1.Status of content analysis of pyrrolizidine alkaloids in food and herbs.
Yan ZHANG ; Ma SI-QI ; Fei-Fei YANG ; Si JIAN-YONG ; Wu QING ; Yong-Hong LIAO
China Journal of Chinese Materia Medica 2020;45(22):5421-5428
Pyrrolizidine alkaloids(PAs) are a group of naturally occurring alkaloids with a pyrrolizidine skeleton which can be found in about 3% of the world's flowering plants. It is notorious that PAs are cause the hepatoxic and genotoxic-carcinogenic effects by taking PA-containing herbs, food and dietary supplements. In order to control the poisoning caused by PAs, European Medicines Agency has set a limit of intake of PAs from herbal medicinal products at 0.007 μg of 1,2-unsaturated PAs/kg body weight. Nonetheless, a systematic overview of the amount of PAs in the herb has not been provided. Therefore, this paper is to systematically review the current status of PAs content analysis of herbal medicines and foods reported in the literature, and to provide theoretical and experimental support for the safety risk assessment and control of PAs in Chinese herbal medicines.
Food
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Herbal Medicine
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Phytotherapy
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Plants, Medicinal
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Pyrrolizidine Alkaloids/toxicity*
2.Research progress of especial toxicity and of pyrrolizidine alkaloids.
Jiayin HAN ; Aihua LIANG ; Shuangrong GAO
China Journal of Chinese Materia Medica 2011;36(10):1397-1401
Pyrrolizidine alkaloids (PAs) are widely distributed in many plants including medicinal herbs. The hepatotoxicity of PAs has been known academically for a long time, however, their reproductive toxicity, mutagenesis and carcinogenicity have been less researched. This article is an overview of the clinical and experimental reports of the reproductive toxicity, mutagenesis and carcinogenicity of PAs, the effective factors and generating mechanism of the toxicity.
Animals
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Biomedical Research
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Humans
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Plant Extracts
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analysis
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toxicity
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Plants, Medicinal
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chemistry
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toxicity
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Pyrrolizidine Alkaloids
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analysis
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toxicity
3.Developmental toxicity of retrorsine on mouse embryos in vitro.
Jiayin HAN ; Aihu LIANG ; Yan YI
China Journal of Chinese Materia Medica 2011;36(14):1901-1904
OBJECTIVETo investigate the fetotoxicity of retrorsine.
METHODMouse whole embryo culture (WEC) was applied. Post-implantation (8.5 d) mouse embryos were isolated from their mothers and put into the medium of immediately centrifuged serum (ICS) prepared from rats. Different concentrations of retrorsine (12.5, 25, 50, 100 mg x L(-1)) were added into the WEC culture. Development (yolk sac diameter, crown-rump length, head length, somite number) and organic morphodifferentiation (yolk sac circulation, allantois, embryonic flexion, heart, brain, optic-otic-olfactory organ, branchial arch, maxillary, mandible, bud) of embryos were observed at 48 h after treatment.
RESULTObvious fetotoxicity could be observed in various retrorsine treatment groups in a dose-dependent manner. Development of embryos was delayed significantly at dose 12.5-100 mg x L(-1). Malformations were shown in all organic morphodifferentiation indexes, especially in otic-olfactory organ, branchial arch, maxillary, mandible, bud.
CONCLUSIONRetrorsine had obvious fetotoxicity in vitro WEC culture, indicating that exposure of pregnant mice to retrorsine may have potential risk on fetals.
Animals ; Dose-Response Relationship, Drug ; Embryo, Mammalian ; drug effects ; Female ; Male ; Mice ; Pregnancy ; Pyrrolizidine Alkaloids ; toxicity ; Rats ; Toxicity Tests ; methods
4.Embryotoxicity of Senecionis Scandentis Hebra on in vitro cultured mouse embryos.
Jia-Yin HAN ; Yan YI ; Ai-Hua LIANG ; Yu-Shi ZHANG ; Chun-Ying LI ; Yong ZHAO ; Hong-Yu CUI ; Yu-Ting LU
Acta Pharmaceutica Sinica 2014;49(9):1267-1272
The purpose of this study is to evaluate the embryotoxicity of alkaloids in Senecionis Scandentis Hebra on in vitro cultured mouse embryos. Mouse whole embryo culture (WEC) was applied in this study. Post-implantation (8.5 d) mouse embryos were isolated from their mothers, and cultured in medium of immediately centrifuged serum (ICS) with different concentrations of seneciphylline (target concentrations were 100, 50, 25 and 12.5 μg x mL(-1)) or senkirkine (target concentrations were 50, 25 and 12.5 μg x mL(-1)) for 48 h. After culturing completed, the development and organic morphodifferentiation of the cultured embryos were evaluated microscopically. Treatment with seneciphylline and senkirkine had adverse effects on the development and organic morphodifferentiation of embryos. The effect also had clear dose-response. Alkaloidals in Senecionis Scandentis Hebra had embryotoxicity on cultured embryos, which indicated that pregnant people exposed to Senecionis Scandentis Hebra may get potential risk on fetus.
Animals
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Embryo Culture Techniques
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Embryo, Mammalian
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drug effects
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Female
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Mice
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Pregnancy
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Pyrrolizidine Alkaloids
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toxicity
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Senecio
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chemistry
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Teratogens
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toxicity
5.Advance on pharmacologic actions, toxicity and pharmacokinetics of pyrrolizidine alkaloids.
Jiangguo GAO ; Changhong WANG ; Yan LI ; Zhengtao WANG
China Journal of Chinese Materia Medica 2009;34(5):506-511
Plants containing pyrrolizidine alkaloids were widely used in traditional medicine. Its hepatotoxicity is main toxicity as well known internationally. In order to providing some foundation for the future studies, the advancement on the pharmacologic actions, toxicity, and pharmacokinetics or toxicokinetics of pyrrolizidine alkaloids was reviewed.
Animals
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Drug-Related Side Effects and Adverse Reactions
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Humans
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Liver
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drug effects
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Plant Extracts
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pharmacokinetics
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pharmacology
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toxicity
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Plants, Medicinal
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chemistry
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Pyrrolizidine Alkaloids
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pharmacokinetics
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pharmacology
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toxicity
6.Pyrrolizidine alkaloids-containing Chinese medicines in the Chinese pharmacopoeia and related safety concerns.
Acta Pharmaceutica Sinica 2011;46(7):762-772
It has been well-known that many medicinal plants used in traditional Chinese medicine contain hepatotoxic pyrrolizidine alkaloids (HPAs), and some even have been recorded in many editions of the Chinese Pharmacopoeia (ChP). In order to clarify the current status of these PAs-containing Chinese materia medica and proprietary Chinese formulae, the ChP 2010, the newest version, and the related safety issues were thoroughly investigated and analyzed on the current advances in research. Total nine crude drugs (not including the processed slices) were found to contain HPAs, which may be present in tens of Chinese proprietary drugs prepared with these crude drugs. Because of the lack of the alkaloid limitation in most monographs, their potential threats to human health may be underestimated. For this reason, attention should be drawn to the importance of the issue. The key point is to conduct the basic studies immediately on these PA-containing herbal plants or products, whose possible hazards need to be carefully assessed. Further efforts should also be made to elevate the criteria for quality control and ensure the drugs' safety in clinic for human health.
China
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Drugs, Chinese Herbal
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adverse effects
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chemistry
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Medicine, Chinese Traditional
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Pharmacopoeias as Topic
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Plants, Medicinal
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adverse effects
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chemistry
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Pyrrolizidine Alkaloids
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analysis
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toxicity
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Quality Control
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Safety
7.General situation of the toxicity researches on Senecio.
China Journal of Chinese Materia Medica 2006;31(2):93-97
This article summarized the toxic components, toxication faeature and mechanism and clinical poisoning reports of Senecio spp. The distribution of major toxic components pyrrolizidine alkaloids (PAs) in Chinese medicinal herbs and the application of Senecio spp. in China were also recapitulated. The proposals for the application and development of Senecio spp. were put forward.
Animals
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Chemical and Drug Induced Liver Injury
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Humans
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Plant Poisoning
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etiology
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veterinary
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Plants, Medicinal
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chemistry
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poisoning
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toxicity
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Plants, Toxic
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chemistry
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poisoning
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toxicity
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Pyrrolizidine Alkaloids
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isolation & purification
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poisoning
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toxicity
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Senecio
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chemistry
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classification
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poisoning
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toxicity
8.Toxic effects of aqueous extract of crotalariae assamicae semen in rats and possible mechanism in association with liver damage.
Min CHENG ; Jun TANG ; Li-Qun JIANG ; Zi-Ming JIA ; Masao HATTORI
China Journal of Chinese Materia Medica 2013;38(11):1800-1805
OBJECTIVETo study the toxic effects of aqueous extract of Crotalariae Assamicae Semen (CAS), one of the pyrrolizidine alkaloid-containing Chinese herbal medicines, in rats and the possible mechanism in association with liver damage.
METHODThe aqueous extract of CAS (CASE) was prepared by the conventional water extracting-alcohol precipitating method. The LD50 value of CASE in rats was determined by Kärber method. Rats were randomly divided into four groups in which three groups were orally administered with different doses of the CASE and one group with distilled water as control. Toxic effects were assessed by morphological, biochemical and histopathological changes. Moreover, in vitro metabolism using rat liver microsomes was also conducted and applied for the exploration of the underlying mechanism of liver damage.
RESULTThe LD50 value of CASE in Wistar rats was (2.36 +/- 0.26) g x kg(-1). The toxic effects were found in all groups of rats dosed with CASE, in which serum levels of ALT and AST were significantly elevated, and the obvious and dose-dependent damages in liver and lung were observed by histopathological examination. Moreover, the liver tissue-bound pyrroles were detected and generated in a dose-dependent manner, and the pyrrole metabolites observed in the in vitro microsomal metabolism. All the evidences suggested a strong correlation between metabolism and toxicity of CASE in rats.
CONCLUSIONCASE could induce the acute toxicity in rats, of which liver and lung were the major targets. Toxic effects were strongly correlated with pyrrolizidine alkaloids in CAS. The possible mechanism for its liver toxicity may be related to the formation of pyrrole metabolites as well as the corresponding tissue-binding products.
Alanine Transaminase ; metabolism ; Animals ; Crotalaria ; chemistry ; Drugs, Chinese Herbal ; administration & dosage ; toxicity ; Lethal Dose 50 ; Liver ; drug effects ; enzymology ; injuries ; Male ; Microsomes, Liver ; drug effects ; enzymology ; Pyrrolizidine Alkaloids ; administration & dosage ; toxicity ; Rats ; Rats, Wistar