Yamamoto Yuko, Hotta Yuji, Tomita Natsumi, Naiki-Ito Aya, Kitagawa Ayae, Kuboshiki Urara, Hagita Tamaki, Noda Misuzu, Sanagawa Akimasa, Kataoka Tomoya, Kondo Masahiro, Furukawa-Hibi Yoko, Takahashi Satoru, Kimura Kazunori
Department of Hospital Pharmacy, Nagoya City University Graduate School of Pharmaceutical Sciences, 3-1 Tanabe do-ri, Mizuho-ku, Nagoya, 467-8603, Japan.
Department of Analytical Chemistry, Aichi Prefectural Institute of Public Health, 7-6, Nagare, Tsuji-machi, Kita-ku, Nagoya, 462-8576, Japan.
Biochem Biophys Rep. 2023 Jan 13;33:101422. doi: 10.1016/j.bbrep.2023.101422. eCollection 2023 Mar.
Cisplatin (CDDP) is a widely used anticancer drug, but acute kidney injury (AKI) is one of the most important dose-limiting factors. Trace metal elements are present in various concentrations in the body and play an important role in maintaining normal vital functions. However, the relationship between CDDP-induced AKI and trace metal elements is unknown. In this study, we cultured human renal proximal tubular epithelial cells in the presence of CDDP (0, 12.5, 25, 50 μM) and analyzed the concentration of trace elements in medium after 24 h. We found that CDDP significantly increased the concentrations of zinc (Zn) and manganese (Mn) in medium and significantly decreased them in lysate. Therefore, we examined the effects of CDDP (3 mg/kg, i.p.) administration on serum and urinary Zn and Mn concentrations in rats. The results showed that urinary excretion of Zn and Mn increased in CDDP-treated rats 5 days after administration. Also, 5 days after administration, pyknosis, nuclear loss, loss of the brush border membrane, and DNA fragmentation were observed, and serum creatinine and blood urea nitrogen levels were found to be significantly increased. These data suggested that 24-h excretion of Zn and Mn might reflect on CDDP induced nephropathy. Monitoring urinary Zn and Mn excretion may be beneficial in detecting AKI, but further studies are needed for clinical application.
顺铂(CDDP)是一种广泛使用的抗癌药物,但急性肾损伤(AKI)是其最重要的剂量限制因素之一。体内存在各种浓度的微量元素,它们在维持正常生命功能中发挥着重要作用。然而,CDDP诱导的AKI与微量元素之间的关系尚不清楚。在本研究中,我们在存在CDDP(0、12.5、25、50 μM)的情况下培养人肾近端小管上皮细胞,并在24小时后分析培养基中微量元素的浓度。我们发现CDDP显著增加了培养基中锌(Zn)和锰(Mn)的浓度,并显著降低了细胞裂解物中的浓度。因此,我们研究了腹腔注射CDDP(3 mg/kg)对大鼠血清和尿液中Zn和Mn浓度的影响。结果显示,给药5天后,CDDP处理的大鼠尿液中Zn和Mn的排泄增加。此外,给药5天后,观察到细胞核固缩、核丢失、刷状缘膜丢失和DNA片段化,并且血清肌酐和血尿素氮水平显著升高。这些数据表明,Zn和Mn的24小时排泄可能反映了CDDP诱导的肾病。监测尿液中Zn和Mn的排泄可能有助于检测AKI,但临床应用还需要进一步研究。