Ok, a question from an oldskooler that hasn't been on here fore ages..
BABY DOC..
you said....
"The reason SSRI's reduce the effects of MDMA is because they have a greater affinity for the reuptake transporter than MDMA does."
But isn't the "effect" of mdma caused by the binding of the molecule to the receptors on the dedradite (SP?), not the reuptake transporter.?
I was under the impression that nuerotransmitters binding with the recepters is what gave the "effects" of the drug, and that the reuptake transporters were simply a method of "controlling" the amount of serotonin floating about in the synapse at any one time. And this was also how ssri's worked.. By blocking the reuptake (or blocking control of levels) of serotonin there is infact more serotonin to bind with the receptors on the dendradite (sp?)
Hence SSRI's been more prone to bond with reuptake transporters than serotonin makes MORE serotonin be availiable to bind with the receptors on the dedradite, hence increasing the "effects" of the drug ?
SO where have i gone wrong.?
Chem