Ohuchi K, Sugawara T, Watanabe M, Hirasawa N, Tsurufuji S, Fujiki H, Sugimura T, Christensen S B
J Cancer Res Clin Oncol. 1987;113(4):319-24. doi: 10.1007/BF00397715.
The effects of thapsigargin, which is a histamine secretagogue and has recently been found to be a non-(12-O-tetradecanoylphorbol-13-acetate) (TPA)-type tumor promoter in two-stage carcinogenesis using mouse skin, on arachidonic acid metabolism in rat peritoneal macrophages were examined. The release of radioactivity from 3H arachidonic acid-labeled macrophages was increased at doses more than 10 ng/ml. Prostaglandin E2 production was also increased dose-dependently without inducing prominent changes in cell morphology. The potency to stimulate prostaglandin E2 production by thapsigargin was stronger than that by TPA at a dose of 10 ng/ml when measured 6 h after the incubation. HPLC analysis revealed that thapsigargin stimulated the production of lipoxygenase products such as leukotriene B4 and 12-hydroxyeicosatetraenoic acid as well as cyclooxygenase products such as prostaglandin E2 and 6-keto prostaglandin F 1 alpha. Thapsigargin, an analogue of thapsigargin, also stimulated prostaglandin E2 production. The mechanism of the action of thapsigargin was discussed. It was confirmed that the tumor promoters are associated with the activity to stimulate arachidonic acid metabolism irrespective of their type, TPA-type or non-TPA-type.
毒胡萝卜素是一种组胺促分泌剂,最近发现在利用小鼠皮肤进行的两阶段致癌过程中,它是一种非(12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯)(TPA)型肿瘤启动剂,本研究检测了其对大鼠腹腔巨噬细胞花生四烯酸代谢的影响。当剂量超过10 ng/ml时,3H花生四烯酸标记的巨噬细胞的放射性释放增加。前列腺素E2的产生也呈剂量依赖性增加,且未引起细胞形态的显著变化。孵育6小时后测量发现,在10 ng/ml的剂量下,毒胡萝卜素刺激前列腺素E2产生的能力比TPA更强。高效液相色谱分析显示,毒胡萝卜素刺激了脂氧合酶产物如白三烯B4和12 - 羟基二十碳四烯酸以及环氧化酶产物如前列腺素E2和6 - 酮前列腺素F1α的产生。毒胡萝卜素的类似物毒胡萝卜素也刺激了前列腺素E2的产生。本文讨论了毒胡萝卜素的作用机制。证实了肿瘤启动剂与刺激花生四烯酸代谢的活性相关,而与它们是TPA型还是非TPA型无关。