首页> 外文期刊>Medical oncology >Protective effect of L-carnitine versus amifostine against cisplatin-induced nephrotoxicity in rats.
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Protective effect of L-carnitine versus amifostine against cisplatin-induced nephrotoxicity in rats.

机译:左旋肉碱与氨磷汀对顺铂诱导的大鼠肾毒性的保护作用。

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摘要

We aimed to compare the protective effect of L-carnitine (CAR) and amifostine (AMF) against cisplatin (CDDP)-induced nephrotoxicity through biochemical markers and histopathological evaluation. Fifty-seven Wistar albino male rats were randomly classified into six groups, which were AMF+CDDP (n = 11; 200 mg/kg AMF 30 min prior to 7 mg/kg CDDP), CAR+CDDP (n = 11; 300 mg/kg CAR 30 min prior to 7 mg/kg CDDP), CDDP (n = 11; 1 mL/kg isotonic saline 30 min prior to 7 mg/kg CDDP), AMF (n = 8; 200 mg/kg AMF alone), CAR (n = 8; 300 mg/kg CAR alone), and control (n = 8; 1 mL/kg isotonic saline alone). All drugs were given intraperitoneally. Five days after medication, animals were killed, and samples of blood and kidney tissues were collected for biochemical and histopathological evaluation. The serum urea level was highest in AMF+CDDP group among CDDP-applied groups without statistical significance (median, range: 88, 56-21 mg/dL; P > 0.05). There was no statistical significance among CDDP-applied groups in terms of creatinine level (P > 0.05). In the AMF+CDDP group, the median glomerular, tubular, and tubulointerstitial inflammatory damage scores were significantly higher than the other CDDP-applied groups (P < 0.001). The difference between CAR+CDDP and CDDP groups was not statistically significant in terms of renal damage scores. AMF+CDDP group had significantly higher median total nephrotoxicity score than all the other groups (P < 0.001). To conclude, AMF or CAR has no protective effect on CDDP-induced nephrotoxicity. Furthermore, our findings suggest that application of AMF before CDDP may enhance CDDP-induced nephrotoxicity histopathologically.
机译:我们旨在通过生物化学标记和组织病理学评估比较左旋肉碱(CAR)和氨磷汀(AMF)对顺铂(CDDP)诱导的肾毒性的保护作用。将57只Wistar白化病雄性大鼠随机分为六组,分别为AMF + CDDP(n = 11; 200 mg / kg AMF,在7 mg / kg CDDP之前30分钟),CAR + CDDP(n = 11; 300 mg / kg在7 mg / kg CDDP之前30分钟的CAR),CDDP(n = 11;在7 mg / kg CDDP之前30 min的1 mL / kg等渗盐水),AMF(n = 8; 200 mg / kg AMF单独) ,CAR(n = 8;仅300 mg / kg CAR)和对照(n = 8;仅1 mL / kg等渗盐水)。腹膜内给予所有药物。用药五天后,将动物处死,并收集血液和肾脏组织样本进行生化和组织病理学评估。在应用CDDP的各组中,AMF + CDDP组的血清尿素水平最高,无统计学意义(中位数,范围:88、56-21 mg / dL; P> 0.05)。在应用CDDP的各组中,肌酐水平无统计学意义(P> 0.05)。在AMF + CDDP组中,肾小球,肾小管和肾小管间质炎性损害中位数明显高于其他应用CDDP的组(P <0.001)。就肾脏损害评分而言,CAR + CDDP组和CDDP组之间的差异无统计学意义。 AMF + CDDP组的总肾毒性中位数明显高于其他所有组(P <0.001)。总之,AMF或CAR对CDDP诱导的肾毒性没有保护作用。此外,我们的发现表明,在CDDP之前应用AMF可能会在组织病理学上增强CDDP诱导的肾毒性。

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