Pacifici G M, Cuoci L, Rane A
Toxicol Pathol. 1984;12(1):69-73. doi: 10.1177/019262338401200111.
The subcellular distribution of (3H )-styrene-7,8-oxide was studied in the rat liver. The compound was added to liver homogenate to give a final concentration of 2 X 10(-5); 2 X 10(-4) and 2 X 10(-3) M. Subcellular fractions were obtained by differential centrifugation. Most of styrene oxide (59-88%) was associated with the cytosolic fraction. Less than 15 percent of the compound was retrieved in each of the nuclear, mitochondrial and microsomal fractions. A considerable percentage of radioactivity was found unextractable with the organic solvents, suggesting that styrene oxide reacted with the endogenous compounds. The intracellular distribution of this epoxide was also studied in the perfused rat liver. Comparable results with those previously described were obtained. The binding of styrene oxide to the cytosolic protein was investigated by equilibrium dialysis and ultrafiltration. Only a small percentage of the compound was bound to protein.
研究了大鼠肝脏中(3H)-苯乙烯-7,8-氧化物的亚细胞分布。将该化合物添加到肝脏匀浆中,使其终浓度分别为2×10⁻⁵、2×10⁻⁴和2×10⁻³ M。通过差速离心获得亚细胞组分。大部分苯乙烯氧化物(59-88%)与胞质组分相关。在核、线粒体和微粒体组分中,该化合物的回收率均低于15%。发现相当一部分放射性不能被有机溶剂提取,这表明苯乙烯氧化物与内源性化合物发生了反应。还在灌注大鼠肝脏中研究了这种环氧化物的细胞内分布。获得了与先前描述结果相当的结果。通过平衡透析和超滤研究了苯乙烯氧化物与胞质蛋白的结合。只有一小部分化合物与蛋白结合。