Huperzine A: A Natural Nootropic

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Huperzine A: A Natural Nootropic

Huperzine A is a compound, specifically a naturally occurring sesquiterpene alkaloid, that functions as an acetylcholinesterase inhibitor. If that seems like a bunch of big words, don’t worry, we’ll translate in a moment.

First, a nod to its origins: it is found in certain kinds of firmoss, especially the “toothed clubmoss”, Huperzia serrata, which grows in many Asian countries.

What’s an acetylcholinesterase inhibitor?

Let’s do this step-by-step:

  • An acetylcholinesterase inhibitor is a compound that inhibits acetylcholinesterase.
  • Acetylcholinesterase is an enzyme that catalyzes (speeds up) the breakdown of acetylcholine.
  • Acetylcholine is a neurotransmitter; it’s an ester of acetic acid and choline.
    • This is the main neurotransmitter of the parasympathetic nervous system, and is also heavily involved in cognitive functions including memory and creative thinking.

What this means: if you take an acetylcholinesterase inhibitor like huperzine A, it will inhibit acetylcholinesterase, meaning you will have more acetylcholine to work with. That’s good.

What can I expect from it?

Huperzine A has been well-studied for a while, mostly for the prevention and treatment of Alzheimer’s disease:

However, research has suggested that huperzine A is much better as a prevention than a treatment:

❝A central event in the pathogenesis of Alzheimer’s disease (AD) is the accumulation of senile plaques composed of aggregated amyloid-β (Aβ) peptides.

Ex vivo electrophysiological experiments showed that 10 μM of Aβ1-40 significantly decreased the effect of the AChE inhibitor huperzine A on the synaptic potential parameters. ❞

~ Dr. Irina Zueva

Source: Can Activation of Acetylcholinesterase by β-Amyloid Peptide Decrease the Effectiveness of Cholinesterase Inhibitors?

In other words: the answer to the titular question is “Yes, yes it can”

And, to translate Dr. Zueva’s words into simple English:

  • People with Alzheimer’s have amyloid-β plaque in their brains
  • That plaque reduces the effectiveness of huperzine A

So, what if we take it in advance? That works much better:

❝Pre-treatment with [huperzine A] at concentrations of 50, 100, and 150 µg/mL completely inhibited the secretion of PGE2, TNF-α, IL-6, and IL-1β compared to post-treatment with [huperzine A].

This suggests that prophylactic treatment is better than post-inflammation treatment. ❞

~ Dr. Thu Kim Dang

Source: Anti-neuroinflammatory effects of alkaloid-enriched extract from Huperzia serrata

As you may know, neuroinflammation is a big part of Alzheimer’s pathology, so we want to keep that down. The above research suggests we should do that sooner rather than later.

Aside from holding off dementia, can it improve memory now, too?

There’s been a lot less research done into this (medicine is generally more concerned with preventing/treating disease, than improving the health of healthy people), but there is some:

Huperzine-A capsules enhance memory and learning performance in 34 pairs of matched adolescent students

^This is a small (n=68) old (1999) study for which the full paper has mysteriously disappeared and we only get to see the abstract. It gave favorable results, though.

The effects of huperzine A and IDRA 21 on visual recognition memory in young macaques

^This, like most non-dementia research into HupA, is an animal study. But we chose to spotlight this one because, unlike most of the studies, it did not chemically lobotomize the animals first; they were and remained healthy. That said, huperzine A improved the memory scores most for the monkeys that performed worst without it initially.

Where can I get it?

As ever, we don’t sell it, but here’s an example product on Amazon for your convenience

Enjoy!

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    woman holds glass of water and has full cheeks
    Rinsing with water could prevent acid damaging your teeth.
    Shutterstock

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    Evangeline Mantzioris, Program Director of Nutrition and Food Sciences, Accredited Practising Dietitian, University of South Australia

    This article is republished from The Conversation under a Creative Commons license. Read the original article.

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