Lewin-Kowalik Joanna, Marcol Wiesław, Larysz-Brysz Magdalena, Wolwender Katarzyna, Pietrucha-Dutczak Marita, Górka Dariusz
Department of Physiology, Silesian Medical University, Katowice, Poland.
Med Sci Monit. 2002 Oct;8(10):BR414-20.
Peripheral nerve regeneration after traumatic injury and standard repair with a nerve autograft is often incomplete and results in neuropathic pain. Peripheral nerve extracts applied to the proximal nerve stump by means of autologous, dead-ended connective tissue chambers (deCTC) are known to accelerate the rate of axon regeneration. This study tested if such extracts would influence autotomy, which is a behavioral measure of neuropathic pain in animal models.
MATERIAL/METHODS: The study was performed on Wistar rats. DeCTCs, filled with postmicrosomal fraction obtained from 7-day-predegenerated nerves (7D group) or fibrin (F group), were implanted into transected sciatic nerve. In the control group (C), sciatic nerve was transected and its distal part was removed. The self-mutilation behavior in rats was assessed daily for seven weeks after sciatic nerve transection. The onset as well as intensity of autotomy was measured. The progress of regeneration was assessed under light microscopy and histochemistry.
The earliest onset and greatest severity of autotomy were found in the 7D group. Regeneration progress was also highest in this group. In the F group, we found weaker regeneration and less autotomy. The control group showed no regeneration, but more autotomy than the F group.
Intensified autotomy may be the price paid for enhanced peripheral nerve regeneration after application of growth-promoting substances.
创伤性损伤后周围神经再生以及采用自体神经移植进行标准修复往往并不完全,且会导致神经性疼痛。已知通过自体、盲端结缔组织腔室(deCTC)将周围神经提取物应用于近端神经残端可加速轴突再生速度。本研究测试了此类提取物是否会影响自残行为,这是动物模型中神经性疼痛的一种行为指标。
材料/方法:本研究以Wistar大鼠为对象。将填充有从7天前退变神经获得的微粒体后组分的deCTC(7D组)或纤维蛋白(F组)植入切断的坐骨神经中。在对照组(C组)中,切断坐骨神经并切除其远端部分。在坐骨神经切断后七周内每天评估大鼠的自残行为。测量自残行为的起始时间和强度。在光学显微镜和组织化学下评估再生进程。
7D组出现了最早的自残行为起始时间和最严重的自残程度。该组的再生进程也最高。在F组中,我们发现再生较弱且自残行为较少。对照组未出现再生,但自残行为比F组更多。
强化的自残行为可能是应用促生长物质后周围神经再生增强所付出的代价。