Özay Rafet, Bekar Ahmet, Kocaeli Hasan, Karlı Necdet, Filiz Gülaydan, Ulus I Hakkı
Department of Neurosurgery, Uludağ University School of Medicine, 16059, Görükle, Bursa, Turkey.
Department of Neurosurgery, Uludağ University School of Medicine, 16059, Görükle, Bursa, Turkey.
Surg Neurol. 2007 Dec;68(6):615-622. doi: 10.1016/j.surneu.2006.12.054.
Citicoline has been shown to have beneficial effects in a variety of CNS injury models. The aim of this study was to test the effects of citicoline on nerve regeneration and scarring in a rat model of peripheral nerve surgery.
Seventy adult Sprague-Dawley rats underwent a surgical procedure involving right sciatic nerve section and epineural suturing. Rats were assigned to the control or experiment groups to receive a topical application of 0.4 mL of saline or 0.4 mL (100 micromol/L) of citicoline, respectively. Macroscopic, histological, functional, and electromyographic assessments of nerves were performed 4 to 12 weeks after surgery.
In the control versus citicoline-treated rats, SFI was -90 +/- 1 versus -84 +/- 1 (P < .001), -76 +/- 4 versus -61 +/- 3 (P < .001), and -66 +/- 2 versus -46 +/- 3 (P < .001) at 4, 8, and 12 weeks after surgery, respectively. At 12 weeks after surgery, axon count and diameter were 16400 +/- 600 number/mm(2) and 5.47 +/- 0.25 microm versus 22250 +/- 660 number/mm(2) (P < .001) and 6.65 +/- 0.28 microm (P < .01) in the control and citicoline-treated groups, respectively. In citicoline-treated rats, histomorphological axonal organization score at the repair site was (3.4 +/- 0.1) significantly better than that in controls (2.6 +/- 0.3) (P < .001). Peripheral nerve regeneration evaluated by EMG at 12 weeks after surgery showed significantly better results in the citicoline group (P < .05). Nerves treated with citicoline demonstrated reduced scarring at the repair site (P < .001).
Our results demonstrate that citicoline promotes regeneration of peripheral nerves subjected to immediate section suturing type surgery and reduces postoperative scarring.
在多种中枢神经系统损伤模型中,已证实胞磷胆碱具有有益作用。本研究旨在测试胞磷胆碱对大鼠周围神经手术模型中神经再生和瘢痕形成的影响。
70只成年Sprague-Dawley大鼠接受了一项手术,包括右侧坐骨神经切断和神经外膜缝合。将大鼠分为对照组和实验组,分别局部应用0.4 mL生理盐水或0.4 mL(100微摩尔/升)胞磷胆碱。术后4至12周对神经进行宏观、组织学、功能和肌电图评估。
在对照组和胞磷胆碱治疗组大鼠中,术后4、8和12周时的坐骨神经功能指数(SFI)分别为-90±1与-84±1(P<.001)、-76±4与-61±3(P<.001)以及-66±2与-46±3(P<.001)。术后12周时,对照组和胞磷胆碱治疗组的轴突计数和直径分别为16400±600个/mm²和5.47±0.25微米,以及22250±660个/mm²(P<.001)和6.65±0.28微米(P<.01)。在胞磷胆碱治疗组大鼠中,修复部位的组织形态学轴突组织评分(3.4±0.1)明显优于对照组(2.6±0.3)(P<.001)。术后12周通过肌电图评估的周围神经再生在胞磷胆碱组显示出明显更好的结果(P<.05)。用胞磷胆碱治疗的神经在修复部位的瘢痕形成减少(P<.001)。
我们的结果表明,胞磷胆碱可促进接受即刻切断缝合型手术的周围神经再生,并减少术后瘢痕形成。