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新生大鼠组织中的鸟氨酸脱羧酶和多胺:鸟氨酸脱羧酶特异性不可逆抑制剂α-二氟甲基鸟氨酸的作用

Ornithine decarboxylase and polyamines in tissues of the neonatal rat: effects of alpha-difluoromethylornithine, a specific, irreversible inhibitor of ornithine decarboxylase.

作者信息

Slotkin T A, Seidler F J, Trepanier P A, Whitmore W L, Lerea L, Barnes G A, Weigel S J, Bartolome J

出版信息

J Pharmacol Exp Ther. 1982 Sep;222(3):741-5.

PMID:6809932
Abstract

To evaluate the role of ornithine decarboxylase (ODC) and the polyamines in tissue growth and development, neonatal rats were given daily injections of alpha-difluoromethylornithine, a specific, irreversible inhibitor of ODC. Enzyme activity in brain, heart and kidney was effectively inhibited, leading to prompt reductions in putrescine levels which were apparent throughout the 4-week period of drug treatment. Deficits in spermidine levels appeared within several days and remained significant in all three tissues, although some recovery toward control levels was apparent after 2 weeks postnatally. Spermine levels were not decreased and in some cases were actually increased during the course of alpha-difluoromethylornithine administration; assessment of total organ content of spermine or total polyamines per organ (putrescine + spermidine + spermine) indicated that the tissues were still actively increasing their net polyamine content despite continued inhibition of ODC. Growth of the kidney and brain were affected within several days of commencing alpha-difluoromethylornithine treatment, well before the onset of body weight or heart weight deficits. By 14 days of age and thereafter, animals displayed delayed eye-opening, deficient fur growth and shorter body length. These data suggest that the ODC/polyamine system does serve as a modulator of tissue growth during neonatal mammalian development and that differences exist among various tissues in the degree and time course of dependence of growth on polyamines, particularly putrescine and/or spermidine.

摘要

为了评估鸟氨酸脱羧酶(ODC)和多胺在组织生长发育中的作用,给新生大鼠每日注射α-二氟甲基鸟氨酸,它是ODC的一种特异性、不可逆抑制剂。脑、心脏和肾脏中的酶活性被有效抑制,导致腐胺水平迅速降低,在整个4周的药物治疗期间这种降低都很明显。亚精胺水平在数天内出现不足,并且在所有这三种组织中都保持显著水平,尽管在出生后2周后向对照水平有一些恢复。精胺水平没有降低,并且在α-二氟甲基鸟氨酸给药过程中某些情况下实际上有所增加;对精胺的总器官含量或每个器官的总多胺(腐胺+亚精胺+精胺)的评估表明,尽管ODC持续受到抑制,但组织仍在积极增加其净多胺含量。在开始α-二氟甲基鸟氨酸治疗的数天内,肾脏和脑的生长就受到影响,这远在体重或心脏重量出现不足之前。到14日龄及之后,动物出现睁眼延迟、毛发生长不足和体长较短的情况。这些数据表明,ODC/多胺系统在新生哺乳动物发育过程中确实作为组织生长的调节剂,并且不同组织在生长对多胺,特别是腐胺和/或亚精胺的依赖程度和时间进程方面存在差异。

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