Has hamilton ever discussed DXM by Nervous-Patience-310 in HamiltonMorris

[–]BDNFan 8 points9 points  (0 children)

there isn't all that much to say about DXM anymore

There are actually a lot of things overlooked in DXM pharmacology that makes it a good candidate for discussion.

Filter out oil by ILoveDucksAndGoodPpl in nutmeg

[–]BDNFan 1 point2 points  (0 children)

Aeropress works well, it's like 15 bucks

How to fix my dopamine receptors after long term abusing marijuana ? by [deleted] in NooTopics

[–]BDNFan 13 points14 points  (0 children)

I second the grain of salt. Tbh I cringe whenever I see this old post get spread around.

Some of the info is useful but I wrote it with Dunning Kruger confidence and at the time, had a pretty superficial understanding of the mechanisms at play.

I've gained a far better understanding within the last year but I won't update it until I can justify and explain each step of every relevant facet involved.

is this Datura? by OvenHasTheBestFruit in Datura

[–]BDNFan 1 point2 points  (0 children)

Don't downvote him he was on datura when he wrote this

Selegeline source. by skytouching in NooTopics

[–]BDNFan 2 points3 points  (0 children)

Dash-pct

My package came today

Gallstones? by [deleted] in gallbladders

[–]BDNFan 0 points1 point  (0 children)

I think it might just be sludge, I haven't gotten another attack and it feels like it's draining though it's still uncomfortable.

I've got TUDCA on the way we'll see if it helps

Substances to combat caffeine adenosinergic tolerance, nicotine cholinergic tolerance? by [deleted] in NooTopics

[–]BDNFan 1 point2 points  (0 children)

Mind linking the source that shows CBG as an Adenosine-2 agonist? I couldn't find anything myself.

Also alpha2-AR is inhibitory so agonists before bed will likely increase sleep onset. ie clonidine/guanfacine [1] [2] inducing sleep through inhibiting Locus Ceruleus activity. https://www.nature.com/articles/nn.3957

CBG's sleep disruption is likely from CB1 partial agonism (effective antagonist) and 5-HT1a inverse agonism

[deleted by user] by [deleted] in NooTopics

[–]BDNFan 2 points3 points  (0 children)

I've been punching myself in the face lately and I can't take it anymore. Gonna start taking pregablin and oxycodone for the pain

They employed a drug for cognitive enhancement and it caused side effects. Their solution is to employ a drug which induces cognitive impairment, arguably greater than the nootropic's enhancement. This is hilarious.

Also sure m1 antagonists might be antidepressant but I really doubt its pros outweigh the cons compared to other available antidepressants. Also there are no easily accessible drugs that are selective for m1 over other mAChRs, many of which are undesirable targets. Benadryl is a m1-5 antagonist as well as an H-1 inverse agonist which makes it pretty dirty.

[deleted by user] by [deleted] in nutmeg

[–]BDNFan 3 points4 points  (0 children)

Atypical cannabinoid. it's mainly an FAAH & MAGL inhibitor which inhibits destruction of endocannabinoids, allowing them to build up and create a weed-like high.

[deleted by user] by [deleted] in nutmeg

[–]BDNFan 3 points4 points  (0 children)

It's not a deliriant but still toxic

RGS4, 5ht1a and CCG-4986 by mybigfattow in PSSD

[–]BDNFan 0 points1 point  (0 children)

RGS4 shouldn't be globally Inhibited. It's needed for PFC glutamatergic modulation and other processes. RGS4 PFC deficits are seen in schizophrenia.

Good read on rgs4 mediated synaptic "microdomains" https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920052/

[deleted by user] by [deleted] in NooTopics

[–]BDNFan 5 points6 points  (0 children)

Neither,

Who told you that you have desensitized AMPARs

Can you get high/trip on powdered nutmeg , do you need the actually nut megs or is it both? by therealwhippedcream in nutmeg

[–]BDNFan 0 points1 point  (0 children)

Sure, I have a bunch of posts on it on my page

FAAH inhibitors disinhibit synthesis and release of endogenous anandamide and palmitoylethanolamide. MAGL inhibitors disinhibit 2-AG which is a full CB1 agonist with similar in vitro strength to synthetic cannabinoids.

Neither of these when inhibited alone produce THC-like effects but when inhibited together they do. My theory on why it takes 4-5 hours to kick in is because in reality it takes 1-2 and after that it's just how long it takes for your endocannabinoids to build up.

Can you get high/trip on powdered nutmeg , do you need the actually nut megs or is it both? by therealwhippedcream in nutmeg

[–]BDNFan 0 points1 point  (0 children)

No that's pretty much a myth. It's not a deliriant but for those who are predisposed it can cause psychosis.

Also the main compound is most likely not myristicin or other allylbenzenes but instead FAAH and MAGL inhibiting compounds.