • Basal ganglia, cerebellum, hippocampus, cerebral cortex and nucleus accumbens (“reward centre of the brain”). • Others: hypothalamus, amygdala, spinal cord, brainstem and nucleus of the solitary tract (visceral sensations of N,V)
  • 6. Behavioral changes that may be symptoms of prolonged marijuana use include: • distorted perceptions • impaired coordination • difficulty in thinking and problem solving • ongoing problems with learning and memory Other signs of marijuana abuse are frequently visible in users: • red, blurry, bloodshot eyes • constant, mucus-filled cough • rapid heartbeat • Hunger & dry mouth • anxiety, paranoia, or fear • poor memory • poor coordination and slow reaction time • Addiction • Cancer of the lungs is also linked to marijuana use because unfiltered marijuana smoke has more carcinogens than cigarettes.
  • 8. AMPHETAMINE ABUSE • CNS stimulants. • Amphetamine is made up of two distinct compounds (enantiomers): pure dextroamphetamine and pure levoamphetamine. • Dextroamphetamine is more potent than levoamphetamine. • Medications containing amphetamines are prescribed for narcolepsy, obesity, and attention deficit/hyperactivity disorder.
  • 9. Methods of Use • Dependence liability: Moderate • Routes: • Medical: Oral, nasal inhalation Recreational: Oral, nasal inhalation, insufflations, rectal, intravenous • Pharmacokinetic data • Bioavailability: Rectal 95–100%; Oral 75–100% • Protein Binding: 15–40% • Metabolism: Hepatic: CYP2D6, BDH, and FMO(flavin monooxygenase) • Half life: D-amph:9–11h; L-amph:11–14h
  • 10.
  • 11. Disorders Medically Treated With Amphetamines • • • • • • Attention deficit hyperactivity disorder Narcolepsy (uncontrolled episodes of sleep) Obesity Parkinson's disease Nasal congestion Causes release of dopamine and norepinephrine in the brain and inhibits their reuptake.
  • 12. Short-Term Effects • • • • • • • • • • • High body temperature Cardiovascular system failure Hostility or paranoia Irregular or increased heart rate Increased blood pressure Increased activity Euphoria Decreased fatigue/drowsiness Decreased appetite Dry mouth Dilated pupils • • • • • • • Increased respiration Heightened alertness/energy Nausea Headache Palpitations Altered sexual behavior Tremor/twitching of small muscles • Release of social inhibitions
  • 13. Long-Term Effects • Toxic psychosis • Physiological and behavioral disorders • Dizziness • Pounding heartbeat • Cardiomyopathies • Difficulty breathing • Mood or mental changes • Unusual fatigue • Cardiac arrhythmias • Repetitive motor activity • • • • • • • Ulcers Malnutrition Mental illness Skin disorders Vitamin deficiency Flush or pale skin Loss of coordination and physical collapse • Convulsions, coma, and death