Fitzwater Joseph L, Grande Kathryn B, Sailors Joseph L, Acevedo Jesus F, Word R Ann, Wai Clifford Y
Division of Female Pelvic Medicine and Reconstructive Surgery, Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Int Urogynecol J. 2015 Feb;26(2):251-6. doi: 10.1007/s00192-014-2496-5. Epub 2014 Sep 25.
The objective was to evaluate the effect of myogenic stem cells on histological properties and the volume of striated muscle of the external anal sphincter after transection and repair.
Histological analysis was performed on the external anal sphincters of 40 young female rats euthanized at 7 or 90 days after transection and repair and randomization to injection of either phosphate buffered solution (PBS) or myogenic stem cells (SC) at the transection site. Sphincter complexes, previously evaluated for neurophysiological function, were processed for histology and analyzed for possible disruption, amount of inflammation, and volume of striated muscle. The relationship between the muscular disruption and contractile force of sphincters was evaluated.
Disruption was seen in 100 % of sphincters 7 days after repair for both SC and control animals. Eighty-nine percent of controls and 78% of SC-administered animals had intact sphincters at 90 days. Significant inflammatory infiltrate was seen in repaired anal sphincters for both the PBS and the SC groups at 7 days, and persisted at 90 days, with no difference between treatment groups. Striated muscle volume increased from 7 to 90 days for both control and SC-administered animals. Although there was no difference in volume between treatments, there was substantial temporal improvement in contractile force generation of the sphincters receiving SC compared with those receiving PBS.
In this animal model, administration of myogenic stem cells to transected/repaired anal sphincters did not alter the amount of inflammation nor the volume of striated muscle, suggesting that stem cells might improve contractile function through other cellular processes.
目的是评估肌源性干细胞对肛门外括约肌横断并修复后组织学特性及横纹肌体积的影响。
对40只年轻雌性大鼠的肛门外括约肌进行组织学分析,这些大鼠在横断并修复后7天或90天安乐死,并随机在横断部位注射磷酸盐缓冲溶液(PBS)或肌源性干细胞(SC)。之前已评估过神经生理功能的括约肌复合体进行组织学处理,并分析其可能的破坏情况、炎症量及横纹肌体积。评估肌肉破坏与括约肌收缩力之间的关系。
修复后7天,SC组和对照组动物的括约肌100%出现破坏。90天时,89%的对照组和78%接受SC注射的动物括约肌完整。PBS组和SC组修复后的肛门括约肌在7天时均出现明显的炎性浸润,并持续至90天,治疗组之间无差异。对照组和接受SC注射的动物横纹肌体积均从7天增加至90天。虽然治疗组之间体积无差异,但与接受PBS的动物相比,接受SC的括约肌在产生收缩力方面有显著的时间性改善。
在该动物模型中,向横断/修复的肛门括约肌施用肌源性干细胞并未改变炎症量或横纹肌体积,这表明干细胞可能通过其他细胞过程改善收缩功能。