Kanamura S, Kanai K, Asaka Y, Watanabe J
Department of Anatomy, Kansai Medical University, Osaka, Japan.
J Ultrastruct Mol Struct Res. 1988 Sep;100(3):269-77. doi: 10.1016/0889-1605(88)90044-4.
Peroxisomes in hepatocytes from mice administered 35, 50, or 100 mg/kg of phenobarbital (PB) were analyzed by quantitative electron microscopy. In perivenular hepatocytes, the volume of peroxisomes per unit cytoplasmic volume decreased to 78 or 57% of that of control animals by administration of 50 or 100 mg/kg. Their average volume also decreased to 78 or 64% of that in control animals in animals injected with 35 or 50 mg/kg. Further, cytochemical catalase activity appeared decreased in peroxisomes of hepatocytes of this zone after administration of 50 or 100 mg/kg. These suggest an inhibitory action of PB administration of biogenesis of peroxisomes in perivenular hepatocytes. In periportal hepatocytes, however, the volume density, average volume, and cytochemical catalase activity of peroxisomes did not change by administration of any doses of PB. Thus, PB administration appears to produce no inhibitory effect on the peroxisome biogenesis in periportal hepatocytes. On the other hand, the number of peroxisomes per unit cytoplasmic volume increased in both periportal and perivenular hepatocytes in animals injected with 50 mg/kg, although it returned to the level of control animals by injection of 100 mg/kg. The inhibitory effect of PB on the peroxisome neogenesis in perivenular hepatocytes may be related to the marked smooth endoplasmic reticulum proliferation by administration of this drug.
通过定量电子显微镜分析给予35、50或100mg/kg苯巴比妥(PB)的小鼠肝细胞中的过氧化物酶体。在肝小叶中央静脉周围的肝细胞中,给予50或100mg/kg时,单位细胞质体积内过氧化物酶体的体积降至对照动物的78%或57%。给予35或50mg/kg时,其平均体积也降至对照动物的78%或64%。此外,给予50或100mg/kg后,该区域肝细胞过氧化物酶体中的细胞化学过氧化氢酶活性似乎降低。这些表明给予PB对肝小叶中央静脉周围肝细胞过氧化物酶体生物合成有抑制作用。然而,在肝小叶门脉周围的肝细胞中,给予任何剂量的PB后,过氧化物酶体的体积密度、平均体积和细胞化学过氧化氢酶活性均未改变。因此,给予PB似乎对肝小叶门脉周围肝细胞的过氧化物酶体生物合成没有抑制作用。另一方面,给予50mg/kg的动物,肝小叶门脉周围和中央静脉周围的肝细胞中单位细胞质体积内过氧化物酶体的数量均增加,尽管给予100mg/kg时其恢复到对照动物的水平。PB对肝小叶中央静脉周围肝细胞过氧化物酶体新生的抑制作用可能与给予该药物后显著的滑面内质网增殖有关。