4.7 Article

Multi-target regulatory mechanism of Yang Xin Tang - a traditional Chinese medicine against dementia

Journal

CHINESE MEDICINE
Volume 18, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13020-023-00813-w

Keywords

Alzheimer's disease; beta amyloid; Chinese medicine; Neural progenitor cell; Neurodegenerative disease; Neuroprotection; Yang Xin Tang

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Yang Xin Tang (YXT), a traditional Chinese herbal preparation, has been reported to improve cognitive function and memory in patients with dementia. This study found that YXT and its major herbal components can regulate gene transcription and molecular targets related to Alzheimer's disease (AD). The neuroprotective and neurogenic actions of YXT suggest its potential as an alternative medicine for treating AD.
Background Yang Xin Tang (YXT) is a traditional Chinese herbal preparation which has been reported to improve cognitive function and memory in patients with dementia. As the underlying mechanism of action of YXT has not been elucidated, we examined the effects of YXT and its major herbal components in regulating gene transcription and molecular targets related to Alzheimer's disease (AD). Methods Aqueous and ethanol extracts of YXT and selected herbal components were prepared and validated by standard methods. A series of biochemical and cellular assays were employed to assess the ability of the herbal extracts to inhibit acetylcholinesterase, reduce beta-amyloid aggregation, stimulate the differentiation of neural progenitor cells, suppress cyclooxygenase, and protect neurons against beta-amyloid or N-methyl-D-aspartate-induced cytotoxicity. The effects of YXT on multiple molecular targets were further corroborated by a panel of nine reporter gene assays. Results Extracts of YXT and two of its constituent herbs, Poria cocos and Poria Sclerotium pararadicis, significantly inhibited beta-amyloid aggregation and beta-amyloid-induced cytotoxicity. A protective effect of the YXT extract was similarly observed against N-methyl-D-aspartate-induced cytotoxicity in primary neurons, and this activity was shared by extracts of Radix Astragali and Rhizoma Chuanxiong. Although the YXT extract was ineffective, extracts of Poria cocos, Poria Sclerotium pararadicis and Radix Polygalae inhibited acetylcholine esterase, with the latter also capable of upregulating choline acetyltransferase. YXT and its components significantly inhibited the activities of the pro-inflammatory cyclooxygenases. Additionally, extracts of YXT and several of its constituent herbs significantly stimulated the phosphorylation of extracellular signal-regulated kinases and cAMP-responsive element binding protein, two molecular targets involved in learning and memory, as well as in the regulation of neurogenesis. Conclusions Several constituents of YXT possess multiple regulatory effects on known therapeutic targets of AD that range from beta-amyloid to acetylcholinesterase. The demonstrated neuroprotective and neurogenic actions of YXT lend credence to its use as an alternative medicine for treating AD.

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