Foxworthy P S, Eacho P I
Toxicol Lett. 1986 Feb;30(2):189-96. doi: 10.1016/0378-4274(86)90102-5.
Leibovitz L-15 medium was superior to RPM11640 in both maintenance and induction of peroxisomal beta-oxidation in cultured rat hepatocytes. Serum was not required for maintenance or induction of beta-oxidation. Cell plating density had only slight effects on maintenance and did not affect induction. Bezafibrate caused time- and dose-related increases in beta-oxidation, as well as increases in catalase, peroxisome volume fraction, and peroxisome number. This system maintained a greater percentage of control beta-oxidation than previously reported, and responded to several hypolipidemics with sizeable increases in activity. The flexibility of this system with respect to serum and cell-plating density facilitates simultaneous studies of cell parameters which are regulated by these variables.
在培养的大鼠肝细胞中,Leibovitz L - 15培养基在维持和诱导过氧化物酶体β - 氧化方面优于RPMI1640。维持或诱导β - 氧化不需要血清。细胞接种密度对维持仅有轻微影响,且不影响诱导。苯扎贝特引起β - 氧化的时间和剂量相关增加,以及过氧化氢酶、过氧化物酶体体积分数和过氧化物酶体数量增加。该系统维持的对照β - 氧化百分比高于先前报道,并对几种降血脂药物有显著的活性增加反应。该系统在血清和细胞接种密度方面的灵活性有助于同时研究受这些变量调节的细胞参数。