1.Study on the effect using hemoperfusion to treat tetramine poisoned patients.
Xiaowei GE ; Xiaohua LI ; Lei GUAN ; Peibin MA ; Haishi WANG
Chinese Journal of Industrial Hygiene and Occupational Diseases 2002;20(6):403-404
OBJECTIVETo evaluate the effect of hemoperfusion on tetramine poisoned patients.
METHODSThree tretramine poisoned cases treated with hemoperfusion were selected. The samples during and after hemoperfusion were collected and analyzed by gas chromatography.
RESULTSTetramine concentration at the inlet of the artificial kidney kept the same level during hemoperfusion. After hemoperfusion, the tetramine concentration in patient plasma changed little in 72 hours. 1.03-1.55 mg of tetramine was adsorbed by the instrument of hemoperfusion after two hours' hemoperfusion.
CONCLUSIONAlthough hemoperfusion was not so effective to reduce blood tetramine concentration in patients, it could clear about 1 mg tetramine for one time.
Bridged-Ring Compounds ; blood ; poisoning ; Chromatography, Gas ; Hemoperfusion ; Humans
2.Autopsy for two cases of acute tetramine poisoning.
Yu-chuan XU ; Bo CHEN ; Jian-zhou CHEN ; Long-chun LEI ; Yan-qiong BAI
Chinese Journal of Industrial Hygiene and Occupational Diseases 2006;24(6):381-381
Acute Disease
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Adult
;
Autopsy
;
Bridged-Ring Compounds
;
poisoning
;
Child
;
Humans
;
Male
;
Poisoning
;
pathology
;
Rodenticides
;
poisoning
3.Microbiological transformation of paeoniflorin and albiflorin.
Xinxin LIU ; Xiaochi MA ; Changhong HUO ; Shuhong YU ; Qiao WANG
China Journal of Chinese Materia Medica 2010;35(7):872-875
OBJECTIVETo investigate the microbiological transformation of paeoniflorin and albiflorin.
METHODThe bacteria strains able to transform paeoniflorin and albiflorin were screened from 18 strains of microorganisms. The products were isolated by chromatography method and their structures were elucidated by spectral technology.
RESULTIt was found that Cunninghamella blakesleana (AS 3.970) and Syncephalastrum racemosum (AS 3.264) could convert paeoniflorin and albiflorin efficiently, respectively. C. blakesleana could convert paeoniflorin to produce albiflorin, while S. racemosum could convert albiflorin to produce paeoniflorin.
CONCLUSIONPaeoniflorin and albiflorin could be converted each other in definited condition.
Benzoates ; metabolism ; Biotransformation ; Bridged-Ring Compounds ; metabolism ; Cunninghamella ; metabolism ; Glucosides ; metabolism ; Monoterpenes ; Mucorales ; metabolism
5.Simultaneous assay of paeoniflorin and albiflorin in Paeoniae Radix Alba by QAMS.
Shanjun HUANG ; Qiwei YANG ; Yanhong SHI ; Rui WANG ; Zhengtao WANG
China Journal of Chinese Materia Medica 2011;36(6):780-783
OBJECTIVETo develop a method of quantitative analysis of multi-components by single marker (QAMS) for simultaneously determining paeoniflorin and albiflorin in Paeoniae Radix Alba.
METHODUsing paeoniflorin as the internal reference substance, the relative correction factor (RCF) of albiflorin was determined by HPLC and UPLC with good reproducibility. The contents of paeoniflorin in 16 samples of Paeoniae Radix Alba were authentically determined by the external standard method, and the content of albiflorin was calculated according to the RCF. The contents of these two components in the samples were determined with the external standard method.
RESULTNo siginificant differences between the quantitative results of QAMS method and external standard method were observe.
CONCLUSIONIt is a convenient and accurate method to determine multi-components when some authentic standard substances were unavailable. It can be used to control the quality of Paeoniae Radix Alba
Benzoates ; analysis ; Bridged-Ring Compounds ; analysis ; Chromatography, High Pressure Liquid ; methods ; Glucosides ; analysis ; Monoterpenes ; Paeonia ; chemistry
7.Clinical analysis of 15 cases of acute tetramine poisoning.
Yong-jun YANG ; Jin-e LI ; Xin-gang YANG
Chinese Journal of Industrial Hygiene and Occupational Diseases 2004;22(5):335-335
Acute Disease
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Adult
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Bridged-Ring Compounds
;
poisoning
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Female
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Humans
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Male
;
Middle Aged
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Rodenticides
;
poisoning
9.Optimization of a cucurbit6uril-based real-time label-free method for analyzing the activity of ornithine decarboxylase.
Jing WANG ; Xiangchen LIU ; Hongyan MA ; Qiang CHEN ; Sen LIU
Chinese Journal of Biotechnology 2021;37(8):2903-2914
Ornithine decarboxylase (ODC) is a key enzyme in the biosynthetic pathway of polyamines and catalyzes the decarboxylation of ornithine to produce putrescine. Inhibition of ODC activity is a potential approach for the prevention and treatment of many diseases including cancer, as the expression levels and the activities of ODC in many abnormal cells and tumor cells are generally higher than those of normal cells. The discovery and evaluation of ODC inhibitors rely on the monitoring of the reaction processes catalyzed by ODC. There are several commonly used methods for analyzing the activity of ODC, such as measuring the yield of putrescine by high performance liquid chromatography, or quantifying the yield of isotope labelled carbon dioxide. However, the cumbersome operation and cost of these assays, as well as the difficulty to achieve high-throughput and real-time detection, hampered their applications. In this work, we optimized a real-time label-free method for analyzing the activity of ODC based on the macromolecule cucurbit[6]uril (CB6) and a fluorescent dye, DSMI (trans-4-[4-(dimethylamino) styryl]-1-methylpyridinium iodide). Finally, the optimized method was used to determine the activities of different ODC inhibitors with different inhibition mechanisms.
Bridged-Ring Compounds
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Imidazoles
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Ornithine
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Ornithine Decarboxylase
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Ornithine Decarboxylase Inhibitors
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Putrescine
10.Identification of genes involved in biosynthesis of paeoniflorin in Paeonia lactiflora based on transcriptome analysis.
Wen-Ding GUO ; Zhi-Min HU ; Jun-Ling BU ; Jian WANG ; Ying MA ; Juan GUO ; Lu-Qi HUANG
China Journal of Chinese Materia Medica 2022;47(16):4347-4357
Paeoniflorin, a representative pinane monoterpene glycoside, is the main active component and quality index of Paeoniae Radix Alba and Paeoniae Radix Rubra.The possible biosynthesis of paeoniflorin is as follows: GPP is derived from mevalonate(MVA) and/or 2-C-methyl-D-erythritol 4-phosphate(MEP) pathway(s) followed by the catalysis with terpene synthase, cytochrome P450(CYP450), UDP-glucuronosyltransferase(UGT), and acyltransferase(AT), respectively.This study aims to explore the genes rela-ted to the biosynthesis of paeoniflorin.To be specific, the cDNA libraries for flowers, leaves, and roots of Paeonia lactiflora were established and sequenced.A total of 30 609 open reading frames(ORFs) were yielded.Through functional annotation and expression analysis of all CYP450 genes in the transcriptome, 11 CYP450 genes belonging to CYP71 A and CYP71 D subfamilies and showing expression trend consistent with monoterpene synthase PlPIN that may be involved in paeoniflorin biosynthesis were screened out.Subsequently, 7 UGT genes and 9 AT genes demonstrating the expression trend consistent with PlPIN which were possibly involved in paeoniflorin biosynthesis were further screened by functional annotation analysis, full-length sequence analysis, expression analysis, and phylogeny analysis.This study provided a systematic screening method with smaller number of candidate genes, thus reducing the workload of functional gene verification.The result laid a foundation for analyzing the biosynthesis pathway of paeoniflorin and the formation mechanism.
Bridged-Ring Compounds
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Gene Expression Profiling
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Glucosides/metabolism*
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Monoterpenes/metabolism*
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Paeonia/genetics*