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首页> 外文期刊>Japanese Journal of Pharmacology >Induction of Drug Metabolizing Enzymes by Polychlorinated Biphenyl in the Parotid Gland and Relation to Changes in Vitamin A Content and Morphological Changes
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Induction of Drug Metabolizing Enzymes by Polychlorinated Biphenyl in the Parotid Gland and Relation to Changes in Vitamin A Content and Morphological Changes

机译:腮腺中多氯联苯对药物代谢酶的诱导及其与维生素A含量和形态变化的关系

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References(25) The relationship between the morphological changes and vitamin A content during the development of acute toxicity induced by polychlorinated biphenyl (PCB) in mouse parotid glands was investigated. PCB was administered intraperitoneally at a single dose of 2 mg/kg. Ultrastructural studies revealed remarkable morphological changes in the rough endoplasmic reticulum, nucleus, Golgi apparatus and the secretory granules at 7 days after the administration of PCB. The activities of adenosine monophosphatase (AMPase) and alkaline phosphatase were increased 1 day after PCB administration. Then the activity of NADPH-cytochrome c reductase increased 4 days after PCB administration. Subsequently, the vitamin A content of the parotid glands significantly decreased at 7 days compared with the control. These sequential changes in enzyme activities implied that the decrease of vitamin A content in the parotid glands may be partly due to catabolism of vitamin A by increased activities of microsomal enzymes induced by PCB. In conclusion, it is suggested that PCB also induces drug metabolizing enzymes in the parotid gland cells and that the acute toxicity of PCB on this tissue may occur, at least partly, through the reduction of vitamin A not only by the secondary effect from liver impairment but also by the locally accelerated catabolism of vitamin A in the mouse parotid gland.
机译:参考文献(25)研究了小鼠腮腺中多氯联苯(PCB)诱发急性毒性过程中形态变化与维生素A含量之间的关系。以2 mg / kg的单剂量腹膜内施用PCB。超微结构研究显示,多氯联苯给药后第7天,粗糙的内质网,细胞核,高尔基体和分泌颗粒的形态发生了显着变化。施用PCB后1天,腺苷单磷酸酶(AMPase)和碱性磷酸酶的活性增加。然后在PCB施用后4天,NADPH-细胞色素c还原酶的活性增加。随后,与对照组相比,腮腺的维生素A含量在第7天显着下降。酶活性的这些顺序变化暗示腮腺中维生素A含量的降低可能部分归因于PCB诱导的微粒体酶活性增加导致维生素A分解代谢。总之,提示PCB还可以在腮腺细胞中诱导药物代谢酶,并且PCB对该组织的急性毒性可能至少部分地通过维生素A的减少而发生,这不仅是由于肝脏损害引起的继发性作用还可以通过小鼠腮腺中维生素A的局部加速分解代谢来实现。

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