AI Article Synopsis

  • The study investigates the active ingredients of a widely used Chinese herbal medicine known for its central nervous system effects, comparing the effectiveness of its ethanol extracts (EES) and water extracts (WES) for the first time.
  • Despite both extracts showing similar anti-depressive effects, EES contained higher levels of many components than WES, raising questions about how they achieve comparable efficacy.
  • Ultimately, the research identified five key lignans that effectively target the brain, suggesting further exploration of these components could enhance understanding of the herbal medicine's active ingredients.

Article Abstract

, a widely used Chinese herbal medicine, was considered as central nervous system (CNS) drug for years. Both ethanol extracts (EES) and water extracts (WES) of it were applied clinically. Unfortunately, the difference of their efficacy and even effective material foundation of remains obscure. In this study, to explore the active constituents of , we compared pharmacodynamics and chemical profiles / of EES/WES for the first time using multiple chemical analysis, pharmacological and data processing approaches. It was proved that there was no significant difference in the anti-depressive effects between WES and EES. However, the contents of most components and in plasma were higher in EES than those in WES, which was unconvincing for their similar efficacy. Therefore, we further explored components of targeted onto brain and the results showed that 5 lignans were identified with definite absorptivity respectively both in EES and WES caused by the limitation of blood-brain barrier. Moreover, bioinformatic analysis predicted their anti-depressive action. Above all, the systematic strategy screened 5 brain-targeted effective substances of and it was suggested that exploring the components into nidi would promote the studies on herbs effective material basis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049611PMC
http://dx.doi.org/10.1016/j.apsb.2019.10.008DOI Listing

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