Bernstein J, Meneses P, Basilio C, Martínez B
Res Commun Chem Pathol Pharmacol. 1984 Oct;46(1):121-36.
A postmitochondrial preparation of rat lung homogenate was able to metabolize ethanol (205.8 mumoles/g X hr) only in the presence of uridine diphosphate glucuroniate, with a Km for ethanol of about 14 mM. Lung slices from the same animals incubated in a Krebs ringer bicarbonate buffer showed a biphasic time-curve for ethanol metabolism. The amount of metabolized ethanol first increased and then decreased. The metabolic product of this system (PET-I) was sensitive to the action of betaglucuronidase. Lung slices from some animals, however, showed a monophasic time-curve for ethanol metabolism. The metabolic product of this system (PET-II) was insensitive to the action of beta-glucuronidase but sensitive to that of sulfatase. These results confirm our previous suggestion that the lung of the rat is able to metabolize ethanol by a conjugation process catalyzed by a glucuronyl-transferase. In addition, the evidence obtained in this work also suggests that in some animals PET is represented by a sulfotransferase.
大鼠肺匀浆的线粒体后制剂仅在存在尿苷二磷酸葡糖醛酸酯的情况下能够代谢乙醇(205.8微摩尔/克×小时),乙醇的Km约为14毫摩尔。在相同动物的肺切片在 Krebs 林格碳酸氢盐缓冲液中孵育时,乙醇代谢呈现双相时间曲线。代谢的乙醇量先增加后减少。该系统的代谢产物(PET-I)对β-葡糖醛酸酶的作用敏感。然而,一些动物的肺切片显示乙醇代谢呈单相时间曲线。该系统的代谢产物(PET-II)对β-葡糖醛酸酶的作用不敏感,但对硫酸酯酶的作用敏感。这些结果证实了我们之前的推测,即大鼠的肺能够通过葡糖醛酸结合过程催化乙醇代谢。此外,这项工作中获得的证据还表明,在一些动物中,PET 由硫酸转移酶代表。