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Huperzine A as a neuroprotective and antiepileptic drug: a review of preclinical research

Journal

EXPERT REVIEW OF NEUROTHERAPEUTICS
Volume 16, Issue 6, Pages 671-680

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/14737175.2016.1175303

Keywords

Huperzine A; acetylcholinesterase; nicotinic receptors; GABAergic transmission; excitotoxicity; neuroprotection

Funding

  1. DoD [09082006]
  2. CIMIT
  3. Harvard Medical School
  4. NIH NINDS [R01NS066019]
  5. NIH NIMH [R21MH104318]
  6. Boston Children's Hospital Translational Research Program
  7. Smith Family Foundation
  8. King Saud University
  9. Sage therapeutics Inc.
  10. Wuhan Yirude Medical Equipment New Technology Co., Ltd.
  11. Neuropace Inc.
  12. Nexstim Inc.
  13. Neuronetics Inc
  14. Brainsway Inc.
  15. Eisai Pharmaceuticals

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Huperzine A (HupA) is an acetylcholinesterase (AChE) inhibitor extracted from Huperzia Serrata, a firmoss, which has been used for various diseases in traditional Chinese medicine for fever and inflammation. More recently, it has been used in Alzheimer's disease and other forms of dementia with a presumed mechanism of action via central nicotinic and muscarinic receptors. HupA is marketed as a dietary supplement in the U.S. This article reviews newly proposed neuroprotective and anticonvulsant HupA properties based on animal studies. HupA exerts its effects mainly via alpha 7nAChRs and alpha 4 beta 2nAChRs, thereby producing a potent anti-inflammatory response by decreasing IL-1 beta, TNF-alpha protein expression, and suppressing transcriptional activation of NF-kappa B signaling. Thus, it provides protection from excitotoxicity and neuronal death as well as increase in GABAergic transmission associated with anticonvulsant activity.

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