TY - JOUR
T1 - Multiple doses of stem cells maintain urethral function in a model of neuromuscular injury resulting in stress urinary incontinence
AU - Janssen, Kristine
AU - Lin, Dan Li
AU - Hanzlicek, Brett
AU - Deng, Kangli
AU - Balog, Brian M
AU - van der Vaart, Carl H
AU - Damaser, Margot S
N1 - Funding Information:
This work was supported by Cleveland Clinic and Rehabilitation Research and Development Service of the Department of Veterans Affairs Merit Review Award I01 RX000228-01A.
Publisher Copyright:
© 2019 American Physiological Society. All rights reserved.
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Stress urinary incontinence (SUI) is more prevalent among women who deliver vaginally than women who have had a cesarean section, suggesting that tissue repair after vaginal delivery is insufficient. A single dose of mesenchymal stem cells (MSCs) has been shown to partially restore urethral function in a model of SUI. The aim of the present study was to determine if increasing the number of doses of MSCs improves urethral and pudendal nerve function and anatomy. We hypothesized that increasing the number of MSC doses would accelerate recovery from SUI compared with vehicle treatment. Rats underwent pudendal nerve crush and vaginal distension or a sham injury and were treated intravenously with vehicle or one, two, or three doses of 2 × 10
6 MSCs at 1 h, 7 days, and 14 days after injury. Urethral leak point pressure testing with simultaneous external urethral sphincter electromyography and pudendal nerve electroneurography were performed 21 days after injury, and the urethrovaginal complex and pudendal nerve were harvested for semiquantitative morphometry of the external urethral sphincter, urethral elastin, and pudendal nerve. Two and three doses of MSCs significantly improved peak pressure; however, a single dose of MSCs did not. Single, as well as repeated, MSC doses improved urethral integrity by restoring urethral connective tissue composition and neuromuscular structures. MSC treatment improved elastogenesis, prevented disruption of the external urethral sphincter, and enhanced pudendal nerve morphology. These results suggest that MSC therapy for postpartum incontinence and SUI can be enhanced with multiple doses.
AB - Stress urinary incontinence (SUI) is more prevalent among women who deliver vaginally than women who have had a cesarean section, suggesting that tissue repair after vaginal delivery is insufficient. A single dose of mesenchymal stem cells (MSCs) has been shown to partially restore urethral function in a model of SUI. The aim of the present study was to determine if increasing the number of doses of MSCs improves urethral and pudendal nerve function and anatomy. We hypothesized that increasing the number of MSC doses would accelerate recovery from SUI compared with vehicle treatment. Rats underwent pudendal nerve crush and vaginal distension or a sham injury and were treated intravenously with vehicle or one, two, or three doses of 2 × 10
6 MSCs at 1 h, 7 days, and 14 days after injury. Urethral leak point pressure testing with simultaneous external urethral sphincter electromyography and pudendal nerve electroneurography were performed 21 days after injury, and the urethrovaginal complex and pudendal nerve were harvested for semiquantitative morphometry of the external urethral sphincter, urethral elastin, and pudendal nerve. Two and three doses of MSCs significantly improved peak pressure; however, a single dose of MSCs did not. Single, as well as repeated, MSC doses improved urethral integrity by restoring urethral connective tissue composition and neuromuscular structures. MSC treatment improved elastogenesis, prevented disruption of the external urethral sphincter, and enhanced pudendal nerve morphology. These results suggest that MSC therapy for postpartum incontinence and SUI can be enhanced with multiple doses.
KW - external urethral sphincter
KW - leak point pressure
KW - mesenchymal stem cells
KW - pudendal nerve
KW - rat
UR - http://www.scopus.com/inward/record.url?scp=85073083412&partnerID=8YFLogxK
U2 - 10.1152/ajprenal.00173.2019
DO - 10.1152/ajprenal.00173.2019
M3 - Article
C2 - 31411077
SN - 1931-857X
VL - 317
SP - F1047-F1057
JO - American journal of physiology. Renal physiology
JF - American journal of physiology. Renal physiology
IS - 4
ER -