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氨磷汀及其代谢产物WR1065对顺铂诱导的神经毒性的体外保护作用。

In vitro protection from cisplatin-induced neurotoxicity by amifostine and its metabolite WR1065.

作者信息

Verstappen C C, Geldof A A, Postma T J, Heimans J J

机构信息

Department of Neurology, University Hospital Vrije Universiteit, Amsterdam, The Netherlands.

出版信息

J Neurooncol. 1999 Aug;44(1):1-5. doi: 10.1023/a:1006241622639.

Abstract

Cisplatin-induced neuropathy is a major dose-limiting toxicity. Counteraction by amifostine and its metabolite WR1065 may reduce peripheral neurotoxicity in a number of patients. Using the nerve growth factor (NGF)-dependent neurite outgrowth from the PC12 pheochromocytoma cell line as an in vitro assay for neurotoxicity, the protective effects of amifostine and WR1065 against cisplatin action on neurite formation by PC12 cells were studied. Cisplatin in a concentration of 10 microg/ml significantly decreased the percentage of neurite forming cells from 84% to 40%. Amifostine in doses of 0.4 and 0.8 mM proved to protect significantly against the cisplatin-induced decrease in neurite formation, when co-incubated with cisplatin. Also the metabolite WR1065 protected significantly against cisplatin neurotoxicity in a dose of 0.12 mM. Our results show a significant protection by amifostine and its main metabolite WR1065 against cisplatin-induced neurotoxicity using an in vitro model.

摘要

顺铂诱导的神经病变是一种主要的剂量限制性毒性。氨磷汀及其代谢产物WR1065的对抗作用可能会降低许多患者的外周神经毒性。使用源自PC12嗜铬细胞瘤细胞系的依赖神经生长因子(NGF)的神经突生长作为神经毒性的体外测定方法,研究了氨磷汀和WR1065对顺铂作用于PC12细胞神经突形成的保护作用。浓度为10微克/毫升的顺铂显著降低了神经突形成细胞的百分比,从84%降至40%。当与顺铂共同孵育时,0.4和0.8毫摩尔剂量的氨磷汀被证明能显著保护细胞免受顺铂诱导的神经突形成减少。代谢产物WR1065在剂量为0.12毫摩尔时也能显著保护细胞免受顺铂神经毒性。我们的结果表明,使用体外模型,氨磷汀及其主要代谢产物WR1065对顺铂诱导的神经毒性具有显著的保护作用。

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