Vendrell M, Zawia N H, Serratosa J, Bondy S C
Department of Pharmacology and Toxicology, C.S.I.C., Barcelona, Spain.
Brain Res. 1991 Mar 29;544(2):291-6. doi: 10.1016/0006-8993(91)90067-6.
An increase of proto-oncogene c-fos expression in cerebral cortex of rats treated with subconvulsant doses of the pesticide organochlorine lindane (gamma-hexachlorocyclohexane) has been detected using Northern blots. Immunohistochemical studies show that Fos protein was already increased in neuronal nuclei 3 h after treatment. The administration of the benzodiazepine diazepam prior to lindane totally blocked the activation of this proto-oncogene expression. Parallel to this increased expression of c-fos an activation of the ornithine decarboxylase (ODC) gene and enzyme was also observed. High levels of ODC mRNA and increased enzyme activity in cortex were found in rats following lindane treatment. These changes were attenuated by prior treatment of animals with diazepam. The co-induction of c-fos and ODC suggests a potential link between the ODC/polyamine system and the short-acting proto-oncogenes in stimulus-transcription coupling events.
利用Northern印迹法已检测到,用亚惊厥剂量的有机氯农药林丹(γ-六氯环己烷)处理的大鼠大脑皮层中,原癌基因c-fos的表达增加。免疫组织化学研究表明,处理后3小时神经元细胞核中的Fos蛋白就已增加。在林丹给药前给予苯二氮䓬类药物地西泮,可完全阻断这种原癌基因表达的激活。与c-fos表达增加同时,还观察到鸟氨酸脱羧酶(ODC)基因和酶的激活。林丹处理后的大鼠皮层中发现ODC mRNA水平升高且酶活性增加。用动物预先用地西泮处理可减弱这些变化。c-fos和ODC的共同诱导表明,在刺激-转录偶联事件中,ODC/多胺系统与短效原癌基因之间存在潜在联系。