Literature DB >> 26376954

Metabolism, Distribution, and Elimination of Mequindox in Pigs, Chickens, and Rats.

Lingli Huang1, Fujun Yin1, Yuanhu Pan1, Dongmei Chen1, Juan Li1, Dan Wan1, Zhenli Liu1, Zonghui Yuan1.   

Abstract

Mequindox (MEQ), a quinoxaline-N,N-dioxide antibacterial agent used to control bacterial enteritis in various food-producing animals, is a potential violative residue in food animal-derived products. The disposition and elimination of MEQ in rats, pigs, and chickens was comprehensively investigated to identify the marker residue and target tissue of MEQ in food animals for residue monitoring. Following a single oral administration, 62-71% of MEQ was rapidly excreted via urine and feces in all species within 24 h. Urinary excretion of radioactivity was 84 and 83.5% of the administered dose in rats and pigs, respectively. More than 92% of the administered dose was excreted in all species within 15 days. Radioactivity was found in nearly all tissues at the first 6 h after dosing, with the majority of radioactivity cleared within 4-6 days. The highest radioactivity and longest persisting time were found to be in the liver and kidney. Totals of 11, 12, and 7 metabolites were identified in rats, chickens, and pigs, respectively. No parent drug could be detected in any of the tissues of pigs and chickens. 3-Methyl-2-acetyl quinoxaline (M1), 3-methyl-2-(1-hydroxyethyl) quinoxaline-N4-monoxide (M4), and 3-methyl-2-(1-hydroxyethyl) quinoxaline-1,4-dioxide (M6) were the common and major metabolites of MEQ in all three species. Additionally, 3-methyl-2-(1-hydroxyethyl) quinoxaline (M5), 3-hydroxymethyl-2-ethanol quinoxaline-1,4-dioxide (M7), and 3-methyl-2-(1-hydroxyethyl) quinoxaline-N1-monoxide (M8) were the major metabolites of MEQ in rats, pigs, and chickens, respectively. M1 was designated to be the marker residue of MEQ in pigs and chickens. These results provide scientific data for the determination of marker residues and withdrawal time of MEQ in food animals and improve the understanding of the toxicity and disposition of MEQ in animals.

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Keywords:  [3H]-mequindox; excretion; isotopic tracing; marker residue; metabolism; target tissue; tissue depletion

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Year:  2015        PMID: 26376954     DOI: 10.1021/acs.jafc.5b02780

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  6 in total

1.  Toxic metabolites, MAPK and Nrf2/Keap1 signaling pathways involved in oxidative toxicity in mice liver after chronic exposure to Mequindox.

Authors:  Qianying Liu; Zhixin Lei; Anxiong Huang; Qinghua Wu; Shuyu Xie; Ihsan Awais; Menghong Dai; Xu Wang; Zonghui Yuan
Journal:  Sci Rep       Date:  2017-02-03       Impact factor: 4.379

2.  UPLC-MS/MS Method for Simultaneous Determination of Three Major Metabolites of Mequindox in Holothurian.

Authors:  Huihui Liu; Chuanbo Ren; Dianfeng Han; Hui Huang; Rongjie Zou; Huawei Zhang; Yingjiang Xu; Xianghong Gong; Xiuzhen Zhang; Yanshen Li
Journal:  J Anal Methods Chem       Date:  2018-04-01       Impact factor: 2.193

3.  Mequindox-Induced Kidney Toxicity Is Associated With Oxidative Stress and Apoptosis in the Mouse.

Authors:  Qianying Liu; Zhixin Lei; Jingchao Guo; Aimei Liu; Qirong Lu; Zainab Fatima; Haseeb Khaliq; Muhammad A B Shabbir; Muhammad Kashif Maan; Qinghua Wu; Menghong Dai; Xu Wang; Yuanhu Pan; Zonghui Yuan
Journal:  Front Pharmacol       Date:  2018-05-01       Impact factor: 5.810

4.  Mechanisms of the Testis Toxicity Induced by Chronic Exposure to Mequindox.

Authors:  Qianying Liu; Zhixin Lei; Anxiong Huang; Qirong Lu; Xu Wang; Saeed Ahmed; Ihsan Awais; Zonghui Yuan
Journal:  Front Pharmacol       Date:  2017-09-26       Impact factor: 5.810

5.  Toxic metabolites, Sertoli cells and Y chromosome related genes are potentially linked to the reproductive toxicity induced by mequindox.

Authors:  Qianying Liu; Zhixin Lei; Menghong Dai; Xu Wang; Zonghui Yuan
Journal:  Oncotarget       Date:  2017-09-15

6.  Simultaneous Quantification and Pharmacokinetic Study of Five Homologs of Dalbavancin in Rat Plasma Using UHPLC-MS/MS.

Authors:  Difeng Zhu; Li Ping; Yawen Hong; Jiale Shen; Qinjie Weng; Qiaojun He
Journal:  Molecules       Date:  2020-09-08       Impact factor: 4.411

  6 in total

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