电针通过CD4和BDNF的协同作用促进脊髓挫伤大鼠神经再生和功能恢复

Ibrain Pub Date : 2022-07-26 DOI:10.1002/ibra.12055
Bao-Lei Zhang, Xi-Liang Guo
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引用次数: 0

摘要

探讨电针对大鼠脊髓损伤(SCI)免疫相关因素和再生相关因素的影响。采用PCI - 3000仪器建立脊髓挫伤模型。选择两种穴位对大鼠进行电针治疗。每周对大鼠进行1次实验,用磁共振成像技术检测纤维重构。对脊髓瘢痕样本进行转录组测序。使用Python编写代码,对转录组测序数据与纤维重建结果的相关性进行统计分析和生物信息学分析。最后,采用定量反转录聚合酶链反应(qRT-PCR)验证脊髓瘢痕组织中CD4和脑源性神经营养因子(BDNF)的表达。电针对脊髓损伤后大鼠运动功能恢复有积极作用。生物信息学分析发现CD4和BDNF之间有直接的相互作用。转录组测序和PCR结果证实,电针可显著降低脊髓损伤大鼠的CD4表达,显著增加BDNF表达,同时与脊髓损伤大鼠的神经再生相对应。我们的研究结果表明,电针干预通过抑制CD4的表达和增加BDNF的表达来改善脊髓损伤大鼠的神经行为。
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Electroacupuncture promotes nerve regeneration and functional recovery in rats with spinal cord contusion through the coordinate interaction of CD4 and BDNF

To explore the effect of electroacupuncture on spinal cord injury (SCI) involving immune-related factors and regeneration-related factors in rats. The model of spinal cord contusion was established by PCI 3000 instrument. Two types of acupuncture points were selected for electroacupuncture treatment on rats. The rats were tested once a week, and the fiber remodeling was detected by magnetic resonance imaging. Transcriptome sequencing was performed on spinal scar samples. Using Python to write code, statistical analysis and bioinformatics analysis of the correlation between transcriptome sequencing data and fiber reconstruction results are carried out. Lastly, the expression of CD4 and brain-derived neurotrophic factor (BDNF) in spinal cord scar was verified by quantitative reverse-transcription polymerase chain reaction (qRT-PCR). Electroacupuncture exhibited a positive effect on the recovery of motor function in rats after SCI. Bioinformatics analysis found a direct interaction between CD4 and BDNF. Transcriptome sequencing and PCR results verified that electroacupuncture significantly reduced the expression of CD4, and increased significantly the expression of BDNF, simultaneously corresponding to nerve regeneration in rats with SCI. Our results showed that electroacupuncture intervention in SCI rats improves neural behavior via inhibiting the expression of CD4 and increasing the expression of BDNF.

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