Quantitation of DNA reactive pyrrolic metabolites of senecionine – A carcinogenic pyrrolizidine alkaloid by LC/MS/MS analysis
Tài liệu tham khảo
Fu, 2004, Pyrrolizidine alkaloids--genotoxicity, metabolism enzymes, metabolic activation, and mechanisms, Drug Metab Rev, 36, 1, 10.1081/DMR-120028426
Mattocks, 1986
Edgar, 2015, Pyrrolizidine alkaloids: potential role in the etiology of cancers, pulmonary hypertension, congenital anomalies, and liver disease, Chem Res Toxicol, 28, 4, 10.1021/tx500403t
Fu, 2017, Detection of pyrrolizidine alkaloid DNA adducts in livers of cattle poisoned with heliotropium europaeum, Chem Res Toxicol, 30, 851, 10.1021/acs.chemrestox.6b00456
Fu, 2010, High-performance liquid chromatography electrospray ionization tandem mass spectrometry for the detection and quantitation of pyrrolizidine alkaloid-derived DNA adducts in vitro and in vivo, Chem Res Toxicol, 23, 637, 10.1021/tx900402x
Fu, 2007, Detection, hepatotoxicity, and tumorigenicity of pyrrolizidine alkaloids in Chinese herbal plants and herbal dietary supplements, J Food Drug Anal, 15, 400
1976
2002, 153
Pyrrolizidine, 1989, 19
Fu, 2017, Pyrrolizidine Alkaloids: metabolic activation pathways leading to liver tumor initiation, Chem Res Toxicol, 30, 81, 10.1021/acs.chemrestox.6b00297
He, 2017, 7-Glutathione-pyrrole and 7-cysteine-pyrrole are potential carcinogenic metabolites of pyrrolizidine alkaloids, J Environ Sci Health, Part C, 35, 69, 10.1080/10590501.2017.1298358
He, 2019, 1-Formyl-7-hydroxy-6,7-dihydro-5 H-pyrrolizine (1-CHO-DHP): a potential proximate carcinogenic metabolite of pyrrolizidine alkaloids, Chem Res Toxicol, 32, 1193, 10.1021/acs.chemrestox.9b00038
He, 2016, 7-Cysteinyl-pyrrole conjugate-a new potential DNA reactive metabolite of pyrrolizidine alkaloids, J Environ Sci Health Part C, 34, 57, 10.1080/10590501.2015.1135593
Xia, 2016, Pyrrolizidine alkaloid-protein adducts-potential non-invasive biomarkers of pyrrolizidine alkaloid-induced liver toxicity and exposure, Chem Res Toxicol, 29, 1282, 10.1021/acs.chemrestox.6b00120
Xia, 2013, Pyrrolizidine alkaloid-derived DNA adducts as a common biological biomarker of pyrrolizidine alkaloid-induced tumorigenicity, Chem Res Toxicol, 26, 1384, 10.1021/tx400241c
Zhu, 2017, The long persistence of pyrrolizidine alkaloid-derived DNA adducts in vivo: kinetic study following single and multiple exposures in male ICR mice, Arch Toxicol, 91, 949, 10.1007/s00204-016-1713-z
He, 2016, 7-N-Acetylcysteine-pyrrole conjugate—a potent DNA reactive metabolite of pyrrolizidine alkaloids, J Food Drug Anal, 24, 682, 10.1016/j.jfda.2016.08.001
Xia, 2015, 7-Glutathione pyrrole adduct: a potential DNA reactive metabolite of pyrrolizidine alkaloids, Chem Res Toxicol, 28, 615, 10.1021/tx500417q
Yang, 2001, Metabolic activation of the tumorigenic pyrrolizidine alkaloid, riddelliine, leading to DNA adduct formation in vivo, Chem Res Toxicol, 14, 101, 10.1021/tx000150n
Seglen, 1972, Preparation of rat liver cells. I. Effect of Ca 2+ on enzymatic dispersion of isolated, perfused liver, Exp Cell Res, 74, 450, 10.1016/0014-4827(72)90400-4
Shi, 2011, Hepatic cytochrome P450s attenuate the cytotoxicity induced by leflunomide and its active metabolite A77 1726 in primary cultured rat hepatocytes, Toxicol Sci, 122, 579, 10.1093/toxsci/kfr106
Eastman, 1982, A new pyrrolizidine alkaloid metabolite, 19-hydroxysenecionine isolated from mouse hepatic microsomes in vitro, Drug Metab Dispos, 10, 696
Estep, 1991, [14C]monocrotaline kinetics and metabolism in the rat, Drug Metab Dispos, 19, 135
Lame, 1991, Metabolism of [14C]monocrotaline by isolated perfused rat liver, Drug Metab Dispos, 19, 516
Lame, 1995, Biliary excretion of pyrrolic metabolites of [14C]monocrotaline in the rat, Drug Metab Dispos, 23, 422
Reid, 1998, Involvement of cytochrome P450 3A in the metabolism and covalent binding of 14C-monocrotaline in rat liver microsomes, J Biochem Mol Toxicol, 12, 157, 10.1002/(SICI)1099-0461(1998)12:3<157::AID-JBT4>3.0.CO;2-K
Huan, 1998, Species differences in the hepatic microsomal enzyme metabolism of the pyrrolizidine alkaloids, Toxicol Lett, 99, 127, 10.1016/S0378-4274(98)00152-0
Xia, 2018, Pyrrolizidine alkaloid secondary pyrrolic metabolites construct multiple activation pathways leading to DNA adduct formation and potential liver tumor initiation, Chem Res Toxicol, 31, 619, 10.1021/acs.chemrestox.8b00096
Ruan, 2014, Metabolic activation of pyrrolizidine alkaloids: insights into the structural and enzymatic basis, Chem Res Toxicol, 27, 1030, 10.1021/tx500071q
Cheeke, 1988, Toxicity and metabolism of pyrrolizidine alkaloids, J Anim Sci, 66, 2343, 10.2527/jas1988.6692343x
Cheeke, 1994, A review of the functional and evolutionary roles of the liver in the detoxification of poisonous plants, with special reference to pyrrolizidine alkaloids, Vet Hum Toxicol, 36, 240