Propranolol (beta blockers)
either lipid soluble (labetalol, oxprenolol, propranolol and timolol) or non lipid soluble (atenolol, nadolol, sotalol)
nonselective beta blocker with lipophilic properties allowing it to cross the BBB
Decreases REM duration
Causes EDS, daytime fatigue, insomnia, nightmares, sleep terrors and hallucinations
case reports describe beta blocker induced REM behavior disorder
PSG-
- increase in wake time after sleep onset
-increase in NREM stage 1 sleep
- increase in REM sleep latency
- decrease in REM sleep (less with atenolol and metoprolol)
Bupropion
Antidepressant that blockes reuptake of NE and Dop
Does not decrease REM duration
Used for depression and for smoking cessation
Reserpine
Depletes catecholamines
Increases REM sleep
Physostigmine
Cholinesterase inhibitor
Increases REM sleep
Donepezil
Centrally acting chplinesterase inhibitor
Increases REM sleep
Dexamethasone (corticosteroids)
Decrease REM sleep
Decrease number of REM periods
Decrease N3 sleep
Increase in REM latency
Increase time spent awake
MAO inhibitors (inhibit enzymes in the metabolism of NE, Dop, Ser)
Most potent REM inhibitors
Decreased TST
Increased wake time after sleep onset
No change in SWS
Increased REM sleep latency
REM rebound upon drug withdrawal
Types: classic- irreversible enzyme in hibition -phenelzine, Trancypromine or
Newer reversible (brofaromine)
Benzodiazepines
Act on GABA receptors and enhance activity of GABA
Increase in TST
Reduces sleep latency
Reduction in frequency of arousals
Reduction in wake time after sleep onset
Increase in N2 sleep
Reduction in N3 sleep (SWS)
Increase in REM sleep latency
Reduction in REM sleep
Increase in spindle density at 12-14 cycles/sec and pseudospindle density
Increase in sleep continuinty
Ropinirole (Requip)
treats RLS
Non effective for non motor symptoms of RBD
In mild RBD with frequent comorbid periodic limb movements pramipexole decreases nocturnal behavior
Baclofen
Agonist at GABA receptor and inhibits transmission of both monosynaptic and polysynaptic reflexes at spinal cord by hyperpolarization of primary afferent fibre terminals
used to treat spasticity
melatonin
initial therapy for RBD symptoms and at high doses at bedtime (6-15mg) augments REM sleep atonia
Obstructive apneas
opiates BDZs by reducing tone in upper airway dilator muscles
alcohol ingestion leading to inhibition of upper airway muscle
Barbs decrease tone in upper airway dilator muscles
Olanzapine- atypical antipsychotic
Binds to Dop receptors D1/D2, serotonin receptor 5HT-2, muscarinic Ach receptors, alpha 1 receptor, Histaminergic receptor H1
Increases REM sleep latency
Decreases REM sleep
Increases REM sleep density (quantitative measure of phasic eye movement)
Opiates
cause central sleep apnea such as methadone in creases risk of cSA in a dose dependent fashion with erratic, ataxic, irregular breaqthing
decreases SWS
Temazepam
can worsen OSA
Tiagabine
GAT-1 inhibitor
Increases SWS
Hydroxyzine (antihistamines)
Modest suppression of REM sleep and increased sleep continuity
Phenobarbital (GABA receptor agonist)
Increases sleep continuity
Decreases both REM and SWS
Minimally affects SWS
Amphetamines
Increase MAO neurotransmitters NE, Dop, Ser by increasing their presynaptic release or blocking reuptake
Enhance wakefulness and alertness producing insomnia
Decrease in sleepiness
Increase in sleep latency
Decrease in sleep efficiency
increase in wake time after sleep onset
Decrease in TST
Increase in sleep fragmentation
Decrease in SWS
Increase in REM sleep latency
Decrease in REM sleep
Discontinuation of amphetamines
increase in sleepiness
increse in SWS
Increase in REM sleep
Carbamazepine works through sodium channels
Increases SWS while decreasing REM sleep
Phenytoin works via sodium channel blockade
Chronic use decreases SWS
Acute use increases SWS
Lamotrigine works via sodium blackade
Decreases SWS
Diazepam works as a GABA agonist
Decreases both REM and SWS