川乌蜜煮解毒机理研究:生物碱转化和超分子聚集的研究。

IF 8.9
Journal of pharmaceutical analysis Pub Date : 2025-09-01 Epub Date: 2025-01-23 DOI:10.1016/j.jpha.2025.101205
Yu Zheng, Nina Wei, Chang Lu, Weidong Li, Xiaobin Jia, Linwei Chen, Rui Chen, Zhipeng Chen
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引用次数: 0

摘要

乌头(Aconitum carmichaelii Debx)的干母根川乌。它是一种著名的传统中药(TCM),以其强大的功效而闻名,但其固有的毒性主要是由于其生物碱含量。传统和现代的解毒方法包括适当的加工方法、合理的配伍方法和专门的煎煮方法,其中尤以蜜煮解毒方法为特色。然而,对水煮蜂蜜解毒机理的研究仍然有限。本研究通过分析生物碱转化和超分子聚集来探讨其机理。比较了蜜煮和水煮CW制剂。采用超高效液相色谱-串联质谱法分析连续波生物碱,特别是双酯生物碱(DDAs)、单酯生物碱(MDAs)和非酯化二萜生物碱(NDAs)。采用透射电子显微镜观察并鉴定了蜂蜜熬制的CW汤中的超分子聚集体。比较了水煮、蜂蜜煮和nades煮CW的体内吸收情况。中位致死剂量(LD50)试验评估毒性,包括肝毒性和肾毒性。体外实验评估了cw给药血清对RAW264.7细胞的安全性、抗炎和镇痛作用,并在小鼠体内进行了验证。结果表明,蜂蜜促进了高毒mda向低毒mda的转化,并阻止了mda水解成NDAs。蜂蜜煮沸的CW形成约250 nm的超分子聚集体,包裹mda,抑制它们向NDAs的转化。这些包封的mda作为一种稳定的给药系统,具有比游离苯甲酰美沙康更高的生物利用度。随后的小鼠实验证实,蜂蜜煮沸的CW显著增加了CW的LD50,同时降低了CW的肝毒性和肾毒性。此外,蜂蜜煮沸的CW显著提高了细胞安全性,增强了抗炎和镇痛作用。我们的研究结果表明,蜂蜜煮沸的CW通过影响生物碱的转化和促进超分子聚集体的形成,显示出一种有效的解毒机制。本研究为蜜煮中药解毒或增效策略的开发奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanistic insights into honey-boiled detoxification of ChuanWu: A study on alkaloid transformation and supramolecular aggregation.

ChuanWu (CW), the dried mother root of Aconitum carmichaelii Debx., is a well-known traditional Chinese medicine (TCM) recognized for its potent efficacy but inherent toxicity, primarily due to its alkaloid content. Traditional and modern detoxification methods for CW include proper processing, rational compatibility, and specialized decoction techniques, among which honey-boiled CW is particularly distinctive. However, research on the detoxification mechanism of honey-boiled CW remains limited. This study investigated this mechanism by analyzing alkaloid transformation and supramolecular aggregation. Honey-boiled and water-boiled CW preparations were compared. Ultra-high-performance liquid chromatography-tandem mass spectrometry was used to analyze CW alkaloids, specifically diester alkaloids (DDAs), monoester alkaloids (MDAs), and non-esterified diterpenoid alkaloids (NDAs). Transmission electron microscopy was employed to observe and identify supramolecular aggregates in the honey-boiled CW decoction. In vivo absorption of water-boiled, honey-boiled, and NADES-boiled CW was compared. Median lethal dose (LD50) tests assessed toxicity, including hepatotoxicity and nephrotoxicity. In vitro experiments evaluated the safety, anti-inflammatory, and analgesic effects of CW-medicated serum on RAW264.7 cells, with in vivo validation in mice. Results showed that honey promoted the conversion of highly toxic DDAs to less toxic MDAs and prevented MDAs from hydrolyzing into NDAs. Honey-boiled CW formed approximately 250 nm supramolecular aggregates that encapsulated MDAs, inhibiting their conversion to NDAs. These encapsulated MDAs acted as a stable delivery system with higher bioavailability than free benzoylmesaconine. Subsequent mouse experiments confirmed that honey-boiled CW significantly increased the LD50 of CW while reducing hepatotoxicity and nephrotoxicity. Additionally, honey-boiled CW significantly improved cell safety and enhanced anti-inflammatory and analgesic effects. Our findings reveal that honey-boiled CW exhibits a potent detoxification mechanism by influencing alkaloid transformation and facilitating the formation of supramolecular aggregates. This study lays the groundwork for developing detoxification or synergistic strategies within honey-boiled TCM.

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