Ou Y H, Lin J K
Institute of Biochemistry, College of Medicine, National Taiwan University, Taipei, Republic of China.
J Toxicol Environ Health. 1992 Jan;35(1):19-28. doi: 10.1080/15287399209531590.
The metabolism of butachlor was studied in rat liver and kidney homogenates. In vitro incubation of butachlor with liver fractions (S9, microsome, and cytosolic fractions) formed a considerable amount of butachlor glutathione conjugate (BGSC), while the conjugating activity was not efficient for the kidney S9 fraction. There is a sex difference in the distribution of glutathione S-transferase in the liver. It seems that more enzyme activity is detected in the female liver microsome, while this is not the case in its cytosolic fraction. Further biotransformation of BGSC to mercapturate was not observed in the liver S9 fraction. This metabolite was further transformed to butachlor acetyl cysteine conjugate (BACC) in the presence of acetyl CoA, but to butachlor cysteine conjugate (BCC) in the absence of acetyl CoA. These findings demonstrated that butachlor is initially conjugated with GSH to form BGSC by the enzyme glutathione S-transferase in the liver. This metabolite is apparently transported to the kidneys, where it is transformed to the mercapturate.
在大鼠肝脏和肾脏匀浆中研究了丁草胺的代谢情况。丁草胺与肝脏组分(S9、微粒体和胞质组分)进行体外孵育时会形成大量的丁草胺谷胱甘肽共轭物(BGSC),而肾脏S9组分的共轭活性则不高。肝脏中谷胱甘肽S-转移酶的分布存在性别差异。似乎在雌性肝脏微粒体中检测到更多的酶活性,而在其胞质组分中并非如此。在肝脏S9组分中未观察到BGSC进一步生物转化为硫醚氨酸。在乙酰辅酶A存在的情况下,这种代谢物进一步转化为丁草胺乙酰半胱氨酸共轭物(BACC),但在没有乙酰辅酶A的情况下则转化为丁草胺半胱氨酸共轭物(BCC)。这些发现表明,丁草胺最初在肝脏中通过谷胱甘肽S-转移酶与谷胱甘肽结合形成BGSC。这种代谢物显然被转运到肾脏,在那里它被转化为硫醚氨酸。