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冈田酸类化合物使小鼠和大鼠胃肠道黏膜的标记指数增加。

Increase of labeling indices in gastrointestinal mucosae of mice and rats by compounds of the okadaic acid type.

作者信息

Yuasa H, Yoshida K, Iwata H, Nakanishi H, Suganuma M, Tatematsu M

机构信息

Laboratory of Pathology, Aichi Cancer Center Research Institute, Nagoya, Japan.

出版信息

J Cancer Res Clin Oncol. 1994;120(4):208-12. doi: 10.1007/BF01372558.

Abstract

Effects of compounds of the okadaic acid type (okadaic acid, dinophysistoxin-1, calyculin A and tautomycin) on proliferation by digestive-tract epithelial cells were investigated in mice and rats. In mice, a single oral administration of these agents caused significant enhancement of BrdU labeling indices in a dose/response manner. Exceptions showing no response were limited to the pyloric mucosa for okadaic acid, the pyloric and fundic mucosa for calyculin A and the pyloric mucosa for tautomycin. Sequential analysis of labeling indices after a single oral administration of dinophysistoxin-1 revealed two peaks of cell proliferation at 18 h and 36 h in the esophagus, ileum and colon. The labeling indices of the forestomach, fundus, pylorus and jejunum, on the other hand, continuously increased from 6 h after the administration. Elevated proliferation was also observed in the skin after 30 h or after, but no effects on the liver or kidney were evident. A single oral administration of the okadaic acid type of compounds also dose-dependently enhanced cell proliferation of the rat digestive tract. These results strongly suggest that the okadaic acid class of compounds may exert promoting potential for the gastrointestinal mucosa when administered orally.

摘要

研究了冈田酸类化合物(冈田酸、鳍藻毒素 -1、花萼海绵诱癌素A和互隔交链孢酚单甲醚)对小鼠和大鼠消化道上皮细胞增殖的影响。在小鼠中,单次口服这些药物会以剂量/反应方式显著提高BrdU标记指数。无反应的例外情况仅限于冈田酸作用于幽门黏膜、花萼海绵诱癌素A作用于幽门和胃底黏膜以及互隔交链孢酚单甲醚作用于幽门黏膜。单次口服鳍藻毒素 -1后对标记指数的连续分析显示,在食管、回肠和结肠中,细胞增殖在18小时和36小时出现两个峰值。另一方面,前胃、胃底、幽门和空肠的标记指数在给药后6小时开始持续增加。30小时及以后在皮肤中也观察到增殖升高,但对肝脏或肾脏没有明显影响。单次口服冈田酸类化合物也会剂量依赖性地增强大鼠消化道的细胞增殖。这些结果强烈表明,冈田酸类化合物口服给药时可能对胃肠道黏膜具有促进作用。

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