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大鼠坐骨神经再生过程中髓鞘蛋白的合成及超微结构研究

Synthesis of myelin proteins and ultrastructural investigations in regenerating rat sciatic nerve.

作者信息

Alberghina M, Bernocchi G, Biggiogera M, Viola M, Karlsson J O, Manfredi-Romanini M G, Giuffrida A M

出版信息

J Neurosci Res. 1985;13(4):551-62. doi: 10.1002/jnr.490130410.

Abstract

Myelin protein synthesis, as well as ultrastructural and morphometric changes in regenerating peripheral nerve, was studied. Sciatic nerves of rats were crushed unilaterally; sham-operated nerves of the contralateral side served as controls. For the in vivo experiments, rats were killed at selected periods after the nerves were crushed (30, 60, 90, and 120 days); seven days prior to killing, the animals were injected intravenously with L-[4,5-3H]leucine. For the in vitro experiments, proximal and distal segments of sciatic nerve and equivalent sham-operated nerves were labeled with 3H-amino acid mixture 90 days after axotomy. Purified myelin was isolated from nerve segments; specific radioactivity and gel electrophoretic patterns of proteins were analyzed. Cross-sectional electron microscope (EM) preparations of proximal, distal, and contralateral segments of nerves also were examined. Results showed that the incorporation of labeled amino acids into total myelin proteins was enhanced significantly in the distal segment of sciatic nerves at all of the periods of regeneration studied. The yield of myelin protein per mm distal nerve segment increased as regeneration proceeded. The remyelination of fibers early after nerve crush was weak, whereas it gradually attained the normal range 90-120 days after axotomy. Morphometric analysis of myelin sheath thickness of regenerating axons was consistent with the data obtained for myelin protein synthesis.

摘要

研究了再生周围神经中的髓鞘蛋白合成以及超微结构和形态计量学变化。对大鼠的坐骨神经进行单侧挤压;对侧假手术神经作为对照。对于体内实验,在神经挤压后的选定时间段(30、60、90和120天)处死大鼠;处死前7天,给动物静脉注射L-[4,5-³H]亮氨酸。对于体外实验,在轴突切断90天后,用³H-氨基酸混合物标记坐骨神经的近端和远端节段以及等效的假手术神经。从神经节段中分离纯化髓鞘;分析蛋白质的比放射性和凝胶电泳图谱。还检查了神经近端、远端和对侧节段的横断面电子显微镜(EM)标本。结果表明,在所研究的所有再生时间段内,坐骨神经远端节段中标记氨基酸掺入总髓鞘蛋白的量均显著增加。随着再生的进行,每毫米远端神经节段的髓鞘蛋白产量增加。神经挤压后早期纤维的髓鞘再生较弱,而在轴突切断后90-120天逐渐达到正常范围。再生轴突髓鞘厚度的形态计量学分析与髓鞘蛋白合成的数据一致。

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