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在大鼠结肠黏膜中应用12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)、脱氧胆酸钠和吲哚后鸟氨酸脱羧酶和组氨酸脱羧酶活性的诱导。

Induction of ornithine decarboxylase and histidine decarboxylase activities in rat colon mucosa after application of 12-o-tetradecanoylphorbol-13-acetate (TPA), sodium deoxycholate and indole.

作者信息

Sun Y, Li Y

机构信息

Department of Biochemistry, Zhejiang Medical University, Hangchou, The People's Republic of China.

出版信息

Cancer Lett. 1988 Feb;39(1):77-84. doi: 10.1016/0304-3835(88)90042-0.

Abstract

Ornithine decarboxylase (ODC) and histidine decarboxylase (HDC) activities of rat colon mucosa were induced after intrarectal instillation of 12-o-tetradecanoylphorbol-13-acetate (TPA) and sodium deoxycholate. After instillation of sodium deoxycholate, ODC and HDC activities increased rapidly and reached a peak at 4 h, then decreased quickly towards control levels. Both enzymes activities also increased significantly 4 h after instillation in animals treated with TPA and sodium deoxycholate plus indole. However, there were no changes in ODC and HDC activities from 0-8 h after indole administration. These data are the first to show the induction of HDC activity in colon mucosa by TPA and sodium deoxycholate and suggest that the induction of activities in these two enzymes might be one mechanism of their action as cancer promoters.

摘要

在大鼠结肠黏膜内直肠灌注12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)和脱氧胆酸钠后,鸟氨酸脱羧酶(ODC)和组氨酸脱羧酶(HDC)的活性被诱导。灌注脱氧胆酸钠后,ODC和HDC的活性迅速增加,并在4小时达到峰值,然后迅速下降至对照水平。在接受TPA和脱氧胆酸钠加吲哚处理的动物中,灌注后4小时这两种酶的活性也显著增加。然而,吲哚给药后0 - 8小时,ODC和HDC的活性没有变化。这些数据首次表明TPA和脱氧胆酸钠可诱导结肠黏膜中HDC的活性,并提示这两种酶活性的诱导可能是它们作为癌症促进剂发挥作用的一种机制。

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