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甲氨蝶呤与吲哚美辛对人正常造血细胞系的相互作用。

Interaction between methotrexate and indomethacin on a human normal haemopoietic cell line.

作者信息

Hollingsworth S J, Shankley N P, Anderson E M, Bennett A

机构信息

Department of Surgery, King's College School of Medicine and Dentistry, Rayne Institute, London.

出版信息

Br J Pharmacol. 1995 Feb;114(3):715-9. doi: 10.1111/j.1476-5381.1995.tb17197.x.

Abstract
  1. The interaction between methotrexate and indomethacin has been examined, at a physiological folate concentration (20 nM), on a human normal lymphoblast-like cell line (RPMI 1788) in vitro. 2. Indomethacin (1 microgram ml-1) increased the reduction of lymphoblast growth caused by methotrexate (10-80 ng ml-1). 3. Indomethacin (0.1 and 1 microgram ml-1) potentiated the cytotoxicity of methotrexate (20 and 40 ng ml-1) after 4 days in culture. 4. Indomethacin (0.4 micrograms ml-1) reduced the accumulation of tritium in lymphoblasts incubated with [3H]-methotrexate after 30 min; therefore initial drug accumulation was not responsible for the potentiation seen after 4 days. 5. If indomethacin increases the killing of human cancer cells by methotrexate in vivo, with a smaller potentiation on lymphoblasts, this combination may be beneficial in treating human malignancy.
摘要
  1. 在生理叶酸浓度(20 nM)下,于体外在人正常淋巴母细胞样细胞系(RPMI 1788)中研究了甲氨蝶呤与吲哚美辛之间的相互作用。2. 吲哚美辛(1微克/毫升)增加了甲氨蝶呤(10 - 80纳克/毫升)所致的淋巴母细胞生长抑制。3. 培养4天后,吲哚美辛(0.1和1微克/毫升)增强了甲氨蝶呤(20和40纳克/毫升)的细胞毒性。4. 吲哚美辛(0.4微克/毫升)在30分钟后降低了与[3H] - 甲氨蝶呤一起孵育的淋巴母细胞中氚的积累;因此,最初的药物积累并非4天后所见增强作用的原因。5. 如果吲哚美辛在体内增加甲氨蝶呤对人癌细胞的杀伤作用,对淋巴母细胞的增强作用较小,那么这种联合用药可能对治疗人类恶性肿瘤有益。

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