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促红细胞生成素通过抑制轴突切断后诱导型一氧化氮合酶的表达来增强面运动神经元的存活。

Erythropoietin enhances survival of facial motor neurons by inhibiting expression of inducible nitric oxide synthase after axotomy.

机构信息

Department of Oral and Maxillofacial Surgery, School of Stomatology, Jilin University, 418 Ziqiang Road, Changchun 130041, Jilin, China.

出版信息

J Clin Neurosci. 2010 Mar;17(3):368-71. doi: 10.1016/j.jocn.2009.08.014. Epub 2010 Jan 20.

DOI:10.1016/j.jocn.2009.08.014
PMID:20089409
Abstract

The aims of this study were (1) to evaluate the effect of high-dose erythropoietin (EPO; 5000 U/kg) on expression of inducible nitric oxide synthase (iNOS) in the facial nucleus after facial nerve transection; and (2) to explore whether this effect is relevant to facial motor neuron survival. Forty-two Wistar rats (250-300 g) of both sexes were used in this study. The right facial nerves of 40 rats were transected at the level of the stylomastoid foramen, with the left sides left untreated. The rats were randomly divided into 2 groups: (1) EPO group (treated with EPO twice per week at a dose of 5000 U/kg bodyweight); (2) saline group (treated with saline). The 2 rats that did not undergo axotomy served as the control group. After axotomy, expression of iNOS in the facial nucleus was detected by iNOS immunohistochemistry at various time points, and the number of surviving motor neurons was counted in coronal paraffin sections of the facial nucleus. In both the EPO and saline groups, axotomy caused a significant increase in iNOS expression in the facial nucleus at 1, 2, 3, and 4 weeks after axotomy. iNOS expression was lower in the EPO group than in the saline group. At 2, 3 and 4 weeks after axotomy, a significantly greater proportion of facial motor neurons survived in the EPO group than in the saline group. These results indicate that a high dose of EPO attenuates the increase in iNOS expression in the facial nucleus after facial nerve transection, and thus may enhance the survival of facial motor neurons.

摘要

本研究的目的是

(1) 评估大剂量促红细胞生成素(EPO;5000 U/kg)对面神经切断后面神经核诱导型一氧化氮合酶(iNOS)表达的影响;(2) 探讨这种作用是否与面运动神经元存活有关。本研究共使用 42 只 Wistar 大鼠(250-300 g),其中 40 只大鼠右侧面神经于茎乳孔处切断,左侧未处理作为对照。大鼠随机分为 2 组:(1) EPO 组(每周 2 次,5000 U/kg 体重);(2) 盐水组。在面神经切断后不同时间点通过 iNOS 免疫组化检测面神经核中 iNOS 的表达,并对面神经核冠状石蜡切片中存活的运动神经元进行计数。在 EPO 和盐水组中,面神经切断后 1、2、3 和 4 周,面神经核中 iNOS 表达明显增加。EPO 组 iNOS 表达低于盐水组。面神经切断后 2、3 和 4 周,EPO 组的面运动神经元存活比例明显高于盐水组。这些结果表明,大剂量 EPO 可减轻面神经切断后面神经核中 iNOS 表达的增加,从而可能增强面运动神经元的存活。

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