Gurkalo V K, Zabezhinskiĭ M A
Vopr Onkol. 1983;29(8):37-40.
The modifying effect of apomorphine and haloperidol - agonist and antagonist of dopamine receptors, respectively - on the development of N-nitrosodiethylamine (NDEA) - induced hepatic tumors was studied in 60 noninbred albino male rats. The study was concerned with an evaluation of the effect of the drugs on tumor frequency as well as on the neoplastic transformation of such cell elements as hepatocytes, cholangiolar epithelium and endothelium. It was found that apomorphine significantly inhibited the carcinogenic effect of NDEA and neoplastic transformation of hepatocytes. Haloperidol revealed a tendency of stimulating NDEA effect on cholangiolar epithelium. The results are discussed in the context of the considerable importance of the functional condition of the presynaptic receptors of catecholaminergic systems in the mechanism of carcinogenic chemical action.
在60只非近交系雄性白化大鼠中,研究了阿扑吗啡和氟哌啶醇(分别为多巴胺受体激动剂和拮抗剂)对N-亚硝基二乙胺(NDEA)诱导的肝肿瘤发生的修饰作用。该研究旨在评估药物对肿瘤发生率以及肝细胞、胆小管上皮和内皮等细胞成分的肿瘤转化的影响。结果发现,阿扑吗啡显著抑制了NDEA的致癌作用以及肝细胞的肿瘤转化。氟哌啶醇显示出刺激NDEA对胆小管上皮作用的趋势。结合儿茶酚胺能系统突触前受体的功能状态在致癌化学作用机制中的重要性,对结果进行了讨论。