Title: Drugs Affecting the Central Nervous System
1Drugs Affecting the Central Nervous System
- Pharmacology 49.222
- Bill Diehl-Jones RN, PhD
- Faculty of Nursing and Department of Zoology
2Agenda
- Zen Review
- CNS drugs
- anxiolytics and hypnotics
- stimulants
- Anaesthetics
- Antidepressants
3Anxiolytics and Hypnotics
4Two Classes
- Benzodiazepines
- pam and lam
- Eg clonazepam, midazolam, lorazepam
- Others
- Buspirone
- Barbiturates
- Non-barbiturates
5Benzodiazopines
- Bind adjacent to GABA receptor
- Enhances affinity of receptor for GABA
- Hyperpolarizes neurons, prevents firing
Cl-
Benzodiazipene
GABA
6Benzodiazopines
- 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
7Buspirone
- Use
- General anxiety disorders
- Mode of action
- Activates 5-HT1a1 receptor (and possibly others)
- Slow onset, less drowsiness, fatigue than most
benzodiazepines
8Barbiturates
- 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?)
9Non-Barbiturates
- Chloral Hydrate
- Antihistamines
- Eg diphenhydramine
- Alcohol
- Eg Laphroiag Single Malt Scotch
NAD
NADH
NAD
NADH
Acetaldehyde
Acetate
Disulfaram
10CNS Stimulants
11Flavours
- Psychomotor Stimulants
- Amphetamine
- Caffeine
- Theophylline
- Nicotine
- Psychotomimetic Drugs
- Lysergic Acid Diethylamide (LSD)
- Phencyclidine (Angel Dust)
- Tetrahydrocannabinol (THC)
Mehylxanthines
12Amphetamines "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
13Mechanisms of Action of Amphetamines
Dopa
MAO
-
Dopamine 5-HT NE
Amphetamine
Increased NT
Receptor
14Clinical Effects of Amphetamines
- CNS
- Increased alertness
- longer-lasting than cocaine
- decreased fatigue/appetite
- Irritability, weakness
- amphetamine psychosis
- Arrhythmias, circulatory collapse
15Methylxanthines
- Clinical Uses
- Cardiovascular (caffeine/theo)
- Positive inotrope/chronotrope
- Apnea/bradycardia
- Asthma (theo)
- Why?
- Other effects
- Diuretic
- stimulant
16Methylxanines
- Modes of Action
- Increases Cai
- Increases cAMP, cGMP
- Blocks adenosine receptors
17Methylxanthine 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
18Nicotine
- Clinical Uses
- None
- Mode of Action
- Low dose
- Ganglionic stimulation
- High dose
- Ganglion blockade
19Nicotine
- Physiological Effects
- CNS
- Crosses blood-brain barrier
- Low dose euphoria, relaxation, arousal
- High dose respiratory effects, hypotension
- Peripheral
- Again, depends on dose
20Psychotomimetic Drugs
21LSD
- Clinical Uses
- ?
- Modes of Action
- 5-HT agonist
- Physiologic Effects
- Sympathetic
- Pupillary dilation, increased BP, piloerection
- CNS
- Altered perceptual states
- True dependence rare
22THC
- 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
23PCP
- Clinical Uses
- Anaesthetic (ketamine -research only)
- Mode of Action
- DO, 5-HT, NE reuptake inhibitor
- Physiological Effects
- Dissociative behaviour, coma
24Anaesthetics
25What is Anaesthesia?
26What Factors are Important in Anaesthetic
Selection?
27Preanaesthetics
- Anticholinergics
- Antiemetics
- Antihistamines
- Barbiturates
- Benzodiazepines
- WHY?
28Phases 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
29Depth 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?
30General Anaesthetics
- Inhaled
- Intravenous
- Local
31Inhaled 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
32Examples of Inhaled Anaestheticsand Relative MAC
Values
Ether
Halothane
Nitrous Oxide
33HomeworkRefer to Table 11.7 for Characteristics
of Inhalation Anaesthetics
34Intravenous Anaesthetics
35Flavours of Intravenous Anaesthetics
- Barbiturates
- Thiopental
- Benzodiazepines
- Midazolam
- Opioids
- Morphine
- Meuroleptanaesthesia
- Droperidol/fentanyl (INNOVAR)
- Ketamine
36Differences Between Inhalation and Intravenous
Anaesthetics
- Inhalation likely no discrete receptors
- Intravenous specific receptors
- For specific differences, refer to Table 11.9
37Local 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
38Antidepressants
39Major Groups
- Tricyclics
- SSRIs
- MAO Inhibitors
- Drugs to treat Mania
40Tricyclics/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
41SSRI 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?
42MAO 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
43Lithium Salts
- Mode of Action
- Affects IP3, blocks Na channels
- Clinical Effects
- Tmt of manic/depressive patients
- VERY TOXIC
44Neuroleptics
- Antischizophrenic/Antipsychotic Drugs
45Categories of Neuroleptics
- Phenothiazines
- Eg Chlorpromazine
- Benziosoxazoles
- Eg Respiridone
- Dibenzodiazepines
- Eg Cloazapine
- Butyrophenones
- Eg Haloperidol
46How do They Work?
- DO receptor blockers
- 5-HT receptor blockers
47Clinical 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?