Active constituents: Huperzine A is an alkaloid found in
huperzia that has been reported to prevent the breakdown of acetylcholine, an important
substance needed by the nervous system to transmit information from cell to cell.2
Animal research has suggested that huperzine A’s ability to preserve acetylcholine may
be greater than that of some prescription drugs.3 4 Loss of
acetylcholine function is a primary feature of several disorders of brain function, including
Alzheimer’s disease. Huperzine A may also have a
protective effect on brain tissue, further increasing its theoretical potential for helping
reduce symptoms of some brain disorders.5 6
In a double-blind trial, people with Alzheimer’s
disease had significant improvement in memory and cognitive and behavioral functions after
taking 200 mcg of huperzine A twice per day for eight weeks.7 Another double-blind
trial using injected huperzine A confirmed a positive effect in people with dementia,
including, but not limited to, Alzheimer’s disease.8 Another double-blind
trial found that huperzine A (100–150 mcg two to three times per day for four to six
weeks) was more effective for improving minor memory loss associated with age-related cognitive decline than the drug
piracetam.9
Huperzine A has also been shown to enhance memory in adolescent middle school students. A
small controlled trial found that 100 mcg of huperizine A two times per day for four weeks was
effective in improving memory and learning performance.10 Although no side effects
were reported in this short trial, long-term safety studies are needed before huperizine A is
recommended for adolescents or younger children to improve memory and learning
performance.
Are there any side effects or interactions? Medications that
prevent acetylcholine breakdown often produce side effects, including nausea, vomiting, excess
saliva and tear production, and sweating. However, while dizziness was reported in a few
people in one study, no severe side effects have been reported in human trials using huperzine
A. Further studies are needed to determine the long-term safety of huperzine A.
Are there any drug interactions? Certain medications may
interact with huperzia. Refer to the drug interactions
safety check for a list of those medications.
References:
1. Kozikowski AP, Tückmantel W. Chemistry, Pharmacology, and
Clinical Efficacy of the Chinese Nootropic Agent Huperzine A. www.huperzine.net/invent.htm, 26
June 2000.
2. Ashani Y, Peggins JO, Doctor BP. Mechanism of inhibition of
cholinesterases by huperzine A. Biochem Biophys Res Commun 1992;184:719–26.
3. Cheng DH, Tang XC. Comparative studies of huperzine A, E2020, and
tacrine on behavior and cholinesterase activities. Pharmacol Biochem Behav
1998;60:377–86.
4. Cheng DH, Ren H, Tang XC. Huperzine A, a novel promising
acetylcholinesterase inhibitor. Neuroreport 1996;8:97–101.
5. Ved HS, Koenig ML, Dave JR, et al. Huperzine A, a potential
therapeutic agent for dementia, reduces neuronal cell death caused by glutamate.
Neuroreport 1997;8:963–8.
6. Skolnick AA. Old Chinese herbal medicine used for fever yields
possible new Alzheimer’s disease therapy [news item]. JAMA 1997;277:776.
7. Xu SS, Gao ZX, Weng Z, et al. Efficacy of tablet huperzine-A on
memory, cognition, and behavior in Alzheimer’s disease. Chung Kuo Yao Li Hsueh
Pao 1995;16:391–5.
8. Zhang RW, Tang XC, Han YY, et al. Drug evaluation of huperzine A in
the treatment of senile memory disorders. Chung Kuo Yao Li Hsueh Pao
1991;12:250–2 [in Chinese].
9. Wang Z, Ren G, Zhao Y, et al. A double-blind study of huperzine A and
piracetam in patients with age-associated memory impairment and dementia. In: Kanba S,
Richelson E (eds). Herbal Medicines for Nonpsychiatric Diseases. Tokyo: Seiwa Shoten
Publishers, 1999, 39–50.
10. Sun QQ, Xu SS, Pan JL, et al. Huperizine-A capsules enhance memory
and learning performance in 34 pairs of matched adolescent students. Acta Pharmacol
Sin 1999;20:601–3.
11. Qian BC, Wang M, Zhou ZF, et al. Pharmacokinetics of tablet huperzine
A in six volunteers. Chung Kuo Yao Li Hsueh Pao 1995;16:396–8.
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purposes only. It is based on scientific studies (human, animal, or in vitro),
clinical experience, or traditional usage as cited in each article. The results reported may
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before making any changes in prescribed medications. Information expires December 2003.