Effects of halothane on the ultrastructure of rat liver cells.

W. T. Ross, R. Cardell
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引用次数: 28

Abstract

The objective was to study the effects of halothane, a volatile anesthetic, on hepatic metabolism of a second volatile anesthetic, methoxyflurane, and to correlate these biochemical findings with hepatic morphological changes. Microsomal fractions isolated from rats treated with halothane and from control animals were assayed for their capacity to dechlorinate methoxyflurane. Microsomes from halothane-treated rats demonstrated about 2.6 times the capacity to dechlorinate methoxyflurane as microsomes from control animals. Electron microscopy showed that liver cells from halothane-treated animals, when compared with hepatocytes from control rats, had increased amounts of smooth endoplasmic reticulum, an increased number of lipid droplets, and more microbodies per cell. Rough endoplasmic reticulum and glycogen were decreased by halothane treatment. We interpret these results to mean that halothane induces the rough endoplasmic reticulum to synthesize enzymes required for the biotransformation of methoxyflurane. It is suggested that these enzymes are placed in membranes of the rough endoplasmic reticulum. This organelle is converted to smooth endoplasmic reticulum and here the biotransforming enzymes function to dechlorinate methoxyflurane.
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氟烷对大鼠肝细胞超微结构的影响。
目的是研究氟烷(一种挥发性麻醉剂)对第二种挥发性麻醉剂甲氧基氟醚的肝脏代谢的影响,并将这些生化结果与肝脏形态学变化联系起来。从经氟烷处理的大鼠和对照动物身上分离的微粒体部分测定了它们对甲氧基氟醚脱氯的能力。经氟烷处理的大鼠的微粒体对甲氧基氟醚的脱氯能力是对照动物的2.6倍。电子显微镜显示,与对照大鼠肝细胞相比,氟烷处理动物肝细胞的光滑内质网数量增加,脂滴数量增加,每个细胞的微体数量增加。氟烷处理使粗面内质网和糖原减少。我们将这些结果解释为氟烷诱导粗内质网合成甲氧基氟烷生物转化所需的酶。这表明这些酶被放置在粗内质网的膜上。这个细胞器被转化为光滑的内质网,在这里生物转化酶的作用是脱氯甲氧基氟醚。
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Effects of halothane on the ultrastructure of rat liver cells. MORPHOLOGIC OBSERVATIONS CONCERNING THE RELEASE AND TRANSPORT OF SECRETORY PRODUCTS IN THE ADENOHYPOPHYSIS. Initiation of cell proliferation in the vaginal and uterine epithelia of the mouse. Malformations in the genito-urinary tract induced by maternal vitamin A deficiency in the rat. The vascular architecture of the rat uterus as influenced by estrogen and progesterone.
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