hallucinogens 2 Flashcards
what do indoleamine and phenethylamine hallucinogens activate and what does this cause?
- activate serotonin receptors
- primary neuropharmacological mechanism = stimulation of 5HT receptors
- stimulation/activation of 5HT receptors = main contributor to psychological effects
what are the two main groups of classical hallucinogens (in terms of chemical structure)
- phenethylamines
- indoleamines
what does the serotonergic raphe in the midbrain do?
- supply large parts of the brain with nerves
what type of receptors are 5HT2A receptors and what effect does activation do?
- G protein-coupled receptors
- stimulatory effects on the neurone (increases transmitter release and increased activity)
- may stimulate excitatory neurones including prefrontal cortex
- stimulating excitatory neurones may be critical for hallucinogenic effects
what have animal studied shown about behavioural effects of classical hallucinogens?
- shown that classical hallucinogens = blocked by selective 5HT2A receptor antagonist
what does MDMA stimulate?
serotonin release
dopamine release (including nucleus accumbens)
what is the primary neuropharmacological mechanism of dissociative anaesthetics?
- blockade of channel pore of NDMA-type glutamate receptor
- this increases neural excitation in many brain areas by disinhibition (reducing activity of inhibitory neurones)
what else does NMDA receptor antagonists stimulate?
- prefrontal cortex
- nucleus accumbens dopamine release
- this may be regulated by increased neural excitation in cortical regions
identify adverse effects of dissociative anaesthetics and MDMA
- dependence
- neurodegeneration
- ketamine bladder
explain dependence as an adverse effect of dissociative anaesthetics and MDMA
- animal studies show evidence that support dissociative anaesthetics and MDMA can cause dependence
- potential for dependence = lower than other drugs of abuse
explain neurodegeneration as an adverse effect of dissociative anaesthetics and MDMA
- studies in animals shown that non-competitive NDMA receptor antagonists, including PCP and ketamine and MDMA cause neurodegeneration
- induced neurodegeneration = selective to serotonergic neurones
- for MDMA = no compelling evidence than recreational use of drug also damages serotonergic neurones in humans
explain ketamine bladder as an adverse effect of dissociative anaesthetics and MDMA
- thickening of bladder
- lower bladder capacity
- kidney dysfunction
- k-cramps
- all reported in chronic ketamine users
explain how classical hallucinogens/MDMA are used in assisted psychotherapy
- drug used in 1 or few occasions
- used to overcome obstacles for successful psychotherapy
- used to treat substance abuse, severe depression, cancer anxiety, PTSD, alcohol-dependence
- needs careful clinical supervision due to potential ‘bad trip’