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基于液相色谱-质谱联用(LC-MS)和核磁共振氢谱(¹H NMR)的43种马兜铃属植物的代谢组学分析及体外毒理学评估

LC-MS- and (1)H NMR-Based Metabolomic Analysis and in Vitro Toxicological Assessment of 43 Aristolochia Species.

作者信息

Michl Johanna, Kite Geoffrey C, Wanke Stefan, Zierau Oliver, Vollmer Guenter, Neinhuis Christoph, Simmonds Monique S J, Heinrich Michael

机构信息

Research Cluster Biodiversity and Medicines/Centre for Pharmacognosy and Phytotherapy, UCL School of Pharmacy , 29-39 Brunswick Square, London, WC1N 1AX, United Kingdom.

Royal Botanic Gardens , Kew, Richmond, Surrey, TW9 3AB, United Kingdom.

出版信息

J Nat Prod. 2016 Jan 22;79(1):30-7. doi: 10.1021/acs.jnatprod.5b00556. Epub 2015 Dec 26.

Abstract

Species of Aristolochia are used as herbal medicines worldwide. They cause aristolochic acid nephropathy (AAN), a devastating disease associated with kidney failure and renal cancer. Aristolochic acids I and II (1 and 2) are considered to be responsible for these nephrotoxic and carcinogenic effects. A wide range of other aristolochic acid analogues (AAAs) exist, and their implication in AAN may have been overlooked. An LC-MS- and (1)H NMR-based metabolomic analysis was carried out on 43 medicinally used Aristolochia species. The cytotoxicity and genotoxicity of 28 Aristolochia extracts were measured in human kidney (HK-2) cells. Compounds 1 and 2 were found to be the most common AAAs. However, AA IV (3), aristolactam I (4), and aristolactam BI (5) were also widespread. No correlation was found between the amounts of 1 or 2 and extract cytotoxicity against HK-2 cells. The genotoxicity and cytotoxicity of the extracts could be linked to their contents of 5, AA D (8), and AA IIIa (10). These results undermine the assumption that 1 and 2 are exclusively responsible for the toxicity of Aristolochia species. Other analogues are likely to contribute to their toxicity and need to be considered as nephrotoxic agents. These findings facilitate understanding of the nephrotoxic mechanisms of Aristolochia and have significance for the regulation of herbal medicines.

摘要

马兜铃属植物在世界各地被用作草药。它们会引发马兜铃酸肾病(AAN),这是一种与肾衰竭和肾癌相关的毁灭性疾病。马兜铃酸I和II(1和2)被认为是造成这些肾毒性和致癌作用的原因。存在多种其他马兜铃酸类似物(AAAs),它们在AAN中的影响可能被忽视了。对43种药用马兜铃属植物进行了基于液相色谱 - 质谱联用和(1)H核磁共振的代谢组学分析。测定了28种马兜铃提取物在人肾(HK - 2)细胞中的细胞毒性和遗传毒性。发现化合物1和2是最常见的AAAs。然而,马兜铃酸IV(3)、马兜铃内酰胺I(4)和马兜铃内酰胺BI(5)也广泛存在。未发现1或2的含量与提取物对HK - 2细胞的细胞毒性之间存在相关性。提取物的遗传毒性和细胞毒性可能与其5、马兜铃酸D(8)和马兜铃酸IIIa(10)的含量有关。这些结果推翻了1和2是马兜铃属植物毒性唯一原因的假设。其他类似物可能对其毒性有贡献,需要被视为肾毒性剂。这些发现有助于理解马兜铃的肾毒性机制,对草药的监管具有重要意义。

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