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Different benzos bind with different selectivity to the parts of the brain ?


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Sorry for being a bit spammy, but I'm trying to figure out what I have to do. C/T, crossover etc. The 'default' methods do not work.

 

I think I had forgotten about this issue. Since each benzodiazepine has a relatively selective affinity for the subunits it binds to, would that mean that there could be significant differences between benzos in binding to respective regions of the brain ?

 

I get the whole concept of saturating the body with diazepam while gradually reducing the original benzo followed by a taper, but it's not as if that's an option for various reasons.

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