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首页> 外文期刊>Archives of Toxicology >TCDD-induced chick cardiotoxicity is abolished by a selective cyclooxygenase-2 (COX-2) inhibitor NS398
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TCDD-induced chick cardiotoxicity is abolished by a selective cyclooxygenase-2 (COX-2) inhibitor NS398

机译:选择性环氧化酶2(COX-2)抑制剂NS398消除了TCDD诱导的雏鸡心脏毒性

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摘要

Halogenated aromatic hydrocarbons, including 2,3,7,8-tetrachlorodibenzo-p- dioxin (TCDD), are known to cause severe heart defects in avian species. However, the mechanism of TCDD-induced chick cardiovascular toxicity is unclear. In this study, we investigated cyclooxygenase-2 (COX-2) as a possible mechanism of TCDD-induced cardiotoxicity. Fertile chicken eggs were injected with TCDD and a COX-2 selective inhibitor, NS398, and we investigated chick heart failure on day 10. We found that the chick heart to body weight ratio and atrial natriuretic factor mRNA expression were increased, but this increase was abolished with treatment of NS398. In addition, the morphological abnormality of an enlarged ventricle resulting from TCDD exposure was also abolished with co-treatment of TCDD and NS398. Our results suggested that TCDD-induced chick heart defects are mediated via the nongenomic pathway and that they do not require the genomic pathway.
机译:众所周知,包括2,3,7,8-四氯二苯并对二恶英(TCDD)在内的卤代芳烃会导致禽类严重的心脏缺陷。但是,TCDD诱发雏鸡心血管毒性的机制尚不清楚。在这项研究中,我们调查了环氧合酶2(COX-2)作为TCDD诱导的心脏毒性的可能机制。给可育的鸡蛋注射TCDD和COX-2选择性抑制剂NS398,并在第10天调查了小鸡心力衰竭。我们发现小鸡心体重比和心房利钠因子mRNA表达增加,但这种增加是废除NS398的治疗。此外,TCDD和NS398的联合治疗也消除了因TCDD暴露而引起的脑室扩大的形态异常。我们的结果表明,TCDD诱导的雏鸡心脏缺陷是通过非基因组途径介导的,并且它们不需要基因组途径。

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