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西咪替丁预防顺铂肾毒性不影响其抗肿瘤活性。

Protecting cisplatin-induced nephrotoxicity with cimetidine does not affect antitumor activity.

机构信息

Department of Medicinal Informatics, Graduate School of Medical Science, Kanazawa University, 13–1 Takara-machi, Kanazawa 920–8641, Japan.

出版信息

Biol Pharm Bull. 2010;33(11):1867-71. doi: 10.1248/bpb.33.1867.

Abstract

The present study examined the influence of cimetidine on the nephrotoxicity and antitumor effects of cisplatin in vitro and in vivo. When the serum concentration of cimetidine was maintained over 20 µg/ml for 4 h by bolus and continuous intravenous infusion, cimetidine prevented nephrotoxicity of cisplatin without influencing antitumor activity. Cimetidine and the antioxidant N-acetylcysteine (NAC) significantly inhibited the in vitro growth inhibition of cisplatin in cells originating from the kidney, but not in SOSN2 osteosarcoma cells. Cimetidine (1 mM) also did not influence platinum concentration in the cells, regardless of whether the organic cation transporter 2 (OCT2) was expressed. Cisplatin did induce reactive oxygen species (ROS) in the KN41 kidney cell line and cimetidine and NAC significantly reduced ROS production. However, cisplatin did not produce ROS in osteosarcoma cells. From these results, cimetidine clearly inhibits nephrotoxicity induced by cisplatin without any influence on the antitumor activity of cisplatin on osteosarcoma in vitro and in vivo.

摘要

本研究考察了西米替丁对顺铂在体外和体内的肾毒性和抗肿瘤作用的影响。当西米替丁通过推注和持续静脉输注将血清浓度维持在 20μg/ml 以上 4 小时时,西米替丁可预防顺铂的肾毒性,而不影响抗肿瘤活性。西米替丁和抗氧化剂 N-乙酰半胱氨酸(NAC)显著抑制了源自肾脏的细胞中顺铂的体外生长抑制作用,但对 SOSN2 骨肉瘤细胞没有影响。西米替丁(1mM)也不影响细胞中的铂浓度,无论是否表达有机阳离子转运体 2(OCT2)。顺铂确实诱导了 KN41 肾细胞系中的活性氧(ROS),西米替丁和 NAC 显著减少了 ROS 的产生。然而,顺铂在骨肉瘤细胞中没有产生 ROS。从这些结果可以清楚地看出,西米替丁可抑制顺铂引起的肾毒性,而对顺铂在体外和体内的骨肉瘤抗肿瘤活性没有任何影响。

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