clincial psych Flashcards
history of bromides
Sir Charles Locock gave potassium bromide to people to calm them down patients’ epilepsy improved, sir Samuel wilks also found this. Bromide sleep, the pills last for 9 days in body, sleeps day and night and cannot wake up.
Bromo-seltzer history
contained potassium bromide (plus sodium bicarbonate and citric acid for fizz), invented by Isaac Emerson in 1888. Continued in over-the-counter form under mid-1970’s. inlincation to kill you if you take too much.
Barbituates
veronal, 30 minute sleep, 8 hour sleep, 9 hour sleep, struggled to get out of bed after higher dose. pentonarbital, given to chidlren as well.
risk of barbituates
major risk over overdoes
they were the cause of two thirds of poisning deaths in the 50s
who started developing benzodiazepines?
Leo Sternbach - making six drugs
what drug was the most perscribed in the US in 1978?
valium
positives of valium
less sideffects than other BD and makes you calm
how do benzodiazepines work?
- GABAA receptors are found in high concentrations in limbic structures such as the amygdala and associated limbic structures.
- Benzodiazepines bind to a specific site on the GABAA receptor.
- This activates GABA chloride ions flood through its center into the neuron, causing it to fire and release GABA downstream.
drain opens when the benzo attaches
alpha sub-units
5 subunits, different distributions around the brain
how many subunits form the GABA receptor?
theres 5 different alpha
where is α1 most spread
cortical and cerebellar regions
where is α2 the most intense
striatum
where is α3
frontal
wehre is α5?
hippocampus
what is the specific function/ side effects of α1?
- sedation
- anti-convulsive
- amnesia
- addictive
what is the specific function/ side effects of α2?
- anxiolysis - relaxing
- muscle relaxation
- addictive
what is the specific function/ side effects of α3?
- muscle relaxation
what is the specific function/ side effects of α5?
- muscle relaxation
- amnesia
Rudolph study using mice to asses the sedative properties of alpha one …
Rudolph - got rid of alpha one subunit in mice, genetic knock out, to assess sedative effects
found dizapem didnt work and its sedative properties rely on alpha one sub unit
Rudolph research into alpha one role in anxiety …
anti anxiety effects measured in an elevated X-maze, where mice got to choose how much time they preferred to spend on its dark (preferred) vs. lighted (anxiety-provoking) areas .
Diazepam increased time on lighted arms (reduced anxiety) even in mice lacking the α1 subunit, therefore its anti-anxiety effects were not dependent on the α1 subunit.
memory test on alpha one sub unit
Passive avoidance memory test, in which mice normally remembered not to enter a dark box that they’d previously encountered an aversive stimulus on entering it. However, mice lacking the α1 subunit did not step through, so they remembered the aversive experience as well as controls. This form of anterograde amnesia therefore depends on the α1 subunit.
since they remebred to not go in clearly drug effects memory
what happens to anxiety levels on a mouse with a a2 knock out?
when given diazepam to the a2 knock outs it doesnt work anymore, still anxious
midazolam procedure on memory a2
Presented patients about to have surgery with pictures to remember before and after midazolam (given 8mins prior full anaesthesia). Following recovery from surgery, patients’ memory for pictures shown just before midazolam was unaffected, but they were really bad at remembering pictures once given midazolam. Midazolam therefore induced anterograde amnesia.
what is the most localised sub unit?
a5 - to the hippocamus
a5 study into hippocampus and a5 knock out
Crestani et al. (2002): being able to remember a conditioned stimulus e.g. a tone across a trace interval before the presentation of an unconditioned stimulus e.g. food depends on the hippocampus. Participants lacking the GABAA α5 subunit actually remembered better than controls!