allthegoodjwh's
Greenlighter
- Joined
- Aug 8, 2012
- Messages
- 41
I have read from numerous websites about lobelia topa having psychadellic effects
which at first I chalked up to Basic anticholingeric activity
But could not find any information on in depth pharmacology
Are there actual psychadellic effects
or Is it just anticholongeric delerium
Ive found that large wellbutrin doseages produce a very weak but noticable headspace
Simmilar to an anticholingeric one but without the confusión delerium anxiety and weird sensations I got
I wonder if there Is a hallucinogenic receptor thats nicontinic
I read somewhere else that 5ht-2a agonisim causes indirect a7a nicontinic repecotor antagonisims and that it Is partially responsable for its effects
I theorize that since it said it has mixed agonist antagonist actions at nicontinic receptors that it could be an a7a antagonist
And that wellbutrin produces a very weak versión of the effect (siezure threshold being too low to be able to get anywhere near high enough doses
Pcp Is an a7a antagonist
And so Is dxm
I belive that deleriant effects of anticholingerics are from mucineric antagonisism
eg Pcp may be a dissociative but it Is not a deleriant or it would be as unpopular as benadryl
In lower rec doses benadryl produced effects equal to synthetic marijuana abliet with more euphoria (belive it or not)
But in higher doses I would lose my shit
Im wiling to bet that either benadryl Is a stronger nicontinic antagonisit than musacaric
And or
mucinaric deleriant receptora take a higher dose than nicontinic hallucinogenic receptors
thus proving this theory or at the very least giving it some more supportv
i Belive its m3 receptor I had the source but lost it it acts bu increasing dopamine in one of the da schizofrenia pathways
I will try to find the 5ht2a source
*I did* ITs not a published Medical statement
but I beleive it as it supports my theory
I as hoping someone could either prove or disprove the 5ht2a thing
which at first I chalked up to Basic anticholingeric activity
But could not find any information on in depth pharmacology
Are there actual psychadellic effects
or Is it just anticholongeric delerium
Ive found that large wellbutrin doseages produce a very weak but noticable headspace
Simmilar to an anticholingeric one but without the confusión delerium anxiety and weird sensations I got
I wonder if there Is a hallucinogenic receptor thats nicontinic
I read somewhere else that 5ht-2a agonisim causes indirect a7a nicontinic repecotor antagonisims and that it Is partially responsable for its effects
I theorize that since it said it has mixed agonist antagonist actions at nicontinic receptors that it could be an a7a antagonist
And that wellbutrin produces a very weak versión of the effect (siezure threshold being too low to be able to get anywhere near high enough doses
Pcp Is an a7a antagonist
And so Is dxm
I belive that deleriant effects of anticholingerics are from mucineric antagonisism
eg Pcp may be a dissociative but it Is not a deleriant or it would be as unpopular as benadryl
In lower rec doses benadryl produced effects equal to synthetic marijuana abliet with more euphoria (belive it or not)
But in higher doses I would lose my shit
Im wiling to bet that either benadryl Is a stronger nicontinic antagonisit than musacaric
And or
mucinaric deleriant receptora take a higher dose than nicontinic hallucinogenic receptors
thus proving this theory or at the very least giving it some more supportv
i Belive its m3 receptor I had the source but lost it it acts bu increasing dopamine in one of the da schizofrenia pathways
I will try to find the 5ht2a source
*I did* ITs not a published Medical statement
but I beleive it as it supports my theory
I as hoping someone could either prove or disprove the 5ht2a thing