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

نویسندگان

  • Hiromu Katsuda
  • Mariko Yamashita
  • Hideyuki Katsura
  • Jia Yu
  • Yoshihiro Waki
  • Naoto Nagata
  • Yoshimichi Sai
  • Ken-Ichi Miyamoto
چکیده

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.

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عنوان ژورنال:
  • Biological & pharmaceutical bulletin

دوره 33 11  شماره 

صفحات  -

تاریخ انتشار 2010