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Abstrakty
In this study, we developed a urine metabolomic method by gas chromatography–mass spectrometry (GC–MS) combination with biomedical results to evaluate the effect of activated carbon on methomyl poisoning rats. The rats were divided into four groups, methomyl group, two activated carbon treatment group, and control group. According to the biochemical results, it indicated that activated carbon treated rats could cause liver and kidney function changes. According to the urine metabolomics results, activated carbon treatment group (10 min) and activated carbon treatment group (30 min) could be distinguished from methomyl group, and activated carbon treatment group (10 min) could be separated from activated carbon treatment group (30 min) rats, which indicated that the treatment of rats by activated carbon in different time had a different effect. The results indicate that metabolomic method by GC–MS may be useful to elucidate activated carbon treated on methomyl poisoning rats.
Słowa kluczowe
Czasopismo
Rocznik
Tom
Strony
21--25
Opis fizyczny
Bibliogr. 18 poz., rys.
Twórcy
autor
- The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou 325000, China
autor
- Department of Pharmacy, The First People's Hospital of Wenling, Wenling 317500, China
autor
- Laboratory Animal Centre of Wenzhou Medical University, Wenzhou 325035, China
autor
- Laboratory Animal Centre of Wenzhou Medical University, Wenzhou 325035, China
autor
- Laboratory Animal Centre of Wenzhou Medical University, Wenzhou 325035, China
autor
- The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou 325000, China
autor
autor
- Analytical and Testing Centre of Wenzhou Medical University, Wenzhou 325035, China
autor
- The Laboratory of Clinical Pharmacy, People's Hospital of Lishui City, Lishui 323000, China
Bibliografia
- [1] Meng, S. L. ; Chen, J. Z. ; Xu, P. ; Qu, J. H. ; Fan, L. M. ; Song, C. ; Qiu, L. P. Bull. Environ. Contam. Toxicol. 2014 , 92 , 388 – 392 .
- [2] Meng, S. L. ; Chen, J. Z. ; Hu, G. D. ; Song, C. ; Fan, L. M. ; Qiu, L. P. ; Xu, P. Ecotoxicol. Environ. Saf. 2014 , 101 , 1 – 6 .
- [3] Lin, C. M. Neurol. Int. 2014 , 6 , 5307 .
- [4] Lee, B. K. ; Jeung, K. W. ; Lee, H. Y. ; Jung, Y. H. Clin. Toxicol. (Phila) 2011 , 49 , 828 – 833 .
- [5] Garg, D. P. ; Kiran, R. ; Bansal, A. K. ; Malhotra, A. ; Dhawan, D. K. Drug Chem. Toxicol. 2008 , 31 , 487 – 499 .
- [6] Djeffal, A. ; Messarah, M. ; Boumendjel, A. ; Kadeche, L. ; Feki, A. E. Toxicol. Ind. Health 2015 , 31 , 31 – 43 .
- [7] Zaitsu, K. ; Hayashi, Y. ; Kusano, M. ; Tsuchihashi, H. ; Ishii, A. Drug Metab. Pharmacokinet. 2016 , 31 , 21 – 26 .
- [8] Yi, L. ; Dong, N. ; Yun, Y. ; Deng, B. ; Ren, D. ; Liu, S. ; Liang, Y. Anal. Chim. Acta 2016 , 914 , 17 – 34 .
- [9] Pallares-Mendez, R. ; Aguilar-Salinas, C. A. ; Cruz-Bautista, I. ; Del Bosque-Plata, L. Ann. Med. 2016 , 48 , 89 – 102 .
- [10] Li, S. ; Dunlop, A. L. ; Jones, D. P. ; Corwin, E. J. Biol. Res. Nurs. 2016 , 18 , 12 – 22 .
- [11] Guasch-Ferre, M. ; Hruby, A. ; Toledo, E. ; Clish, C. B. ; Martinez-Gonzalez, M. A. ; Salas-Salvado, J. ; Hu, F. B. Diabetes Care 2016 , 39 , 833 – 846 .
- [12] Zhang, M. ; Deng, M. ; Ma, J. ; Wang X. Chem. Pharm. Bull. (Tokyo) 2014 , 62 , 505 – 507 .
- [13] Zhang, Q. ; Wu, H. ; Wen, C. ; Sun, F. ; Yang, X. ; Hu, L. Int. J. Clin. Exp. Pathol. 2015 , 8 , 9320 – 9325 .
- [14] Juurlink, D. N. Br. J. Clin. Pharmacol. 2016 , 81 , 482 – 487 .
- [15] Patti, G. J. ; Yanes, O. ; Siuzdak, G. Nat. Rev. Mol. Cell Biol. 2012 , 13 , 263 – 269 .
- [16] Wang, Z. ; Ma, J. ; Zhang, M. ; Wen, C. ; Huang, X. ; Sun, F. ; Wang, S. ; Hu, L. ; Lin, G. ; Wang, X. Biol. Pharm. Bull. 2015 , 38 , 1049 – 1053 .
- [17] Wen, C. ; Zhang, M. ; Zhang, Y. ; Sun, F. ; Ma, J. ; Hu, L. ; Lin, G. ; Wang, X. Biomed. Chromatogr. 2016 , 30 , 81 – 84 .
- [18] Wen, C. ; Wang, Z. ; Zhang, M. ; Wang, S. ; Geng, P. ; Sun, F. ; Chen, M. ; Lin, G. ; Hu, L. ; Ma, J. ; Wang, X. Biomed. Chromatogr. 2016 , 30 , 75 – 80 .
Uwagi
PL
Opracowanie rekordu w ramach umowy 509/P-DUN/2018 ze środków MNiSW przeznaczonych na działalność upowszechniającą naukę (2018).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-7c0980a9-030b-4431-a4e8-45299d9cb988