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CNS Depressants

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CNS Depressants Concepts, principles, and examples Terms and concepts Depressant, sedative, tranquillizer, anxiolytic, hypnotic Levels of sedation: Conscious levels ... – PowerPoint PPT presentation

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Title: CNS Depressants


1
CNS Depressants
  • Concepts, principles, and examples

2
Terms and concepts
  • Depressant, sedative, tranquillizer, anxiolytic,
    hypnotic
  • Levels of sedation
  • Conscious levels Anxiolytic, behavioral
    disinhibition, sedation
  • Unconscious levels Hypnagogic state, sleep,
    anaesthesia, coma.

3
Juliens principles of CNS depressants
  • CNS depressants are additive with each other and
    with the behavioral state of the user.
    Supradditive synergistic.
  • CNS depressants are antagonists of the behavioral
    stimulants, but in a non-specific fashion.
  • Rebound or withdrawal is unlikely after a single
    dose of a CNS depressant.
  • Dependence, psychological dependence, and
    tolerance do occur to CNS depressants.

4
Mechanisms of action
  • Reversible depression of excitable tissue
    barbiturates and non-barbiturates, ethyl alcohol,
    and general anaesthetics.
  • Greater depression of polysynaptic pathways, such
    as the reticular activating system (RAS).
  • Potentiating the GABAA receptor complex
    barbiturates prolong Cl- access 4 to 5 times.

5
The mental status exam
  • 1. General appearance
  • 2. Sensorium
  • a. Orientation
  • b. Clarity/cloudiness
  • 3. Behavior/manner
  • 4. Stream of talk
  • 5. Cooperativeness
  • 6. Mood (Feeling)
  • 7. Affect (expression)
  • 8. Perception
  • a. Illusions
  • b. Hallucinations
  • 9. Logical thought?
  • 10. Knowledge
  • 11. Intellect function
  • 12. Insight/judgment

6
General CNS depressants
  • Barbiturates A family of over 2500 derivatives
    of barbituric acid, of which about 50 have been
    marketed. First used in 1912 (phenobarbital).
  • Nonbarbiturate hypnotics Early 1950s
  • Tranquillizers
  • General anaesthetics
  • Abused inhalants

7
The barbiturates
  • Pharmacological phenomena
  • Pharmacokinetics
  • Ultra-short acting Short (re)distribution
    half-lives
  • Short- to long-acting Long elimination
    half-lives
  • Low selectivity and low TI
  • Sleep abnormalities
  • REM suppression
  • REM rebound and rescidivism

8
Barbiturates, continued
  • Psychopharmacological phenomena
  • Repeated use leads to tolerance and dependence
  • Individual reactions may be be different from
    sedation depression, agitation, and aggressive
    behavior may occur, influenced by
  • mental set
  • social setting
  • pain
  • Affects movement and judgment like alcohol

9
Nonbarbiturate hypnotics
  • Glutethimide (Doriden), ethchlorvynol (Placidyl),
    and methyprylon (Noludar) in early 1950s
  • The methaqualone (Quaalude) episode
  • 1951 Malaria treatment
  • 1965 Tranquillizer and panacea
  • 1972-73 Abuse epidemic
  • 1973 Placed on Schedule II
  • 1984 Withdrawn from market by manufacturer

10
Antianxiety agents
  • Dicarbamate derivatives
  • Meprobamate (Equanil, Miltown)
  • Mebutamate (Capla), tybamate (Solacen)
  • Carisoprodol (Rela, Soma)
  • Benzodiazepines

11
General anaesthetics
  • Membrane fluidization and ion channel
    perturbation
  • Gas Nitrous oxide
  • Volatile liquids
  • Ether
  • Halothane
  • -fluranes ( iso-, des-, en-, and sevo-)
  • Injectable GABA agonists
  • Barbiturates, propofol (Diprovan), etomidate

12
The GABAA Receptor Complex
Cl-
Cl-
Cl-
Cl-
Cl-
Inside
Cl- ion channel
B A R B
B A R B
G A B A
G A B A
Cl-
E t O H
B D Z
Cl-
Cl-
Cl-
Cl-
Cl-
Outside
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