Kiessling K H, Pettersson H
Acta Pharmacol Toxicol (Copenh). 1978 Oct;43(4):285-90. doi: 10.1111/j.1600-0773.1978.tb02267.x.
The metabolism of zearalenone in rat liver has been investigated. The studies were performed mainly with liver homogenate, though isolated microsomes and hepatocytes have also been used. Zearalenone was metabolized along two principal pathways, conjugation with glucuronic acid, which was the main route and reduction to an isomer of zearalenol. In no case, however, could all zearalenone metabolized be accounted for as conjugated zearalenone and free and conjugated zearalenol. Therefore another, so far unknown metabolite cannot be excluded. Reduction to zearalenol could be increased three times by the addition of NADH (or NADPH) and is probably catalyzed by a hydroxysteroid dehydrogenase. Some 25-50 per cent of the zearalenol could be conjugated, depending on the incubation conditions. The capacity of hepatocytes to eliminate zearalenone was estimated to be about 100 microgram per gram of liver in one hour. With a liver homogenate the highest value obtained was 82 microgram.
已对玉米赤霉烯酮在大鼠肝脏中的代谢进行了研究。这些研究主要是使用肝脏匀浆进行的,不过也使用了分离的微粒体和肝细胞。玉米赤霉烯酮沿两条主要途径代谢,一条是与葡萄糖醛酸结合,这是主要途径,另一条是还原为玉米赤霉烯醇的异构体。然而,在任何情况下,所有代谢的玉米赤霉烯酮都不能仅解释为结合型玉米赤霉烯酮以及游离和结合型玉米赤霉烯醇。因此,不能排除另一种迄今未知的代谢产物。添加NADH(或NADPH)可使还原为玉米赤霉烯醇的反应增加三倍,该反应可能由一种羟基类固醇脱氢酶催化。根据孵育条件,约25%至50%的玉米赤霉烯醇可被结合。据估计,肝细胞消除玉米赤霉烯酮的能力约为每克肝脏每小时100微克。使用肝脏匀浆时,获得的最高值为82微克。