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Article Abstract

Aristolochic acids (AAs) are an important group of secondary metabolites in the genus Aristolochia. The presence of aristolochic acids infers the potency of many Aristolochia herbs used for ages in traditional medicine of China, Europe, Central America, India, and some other countries. Although being moderately cytotoxic, intake of AAs is associated with serious health problems, such as nephrotoxicity and carcinogenicity. Analyzing AAs in Aristolochia herbs is crucial for regulating their efficacy and toxicity because phytochemistry works have shown the occurrence of AAs in almost all Aristolochia herbs studied. Using two-dimensional parameters, chemical shifts and coupling constants, NMR spectroscopy is a modern, accurate, and reliable method in the analysis of secondary metabolites. Comparing experimental spectroscopic data with those of known and related compounds helps simplify the structural identification of secondary metabolites. The compilation of an NMR database of AAs from scattered sources would also be useful in NMR-based metabolomics. The present review provides updated information on sources and NMR spectroscopic data of 54 aristolochic acid derivatives, including AAs and their methyl esters, denitroaristolochic acids and their derivatives, and sesqui- and diterpene esters of AAs. The report also covers the newest development of analytical and preparative methods used in separation, identification, and quantification of AAs in Aristolochia herbal samples.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12187629PMC
http://dx.doi.org/10.1007/s13659-025-00506-xDOI Listing

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Aristolochic acids (AAs) are an important group of secondary metabolites in the genus Aristolochia. The presence of aristolochic acids infers the potency of many Aristolochia herbs used for ages in traditional medicine of China, Europe, Central America, India, and some other countries. Although being moderately cytotoxic, intake of AAs is associated with serious health problems, such as nephrotoxicity and carcinogenicity.

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An untargeted, data-independent acquisition high-resolution accurate tandem mass spectrometry method using an Orbitrap mass spectrometer was employed to screen for DNA adducts formed from 11 environmental and dietary aromatic or substituted aromatic carcinogens in the kidney, urinary bladder, prostate, pancreas, liver, and the lung of male rats 24 h after treatment. Among the carcinogens investigated, DNA adducts of the structurally related nitrophenanthrenes 3-nitrobenzanthrone (3-NBA), an atmospheric pollutant, and 8-methoxy-6-nitrophenanthro[3,4-]-1,3-dioxole-5-carboxylic acid (AA-I), a naturally occurring genotoxicant from Aristolochiaceae plants, were the most abundant across most organs, forming both 2'-deoxyguanosine (dG) and 2'-deoxyadenosine (dA) adducts. In contrast, significantly lower DNA adduct levels were formed with the aromatic amine 4-aminobiphenyl and 2-nitrofluorene, an oxidized derivative of 2-aminofluorene; the heterocyclic aromatic amines 2-amino-3,8-dimethylimidazo[4,5-]quinoxaline, 2-amino-1-methyl-6-phenylimidazo[4,5-]pyridine, 2-amino-α-carboline, and 2-amino-3-methyl-α-carboline; and the polycyclic aromatic hydrocarbon benzo[]pyrene.

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Article Synopsis
  • Aristolochic acids, found in aristolochia plants, are harmful as they can damage kidneys and cause cancer.
  • A new detection method was developed using advanced mass spectrometry to identify these acids and their DNA adducts in various herbs, refining solid phase extraction for better sensitivity.
  • The research employed complex data analysis techniques to validate the method, achieving significant confidence levels in detecting these toxic compounds and their effects on DNA.
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