Shull L R, Rush G F, Olson B A, Sleight S D, Aulerich R J, Wisniewski J A
Drug Metab Dispos. 1983 Sep-Oct;11(5):441-5.
Mink were injected (ip) daily with 20 mg/kg of 3-methylcholanthrene (MC) or 40 mg/kg of phenobarbital (PB) for 3 days and killed 48 hr after the last injection. The duration of anesthetic action of PB increased after each injection. MC-treated mink became anorexic and lost substantial body weight. PB caused enlargement of liver and lungs, whereas MC caused liver atrophy. No major treatment-related morphologic changes including amount of endoplasmic reticulum (ER) in liver were revealed by electron microscopic examination. Microsomal protein content was not increased and NADPH cytochrome P-450 reductase was not induced in liver by either PB or MC. Cytochrome P-450 (448) was increased 3.2-fold by PB and 2.5-fold by MC. Cytochrome b5 was increased 2.3-fold by MC but was not affected by PB. Aminopyrine N-demethylase was enhanced 5.1-fold in activity by PB whereas hexobarbital hydroxylase was not induced. MC-treatment moderately increased the activities of benzo(a)pyrene hydroxylase (1.7-fold) and ethoxyresorufin O-deethylase (2.1-fold) but had no effect on ethoxycoumarin O-deethylase. The most distinctive features of the mink revealed by this study are a) lack of PB induction of the ER, microsomal protein content, NADPH-cytochrome P-450 reductase, and hexobarbital hydroxylase, and b) lack of MC induction of cytochrome P-448-associated mixed function oxidases that are known to be highly responsive to MC in other species.
水貂每天腹腔注射20毫克/千克的3-甲基胆蒽(MC)或40毫克/千克的苯巴比妥(PB),连续注射3天,并在最后一次注射后48小时处死。每次注射后,PB的麻醉作用持续时间延长。用MC处理的水貂出现厌食并体重显著减轻。PB导致肝脏和肺脏肿大,而MC导致肝脏萎缩。电子显微镜检查未发现包括肝脏内质网(ER)数量在内的与治疗相关的主要形态学变化。PB或MC均未使肝脏微粒体蛋白含量增加,也未诱导肝脏中的NADPH细胞色素P-450还原酶。细胞色素P-450(448)经PB处理后增加3.2倍,经MC处理后增加2.5倍。细胞色素b5经MC处理后增加2.3倍,但不受PB影响。PB使氨基比林N-脱甲基酶活性增强5.1倍,而己巴比妥羟化酶未被诱导。MC处理适度增加了苯并(a)芘羟化酶(1.7倍)和乙氧基试卤灵O-脱乙基酶(2.1倍)的活性,但对乙氧基香豆素O-脱乙基酶无影响。本研究揭示的水貂最显著特征是:a)PB未诱导ER、微粒体蛋白含量、NADPH-细胞色素P-450还原酶和己巴比妥羟化酶;b)MC未诱导已知在其他物种中对MC高度敏感的细胞色素P-448相关混合功能氧化酶。