Morris W B, Smith G D, Peters T J
Biochem Pharmacol. 1986 Jul 1;35(13):2187-91. doi: 10.1016/0006-2952(86)90590-3.
Counter-current partition, sucrose density gradient centrifugation and enzymic analysis were used to explore the changes in rat liver organelles induced by phenobarbital. There was a small increase in partition coefficient and marker enzyme activity of the endoplasmic reticulum. The modal density of the marker enzyme showed a significant decrease reflecting the proliferation of the smooth endoplasmic reticulum. The mitochondria showed a bimodal distribution with a small reduction of marker enzyme activity. In contrast, lysosomes and peroxisomes were relatively unaffected by phenobarbital treatment. Phenobarbital caused a small but statistically insignificant increase in gamma-glutamyl transferase activity: density gradient centrifugation studies indicated that the increased activity was predominantly in the biliary canalicular elements. In contrast, cytosolic gamma-glutamyl hydrolase activity was strikingly reduced by phenobarbital treatment.
采用逆流分配法、蔗糖密度梯度离心法和酶分析方法,探究苯巴比妥诱导的大鼠肝脏细胞器变化。内质网的分配系数和标志酶活性有小幅增加。标志酶的模态密度显著降低,反映出滑面内质网的增殖。线粒体呈现双峰分布,标志酶活性略有降低。相比之下,溶酶体和过氧化物酶体受苯巴比妥处理的影响相对较小。苯巴比妥使γ-谷氨酰转移酶活性有小幅增加,但在统计学上无显著意义:密度梯度离心研究表明,增加的活性主要存在于胆小管成分中。相反,苯巴比妥处理使胞质γ-谷氨酰水解酶活性显著降低。