Harrison G G, Ivanetich K, Kaminsky L, Halsey M J
Anesth Analg. 1976 Jul-Aug;55(4):529-33. doi: 10.1213/00000539-197607000-00016.
Fluroxene is highly toxic to several animal species. This toxicity is enhanced by induction of raised levels of hepatic microsomal enzymes. Experiments in rats are described which seek to assess the rleative contribution to this toxicity of the individual component groups of the fluroxene molecule. Though results point to the trifluoroethyl moiety of fluroxene as that aspect of the molecule most responsible for the observed mortality, reduction of the vinyl group modifies the pattern of liver injury. That the liver necrosis, manifest following fluroxene anesthesia in the presence of microsomal induction, is alone the direct cause of the acute death of experimental animals is questioned.
氟烷对多种动物具有高毒性。肝微粒体酶水平升高会增强这种毒性。本文描述了在大鼠身上进行的实验,旨在评估氟烷分子各个组成基团对这种毒性的相对贡献。尽管结果表明氟烷的三氟乙基部分是分子中导致观察到的死亡率的最主要方面,但乙烯基的减少会改变肝损伤模式。有人质疑,在微粒体诱导存在的情况下,氟烷麻醉后出现的肝坏死是否是实验动物急性死亡的直接原因。