首页> 美国卫生研究院文献>Applied and Environmental Microbiology >In vitro formation of 3-hydroxy T-2 and 3-hydroxy HT-2 toxins from T-2 toxin by liver homogenates from mice and monkeys.
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In vitro formation of 3-hydroxy T-2 and 3-hydroxy HT-2 toxins from T-2 toxin by liver homogenates from mice and monkeys.

机译:通过小鼠和猴子的肝脏匀浆从T-2毒素体外形成3-羟基T-2和3-羟基HT-2毒素。

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摘要

In vitro metabolism of T-2 toxin was studied in homogenates of mouse and monkey livers. In addition to several hydrolyzed products, including HT-2 toxin, neosolaniol, 4-deacetylneosolaniol, 15-deacetylneosolaniol, and T-2 tetraol, two metabolic products were isolated from the incubation mixture. Their structures were confirmed as 3'-hydroxy T-2 toxin and 3'-hydroxy HT-2 toxin on the basis of mass and nuclear magnetic resonance spectroscopy. The formation of these hydroxylated metabolites was found in the microsomes in the presence of NADPH, and the hydroxylation reaction was enhanced by treating mice with phenobarbital. The results suggest that a cytochrome P-450 is catalyzing the hydroxylation at the C-3' position of T-2 and HT-2 toxins. An in vitro metabolic pathway of T-2 toxin in the hepatic homogenates containing the NADPH-generating system is proposed.
机译:在小鼠和猴肝脏匀浆中研究了T-2毒素的体外代谢。除了几种水解产物,包括HT-2毒素,新松香酚,4-脱乙酰新松香酚,15-脱乙酰新松香酚和T-2四醇之外,还从孵育混合物中分离了两种代谢产物。根据质谱和核磁共振波谱,证实它们的结构为3'-羟基T-2毒素和3'-羟基HT-2毒素。在NADPH存在下,在微粒体中发现了这些羟基化代谢物的形成,并且通过苯巴比妥治疗小鼠增强了羟基化反应。结果表明,细胞色素P-450催化T-2和HT-2毒素的C-3'位置处的羟基化。提出了含有NADPH生成系统的肝匀浆中T-2毒素的体外代谢途径。

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