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面神经切断术和633纳米低功率激光治疗后,面神经运动核中降钙素基因相关肽mRNA的定量及神经元细胞死亡情况

Quantitation of calcitonin gene-related peptide mRNA and neuronal cell death in facial motor nuclei following axotomy and 633 nm low power laser treatment.

作者信息

Snyder Sara K, Byrnes Kimberly R, Borke Rosemary C, Sanchez Ana, Anders Juanita J

机构信息

Laboratory for Receptor Biology and Gene Expression, National Cancer Institute, Bethesda, Maryland 20892, USA.

出版信息

Lasers Surg Med. 2002;31(3):216-22. doi: 10.1002/lsm.10098.

Abstract

BACKGROUND AND OBJECTIVES

A persistent increase in calcitonin gene-related peptide (CGRP) immunoreactivity in motoneurons may serve as an indicator for regeneration after peripheral nerve injury [Borke et al., J Neurocytol 1993;22:141-153].

STUDY DESIGN/MATERIALS AND METHODS: We examined the effects of low power laser treatment (633 nm) on axotomy-induced changes in alpha-CGRP mRNA and long-term neuronal survival in facial motoneurons. A quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) assay for alpha-CGRP mRNA was used to detect changes in the response to axotomy and laser irradiation. Cell counts of neurons in injured and non-injured facial motor nuclei of laser-treated and non-treated rats were done to estimate neuronal survival.

RESULTS

A 10-fold increase (P < 0.0001) in mRNA for alpha-CGRP at 11 days post-transection and an almost threefold increase (P < 0.0001) in neuronal survival at 6-9 months post-transection were found in 633 nm light treated rats.

DISCUSSION

These findings demonstrate that 633 nm laser light upregulates CGRP mRNA and support the theory that laser irradiation increases the rate of regeneration, target reinnervation, and neuronal survival of the axotomized neuron.

摘要

背景与目的

运动神经元中降钙素基因相关肽(CGRP)免疫反应性持续增加可能是周围神经损伤后再生的一个指标[博尔克等人,《神经细胞杂志》1993年;22:141 - 153]。

研究设计/材料与方法:我们研究了低功率激光治疗(633纳米)对面神经运动神经元轴突切断诱导的α - CGRP mRNA变化及长期神经元存活的影响。采用针对α - CGRP mRNA的定量逆转录聚合酶链反应(RT - PCR)分析来检测对轴突切断和激光照射反应的变化。对激光治疗和未治疗大鼠的受伤和未受伤面神经运动核中的神经元进行细胞计数,以评估神经元存活情况。

结果

在633纳米光治疗的大鼠中,横断后11天α - CGRP mRNA增加了10倍(P < 0.0001),横断后6 - 9个月神经元存活增加了近3倍(P < 0.0001)。

讨论

这些发现表明633纳米激光上调CGRP mRNA,并支持激光照射增加轴突切断神经元的再生速率、靶标再支配和神经元存活的理论。

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