Toxicity Assessment of Nine Types of Decoction Pieces from the Daughter Root of Aconitum carmichaeli (Fuzi) Based on the Chemical Analysis of their Diester Diterpenoid Alkaloids

被引:93
作者
Lu, Guanghua
Dong, Zhengqi
Wang, Qing
Qian, Guangsheng
Huang, Wenhua
Jiang, Zhihong
Leung, Kelvin Sze-Yin
Zhao, Zhongzhen [1 ]
机构
[1] Hong Kong Baptist Univ, Sch Chinese Med, Teaching Div, Kowloon Tong, Hong Kong, Peoples R China
关键词
Aconitum carmichaeli Debx; Ranunculaceae; daughter root; diester diterpenoid alkaloids; toxicity; QUANTITATIVE-ANALYSIS; LIQUID; JAPONICUM;
D O I
10.1055/s-0029-1240688
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Various processed types of Fuzi (the daughter roots of the highly toxic plant Aconitum carmichaeli Debx, FZ) decoction pieces (the herbal materials processed according to the specifications of Chinese medicine manuals; "Yinpian" in Chinese transliteration) are widely used in traditional medicine to treat various diseases, but their toxicities are not known. Nine types of FZ decoction pieces, including one raw slice and eight processed forms, were therefore prepared, each in 7 to 10 batches, to assess for their toxicity. Altogether 84 FZ samples were quantified on the amount of highly toxic diester diterpenoid alkaloids, i.e., aconitine, mesaconitine and hypaconitine by a newly developed HPLC method with HPLC-DAD and LC-MS techniques. The comparison of the processed FZ to raw slices of the root showed that the amount of each analyte in the processed FZ was drastically decreased. The sum of the three toxic compounds in the 8 types of processed FZ was only 3.91-34.80% of this value in the FZ raw slice. This implies that the toxicity of processed FZ was decreased significantly. The amounts of toxic components in the 8 types of processed FZ varied significantly, often by a power of ten, indicating that the dosage of these herbs, when prescribed for clinical uses, should be cautiously set in order to avoid poisoning incidents.
引用
收藏
页码:825 / 830
页数:6
相关论文
共 32 条
[1]   The effects of Aconitum alkaloids on the central nervous system [J].
Ameri, A .
PROGRESS IN NEUROBIOLOGY, 1998, 56 (02) :211-235
[2]   Determination of aconitine in body fluids by LC-MS-MS [J].
Beike, J ;
Frommherz, L ;
Wood, M ;
Brinkmann, B ;
Köhler, H .
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 2004, 118 (05) :289-293
[3]   The local anesthetic activity of Aconitum alkaloids can be explained by their structural properties:: a QSAR analysis [J].
Bello-Ramírez, AM ;
Nava-Ocampo, AA .
FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2004, 18 (02) :157-161
[4]   A QSAR analysis to explain the analgesic properties of Aconitum alkaloids [J].
Bello-Ramírez, AM ;
Buendía-Orozco, J ;
Nava-Ocampo, AA .
FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2003, 17 (05) :575-580
[5]   ACONITINE POISONING FOLLOWING THE INGESTION OF CHINESE HERBAL MEDICINES - A REPORT OF 8 CASES [J].
CHAN, TYK ;
TOMLINSON, B ;
CRITCHLEY, JAJH .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE, 1993, 23 (03) :268-271
[6]  
CHAN TYK, 1993, J TROP MED HYG, V96, P62
[7]  
[董兰凤 Dong Lanfeng], 2003, [中国药科大学学报, Journal of China Pharmaceutical University], V34, P549
[8]  
Huang Qin-An, 2007, Zhongguo Zhong Yao Za Zhi, V32, P2143
[9]   Determination of Aconitum alkaloids in the tubers of Aconitum japonicum using gas chromatography selected ion monitoring [J].
Ito, K ;
Ohyama, Y ;
Hishinuma, T ;
Mizugaki, M .
PLANTA MEDICA, 1996, 62 (01) :57-59
[10]  
Jiao S., 2003, Ten lectures on the use of medicinals, P339