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免疫调节剂AS101对环磷酰胺诱导的小鼠睾丸损伤的保护作用。

Protective effect of the immunomodulator AS101 against cyclophosphamide-induced testicular damage in mice.

作者信息

Carmely A, Meirow D, Peretz A, Albeck M, Bartoov B, Sredni B

机构信息

The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.

出版信息

Hum Reprod. 2009 Jun;24(6):1322-9. doi: 10.1093/humrep/den481. Epub 2009 Feb 24.

Abstract

BACKGROUND

Cyclophosphamide (Cy), a widely used anticancer drug, is associated with significant testicular damage and sterility. Co-administration of the immunomodulating compound AS101 during chemotherapy treatments was previously shown to protect organs against cytotoxic damage, without attenuating the drug's anticancer effect. In this animal study, we investigated the effect of AS101 on testicular damage, sperm DNA damage and infertility induced by Cy. Akt and glycogen synthase kinase-3beta (GSK-3beta) phosphorylation were investigated as a possible chemoprotective mechanism.

METHODS

Mature male mice, 10 in each group, were injected intraperitoneally with 200 mg/kg Cy once a week for 5 weeks, with or without concurrent treatment with 10 microg per mouse AS101 three times per week. Damage to testicular tubules and sperm production was determined, sperm chromatin damage was analyzed and fertility was gauged. Akt and GSK-3beta phosphorylation were evaluated.

RESULTS

Co-treatment with AS101 during the course of Cy administration significantly reduced the percentage of damaged seminiferous tubules (76.0 +/- 10.8% versus 40.3 +/- 2.6%), and reduced sperm DNA fragmentation (%DFI) from 44.7 +/- 1.0% to 25 +/- 6.5%. Co-treatment with AS101 also partially protected against the decrease in numbers of impregnated females and litter size. AS101 increased Akt and GSK-3beta phosphorylation.

CONCLUSIONS

Our results indicate that AS101 can significantly protect against Cy-induced testicular damage and sperm DNA damage, probably by acting through Akt/GSK-3beta phosphorylation.

摘要

背景

环磷酰胺(Cy)是一种广泛使用的抗癌药物,与严重的睾丸损伤和不育有关。先前的研究表明,在化疗期间联合使用免疫调节化合物AS101可保护器官免受细胞毒性损伤,同时不减弱药物的抗癌效果。在本动物研究中,我们调查了AS101对Cy诱导的睾丸损伤、精子DNA损伤和不育的影响。研究了Akt和糖原合酶激酶-3β(GSK-3β)磷酸化作为一种可能的化学保护机制。

方法

每组10只成熟雄性小鼠,每周腹腔注射一次200mg/kg Cy,共5周,同时或不同时每周三次给予每只小鼠10μg AS101。测定睾丸小管损伤和精子生成情况,分析精子染色质损伤并评估生育能力。评估Akt和GSK-3β磷酸化情况。

结果

在Cy给药过程中联合使用AS101可显著降低受损生精小管的百分比(76.0±10.8%对40.3±2.6%),并将精子DNA碎片率(%DFI)从44.7±1.0%降至25±6.5%。联合使用AS101还部分预防了受孕雌性数量和窝仔数的减少。AS101增加了Akt和GSK-3β磷酸化。

结论

我们的结果表明,AS101可能通过Akt/GSK-3β磷酸化作用,显著预防Cy诱导的睾丸损伤和精子DNA损伤。

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