Introduced paeoniflorin reduces the main toxicity induced by diosbulbin B, the major toxic compound of Dioscorea bulbifera L.: involved inhibiting inflammation and ferroptosis.

IF 2.1 4区 医学 Q3 CHEMISTRY, MULTIDISCIPLINARY Drug and Chemical Toxicology Pub Date : 2024-12-16 DOI:10.1080/01480545.2024.2440451
Tianzhu Zhang, Bingyin Li, Junming Wang, Xiaohui Wu, Lingling Song, Yanmei Wang, Yueyue Zhang, Yamin Li
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Abstract

Rhizoma Dioscoreae Bulbiferae (HYZ) is a widely utilized herb in clinical practice, known for its significant biological activities. However, the associated hepatotoxicity poses limitations to its application. Our previous research indicated that the effective mitigation of HYZ-induced hepatotoxicity through the concoction with Radix Paeoniae Alba medicinal juice involves the incorporation of paeoniflorin (Pae) and a reduction in diosbulbin B (DB), the primary toxic compound in HYZ. This finding suggests that the introduced Pae may exert a direct attenuating effect on DB. In light of this, this study represents the first investigation into Pae's detoxification effect against DB-induced hepatotoxicity after administration for 2 months in mice vivo while also exploring underlying mechanisms related to inflammation and ferroptosis based on network pharmacology results. Our findings demonstrate that Pae significantly alleviates DB-induced hepatotoxicity in a dose-dependent manner. Western blotting and ELISA analyses revealed that Pae effectively reversed elevated levels of hepatic inflammation-related markers-such as NF-κB, p38 MAPK, NLRP3, TNF-α, and IL-1β-as well as excessively high concentrations of ferroptosis-related MDA and Fe2+. Furthermore, it restored low levels of GSH, SOD, GPX4, and FTH1. In summary, introduced Pae substantially mitigated DB-induced hepatotoxicity by inhibiting both hepatocyte inflammation and ferroptosis.

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引入芍药苷降低了黄药苷B的主要毒性作用,黄药苷B是黄药苷的主要毒性成分,主要参与抑制炎症和铁凋亡。
黄薯蓣(Dioscoreae Bulbiferae, HYZ)是一种被广泛应用于临床的草药,具有重要的生物活性。然而,相关的肝毒性限制了其应用。我们的前期研究表明,通过与白芍药汁配伍,可以有效减轻HYZ诱导的肝毒性,其机制包括芍药苷(Pae)的掺入和HYZ主要毒性化合物黄芩苷B (DB)的减少。这一发现表明,引入的Pae可能对DB有直接的衰减作用。因此,本研究首次在小鼠体内研究Pae在给药2个月后对db诱导的肝毒性的解毒作用,并基于网络药理学结果探索其与炎症和铁中毒相关的潜在机制。我们的研究结果表明,Pae以剂量依赖的方式显著减轻db诱导的肝毒性。Western blotting和ELISA分析显示,Pae有效地逆转了肝脏炎症相关标志物(如NF-κB、p38 MAPK、NLRP3、TNF-α和il -1β)水平升高,以及与铁中毒相关的MDA和Fe2+浓度过高。此外,它还能恢复低水平的GSH、SOD、GPX4和FTH1。综上所述,引入的Pae通过抑制肝细胞炎症和铁下垂显著减轻了db诱导的肝毒性。
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来源期刊
Drug and Chemical Toxicology
Drug and Chemical Toxicology 医学-毒理学
CiteScore
6.00
自引率
3.80%
发文量
99
审稿时长
3 months
期刊介绍: Drug and Chemical Toxicology publishes full-length research papers, review articles and short communications that encompass a broad spectrum of toxicological data surrounding risk assessment and harmful exposure. Manuscripts are considered according to their relevance to the journal. Topics include both descriptive and mechanics research that illustrates the risk assessment implications of exposure to toxic agents. Examples of suitable topics include toxicological studies, which are structural examinations on the effects of dose, metabolism, and statistical or mechanism-based approaches to risk assessment. New findings and methods, along with safety evaluations, are also acceptable. Special issues may be reserved to publish symposium summaries, reviews in toxicology, and overviews of the practical interpretation and application of toxicological data.
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