Iwase T, Arishima K, Ohyama N, Inazawa K, Iwase Y, Ikeda Y, Shirai M, Yamamoto M, Somiya H, Eguchi Y
Toxicology Laboratory, Mitsubishi Kasei Co., Kanagawa, Japan.
J Vet Med Sci. 1994 Jun;56(3):619-21. doi: 10.1292/jvms.56.619.
The teratogenic potential of caffeine was examined in vitro by a whole embryo culture system (WECS) and an embryonic cell culture system (micromas teratogen assay: MTA) in the rat. In the WECS, hyperemia of the tail, and a reduction of the placental size was induced by caffeine at concentrations higher than 50 micrograms/ml; hypoplasia of the forelimb bud was induced at concentrations higher than 100 micrograms/ml; hematoma in the yolk sac and dysmorphogenesis of the fore- and hind-limb buds, prosencephalon and tail were induced by 200 micrograms/ml caffeine. In the MTA, even with 200 micrograms/ml caffeine, the toxicological parameters obtained by proliferation and differentiation assays of the midbrain and limb bud cells were almost the same as in the control. In conclusion, caffeine induced various morphological anomalies, but did not affect proliferation or differentiation of cells in these experimental systems.
通过大鼠全胚胎培养系统(WECS)和胚胎细胞培养系统(微团致畸试验:MTA)在体外研究了咖啡因的致畸潜力。在WECS中,浓度高于50微克/毫升的咖啡因可导致尾部充血和胎盘大小减小;浓度高于100微克/毫升时可导致前肢芽发育不全;200微克/毫升的咖啡因可导致卵黄囊血肿以及前、后肢芽、前脑和尾部的畸形发生。在MTA中,即使使用200微克/毫升的咖啡因,通过中脑和肢芽细胞增殖及分化试验获得的毒理学参数与对照组几乎相同。总之,咖啡因可诱导各种形态异常,但在这些实验系统中不影响细胞的增殖或分化。