Cui Diansheng, Hu Liquan, Li Shiwen, Zheng Xinmin
Department of Urology, Zhongnan Hospital, Wuhan University, Wuhan, Hubei 430071, China.
Zhonghua Nan Ke Xue. 2004 May;10(5):330-3.
To investigate the restoration of erectile function by reconstructing cavernous nerves with sural nerve grafts.
Forty-eight male Sprague-Dawley rats(3-4 m old and 300-400 g) were randomly divided into three groups: the sham-operated group (n = 16) underwent pelvic exploration without transection of the cavernous nerve; the nerve ablation group (n = 16) had a 5 mm segment of the cavernous nerve excised bilaterally; the graft group (n = 16) had a 5 mm segment of the cavernous nerve excised bilaterally, followed by immediate microsurgical reconstruction with an interposition graft of the sural nerve. The cavernous nerves of each group were electrostimulated to determine their potency after 2 and 4 months. And fluorescent retrograde-transported material Fluoro-Gold(FG) was injected into the penis. FG-labeled neuron cells in whole mounts of major pelvic ganglions were observed five days after injection.
Electrical stimulation produced no erection in either the nerve ablation or the graft group, but 100% erection in the sham-operated group after 2 months. The numbers of FG-labeled neurons significantly differed between the nerve ablation group and the graft group. After 4 months erection examination showed statistical significance in the difference between the graft group and the nerve ablation group(P < 0.05). The FG-labeled neurons in the graft group significantly differed from those in the ablation (P < 0.05), and almost reached the level of the sham-operated(P < 0.05).
Cavernous nerve grafting can successfully restore erectile dysfunction in rats after surgical injury.
通过用腓肠神经移植重建海绵体神经来研究勃起功能的恢复情况。
48只雄性Sprague-Dawley大鼠(3 - 4月龄,体重300 - 400克)随机分为三组:假手术组(n = 16)进行盆腔探查但不切断海绵体神经;神经切除组(n = 16)双侧切除5毫米长的海绵体神经段;移植组(n = 16)双侧切除5毫米长的海绵体神经段,随后立即用腓肠神经进行显微外科间置移植重建。在2个月和4个月后对每组的海绵体神经进行电刺激以确定其功能。并将荧光逆行转运物质氟金(FG)注入阴茎。注射后五天观察主要盆腔神经节整装片中FG标记的神经元细胞。
电刺激在神经切除组和移植组均未引起勃起,但假手术组在2个月后100%勃起。神经切除组和移植组中FG标记的神经元数量有显著差异。4个月后的勃起检查显示移植组和神经切除组之间的差异具有统计学意义(P < 0.05)。移植组中FG标记的神经元与切除组有显著差异(P < 0.05),且几乎达到假手术组水平(P < 0.05)。
海绵体神经移植可成功恢复大鼠手术损伤后的勃起功能障碍。