[Effect of acupuncture on the expression of NT3 in the process of spinal plasticity].

Tinghua Wang, Liangfang Wu, Deyang Liao, Xue Zhou, Yanhong Chen, A Takeda
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Abstract

Objective: To explore the change in the expression of NT3 in the process of promoting the plasticity of spinal cord by acupuncture.

Methods: Five adult cats were subjected to unilateral spared root rhizotomy; their L1-L5, L7-S2 dorsal root ganglia (DRG) were sectioned, but L4 was spared. And two groups of acupoints [Zusani (St.36) and Xuanzhong (G. B.39); Futu (St.32) and Sanyingjiao (Sp.6)] located in hind limb were electro-stimulated for thirty minutes q.d. x 7. At seven days, after acupuncture, the L5 segment of spinal cord and spared dorsal root ganglion (L6) were taken and made into frozen section 20 microns in thickness. Immunohistochemistry (NT3 antibody 1:1500) and in situ hybridization (NT3 cRNA probe 1:100) techniques were used. The numbers of positive neuron for NT3 and it's mRNA in large, medium, small neuron of L6 DRG and the numbers of positive neurons and glia cells for NT3 in lamina II were counted respectively.

Results: The numbers of positive large, small neurons for NT3 and its mRNA in DRG and the number of positive neurons and glia cells for NT3 in lamina II on the acupuncture side increased apparently than those on the non-acupuncture side (P < 0.05). However, the positive signal of NT3 mRNA in lamina II was not seen in our study.

Conclusion: The results indicate that acupuncture promoting the plasticity of spinal cord involves both the increase in expression of NT3 in large and small neurons of spared DRG and the increase in number of NT3 positive neurons and glia cells in spinal lamina II. Moreover, NT3 may play a role in the process of promoting the plasticity of spinal cord by acupuncture.

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针刺对脊柱可塑性过程中NT3表达的影响。
目的:探讨针刺促进脊髓可塑性过程中NT3表达的变化。方法:对5只成年猫进行单侧留根切断术;切除L1-L5、L7-S2背根神经节(DRG),保留L4。两组穴位[足尼穴(St.36)和宣中穴(G. B.39);后肢扶背(St.32)和三阴角(Sp.6)]每隔7天电刺激30分钟。针刺后第7天,取脊髓L5节段和余留的背根神经节(L6)制成厚度为20微米的冷冻切片。采用免疫组化(NT3抗体1:1500)和原位杂交(NT3 cRNA探针1:10 00)技术。分别计数L6 DRG大、中、小神经元中NT3阳性神经元及其mRNA的数量,II层中NT3阳性神经元及胶质细胞的数量。结果:针刺侧大鼠DRG中NT3大、小阳性神经元及其mRNA数量、II层NT3阳性神经元及胶质细胞数量均明显高于非针刺侧(P < 0.05)。然而,在我们的研究中没有看到II层nt3mrna的阳性信号。结论:针刺对脊髓可塑性的促进作用既涉及到保留DRG大、小神经元中NT3表达的增加,也涉及到脊髓II层中NT3阳性神经元和胶质细胞数量的增加。此外,NT3可能在针刺促进脊髓可塑性的过程中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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