I can recommend his extensive research on Nootropics [1] for actionable advice.
I can recommend his extensive research on Nootropics [1] for actionable advice.
The following are not nootropics:
* Modafinil and Armodafinil
* Adderall (Amphetamine)
* Caffeine
* Kratom
* Nicotine (this is a border case, in my opinion)
* Selegiline
Stay away from the above, unless taken very occasionally, if you value your health. Drugs like these rapidly build tolerance and become a liability in the long run. If you insist on using stimulants such as amphetamine, learn about how to reduce tolerance with things such as NMDA antagonists and take things to prevent neurotoxicity.
He should also get on with trying Noopept - it's one of the best nootropics of recent times.
From experience, anybody who is a programmer or does similarly demanding intellectual work will stand to benefit from learning about and using nootropics. They're not a silver bullet but quite a few of them are most certainly effective.
> Stay away from the above, unless taken very occasionally
Caffeine, amphetamines, and modafinil are not neurotoxic. I believe the others aren't either but I haven't read up on them. Methamphetamine is neurotoxic but non-methylated amphetamines are not.
http://en.wikipedia.org/wiki/Health_effects_of_caffeine
> Short term side effects such as headache, nausea, and anxiety have been shown as symptoms of mild caffeine consumption.
When assessing the health impact of a drug, it is important to look at the whole picture.
Amp is indeed neurotoxic, though the exact effect is a little nuanced and dose-dependent.
http://www.ncbi.nlm.nih.gov/pubmed/15019431
> In addition to the social, cultural and indirect medical complications of amphetamine analog abuse, this class of drugs is also known to have the potential to damage brain monoaminergic cells directly.
http://www.ncbi.nlm.nih.gov/pubmed/17606768
> In early studies, high doses of amphetamine, comparable to amounts used by addicts, were shown to damage dopaminergic pathways. More recent studies, using therapeutic regimens, appear contradictory. One paradigm shows significant decreases in striatal dopamine and transporter density after oral administration of "therapeutic" doses in primates. Another shows morphological evidence of "trophic" dendritic growth in the brains of adult and juvenile rats given systemic injections mimicking "therapeutic" treatment. Imaging studies of ADHD-diagnosed individuals show an increase in striatal dopamine transporter availability that may be reduced by methylphenidate treatment.
I did not claim that caffeine and modafinil are neurotoxic, just amphetamine.
If you insist on using stimulants such as amphetamine,
learn about how to reduce tolerance with things such as
NMDA antagonists and take things to prevent neurotoxicity.
He should also get on with trying Noopept - it's one of
the best nootropics of recent times.
Care to expound on those points?Noopept is quite good. I stopped taking it because for me it seemed acutely enough anxiolytic to cause rebound anxiety.
http://en.wikipedia.org/wiki/Amphetamine
>The increase of cytosolic dopamine appears to trigger neurotoxicity, as dopamine readily auto-oxidizes, so that amphetamine or methamphetamine's increase in cytosolic dopamine can lead to oxidative stress in the cytosol that in turn promotes autophagy-related degradation of dopamine axons and dendrites
NMDA antagonists such as magnesium (as mentioned by rms), zinc, DXM, MK-801, Memantine and Ketamine can reduce/prevent tolerance as well as nerotoxicity.
http://www.acnp.org/g4/gn401000166/ch162.htm
> Methamphetamine toxicity is inhibited by a variety of drug treatments, including: ... 3) NMDA receptor antagonists
http://www.socialanxietysupport.com/forum/f30/evidence-for-n...
However selegine in microdoses is a true neuroprotective in that sense..