Savage R E, Weigel W W, Krieg E F
National Institute for Occupational Safety and Health, Division of Biomedical and Behavioral Science, Cincinnati, OH 45226-1998.
Cancer Lett. 1992 Feb 14;62(1):63-8. doi: 10.1016/0304-3835(92)90199-6.
The effects of the curative extender 4,4'-methylene bis (2-chloraniline) (MOCA), an established experimental carcinogen that exhibits activity in rat liver, on hepatic ornithine decarboxylase (ODC) activity was investigated. Male Sprague-Dawley rats were injected i.p. with 75 mg/kg MOCA and killed 6, 12, 18, 24, 42 and 48 h later. Stimulation with MOCA of liver cytosolic ODC was first evident at 6 h, peaked at 12 h and returned to control levels by 42 h. The liver enzyme was refractory to stimulation by a second treatment of MOCA within the dosing intervals examined. The magnitude of stimulation of the enzyme by this aromatic amine was dependent on dose and route of administration.
研究了固化剂4,4'-亚甲基双(2-氯苯胺)(MOCA)对肝鸟氨酸脱羧酶(ODC)活性的影响。MOCA是一种已确定的实验性致癌物,在大鼠肝脏中具有活性。给雄性Sprague-Dawley大鼠腹腔注射75 mg/kg MOCA,并在6、12、18、24、42和48小时后处死。MOCA对肝细胞溶质ODC的刺激在6小时时首次明显,在12小时达到峰值,并在42小时恢复到对照水平。在所检查的给药间隔内,肝脏酶对第二次MOCA处理的刺激无反应。这种芳香胺对该酶的刺激程度取决于剂量和给药途径。