Specified
Ex-Bluelighter
Do magic mushrooms work on antipsychotics or are the effects dulled?
What about l dopa? Doesn't that increase dopamine?From my understanding the older, 1st generation antipsychotics had a lower affinity to serotonin sites like 5-HT2a, which shrooms bind to, but had a higher affinity to dopamine sites - which leads to higher incidents of the horrible side effects like tardive dyskinesia.
Affinity = how strongly a drug binds to a certain receptor (in the case of antipsychotics, they are antagonists and BLOCK the receptor). Most drugs that get you are agonists and "excite" the receptor.
Again, I am unfamiliar with the drug you are taking so I'd have to do my research... but chances are if you just don't take it for 2-3 weeks you'll be able to get high.
So what's my best bet? Smoke cigarettes? LolL Dopa is a precursor to dopamine and, technically yes, it can increase dopamine levels if you are lacking in this specific area... but it's not going to help you get high.
If you're taking antipsychotics which antagonize dopamine receptors this actually upregulates the amount of dopamine in your system because you're sites are blocked so your body naturally produces more dopamine... (or less? god it's been awhile since I studied this shit - I'm no doctor)
but this has nothing to do with mushrooms, which are serotonergic and act mainly at the 5-HT2a site.
Fuck
i read up on tagamet and it's the same thing as prilosec. I've been taking these for ages! Everyday about two years ago and I started about a month ago again. Says liver failure...but I've been eating on a full stomach.The In vitro study suggests zuclopenthixol is metabolised primarily by CYP2D6 and CYP3A4.
There are also other CYPD2D6 and CYP3A4 inducers like prilosec OTC... but you need to be careful taking things like that, because they can fuck up your stomach if abused.
So will prilosec reduce the antipsychotic in my blood or the tagamet or none at all?Wiki does, of course!
The executive summary: Cimetidine (which is not the same as omeprazole/Prilosec at all, but has a similar effect on stomach acid). It is primarily a histamine H2 antagonist, acting to reduce acid production, but also happens to be a broad spectrum CYP enzyme inhibitor
Clinically significant drug interactions with the CYP1A2, CYP2C9, CYP2D6 and CYP3A4 enzymes are noted. That is, any drugs reliant on those enzymes to be deactivated will have their duration lengthened because it is not metabolized as fast.
Prodrugs that rely on same enzymes to become 'activated' (codeine -> morphine, DXM -> DXO) will not be converted to their active metabolites and hence have much decreased effects.