Fowler B A, Hook G E, Lucier G W
J Pharmacol Exp Ther. 1977 Dec;203(3):712-21.
A single oral administration of 2,3,7,8-tetrachlorodibenzo-p-dioxin to rats at a dose level of 25 microgram/kg produced marked proliferation of smooth endoplasmic reticulum in renal proximal tubule cells of the straight (S3) segments. This ultrastructural effect was associated with a pronounced induction of the microsomal enzymes glucuronyl transferase and benzopyrene hydroxylase which persisted for at least 16 days after treatment. Renal dissection studies disclosed that the activities of these enzymes in 2,3,7,8-tetrachlorodibenzo-p-dioxin-treated animals were not uniformly distributed within the kidney but followed the general known distribution of S3 cells. Enzyme activities were highest in the outer stripe of the medulla and cortex and lowest in the medulla. These studies demonstrate that the kidney does possess inducible microsomal enzyme systems, capabilities of which have not been appreciated previously due to the lack of a suitable inducing agent and their apparent concentration in a relatively small population of proximal tubule cells.
以25微克/千克的剂量给大鼠单次口服2,3,7,8-四氯二苯并对二恶英,可使直部(S3)段肾近端小管细胞的滑面内质网显著增生。这种超微结构效应与微粒体酶葡糖醛酸转移酶和苯并芘羟化酶的明显诱导有关,该诱导在治疗后至少持续16天。肾脏解剖研究表明,在经2,3,7,8-四氯二苯并对二恶英处理的动物中,这些酶的活性在肾脏内并非均匀分布,而是遵循S3细胞的一般已知分布。酶活性在髓质外层和皮质最高,在髓质最低。这些研究表明,肾脏确实拥有可诱导的微粒体酶系统,由于缺乏合适的诱导剂以及它们在相对较少的近端小管细胞群体中的明显浓度,其能力此前未被认识到。