
Extreme Nootropics
#31
Posted 12 October 2012 - 10:12 AM
#32
Posted 12 October 2012 - 11:26 PM
#33
Posted 15 October 2012 - 11:30 PM
This occurs when receptors for the excitatory neurotransmitter glutamate (glutamate receptors) such as the NMDA receptor and AMPA receptor are overactivated. Excitotoxins like NMDA and kainic acid which bind to these receptors, as well as pathologically high levels of glutamate, can cause excitotoxicity by allowing high levels of calcium ions (Ca2+) to enter the cell. Ca2+ influx into cells activates a number of enzymes, including phospholipases, endonucleases, and proteases such as calpain. These enzymes go on to damage cell structures such as components of the cytoskeleton, membrane, and DNA.
What about calcium channel blockers ? Maybe that's the solution, is there a calcium channel blocker that targets the brain specifically ?
#34
Posted 22 October 2012 - 05:41 AM
personally, i think the "uppers" need to be balanced with the "downers" - being high and inspired requires very firm grounding - so i do tend to focus on things like adaptogens (reishi, ginseng, astragalus, etc), pro-hormones (oxytocin, pregnenolone) and certain other substances (theanine) to deal with any added stresses (adrenaline, cortisol, inflammation) that may come from experimenting with things like the stack above or low dose lsd.
#35
Posted 22 October 2012 - 09:20 AM
#36
Posted 23 October 2012 - 07:53 AM
I agree. I used to lead a very extreme lifestyle some years ago and it took its toll. So I have some leftover generalized anxiety disorder which I have almost fully tamed. I'm currently doing some Himalaya Mentat (great stuff) and will probably include some Selank before I move into hardcore Nootropics. Selank is a powerful endorphine anxyolitic with mild nootropic effects which is safe and will be a great addition to my stack I think.
the injectable peptides seem a bit crazy lol, but i can understand the desire to go there. i only ever experimented that route with hcg, but would like to try peptides or AAS if i understood more about how to recover from any negative sides. not counting the burgeoning costs of experimenting with the infinite combinations of diet, supplementation, exercise and lifestyle choices haha
i did add 60mg hordenine to my chocamine/guarana/carnitine/choline/theanine stack today and it definitely prolonged a very anxiolytic/euphoric effect, seeing as how hordenine is an maoi (B i think...?) and will prolong any effects of the xanthines and pea it makes sense as to why the combo of dmaa/pea/hordenine is talked about on the net. add theobromine, caffeine, naringin and i could see how it would be very stimulating as well as euphorically relaxing, but i'm cautious of the dmaa's effect on the adrenal system - just not sure that stimulating that frequently over time is actually healthy.
have you tried doubling the dose on the Mentat? something i've noticed over the years using herbal extracts is that the recced dose is usually the lowest possible, basically for a middle aged asian housewife, not an athletic 20-30-something western male. (not being prejudiced, just trying to paint a picture)
if the double dose works, go with that for a while and add more meditation and breathing techniques, you may not need to even try the selank.
looking forward to the ongoing explorations!
#37
Posted 23 October 2012 - 03:08 PM
Other than that I'm into or used to be into bodybuilding A LOT. I have tons of experience with AAS personal as well and I run my own peptide business. Peptide injection are subcutaneous so no pain is felt at all. Diabetics shoot insulin SubQ a couple times a day - no pain.
I'm taking it very slowly. If that was a couple of years ago I'd probably be stacking all kinds of dangerous crap and reporting experiences here, but I'm not the same person I used to be.
#38
Posted 26 October 2012 - 06:12 PM
Ok so noone said anything about excitotoxicity caused by pathological levels of glutamate. If I am able to get my hand on potent ampakines and combine them with other ampa-oriented drugs like aniracetam and whatnot, isn't there a chance for an opposite to nootropic effect caused by too much glutamate destroying neurons ?
Quote
This occurs when receptors for the excitatory neurotransmitter glutamate (glutamate receptors) such as the NMDA receptor and AMPA receptor are overactivated. Excitotoxins like NMDA and kainic acid which bind to these receptors, as well as pathologically high levels of glutamate, can cause excitotoxicity by allowing high levels of calcium ions (Ca2+) to enter the cell. Ca2+ influx into cells activates a number of enzymes, including phospholipases, endonucleases, and proteases such as calpain. These enzymes go on to damage cell structures such as components of the cytoskeleton, membrane, and DNA.
What about calcium channel blockers ? Maybe that's the solution, is there a calcium channel blocker that targets the brain specifically ?
memantine solves this problem.
#39
Posted 26 October 2012 - 06:55 PM
#40
Posted 26 October 2012 - 07:00 PM
"Memantine is a low-affinity voltage-dependent uncompetitive antagonist at glutamatergic NMDA receptors.[14][15][16][17][18] By binding to the NMDA receptor with a higher affinity than Mg2+ ions, memantine is able to inhibit the prolonged influx of Ca2+ ions, particularly from extrasynaptic receptors, which forms the basis of neuronal excitotoxicity. The low affinity, uncompetitive nature, and rapid off-rate kinetics of memantine at the level of the NMDA receptor-channel, however, preserves the function of the receptor at synapses, as it can still be activated by physiological release of glutamate following depolarization of the presynaptic neuron"
#41
Posted 26 October 2012 - 07:10 PM
#42
Posted 03 November 2012 - 09:36 PM
Edited by Tatsumaru, 03 November 2012 - 09:37 PM.
#43
Posted 03 November 2012 - 10:22 PM
What about extracellular glutamate, isn't it causing excitotoxicity too? If glutamatergic NMDA receptors are inhibited then extracellular glutamate builds up as neurotransmission is low therefore this can cause a lot of problems too.I qoute from wikipedia:
"Memantine is a low-affinity voltage-dependent uncompetitive antagonist at glutamatergic NMDA receptors.[14][15][16][17][18] By binding to the NMDA receptor with a higher affinity than Mg2+ ions, memantine is able to inhibit the prolonged influx of Ca2+ ions, particularly from extrasynaptic receptors, which forms the basis of neuronal excitotoxicity. The low affinity, uncompetitive nature, and rapid off-rate kinetics of memantine at the level of the NMDA receptor-channel, however, preserves the function of the receptor at synapses, as it can still be activated by physiological release of glutamate following depolarization of the presynaptic neuron"
#44
Posted 04 December 2012 - 05:06 AM
#45
Posted 04 December 2012 - 10:21 AM
True but as an example MB speeds up mitochondria 40% do that with a cars engine and it will handle to n2o alot better and much longer, even in lower ammounts the whole time fine if we are optimistic.Amp looks like what N2O is for sports cars lol.
Lifelong amp addicts for 40 years return to normal health after addiction and can make dramatic improvement, wich allready shows you can push the body to its limits without too much problems.
Throw in semax for what it matters, it dramatically help cognition while also helps the brain, you really CAn go pretty far imo.
#46
Posted 04 December 2012 - 12:20 PM
Edited by Tatsumaru, 04 December 2012 - 12:26 PM.
#47
Posted 04 December 2012 - 12:23 PM
I know my stacks sound extreme haha but thats how i am and i beleive the body can be made capable of doing alot. (look at top athletes, einstein etc).
or ppl with that disorder that remember the exact details of every past day of their life.
#48
Posted 04 December 2012 - 12:27 PM
#49
Posted 31 January 2013 - 10:36 PM
I had been using a product called Sleep Eaze as a dual purpose supplement. It was an unusual formulation, just whole herb and extract combo of Bacopa monnieri and Nardostachys jatamansi. I enjoyed the fact that it helped slow the racetam-induced thought generation insomnia I had been experiencing, as well as provide me with the benefits of daily supplementation with bacopa.
I liked the look of the formula for Mentat DS, so I ordered some from India to use instead after I ran out of Sleep Eaze. Like bacopa (and many other nootropics,) the effects of the product are expected to be cumulative over time. As a treatment for insomnia, though, I hoped that a double dose would work immediately. Unlike Sleep Eaze, however, Mentat appears to be both noticeably (if mildly) anxiolytic and simultaneously mildy pushy. This pushiness offsets the sedating action of the jatamansi and bacopa, which is great when taken during the day, but totally ruined it for me as a sleep aid.
In short, I think it's a good supplement, but a double dose doesn't improve its action and may in fact detract from its efficacy. Everyone's brain chemistry is different, though, so try it out.
#50
Posted 01 February 2013 - 01:21 AM
I know this is a bold statement but I think this combo cured 50-60% of my anxiety disorder in just 2-3 months. I haven't been taking anything since then and I feel great.
And I have to tell you, while my anxiety case wasn't the absolutely insanity nuts-like case, it was still a major major pain in the ass. Couldn't sleep, couldn't not sleep. Constantly afraid for my life, counting calories, being afraid even of vitamin supplements. Now I'm just fine.
#51
Posted 01 February 2013 - 01:31 AM
#52
Posted 01 February 2013 - 03:22 PM
First or I'm crazy or the world is crazy. I wan't to tell everyone that modafinil litterally killed me. I've take it for 1 month before my med exam and it was terrible first day of the exam I was unable to read what it was wrote on the paper. Second day I was too focused that I've done very well 1/3 of the subject... And on physical/mathematical stuff no imagination no creation... So I'm very very very bad for the end of the year. I'm kind of disgusted by noots
But I'm still attracted by the perfect stack but does it exist. I think if you're already smart or a bit crazy you don't need that stuff. Not sure I will retry some prami CDP choline. I wish i can have the perfect stimulant but I don't know how to get anything else that this shitty modafinil which have a looooot of side effect more than MDMA for me haha
#53
Posted 02 February 2013 - 02:58 PM
the brain have multiple directions not just forward glutamate is more vertical spike amplitudes
This is one of the funniest sentences I have ever read. Hahaha I am still laughing aloud every time I read it.
seligiline vs modafinil...which should i go with?
Both. At the same time.
#54
Posted 03 February 2013 - 09:47 AM

#55
Posted 04 February 2013 - 01:28 AM
and how do you get selegiline huh ?
I've PM'd you a resource because I'm feeling kind today

#56
Posted 15 February 2013 - 02:40 AM
#57
Posted 15 February 2013 - 12:58 PM
#58
Posted 16 February 2013 - 09:09 AM
and how do you get selegiline huh ?
Selegiline made me feel quite depressed. It really messed with my mood and didn't motivate me as I'd hoped it would. If you're gonna try it, be careful.
I'd choose modafinil but maybe that's just me.
#59
Posted 17 February 2013 - 01:30 PM
I'm pretty sure that Modafinil + Selegiline + AChI + (if anxious) ISRS or diazépam could be a pretty cool combo for working.
Edited by Babychris, 17 February 2013 - 01:30 PM.
#60
Posted 16 March 2014 - 10:19 PM
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