Literature DB >> 20371258

Acute and subchronic toxicological evaluation of Mequindox in Wistar rats.

Awais Ihsan1, Xu Wang, Xian-ju Huang, Yu Liu, Qin Liu, Wen Zhou, Zong-hui Yuan.   

Abstract

We studied an acute and subchronic oral toxicity of Mequindox (MEQ), a quinoxaline 1,4-dioxide antimicrobial promoter, in Wistar rats according to OECD guidelines. For acute toxicity study, single doses of MEQ at 175, 550 and 2000 mg/kg b.w. were administered to rats by oral gavage. The calculated LD(50) was 550 mg/kg b.w. In subchronic study, rats were fed diets containing 0, 55, 110 or 275 mg MEQ/kg. There was a reduction in body weight of rats fed 275 mg MEQ/kg diet. At 90 days autopsy, a significant decrease in the kidney weight was observed in males while an increase in relative liver and adrenal weights were observed in females fed 275 mg MEQ/kg diet. There was a significant increased in alanineaminotransferase (ALT) and malondialdehyde (MDA) concentrations in males, superoxide dismutase (SOD) activities in females, and aspartateaminotransferase (AST) levels in serum of both genders fed 275 mg MEQ/kg diet. Other toxic effects of 275 mg MEQ/kg diet included significant decrease in sodium and significant increase in potassium concentrations in serum in both genders. We may conclude that MEQ can induce hepatic and adrenal histological changes as well as leaking of different serum constituents in Wistar rats. Copyright 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20371258     DOI: 10.1016/j.yrtph.2010.03.011

Source DB:  PubMed          Journal:  Regul Toxicol Pharmacol        ISSN: 0273-2300            Impact factor:   3.271


  11 in total

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3.  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

4.  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
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Review 6.  Quinoxaline 1,4-di-N-Oxides: Biological Activities and Mechanisms of Actions.

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7.  Mequindox Induced Genotoxicity and Carcinogenicity in Mice.

Authors:  Qianying Liu; Zhixin Lei; Qin Wu; Deyu Huang; Shuyu Xie; Xu Wang; Yuanhu Pan; Zonghui Yuan
Journal:  Front Pharmacol       Date:  2018-04-10       Impact factor: 5.810

8.  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
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9.  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

10.  The Reproductive Toxicity of Mequindox in a Two-Generation Study in Wistar Rats.

Authors:  Qianying Liu; Zhixin Lei; Qin Wu; Ihsan Awais; Muhammad A B Shabbir; Saeed Ahmed; Zainab Fatima; Xu Wang; Yuanhu Pan; Shuyu Xie; Zonghui Yuan
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