Maudsley D V, Leif J, Kobayashi Y
Am J Physiol. 1976 Nov;231(5 Pt. 1):1557-61. doi: 10.1152/ajplegacy.1976.231.5.1557.
Ornithine decarboxylase in the small intestine of starved rats was stimulated 3- to 10-fold by refeeding or administration of insulin. A peak is observed 3-5 h following treatment after which the enzyme activity rapidly declines. The rise in ornithine decarboxylase is reduced by actinomycin D or cycloheximide. The increase in enzyme activity occurs mainly in the duodenum and jejunum with less than a twofold change being observed in the ileum. A small (twofold) increase in S-adenosylmethionine decarboxylase activity in the small intestine was observed after food, but there was no change in diamine oxidase activity. Whereas pentagastrin and metiamide administration markedly stimulated histidine decarbosylase in the gastric mucosa, no consistent effect of these agents on ornithine decarboxylase in the small intestine was observed. The similarities and differences between histidine decarboxylase and ornithine decarboxylase are discussed.
饥饿大鼠小肠中的鸟氨酸脱羧酶在重新喂食或注射胰岛素后被刺激3至10倍。在处理后3至5小时观察到一个峰值,之后酶活性迅速下降。放线菌素D或环己酰亚胺可降低鸟氨酸脱羧酶的升高。酶活性的增加主要发生在十二指肠和空肠,回肠中的变化不到两倍。喂食后小肠中S-腺苷甲硫氨酸脱羧酶活性有小幅(两倍)增加,但二胺氧化酶活性没有变化。虽然注射五肽胃泌素和甲硫咪胺可显著刺激胃黏膜中的组氨酸脱羧酶,但未观察到这些药物对小肠中鸟氨酸脱羧酶有一致的影响。文中讨论了组氨酸脱羧酶和鸟氨酸脱羧酶之间的异同。