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化疗诱导的周围神经病中髓鞘结构保持不变。

Myelin structure is unaltered in chemotherapy-induced peripheral neuropathy.

机构信息

Department of Neuroscience and Biomedical Technologies, University of Milan-Bicocca, Monza, Italy.

出版信息

Neurotoxicology. 2012 Jan;33(1):1-7. doi: 10.1016/j.neuro.2011.10.010. Epub 2011 Nov 4.

Abstract

PURPOSE

Alterations in mRNA for myelin proteins are reported in animal models of chemotherapy-induced peripheral neuropathies (CIPN); however, ultrastructural changes in aldehyde-fixed and plastic-embedded myelin are not evident by electron microscopy. Therefore, we used X-ray diffraction (XRD) to investigate more subtle changes in myelin sheath structure from unfixed nerves.

EXPERIMENTAL DESIGN

We used in vivo chronic animal models of CIPN in female Wistar rats, administering cisplatin (CDDP 2mg/kg, i.p. twice/week), paclitaxel (PT 10mg/kg, i.v. once/week) or bortezomib (0.20mg/kg, i.v. three times/week) over a total period of 4weeks. Animal weights were monitored, and tail nerve conduction velocity (NCV) was determined at the end of the treatments to assess the occurrence of peripheral neuropathy. Sciatic nerves were collected and the myelin structure was analyzed using electron microscopy (EM) and XRD.

RESULTS

All the rats treated with the chemotherapy agents developed peripheral neuropathy, as indicated by a decrease in NCV values; however, light and electron microscopy indicated no severe pathological alterations of the myelin morphology. XRD also did not demonstrate significant differences between sciatic nerves in treated vs. control rats with respect to myelin period, relative amount of myelin, membrane structure, and regularity of membrane packing.

CONCLUSIONS

These results indicate that experimental peripheral neuropathy caused by CDDP, PT, and bortezomib-which are among the most widely used chemotherapy agents-does not significantly affect the structure of internodal myelin in peripheral nerve.

摘要

目的

据报道,在化疗诱导的周围神经病(CIPN)的动物模型中,髓鞘蛋白的 mRNA 发生改变;然而,电镜下醛固定和塑料包埋的髓鞘的超微结构变化并不明显。因此,我们使用 X 射线衍射(XRD)来研究未固定神经的髓鞘结构的更细微变化。

实验设计

我们使用了雌性 Wistar 大鼠的体内慢性 CIPN 动物模型,给予顺铂(CDDP 2mg/kg,腹腔内注射,每周两次)、紫杉醇(PT 10mg/kg,静脉内注射,每周一次)或硼替佐米(0.20mg/kg,静脉内注射,每周三次),总疗程为 4 周。监测动物体重,并在治疗结束时测定尾部神经传导速度(NCV),以评估周围神经病的发生。收集坐骨神经并使用电子显微镜(EM)和 XRD 分析髓鞘结构。

结果

所有接受化疗药物治疗的大鼠均发生周围神经病,表现为 NCV 值降低;然而,光镜和电镜检查均未显示髓鞘形态有严重的病理改变。XRD 也未显示与对照组相比,用 CDDP、PT 和硼替佐米治疗的大鼠坐骨神经在髓鞘周期、髓鞘相对含量、膜结构和膜包装规则性方面有显著差异。

结论

这些结果表明,顺铂、紫杉醇和硼替佐米引起的实验性周围神经病(这些药物是最广泛使用的化疗药物之一)不会显著影响周围神经节段性髓鞘的结构。

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