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Toxicokinetics of methomyl in rabbits |
1.Department of Emergency, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325027; 2.School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou , 325035; 3.Analytical and Testing Center, Wenzhou Medical University, Wenzhou, 325035 |
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Cite this article: |
WANG Zhiyi1,WANG Chunlong2,WANG Xianqin3, et al. Toxicokinetics of methomyl in rabbits[J]. JOURNAL OF WEZHOU MEDICAL UNIVERSITY, 2015, 45(7): 469-.
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Abstract Objective: To observe the toxicokinetics of acute methomyl poisoning in rabbits, and to explore its damaging effects on tissue and organ. Methods: Disposable gavageing methomyl dose 12 mg/kg, to observed symptoms and signs at different time points. The process of metabolism and absorption of methomyl were detected by Liquid chromatography-mass spectrometry/mass spectrometry in rabbit plasma, drawing concentration-time curve. The toxicokinetic parameters were analyzed and calculated by DAS 2.0 software. The pathological changes of brain, heart, liver, kidney were observed under inverted fluorescence microscope. Blood biochemistry was analyzed with biochemical analyzer at each time point. Results: The parameters were AUC0-t (1 209.734± 219.542) μg/L·h. MRT0-t (1.731±0.144) h, t1/2z (1.471±0.277) h, Tmax 0.25 h, CLz/F (9.576±1.816) L·h-1·kg-1, Vz/F (20.225±4.703) L/kg in methomyl toxicokinetics. The pathological changes, cellular infiltration and edema were visible under light microscope in heart, liver, brain. Compared with previous exposure, the Alanine aminotransferase (ALT), aspartate aminotransferase (AST), lactate dehydrogenase (LDH), creatine kinase (CK) elevated after exposure for 6 h, the differences were statistically significant (P<0.05). Troponin-I (cTn-I) increased at 2 h after exposure, the differences were statistically significant (P<0.05). Cholinesterase (AchE) activity decreased rapidly after 0.25 h exposure, the differences were statistically significant (P<0.05), returned to normal levels after exposure for 6 h. Conclusion: The toxicokinetics of Methomyl gavaged poison is in accordance with two-compartment model, its half-life in vivo is short, metabolism is rapid after poisoning, different degrees damages are detected in the brain, heart, liver, kidney organs.
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Received: 23 January 2015
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[1] 徐俊南, 王荣荣, 王志翊, 等. 264例急性中重度中毒临床与流行病学分析[J]. 中国现代医生, 2012, 50(29): 22-24.
[2] Aktar MW, Sengupta D, Chowdhury A. Degradation dynamics and persistence of Quinolphos and Methomyl in/on Okra(Ablemoschus esculentus) fruits and cropped soil[J]. Bull Environ Contam Toxicol, 2008, 80(1): 74-77.[3] Wei G, Li Y, Wang X. Application of dispersive liquid-liquid microextraction combined with high-performance liquid chromatography for the determination of methomyl in natural waters [J]. J Sep Sci, 2007, 30(18): 3262-3267.
[4] Moser VC, McDaniel KL, Phillips PM, et al. Time-course, dose-response, and age comparative sensitivity of N-methyl carbamates in rats[J]. Toxicol Sci, 2010, 114(1): 113-123.
[5] 黄胜利. 阿托品治疗急性灭多威中毒30例[J]. 中国药业,2012, 21(9): 66.
[6] 赵丹. 灭多威诱导MDEC-07114细胞凋亡的实验研究[D].贵州: 遵义医学院, 2012.
[7] 李宁. 百草枯和灭多威中毒应用不同吸附剂血液灌流清除效果的实验研究[D]. 济南: 山东大学, 2009.
[8] 刘宝华, 汤鲁明, 马建设, 等. 血液灌流对灭多威中毒兔中枢神经系统保护作用研究[J]. 中风与神经疾病杂志, 2014, 31(5): 433-435.
[9] Hoizey G, Canas F, Binet L, et al. Thiodicarb and methomyl tissue distribution in a fatal multiple compounds poisoning [J]. J Forensic Sci, 2008, 53(2): 499-502.
[10] 马文翔, 官大威, 张国华, 等. 灭多威中毒死亡1例[J]. 法医学杂志, 2010, 26(3): 227-228.
[11] 石凯, 张慧庚, 王茂旭. 急性灭多威中毒死亡1例[J]. 中国法医学杂志, 2004. 19(5): 310.
[12] 张凯, 林立, 张强, 等. 灭多威染毒家兔周围神经功能的变化[J]. 中国职业医学, 2003, 30(1): 25-26.
[13] Mansour SA, Mossa AT, Heikal TM. Effects of methomyl on lipid peroxidation and antioxidant enzymes in rat erythrocytes: in vitro studies[J]. Toxicol Ind Health, 2009, 25(8): 557-563. |
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