Soames A R, Foster J R
Pathology Section, Zeneca Central Toxicology Laboratory, Alderley Park, Macclesfield, UK.
Int J Exp Pathol. 1994 Dec;75(6):405-14.
Administration of 25 mg/kg/day methyl clofenapate to Alpk/APfSD rats for up to 4 days gave rise to hepatomegaly resulting from a combination of hepatocyte hyperplasia, mainly in the periportal region of the lobule, and centrilobular cell hypertrophy. In hepatocytes undergoing mitosis there was a redistribution of dense vesicles and some peroxisomes to the perinuclear region of the cytoplasm. With increasing length of exposure to methyl clofenapate the number of peroxisomes located in this region during mitosis increased. Chromosomes observed by electron microscopy were seen to lie in close apposition to these organelles. Immunocytochemical localization of the Phase II conjugating enzymes glutathione-S transferase B, C and E showed a dramatic reduction and redistribution of those enzymes in mitotic cells and their absence in the region of the chromosomes. These events may increase the vulnerability of DNA to damage in specific cells.
对Alpk/APfSD大鼠每天给予25mg/kg的氯苯那酯,持续4天,会导致肝脏肿大,这是由肝细胞增生(主要在小叶的汇管区周围)和中央小叶细胞肥大共同引起的。在进行有丝分裂的肝细胞中,致密小泡和一些过氧化物酶体重新分布到细胞质的核周区域。随着接触氯苯那酯时间的延长,有丝分裂期间位于该区域的过氧化物酶体数量增加。通过电子显微镜观察到染色体与这些细胞器紧密相邻。II期结合酶谷胱甘肽-S转移酶B、C和E的免疫细胞化学定位显示,这些酶在有丝分裂细胞中显著减少并重新分布,且在染色体区域不存在。这些事件可能会增加特定细胞中DNA受损的易感性。