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Drugs Affecting the Central Nervous System

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Title: Drugs Affecting the Central Nervous System


1
Drugs Affecting the Central Nervous System
  • Pharmacology 49.222
  • Bill Diehl-Jones RN, PhD
  • Faculty of Nursing and Department of Zoology

2
Agenda
  • Zen Review
  • CNS drugs
  • anxiolytics and hypnotics
  • stimulants
  • Anaesthetics
  • Antidepressants

3
Anxiolytics and Hypnotics
4
Two Classes
  • Benzodiazepines
  • pam and lam
  • Eg clonazepam, midazolam, lorazepam
  • Others
  • Buspirone
  • Barbiturates
  • Non-barbiturates

5
Benzodiazopines
  • Bind adjacent to GABA receptor
  • Enhances affinity of receptor for GABA
  • Hyperpolarizes neurons, prevents firing

Cl-
Benzodiazipene
GABA
6
Benzodiazopines
  • Currently, mainstay of anxiolytic therapy
  • Whats good about benzodiazepines
  • Relatively high therapeutic index (O/D is rare)
  • Also useful for treating muscle (diazepam) and
    sleep (lorazepam) disorders, seizures
    (clonazepam)
  • Whats bad about benzodiazepines
  • Effects potentiated by alcohol

7
Buspirone
  • Use
  • General anxiety disorders
  • Mode of action
  • Activates 5-HT1a1 receptor (and possibly others)
  • Slow onset, less drowsiness, fatigue than most
    benzodiazepines

8
Barbiturates
  • Examples pentobarbital (als)
  • Clinical Use
  • Formerly, main anxiolytics
  • Now, used for anaesthesia, anticonvulsant
  • Mode of action
  • Inhibits Na/K transport in portion of RAS
  • Whats bad
  • Drowsiness, hangover
  • Induce P450 enzymes (so what?)

9
Non-Barbiturates
  • Chloral Hydrate
  • Antihistamines
  • Eg diphenhydramine
  • Alcohol
  • Eg Laphroiag Single Malt Scotch










NAD
NADH
NAD
NADH
Acetaldehyde
Acetate
Disulfaram
10
CNS Stimulants
11
Flavours
  • Psychomotor Stimulants
  • Amphetamine
  • Caffeine
  • Theophylline
  • Nicotine
  • Psychotomimetic Drugs
  • Lysergic Acid Diethylamide (LSD)
  • Phencyclidine (Angel Dust)
  • Tetrahydrocannabinol (THC)


Mehylxanthines
12
Amphetamines "Faster, faster, until the thrill
of speed overcomes the fear of death."Hunter S.
Thompson
  • Clinical Use
  • Few, due to side effects
  • ADHD and Narcolepsy
  • Mode of Action
  • Releases intracellular catecholamines
  • Blocks MAO
  • Stimulates entire CNS and sympathetic branch of
    ANS

13
Mechanisms of Action of Amphetamines
Dopa
MAO
-
Dopamine 5-HT NE

Amphetamine
Increased NT
Receptor
14
Clinical Effects of Amphetamines
  • CNS
  • Increased alertness
  • longer-lasting than cocaine
  • decreased fatigue/appetite
  • Irritability, weakness
  • amphetamine psychosis
  • Arrhythmias, circulatory collapse

15
Methylxanthines
  • Clinical Uses
  • Cardiovascular (caffeine/theo)
  • Positive inotrope/chronotrope
  • Apnea/bradycardia
  • Asthma (theo)
  • Why?
  • Other effects
  • Diuretic
  • stimulant

16
Methylxanines
  • Modes of Action
  • Increases Cai
  • Increases cAMP, cGMP
  • Blocks adenosine receptors

17
Methylxanthine Facts
  • Caffeine
  • Lethal dose is 10 g (100 cups)
  • Withdrawal symptoms in people who routinely have
    more than 600 mg/day (6 cups)
  • Theophylline
  • LOTS in tea

18
Nicotine
  • Clinical Uses
  • None
  • Mode of Action
  • Low dose
  • Ganglionic stimulation
  • High dose
  • Ganglion blockade

19
Nicotine
  • Physiological Effects
  • CNS
  • Crosses blood-brain barrier
  • Low dose euphoria, relaxation, arousal
  • High dose respiratory effects, hypotension
  • Peripheral
  • Again, depends on dose

20
Psychotomimetic Drugs
21
LSD
  • Clinical Uses
  • ?
  • Modes of Action
  • 5-HT agonist
  • Physiologic Effects
  • Sympathetic
  • Pupillary dilation, increased BP, piloerection
  • CNS
  • Altered perceptual states
  • True dependence rare

22
THC
  • Clinical Uses
  • ?
  • Modes of Action
  • THC receptors exist in CNS, but mode unknown
  • Physiological effects
  • Immediate, peak at 20 min
  • Impairs short term memory, produces euphoria,
    increases apetite, increase HR, decrease BP

23
PCP
  • Clinical Uses
  • Anaesthetic (ketamine -research only)
  • Mode of Action
  • DO, 5-HT, NE reuptake inhibitor
  • Physiological Effects
  • Dissociative behaviour, coma

24
Anaesthetics
25
What is Anaesthesia?
26
What Factors are Important in Anaesthetic
Selection?
27
Preanaesthetics
  • Anticholinergics
  • Antiemetics
  • Antihistamines
  • Barbiturates
  • Benzodiazepines
  • WHY?

28
Phases of Anaesthesia
  • Induction
  • Unconsciousness rapidly produced (thiopental)
  • Muscle relaxants - vecuronium
  • Maintenance
  • Vital signs, response to stimuli gauged
  • Volatile gases usually used. Why?
  • Recovery
  • Involves redistribution rather than metabolism

29
Depth of Anaesthesia
  • Stage I Analgesia
  • Loss of pain sensation
  • At level of spinothalamic tract
  • Stage II Excitement
  • Delerium, combative behaviour, BP increase
  • Barbiturates used to manage this
  • Stage III Surgical Anaesthesia
  • Regular respiration, muscle relaxation, eye
    movements cease
  • Stage IV Medullary Paralysis
  • Depression of vasomotor/respiratory centers
  • Implications?

30
General Anaesthetics
  • Inhaled
  • Intravenous
  • Local

31
Inhaled Anaesthetics
  • Primarily used for maintenance
  • Concentration can be rapidly altered
  • Physiological Effects
  • Bronchodilation, decr. ventilation, incr. brain
    perfusion
  • Potency a factor of lipid solubility. Why?
  • Measured as a function of MAC

32
Examples of Inhaled Anaestheticsand Relative MAC
Values
Ether
Halothane
Nitrous Oxide
33
HomeworkRefer to Table 11.7 for Characteristics
of Inhalation Anaesthetics
34
Intravenous Anaesthetics
35
Flavours of Intravenous Anaesthetics
  • Barbiturates
  • Thiopental
  • Benzodiazepines
  • Midazolam
  • Opioids
  • Morphine
  • Meuroleptanaesthesia
  • Droperidol/fentanyl (INNOVAR)
  • Ketamine

36
Differences Between Inhalation and Intravenous
Anaesthetics
  • Inhalation likely no discrete receptors
  • Intravenous specific receptors
  • For specific differences, refer to Table 11.9

37
Local Anaesthetics
  • Applied topically
  • All have amino group linked to lipophilic portion
  • Block conduction of nerve impulses to CNS
  • Generally, these inhibit Na channels
  • How would this affect action potentials?
  • Examples Procaine, lidocaine

38
Antidepressants
39
Major Groups
  • Tricyclics
  • SSRIs
  • MAO Inhibitors
  • Drugs to treat Mania

40
Tricyclics/Polycyclics
  • Examples
  • Amitriptyline, imipramine
  • Mode of Action
  • Inhibit NE, 5-HT, DO re-uptake
  • Also have muscarinic and adrenergic effects
  • How is this manifested in terms of side effects
  • Clinical Effects
  • Elevate mood, mental alertness, reduces morbid
    preoccupation in 50 70 of patients

41
SSRI Inhibitors
  • Examples
  • Fluoxetine, Zoloft, Paxil
  • Mode of Action
  • Selectively block 5-HT reuptake
  • Clinical Effects
  • Effective in treating depression, OCD
  • Fewer side effects than TCAs. Why?

42
MAO Inhibitors
  • Examples
  • Phenylzine, isocarboxazide
  • Mode of Action
  • MAO inactivates excess NE, DO, 5-HT
  • Inhibitors increase the amounts of these
    neurotranmitters
  • Physiological Effects
  • Depression
  • problems with this drug

43
Lithium Salts
  • Mode of Action
  • Affects IP3, blocks Na channels
  • Clinical Effects
  • Tmt of manic/depressive patients
  • VERY TOXIC

44
Neuroleptics
  • Antischizophrenic/Antipsychotic Drugs

45
Categories of Neuroleptics
  • Phenothiazines
  • Eg Chlorpromazine
  • Benziosoxazoles
  • Eg Respiridone
  • Dibenzodiazepines
  • Eg Cloazapine
  • Butyrophenones
  • Eg Haloperidol

46
How do They Work?
  • DO receptor blockers
  • 5-HT receptor blockers

47
Clinical Effects
  • Affect corticostriatial pathways in brain
  • However, also affect Nigrostriatial pathways
  • What type of side effects might this cause?
  • Often have anti-muscarinic effects
  • Again, what types of side effects?
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