I don't post, and I am unsure whether to do so or not in light (oh the irony) of the responses here.
Egotistical masturbation = insecurities about your own prowess within the field that make you deny that anyone could have superior understanding without a shedload of qualifications and respect in the field.
So, you post that you were delusional from ketamine and whatnot, and then you retract it? Why? So lying isn't an issue?
No one is rejecting what you say because you lack credentials- because no one here knew that until you said so, although your confusion of simple concepts makes this obvious.
People sending me PMs is neither depraved (are you familiar with the meaning?) insecure or disgusting. It's because we try to keep a minimum level of discussion which you're not begining to approach.
If you want to discuss egos, why not look at your own? Everything you're writing is based upon the messiah complex you've developed. You've somehow arrived at the conclusion that your few months of study were enough for you to figure 'everything' out. You're mocking everyone who actually worked to learn what they know. Yet you managed to figure everything out without any effort on your part whatsoever.
That's an impressive display of ego.
For someone who claims to have everything regarding serotonergic psychedelics figured out, you know so very little.
Things you've said recently that are nonsense:
BK MBDB by itself is a pure stimulant with high adrenaline facility and dopamine effects.
D2 burn out is the primary factor in stimulant binge mediated anxiety is it not?
MDMA won't cause primary noradrenaline release as it won't bind to the beta carbon electropositive site on the NEVMAT or reuptake site on the NET, it would be as a secondary function of it'a ability to antagonise both of these sites causing decreased reuptake and increased vesicle release akin to DA NEVMAT antagonism inspiring this mechanism.
MDMA won't cause primary noradrenaline release as it won't bind to the beta carbon electropositive site on the NEVMAT or reuptake site on the NET, it would be as a secondary function of it'a ability to antagonise both of these sites causing decreased reuptake and increased vesicle release akin to DA NEVMAT antagonism inspiring this mechanism.
(see: Psychopharmacology (Berl). 2007 Jan;189(4):489-503. Epub 2005 Oct 12. Links
MDMA (Ecstasy) and human dopamine, norepinephrine, and serotonin transporters: implications for MDMA-induced neurotoxicity and treatment.Verrico CD, Miller GM, Madras BK.
Department of Psychiatry, Division of Neurochemistry, New England Primate Research Center, Harvard Medical School, 1 Pine Hill Drive, Southborough, MA 01772-9102, USA.)
The compound, being far far too big (and having a double bonded ketone) to fit through a DA transporter should be almost un-neurotoxic due to not actually releasing harmful breakdown products, the idiotic length of that side change must change DAT conformation over time slightly, as many reports have said that is lessens the ability to enjoy amphetamines and other cascaders
I realise that my posts in the last apologies thread just turned into an egomaniacal rant. I guess there is only so much spam this forum can take.
(oops, that actually makes sense for a change!)
And this doesn't even get into the garbage you spew in the lounge.