Raunio H, Skurnik M, Korhonen P, Pelkonen O
Biochem Pharmacol. 1982 Jan 15;31(2):189-93. doi: 10.1016/0006-2952(82)90209-x.
The induction of aryl hydrocarbon and ornithine decarboxylase by benz[a]-anthracene in the presence or absence of ornithine decarboxylase inhibitors was studied in three different cell culture systems. An almost complete abolishment of ornithine decarboxylase activity by 1,3-diamino-2-propanol or alpha-difluoremethyl ornithine before the addition of the inducer did not affect appreciably the induction of aryl hydrocarbon hydroxylase by benz[a]anthracene in human embryo, HeLa and Rueber H-II-4-E cells in culture. These results suggest that the induction of aryl hydrocarbon hydroxylase does not require ornithine decarboxylase activity per se and can be expressed in the absence of continuous polyamine synthesis.
在三种不同的细胞培养系统中,研究了在存在或不存在鸟氨酸脱羧酶抑制剂的情况下,苯并[a]蒽对芳烃和鸟氨酸脱羧酶的诱导作用。在添加诱导剂之前,1,3-二氨基-2-丙醇或α-二氟甲基鸟氨酸几乎完全消除鸟氨酸脱羧酶活性,这对苯并[a]蒽在人胚胎、HeLa和Rueber H-II-4-E细胞培养物中诱导芳烃羟化酶的作用没有明显影响。这些结果表明,芳烃羟化酶的诱导本身并不需要鸟氨酸脱羧酶活性,并且可以在不存在持续多胺合成的情况下表达。