Journal
EXPERT REVIEW OF NEUROTHERAPEUTICS
Volume 16, Issue 6, Pages 671-680Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/14737175.2016.1175303
Keywords
Huperzine A; acetylcholinesterase; nicotinic receptors; GABAergic transmission; excitotoxicity; neuroprotection
Categories
Funding
- DoD [09082006]
- CIMIT
- Harvard Medical School
- NIH NINDS [R01NS066019]
- NIH NIMH [R21MH104318]
- Boston Children's Hospital Translational Research Program
- Smith Family Foundation
- King Saud University
- Sage therapeutics Inc.
- Wuhan Yirude Medical Equipment New Technology Co., Ltd.
- Neuropace Inc.
- Nexstim Inc.
- Neuronetics Inc
- Brainsway Inc.
- 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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