1 Division of Urogynecology, Department of Obstetrics and Gynecology, University of California-Irvine, Orange, California 2 Department of Anatomy and Neurobiology, Reeve-Irvine Research Center, University of California-Irvine, Orange, California.
Dis Colon Rectum. 2013 Nov;56(11):1290-7. doi: 10.1097/DCR.0b013e3182a4adfb.
This study aims to evaluate in vivo function of the external anal sphincter after transection and repair augmented with myogenic stem cells, and to establish normative electromyography parameters of the rodent external anal sphincter.
Thirty-three Sprague-Dawley rodents underwent baseline needle electromyography of the external anal sphincter. Motor unit action potentials were obtained and normative parameters established. Animals were randomly assigned to a myogenic stem cell group (n = 24) or control group (n = 9). All underwent proctoepisiotomy. The control group underwent layered repair with phosphate-buffered saline injection to the external anal sphincter. The treatment group underwent identical repair with injection of myogenic stem cells 5.0 × 10. Baseline anal pressure recordings were collected and repeated 2 weeks postintervention, and electromyography was repeated at 2 and 4 weeks. Groups were compared across 3 time points with the use of repeated measures ANOVA.
The primary outcomes measured were the functional recovery of rat anal sphincters after stem cell transplantation as assessed by objective electromyography and anal pressure measures.
A mean of 17 motor unit action potentials were sampled per animal. At 2 weeks postrepair, there was a significant difference between control and transplant groups with respect to amplitude, duration, turns, and phases (p < 0.01 for each). No significant electromyography differences were seen at 4 weeks. Resting and peak anal pressures declined significantly at 2 weeks postinjury in the control but not in the stem cell group.
Use of a murine animal population limited the subjective feedback and wider applicability.
In vivo functional studies show recovery of anal sphincter pressures and electromyography to preinjury levels by day 14 in the myogenic stem cell group but not controls. At 4 weeks, all electromyography parameters returned to baseline irrespective of group. Restoration of function may be accelerated by the transplantation of myogenic stem cells and associated trophic factors.
本研究旨在评估经切断和修复后,外括约肌的体内功能,并建立啮齿动物外括约肌肌源性干细胞的正常肌电图参数。
33 只 Sprague-Dawley 大鼠进行了外括约肌针式肌电图的基线检查。获得运动单位动作电位并建立正常参数。动物随机分为肌源性干细胞组(n=24)或对照组(n=9)。所有动物均行直肠-肛门切开术。对照组行外括约肌分层修复,用磷酸盐缓冲盐水注射。治疗组行相同修复,注射肌源性干细胞 5.0×10。收集基线肛门压力记录,并在干预后 2 周重复,2 周和 4 周时重复肌电图。使用重复测量方差分析比较 3 个时间点的组间差异。
主要观察指标是通过客观肌电图和肛门压力测量评估干细胞移植后大鼠肛门括约肌的功能恢复情况。
每只动物平均采集 17 个运动单位动作电位。修复后 2 周,对照组和移植组在振幅、持续时间、匝数和相位方面存在显著差异(p<0.01)。4 周时未见明显肌电图差异。对照组在损伤后 2 周时,静息和峰值肛门压力显著下降,但干细胞组无此变化。
使用鼠类动物种群限制了主观反馈和更广泛的适用性。
体内功能研究显示,在肌源性干细胞组,外括约肌压力和肌电图在 14 天内恢复到损伤前水平,但对照组没有。4 周时,所有肌电图参数均恢复到基线水平,与组无关。移植肌源性干细胞和相关营养因子可能加速功能恢复。