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血小板活化因子拮抗剂BN-52021可保护大鼠免受顺式二氨基二氯铂的肾毒性作用。

Platelet-activating factor antagonist, BN-52021 protects against cis-diamminedichloroplatinum nephrotoxicity in the rat.

作者信息

Pirotzky E, Guilmard C, Sidoti C, Ivanow F, Principe P, Braquet P

机构信息

Institut Henri Beaufour Research Labs., Les Ulis, France.

出版信息

Ren Fail. 1990;12(3):171-6. doi: 10.3109/08860229009065560.

Abstract

The protective effect of the platelet-activating factor (PAF) antagonist, BN 52021, was assessed on cis-diammine-dichloroplatinum (CDDP)-induced nephrotoxicity. Wistar male rats were treated with either a single dose of CDDP (10 mg/kg b.w. ip) alone or in association with 7 daily doses of BN 52021 (10 mg/kg b.w. ip). At the end of the experiment, the CDDP-treated rats lost 25% of body weight and serum creatinine and urea increased from 0.041 +/- 0.006 mmol/l and 0.165 +/- 0.007 g/l for the control group to 0.202 +/- 0.019 mmol/l and 1.51 +/- 0.131 g/l versus CDDP respectively. Body weight, serum creatinine, serum urea and creatinine clearances were similar to the control group in animals treated with CDDP and BN 52021. CDDP caused proximal tubular necrosis and dilatation of cortical collecting tubes, changes that were markedly less in the BN 52021-protected animals. The concomitant administration of BN 52021 with CDDP did not modify the plasma pharmacokinetic of CDDP. In addition, BN 52021 did not interfere with the antiproliferative and antitumoral actions of CDDP in cultured human tumor cells. BN 52021 therefore could prevent the nephrotoxicity of CDDP.

摘要

评估了血小板活化因子(PAF)拮抗剂BN 52021对顺二氨二氯铂(CDDP)诱导的肾毒性的保护作用。Wistar雄性大鼠单独接受单剂量的CDDP(10 mg/kg体重,腹腔注射),或与7天的BN 52021(10 mg/kg体重,腹腔注射)联合使用。实验结束时,接受CDDP治疗的大鼠体重减轻了25%,血清肌酐和尿素从对照组的0.041±0.006 mmol/l和0.165±0.007 g/l分别增加到CDDP组的0.202±0.019 mmol/l和1.51±0.131 g/l。在接受CDDP和BN 52021治疗的动物中,体重、血清肌酐、血清尿素和肌酐清除率与对照组相似。CDDP导致近端肾小管坏死和皮质集合管扩张,而在BN 52021保护的动物中,这些变化明显减轻。BN 52021与CDDP同时给药并未改变CDDP的血浆药代动力学。此外,BN 52021不干扰CDDP在培养的人肿瘤细胞中的抗增殖和抗肿瘤作用。因此,BN 52021可以预防CDDP的肾毒性。

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