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Anti-acetylcholinesterase activities of traditional Chinese medicine for treating Alzheimer's disease. | LitMetric

AI Article Synopsis

  • Alzheimer's disease (AD) is a common neurodegenerative disease leading to memory loss and cognitive decline, primarily due to the loss of cholinergic neurons.
  • Acetylcholinesterase inhibitors (AChEI), including plant-derived drugs like huperzine and galanthamine, are currently FDA-approved for treating mild to moderate AD.
  • A study assessed the AChE inhibitory effects of 26 traditional Chinese medicinal herbs, revealing six with significant dose-dependent activity, indicating promising potential for new AD treatments.

Article Abstract

Alzheimer's disease (AD) is a neurodegenerative disease characterized by progressive memory loss and cognitive impairment. It is the most common type of dementia in the ageing population due to a severe loss of cholinergic neurons in selected brain area. At present, acetylcholinesterase inhibitors (AChEI) are the first group of drugs approved by the FDA to treat mild to moderate Alzheimer's disease. Most of these drugs such as huperzine and galanthamine are originally isolated from plants. In this study, the AChE inhibitory activities from extracts of Chinese medicinal herbs that have traditionally been prescribed to treat insomnia and brain function disorders were examined in a 96-well plate assay based on Ellman's method. Both ethanol and aqueous extracts of 26 traditional Chinese medicinal herbs were tested. Inhibitory effects were expressed as the percentage of inhibition. For the herbal extracts that were shown to exert a significant inhibition, dose-dependent inhibitory assays were also performed. Ethanol and aqueous extracts of six herbs were found to have high AChE inhibitory activities in a dose-dependent manner. The IC(50) of these herbal extracts on inhibition of AChE are at around 5-85 microm/ml. The results of this study indicate that there is a great potential to search for novel usage of these medicinal herbs for the treatment of AD.

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Source
http://dx.doi.org/10.1016/j.cbi.2008.05.030DOI Listing

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