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Identification of Potential Biomarkers from Aconitum carmichaelii, a Traditional Chinese Medicine, Using a Metabolomic Approach

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2017

Year

Abstract

Despite their well-known toxicity, <i>Aconitum</i> species are important traditional medicines worldwide. <i>Aconitum carmichaelii</i>, known in Chinese as (fuzi), is an officially recognized traditional Chinese medicine with characteristic analgesic and anti-inflammatory activities, whose principal pharmacological ingredients are considered as aconitine-type diterpene alkaloids. Notwithstanding the long-recorded use of <i>A. carmichaelii</i> in traditional Chinese medicine, no single-entity aconitum alkaloid drug has been developed for clinical use. UPLC-Q-TOF-MS was used to investigate the marker compounds that can be used to differentiate <i>A. carmichaelii</i> from seven other <i>Aconitum</i> species collected in Yunnan Province. Nontargeted principle component analysis scores plots found that all the tested <i>Aconitum</i> species clustered into three distinct groups, and <i>A. carmichaelii</i> was significantly different chemically than the other seven species. Furthermore, the primary and lateral roots of <i>A. carmichaelii</i> also showed significant differences. Using orthogonal partial least squares discriminate analysis analysis, eight marker compounds were identified, including 14-acetylkarakoline, aconitine, carmichaeline, fuziline, hypaconitine, mesaconitine, neoline, and talatisamine. Four of these aconitum alkaloids, fuziline, hypaconitine, mesaconitine, and neoline, showed significant analgesic activity in a dose-dependent manner compared to the negative and positive controls. However, hypaconitine, mesaconitine, and neoline exhibited significant acute toxicity activity, while fuziline showed no acute toxicity in mice, suggesting the relative safety of this alkaloid. This study provides a good example of how to differentiate an authentic medicinal plant from common adulterants using a metabolomics approach, and to identify compounds that may be developed into new drugs.

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