McCann P P, Pegg A E
Marion Merrell Dow Inc., Indianapolis, IN 46268-0470.
Pharmacol Ther. 1992;54(2):195-215. doi: 10.1016/0163-7258(92)90032-u.
Interest in ornithine decarboxylase (ODC) and the therapeutic effects of its inhibition with the consequent depletion of polyamine biosynthesis has been widespread since the late 1970s and 1980s. This review covers new information about the properties of ODC, recent findings with ODC inhibitors and a discussion of the mechanism of inactivation of ODC by eflornithine. Recent in vivo therapeutic approaches of ODC inhibition are also discussed including: cancer and cancer chemoprevention; autoimmune diseases; polyamines and the blood-brain barrier, ischemia and hyperplasia; the NMDA receptor and modulation by polyamines; hearing loss; African trypanosomiasis; Pneumocystis carinii pneumonia and Cryptosporidium in AIDS; and other infectious diseases/organisms.
自20世纪70年代末和80年代以来,人们对鸟氨酸脱羧酶(ODC)及其抑制作用(从而导致多胺生物合成减少)的治疗效果一直有着广泛的兴趣。本综述涵盖了有关ODC特性的新信息、ODC抑制剂的最新研究结果以及对依氟鸟氨酸使ODC失活机制的讨论。还讨论了ODC抑制的近期体内治疗方法,包括:癌症与癌症化学预防;自身免疫性疾病;多胺与血脑屏障、缺血和增生;NMDA受体与多胺调节;听力损失;非洲锥虫病;艾滋病中的卡氏肺孢子虫肺炎和隐孢子虫;以及其他传染病/病原体。