[Protective mechanism of electroacupuncture combined with acellular nerve allografts on spinal ganglia in rats with sciatic nerve injury].

An-Te Li, Ze-Yu Zhou, Yun-Han Ma, Yu-Meng Hu, Jia-Rui Li, Zi-Ye Wang, Zi-Xuan Wang, Jia-Zhang Wang, Xiu-Mei Fu
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Abstract

Objective: To observe the effects of electroacupuncture (EA) combined with acellular nerve allograft (ANA) on the morphological structure of spinal ganglion cells and the protein expressions of nerve growth factor (NGF) and phosphorylated protein kinase B (p-Akt) in rats with sciatic nerve injury (SNI), so as to explore the protective mechanism of EA combined with ANA on spinal ganglia.

Methods: SPF male SD rats were randomly divided into normal, model, single ANA bridging (bridging) and EA + ANA (combination) groups, with 10 rats in each group. The SNI rat model was established by right sciatic nerve transection. Rats in the bridging group were bridged with ANA to the two broken ends of injured sciatic nerves. Rats in the combination group were treated with EA at "Yanglingquan" (GB34) and "Huantiao" (GB30) 2 d after ANA bridging, with dilatational wave, frequency of 1 Hz/20 Hz, intensity of 1 mA, 15 min/d, 7 d as a course of treatment for 4 consecutive courses. Sciatic function index (SFI) was observed by footprint test. Wet weight ratio of tibialis anterior muscle was calculated after weighing. Morphology of rat spinal ganglion cells was observed after Nissl staining. The protein expressions of NGF and p-Akt were detected by immunofluorescence and Western blot.

Results: Compared with the normal group, the SFI and wet weight ratio of tibialis anterior muscle were significantly decreased (P<0.05), the number of Nissl bodies in spinal ganglion cells was significantly reduced (P<0.05) with dissolution and incomplete structure, the protein expressions of NGF and p-Akt in ganglion cells were significantly decreased (P<0.05) in the model group. Following the interventions and in comparison with the model group, the SFI and the wet weight ratio of tibialis anterior muscle were significantly increased (P<0.05), the damage of Nissl bodies in ganglion cells was reduced and the number was obviously increased (P<0.05), and the protein expressions of NGF and p-Akt in ganglion cells were significantly increased (P<0.05) in the bridging and combination groups. Compared with the bridging group, the SFI and the wet weight ratio of tibialis anterior muscle were increased (P<0.05), the morphology of Nissl bodies in ganglion cells was more regular and the number was increased (P<0.05), the protein expressions of NGF and p-Akt in spinal ganglion cells were significantly increased (P<0.05) in the combination group.

Conclusion: EA combined with ANA can improve the SFI and the wet weight ratio of tibialis anterior muscle in SNI rats, improve the morphology and structure of Nissl bodies in spinal ganglion cells, and increase the protein expressions of NGF and p-Akt in spinal ganglion, so as to play a protective role on spinal ganglia.

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[电针联合脱细胞神经同种异体移植对坐骨神经损伤大鼠脊髓神经节的保护机制]。
目的:观察电针(EA)联合脱细胞神经异体移植(ANA)对坐骨神经损伤大鼠脊髓神经节细胞形态结构及神经生长因子(NGF)、磷酸化蛋白激酶B (p-Akt)蛋白表达的影响,探讨电针(EA)联合脱细胞神经异体移植(ANA)对脊髓神经节的保护机制。方法:将SPF级雄性SD大鼠随机分为正常组、模型组、单ANA桥接组(桥接)和EA + ANA(联合)组,每组10只。采用右侧坐骨神经横断法建立SNI大鼠模型。桥接组大鼠用ANA桥接损伤坐骨神经断端。联合组大鼠于ANA桥接后2 d给予“阳陵泉”(GB34)和“欢条”(GB30) EA,以扩张波治疗,频率为1 Hz/20 Hz,强度为1 mA, 15 min/d, 7 d为一个疗程,连续4个疗程。采用足迹法观察坐骨功能指数(SFI)。称重后计算胫骨前肌湿重比。采用尼氏染色法观察大鼠脊髓神经节细胞形态。免疫荧光和Western blot检测NGF和p-Akt蛋白的表达。结果:与正常组比较,大鼠胫前肌SFI和湿重比明显降低(ppppppppppp)。结论:EA联合ANA可改善SNI大鼠胫前肌SFI和湿重比,改善脊髓神经节细胞内尼氏体的形态和结构,增加脊髓神经节内NGF和p-Akt的蛋白表达,从而对脊髓神经节起到保护作用。
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