misplaced energy
Bluelighter
- Joined
- Jul 22, 2013
- Messages
- 294
Sober right now but i have a nice stash of speed, mdma, ket, xanax and diazepam.
Not sure what im feeling just yet.....hmmmmm
Not sure what im feeling just yet.....hmmmmm
Just took 300mg lyrica (on top of all the other shit I already took, see a few posts above this one)
Mainly oxy, some methadone this morning and benzos. I took another 120mg oxy, 0.125mg brotizolam, 1mg xanax & 6mg bromazepam since then.
I'm actually lyrica rolling at the moment....it only comes in little waves or rushes that last a few minutes and u have to concentrate on it to really feel it good
Gonna stack more lyrica with 30min intervals, 150mg each half hour until I'm where I wanna be. I (obviously) started with 300mg which I took like 3 minutes ago, so in 27min I'll be taking more. If I get report-worthy effects I'll edit this post with them. :D
3tbsp Kratom
Unknown amount of clonazolam powder (haven't found a proper bottle to make a solution yet, but I can generally gauge how much I take (no blackouts haha))
Residual trazadone 100mg
Hallelujah, Kratom came through for me while I have no subs. Fuck that synthetic bullshit. (Btw Joe I totally feel like subs messed up my brain, even heroin euphoria is just okay to me. Then again that might be tolerance.)
@BD: how would you compare 3-HO-PCP to an actual opioid? I'm always looking for alternatives.
Since I have a heavy codeine tolerance, it's hard for me to judge from an opioid-nontolerant person's perspective, but it does seem to have *some* opioid activity, though not very similar to that of codeine/morphine - less warmth and physical pleasure, mostly just mental. It's still a very strong dissociative first, a weak to mild opioid second.
OT:
2 lines and now 3 bumps of (supposed 80% ) sinaloan brown #4, (not of fan of the tar-based dope but this stuff is decent, not as much fent either)
4mg etizolam 2 hours before, 2mg now
Drinking Not Your Whatever's w/family and baking cookies
Back on topic, does anyone use dope intranasally? I have a short duration with the grey AND pure brown. Psychonaut states 5 hours but it's like 1.
Also I fell asleep and woke up 3 times while trying to edit this. Not even create a post, edit one....dope.
Hmmm well if this Brown powdered #4 you speak of is anything like the light Brown powder dope that's has been floating around San Francsico for a bit now it's fentanyl cut for sure (seen positive tests using test strips the needle exchange hands out)
Light Brown in color a bit lighter than gun-powder which is tar cut onto lactose powder but still has strongly acetic odour
But the biggest criteria pointing me towards that conclusion is the duration you say the effects last for
Since I have a heavy codeine tolerance, it's hard for me to judge from an opioid-nontolerant person's perspective, but it does seem to have *some* opioid activity, though not very similar to that of codeine/morphine - less warmth and physical pleasure, mostly just mental. It's still a very strong dissociative first, a weak to mild opioid second.
In my opinion after about 15 minutes of reviewing the abstract and other scientific papers...3 oh PCP cannot be said to have opioid activity...in fact ..it has antagonist activity...which is the had kind, the opposite of opioid effects.
First the paper cited by psychowiki that everyone on redditt or BL has used to propogate this myth is from the 80s and not exactly from a Harvard group. The paper says that it has antagonist activity in a rat bioassy...so opposite of good stuff.
Then it talks about bindi g to morphine receotirs...binding does not mean agonistic or "high" activity...someone please get the full paper from their university
Phencyclidine (PCP) and its 3-hydroxy derivative (PCP-3-OH) caused a dose-dependent, naloxone reversible inhibition of the response of the guinea pig ileum to electrical stimulation. Unlike PCP, PCP-3-OH exerted an opioid antagonistic effect in the mouse vas deferens bioassay. Whereas both compounds displayed a high affinity in displacing [3H]SKF-10047 binding to rat brain membranes, PCP-3-OH displayed a high affinity to [3H]morphine receptors also. The mediation of σ- and μ-receptors in the opioid effects of these drugs is discussed.
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