Pegg A E, Conover C, Wrona A
Biochem J. 1978 Mar 15;170(3):651-60. doi: 10.1042/bj1700651.
Rat liver ornithine decarboxylase activity was decreased by administration of putrescine (1,4-diaminobutane) or other diamines, including 1,3-diaminopropane, 1,5-diaminopentane and 1,6-diaminohexane. This effect was seen in control rats and in rats in which hepatic ornithine decarboxylase activity had been increased by administration of growth hormone (somatotropin) or thioacetamide. Loss of activity was not dependent on the conversion of putrescine into polyamines and was short-lived. Within 6h after intraperitoneal administration of 0.8 mmol/kg body wt., ornithine decarboxylase activity had returned to normal values. This return correlated with the rapid loss of the diamines from the liver, and the decrease in activity could be slightly prolonged by treatment with aminoguanidine, a diamine oxidase inhibitor. A decrease in ornithine decarboxylase activity by these diamines was accompanied by the accumulation in the liver of a nondiffusible inhibitor that decreased the activity of a purified ornithine decarboxylase preparation. The possibility that administration of non-physiological diamines that are not converted into polyamines might be useful for the inhibition of polyamine synthesis is discussed.
给予腐胺(1,4 - 二氨基丁烷)或其他二胺,包括1,3 - 二氨基丙烷、1,5 - 二氨基戊烷和1,6 - 二氨基己烷后,大鼠肝脏鸟氨酸脱羧酶活性降低。在对照大鼠以及通过给予生长激素(促生长素)或硫代乙酰胺使肝脏鸟氨酸脱羧酶活性升高的大鼠中均观察到这种效应。活性丧失不依赖于腐胺向多胺的转化,且是短暂的。腹腔注射0.8 mmol/kg体重的腐胺后6小时内,鸟氨酸脱羧酶活性已恢复到正常值。这种恢复与二胺从肝脏的快速清除相关,并且通过用二胺氧化酶抑制剂氨基胍处理,活性降低可稍有延长。这些二胺使鸟氨酸脱羧酶活性降低的同时,肝脏中会积累一种不可扩散的抑制剂,该抑制剂会降低纯化的鸟氨酸脱羧酶制剂的活性。本文讨论了给予不能转化为多胺的非生理性二胺可能对抑制多胺合成有用的可能性。