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Repair of nerve injury wrapped by encapsulated Schwann cells

Repair of nerve injury wrapped by encapsulated Schwann cells
包裹雪旺细胞包裹神经损伤的修复
批准号:
08671579
负责人:
SAITOH Youichi
金额:
$1.41万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1996
资助国家:
日本
项目状态:
已结题
起止时间:
1996 至 1997

项目摘要

项目成果

SAITOH Youichi的其他基金

相关文献

中文摘要
翻译
为了促进面神经损伤再生,将纯化的雪旺细胞置于面神经损伤周围。根据Kim等人的描述,从SD大鼠背根神经节中获得成熟的雪旺细胞。每只SD大鼠(10周龄)暴露左侧面神经两外周支,用动脉瘤夹(Sugita 1号)夹持2分钟。以8mA恒电流刺激外露面神经近端和远端,记录诱发肌电图。两个刺激点之间的平均距离为25mm,分别在损伤前、损伤后和损伤后14天计算神经传导速度(NCV)。10份压伤部分覆盖含有雪旺细胞(1.0*10<@D18@>D1/ml)的胶原凝胶(0.3ml)(雪旺组),其余8份仅覆盖胶原凝胶(对照组)。电生理研究结束后,用4%多聚甲醛灌注大鼠神经,取出神经,石蜡包埋。用免疫细胞化学方法对5 mm厚切片进行HE和S-100蛋白染色。基线中译为47.6 (SY。+ -。[)6.8米/秒(平均(SY。+ -。[)SE),损伤后显著降低(11.8(]SY.+- . [)2.7m/s)。伤后14 d,雪旺组NCV (30.3(]SY.+- . [)8.6m/s)显著大于对照组(11.2(]SY.+- . [)3.6m/s)。然而,免疫细胞化学未能显示在压伤神经周围移植的雪旺细胞。结果表明,在面神经周围移植雪旺细胞可促进面神经损伤后早期的神经再生。但其促进损伤神经修复的物质和机制尚不明确。
英文摘要
To facilitate the regeneration of crush-injured facial nerve, purified Schwann cells were placed around the crush-injured nerve.Mature Schwann cells were obtained from dorsal root ganglia of SD rats as described by Kim et al. The two peripheral branches of left facial nerve of each SD rat (10 weeks old) were exposed, and pinched with aneurysm clip (Sugita No.1) for 2 minutes. The evoked electromyograms were recorded by stimulating the proximal and distal portions of the exposed facial nerve (8mA constant current). The mean distance between the two stimulation points was 25mm, and nerve conduction velocity (NCV) was calculated before injury, just after injury, and 14 days after injury. Ten crush-injured portions were covered with collagen gel (0.3ml) containing Schwann cells (1.0*10<@D18@>D1/ml) (Schwann group), and the other 8 were covered with collagen gel only (control group). After electrophysiological studies, the rats were perfused with 4% paraformaldehyde, and the nerves were removed and embedded in paraffin. The 5 mum-thick slices were stained for HE and S-100 protein immunocytochemically. The baseline NCV was 47.6(]SY.+-。[)6.8m/s (mean(]SY.+-。[)SE), and it reduced remarkably just after injury (11.8(]SY.+-。[)2.7m/s). Fourteen days after injury, NCV of Schwann group (30.3(]SY.+-。[)8.6m/s) was significantly greater than that of control group (11.2(]SY.+-。[)3.6m/s). However, immunocytochemistry failed to reveal transplanted Schwann cells around crush-injured nerve.From these results, transplantation of Schwann cells around crush-injured facial nerve may facilitate the nerve regeneration in the early period after crush-injury. However, it was difficult to determine the substance and mechanism of facilitation of the repair of injured nerves.
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S M Ekramullarh et al: "The correlation of Ki-67 staiing indices with tumour doubling times in recurrent non-functionig pituitary adenomas" Acta Neurochir. 138. 1449-1455 (1996)
S M Ekramullarh 等人:“复发性无功能垂体腺瘤中 Ki-67 染色指数与肿瘤倍增时间的相关性”Acta Neurochir。
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通讯作者:
Y.Saitoh et al.: "Absence of apoptosis in somato tropinomas treated with octreotide" Acta Neurochir. 139. 851-856 (1997)
Y.Saitoh 等人:“用奥曲肽治疗的体细胞促细胞凋亡不存在”Acta Neurochir。
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Y.Hagiwara et al: "Transplantation of the xencgeneic cells secreting β-endorphin for pain treatment : Aralysis of the permeability of complements through polymer capsules" Cell Transplantation. 6. 527-530 (1997)
Y.Hagiwara 等人:“分泌 β-内啡肽的异基因细胞移植用于疼痛治疗:补体通过聚合物胶囊的渗透性分析”细胞移植。
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S.Hiraga et al: "Establishment of spontaneously immortalized rat type 1 astroglial cell lines : The role of p53 in astroglial carcinogenesis." Glia. 18. 185-199 (1996)
S.Hiraga 等人:“自发永生化大鼠 1 型星形胶质细胞系的建立:p53 在星形胶质细胞癌变中的作用。”
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