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黄芪和伊利尼黄芪提取物的比较细胞毒性:分馏和马钱子碱以外毒性的证据

Comparative cytotoxicity of Astragalus pehuenches and Astragalus illini extracts: Fractionation and evidence of toxicity beyond swainsonine.

科研进展PubMed 论文(药材)机译
  • 期刊Research in veterinary science(Res Vet Sci)
  • 发表时间2026-10-12
  • 作者Cholich LA, Torres AM, Gómez TY, Ojeda GA, Arnt F, Gardner D, Bustillo S
  • 卷期页码V213 : 106438
  • DOI10.1016/j.rvsc.2026.106438
  • PMID42914944

摘要机译

黄芪是家畜中毒的主要原因,传统上归因于马钱子碱(SW)。本研究比较了黄芪和伊利尼黄芪,以确定细胞毒性差异是否可以仅用SW来解释,或者可能涉及其他成分。生物碱富集提取物(AEEs)通过植物化学分析和SW标准化细胞毒性测定进行评估,然后进行伊利尼黄芪提取物分级。

SW通过HPLC-MS/MS进行定量,评估硒和硝基化合物,并估计皂苷当量含量。虽然A. pehuenches比A.illini含有更多的SW(4.70比1.49μg SW/mg AEE),但A.illini提取物在SW归一化暴露下导致C6胶质瘤活力的更大降低。对于A.pehuenches和A.illini AEEs,CC值分别为802.79和447.74μM SW当量。

这两种提取物都没有诱导可检测到的LDH释放。定性AO/EB和凝集素染色显示酸性水泡染色模式和细胞内糖缀合染色模式的变化与SW相关的细胞改变一致。然而,由于等效的SW暴露需要不同的总提取物浓度,它们的内在细胞毒性效力不能直接比较。A的分馏。

伊利尼提取物的细胞毒性与SW浓度不平行,而一些细胞毒性最强的组分含有丰富的皂苷相关化合物。非SW代谢物,可能包括皂苷,可能与观察到的细胞毒性有关;然而,它们的具体贡献仍未得到证实。

这些发现支持综合植物化学和生物学分析,以研究黄芪提取物中SW以外成分的细胞毒性。未来的研究应从结构上表征候选化合物,并测试其个体效应,以确定它们在观察到的细胞毒性中的因果作用。

展开英文摘要原文

Astragalus species are major causes of livestock poisoning, traditionally attributed to swainsonine (SW). This study compared Astragalus pehuenches and Astragalus illini to determine whether cytotoxicity differences could be explained solely by SW or might involve other constituents. Alkaloid-enriched extracts (AEEs) were evaluated using phytochemical analyses and SW-normalised cytotoxicity assays, followed by A. illini extract fractionation. SW was quantified by HPLC-MS/MS, selenium and nitro compounds were assessed, and saponin-equivalent content was estimated. Although A. pehuenches contained more SW than A. illini (4.70 vs. 1.49 μg SW/mg AEE), the A. illini extract caused a greater reduction in C6 glioma viability under SW-normalised exposure. CC₅₀ values were 802.79 and 447.74 μM SW equivalents for A. pehuenches and A. illini AEEs, respectively. Neither extract induced detectable LDH release. Qualitative AO/EB and lectin staining showed changes in acidic vesicular staining patterns and intracellular glycoconjugate staining patterns consistent with SW-associated cellular alterations. However, because equivalent SW exposure required different total extract concentrations, their intrinsic cytotoxic potencies could not be directly compared. Fractionation of the A. illini extract showed that cytotoxicity did not parallel SW concentration, while some of the most cytotoxic fractions contained abundant saponin-related compounds. Non-SW metabolites, potentially including saponins, may be associated with the observed cytotoxicity; however, their specific contributions remain unconfirmed. These findings support integrated phytochemical and biological analyses for investigating cytotoxicity associated with constituents other than SW in Astragalus extracts. Future studies should structurally characterise candidate compounds and test their individual effects to establish their causal roles in the observed cytotoxicity.

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