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作 者:孔天翰[1] 范天生[1] 韩雪飞[1] 张建民[1] 雷留根[1] 马钊[1]
机构地区:[1]河南医科大学人体解剖学教研室
出 处:《神经解剖学杂志》1994年第3期223-228,共6页Chinese Journal of Neuroanatomy
摘 要:本实验利用大鼠坐骨神经钳夹损伤模型,观察了电针(A组)、直流刺激器(B组)及双向平衡电脉冲刺激器(C组)对神经损伤后自残及神经再生的影响,D组为对照。结果:(1)术后17d,C组的右后足趾自残率为13%,而A、B及D组分别为46%、53%及80%,C组的自残率显著低于其它各组(P<0.001);(2)右侧屈肌反射阈:当刺激强度为35±5V(C组)、45±5V(A和B组)时,可引出短潜伏期(45~150ms)的A类及长潜伏期(125~525ms)C类传入纤维反应,而当刺激强度增至65±5V时,于D组仅见长潜伏期(190~600ms)的C类传入纤维反应;(3)术后17d脊神经节的标记细胞百分享分别为11.1%(C组)、5.7%(B组)、5.2%(A组)及1.1%(D组);脊髓前角的标记细胞百分率分别为16.6%(C组)、8.1%(8组)、7.4%(A组)及1.9%(D组)。上述结果表明:双向平衡电脉冲刺激器在抑制神经损伤后自残及促进周围神经再生等方面具有更显著的生理功效。In order to evaluate the effect of three kinds of electrical stimulation in relieving the neuropathic pain and in promoting the regeneration of peripheral nerves, an animal model of autotomy following sciatic nerve lesion was used in this study. 65 adult male Wistar rats were divided into 4(A, B, C and D) groups and the sciatic nerve of right side were crushed. 3days after operation, group A were treated with electroacupuncture(EA, 30 min/day, 10 Hz, 0.4 mA). group B with directcurrent(DC, 24h/day, 0.6 μA), group C with pulse current(MS, 24h/day, 10 Hz, 8μA)and group D as control. The anodic electrode of electrical stimulation in Huantiao (+) point and the cathode in Sanyinchiao(-) point. 17 days after operation.autotomy were checked first, then following experiment on bilateral side : (1)Saphenous nerve were transected;(2)The medial and lateral gastrocnemius were placed in recording electrode, the paw pad were placed in stimulating electrode, the pain threshold of the flexion reflex were observed ; (3) HRP injected into the gastrocnemius and the hypodermis of the paw pad, the labeled cells in the ganglion spinal (L4~L6) and cornu ventrale of spinal cord (L4~L6) were checked. (1)The percentage of autotomy in group C was 13%, 46% in group A, 53% in group B, 80% in group D; (2) The electromyographs(EMGs) from medial and latetal gastrocnemius on left side were evoked by both A-afferent fibers with a short latency (12ms) and C-afferent fibers with a longer latency(87 ms), the threshold of the flexion reflexis 4±0.5V. The stimulus strength from 35±5V (for group C) to 45±5V (for group A and B), the flexion reflex on right side were evoked by both A-afferent fibers with a short latency(45-150 ms)and C-afferent fibers with a longer latency(125-525 ms). Increasing the stimulus strength to 65±5V only produced a long latency (190~600ms) with a very long after-discharge in the gastrocnemius on right side of group D; (3) The small round labeled cells with heavy stain and the big round ones with light stain were
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