Staneva-Stoĭcheva D, Krustev L, Kitova E
Eksp Med Morfol. 1977;16(2):90-6.
The authors carried out histologic and electrone microscopic studies of liver in rats, treated with phenobarbital, methylphenobarbital, with their N-substituted morpholinoethye derivatives as well as in rats from the control group of animals. It was established that phenobarbital and methylphenobarbital caused hypertrophy and vacuolization of endoplasmatic reticulum, but the first preparation of the myelin degeneration of mitochindria as well. Morpholinethyl derivatives of the mentioned two compounds induced above all activation of lysosomes as well as reaction of Goldgi apparatus in the parenchymatous cells of liver. The observed ultrastructural changes were connected with differences in the induced drug-metabolizing enzymic properties of the two groups of compounds, established by the authors in their previous studies.
作者对用苯巴比妥、甲基苯巴比妥及其N-取代吗啉乙基衍生物处理过的大鼠肝脏,以及对照组动物的肝脏进行了组织学和电子显微镜研究。结果发现,苯巴比妥和甲基苯巴比妥可导致内质网肥大和空泡化,但第一种制剂还会引起线粒体髓鞘样变性。上述两种化合物的吗啉乙基衍生物首先诱导肝实质细胞溶酶体激活以及高尔基体反应。观察到的超微结构变化与作者在先前研究中确定的两组化合物诱导的药物代谢酶特性差异有关。