Tutton P J, Barkla D H
Virchows Arch B Cell Pathol. 1978 Aug 25;28(2):151-6. doi: 10.1007/BF02889065.
A stathmokinetic technique was used to study cell proliferation in dimethylhydrazine-induced adenocarcinomata of rat colon following treatment with cytotoxic drugs. The rate of cell division was significantly increased three days after treatment with 5,7-dihydroxytryptamine and seven days after treatment with 5-fluorouracil. Acceleration of tumour cell proliferation following 5,7-dihydroxytryptamine treatment was inhibited by treating animals with the antiseritoninergic drug Xylamidine Tosylate. Acceleration of tumour cell proliferation following 5-fluorouracil treatment was inhibited by treating animals either with the antiseritoninergic drug BW501 or with the histamine H2-receptor blocking drug Cimetidine.
采用静止期细胞动力学技术研究了细胞毒性药物处理后二甲基肼诱导的大鼠结肠癌的细胞增殖情况。用5,7-二羟基色胺处理三天后以及用5-氟尿嘧啶处理七天后,细胞分裂速率显著增加。用抗5-羟色胺能药物甲苯磺酸赛拉米定处理动物,可抑制5,7-二羟基色胺处理后肿瘤细胞增殖的加速。用抗5-羟色胺能药物BW501或组胺H2受体阻断药物西咪替丁处理动物,可抑制5-氟尿嘧啶处理后肿瘤细胞增殖的加速。