22 sedative hypnotic drugs
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Transcript of 22 sedative hypnotic drugs
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
Anita Q. Sangalang, MD, FPOGSFACULTY OF PHARMACY
UNIVERSITY OF SANTO TOMAS
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTICS
Benzodiazepines Barbiturates Miscellaneous agents
Short Ultra
action action
Intermediate Short Buspirone
action action Chloral hydrate
Long Long Zaleplon
action action Zolpidem
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
SEDATION• Reduction of anxiety• Calming effectANXIOLYTIC• Drug that reduces anxiety• SedativeHYPNOSIS• Induction of sleep
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
• Lipid soluble
• Absorbed well from the GIT
• Good distribution to the brain
• Metabolized before elimination from the body by hepatic enzymes
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BENZODIAZEPINES
• Converted initially to active metabolites with long half-lives
• Diazepam and flurazepam After several days of therapy
accumulation of active metabolites can lead to excessive sedation
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BENZODIAZEPINES
• Lorazepam and oxazepam Undergo extrahepatic conjugation
and do not form active metabolites
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BENZODIAZEPINES
• Bz receptors Form part of GABAA receptor-chloride
ion channel macromolecular structure Binding facilitates the inhibitory actions
of GABA Increased GABA mediated chloride ion
conductance
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BENZODIAZEPINES
• Flumazenil Reverses the CNS effects of
benzodiazepines Antagonist at the Bz receptor
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BENZODIAZEPINES
• Beta-carbolines High affinity for Bz receptors Can elicit anxiogenic and convulsant
effects Inverse agonists
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BENZODIAZEPINES
• Diazepam
desmathyldiazepam active
oxazepam metabolites
conjugation
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BENZODIAZEPINES
• Chlorazepam
• Estazolam immediately converted to • Oxazepam inactive metabolites
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BARBITURATES
• Extensively metabolized
• Depress the neuronal activity
• Facilitates and prolongs the inhibitory effects of GABA and glycine
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BARBITURATES
• Bind to multiple isoforms of GABAA
receptor but at different sites from those with which benzodiazepines interact
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BARBITURATES
• Not antagonize by flumazenil
• Increase the duration of GABA- mediated chloride ion channel opening
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BARBITURATES
• Block the excitatory transmitter glutamic acid and at high concentration, sodium channels
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BARBITURATES
• Thiopental Drug with highest lipid solubility enter
the CNS rapidly Used as induction agents in anesthesia
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BARBITURATES
• Thiopental CNS effects are terminated by rapid
redistribution of the drug from the brain to other highly perfused tissues (skeletal muscles)
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BARBITURATES
• Thiopental Metabolism occur via oxidation
and glucoronidation Converted to active metabolite
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
BARBITURATES
• Phenobarbital Goes to the liver to be oxidized Excreted partly unchanged in the urine Alkalinizes the urine Half-life of 4-5 days Requires loading dose
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
OTHER DRUGS
• Buspirone Partial agonist at serotonin receptor
(5-HT receptor) Impairment of mental activity Psychomotor impairment Selective with minimal depressant
effects on the CNS
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
OTHER DRUGS
• Zolpidem and zaleplon Exert their CNS effects via interaction
with benzodiazepine receptors Bind more selectively Antagonize by flumazenil
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
DRUG A - BARBITURATES dose = CNS depression
DRUG B - BENZODIAZEPINES - flatter dose response curve - greater margin of safety
DRUG A
DRUG B
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN SYSTEM EFFECTS1. Sedation2. Hypnosis• Promote sleep onset• Increase the duration of the sleep stateSTAGES OF SLEEPa. REM (Rapid eye movement)• Dream• Decreases at high dosesb. Non-REM• 70-75%
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN SYSTEM EFFECTS3. Anesthesia• Thiopental (barbiturate)• Midazolam (benzodiazepine)• Loss of consciousness, amnesia
and suppression of reflexes
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN SYSTEM EFFECTS4. Anticonvulsant actions• Phenobarbital, clonazepam
Suppression of seizure activity Selective because they do not
cause severe sedation
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN SYSTEM EFFECTS4. Anticonvulsant actions• Diazepam, lorazepam and phenobarbital
Given IV Used in status epilepticus Heavy sedation is needed
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN SYSTEM EFFECTS5. Muscle relaxation• Diazepam
Spasticity states Cerebral palsy
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN SYSTEM EFFECTS6. Medullary depression• High doses can lead to
Respiratory arrest Hypotension CVS collapse Death in suicidal overdose
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN SYSTEM EFFECTS
7. Tolerance and dependence
• Tolerance Decrease in responsiveness Used chronically or in high dosage
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN SYSTEM EFFECTS
7. Tolerance and dependence
• Tolerance Metabolic tolerance
Occurs with phenobarbital Induces its own metabolism Decreases CNS response to the
drug itself
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN SYSTEM EFFECTS
7. Tolerance and dependence
• Dependence
Physiologic State of response to a drug Removal of the drug evokes
unpleasant symptoms Opposite of the drug’s effects
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN SYSTEM EFFECTS
7. Tolerance and dependence
• Dependence
Physiologic Leads to abstinence syndrome
(withdrawal state) when the drug is discontinued
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN –SYSTEM EFFECTS7. Tolerance and dependence• Dependence
Physiologic Withdrawal signs
Anxiety Tremors Hyperreflexia Seizures
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN SYSTEM EFFECTS
7. Tolerance and dependence
• Dependence
Physiologic Occur more commonly with short-
acting drugs Pentobarbital and secobarbital Dependence is unlikely to occur
with buspirone
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
ORGAN SYSTEM EFFECTS7. Tolerance and dependence• Dependence
Psychological State of response to a drug Drug taker feels compelled to use
the drug Suffers anxiety when separated
from the drug
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
CLINICAL USES1. Anxiety states• Benzodiazepines with intermediate or
long durations of action are favored• Buspirone
Used for generalized anxiety disorders• Alprazolam
Phobic and panic attacks
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
CLINICAL USES2. Sleep disorders• Used to treat primary insomnia and
other sleep disorders
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
CLINICAL USES3. Sedation • Prior to medical/surgical procedures• Conscious sedation-anterograde
amnesia4. Treatment of seizures and convulsions
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
CLINICAL USES4. Detoxification of alcoholics• Chlordiazepoxide• Diazepam6. Muscle relaxation7. Manias, major depression, phobias
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
TOXICITY
1. Psychomotor dysfunction
• Cognitive impairment
• Decreased psychomotor skills
• Unwanted daytime sedation
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
TOXICITY
2. Additive CNS depression
• When used with Alcoholic beverages Antihistamines Antipsychotic drugs Opioid analgesics Tricyclic antidepressants
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
TOXICITY
3. Overdosage causes severe respiratory and cardiovascular depression
4. Terratogenic
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SEDATIVE-HYPNOTIC DRUGS
SEDATIVE-HYPNOTIC DRUGS
TOXICITY
3. Induce formation of liver microsomal enzymes
• Metabolize drugs multiple drug interactions
• Chloral hydrate displaces coumarin from protein binding sites and increases anticoagulant effects