Targeting p75 neurotrophin receptors ameliorates spinal cord injury‐induced detrusor sphincter dyssynergia in mice

摘要

Aims To determine the role of p75 neurotrophin receptor (p75 NTR ) and the therapeutic effect of the selective small molecule p75 NTR modulator, LM11A‐31, in spinal cord injury (SCI) induced lower urinary tract dysfunction (LTUD) using a mouse model. Methods Adult female T 8 ‐T 9 transected mice were gavaged daily with LM11A‐31 (100?mg/kg) for up to 6 weeks, starting 1 day before, or 7 days following injury. Mice were evaluated in vivo using urine spot analysis, cystometrograms (CMGs), and external urethral sphincter (EUS) electromyograms (EMGs); and in vitro using histology, immunohistochemistry, and Western blot. Results Our studies confirm highest expression of p75 NTRs in the detrusor layer of the mouse bladder and lamina II region of the dorsal horn of the lumbar‐sacral (L 6 ‐S 1 ) spinal cord which significantly decreased following SCI. LM11A‐31 prevented or ameliorated the detrusor sphincter dyssynergia (DSD) and detrusor overactivity (DO) in SCI mice, significantly improving bladder compliance. Furthermore, LM11A‐31 treatment blocked the SCI‐related urothelial damage and bladder wall remodeling. Conclusion Drugs targeting p75 NTRs can moderate DSD and DO in SCI mice, may identify pathophysiological mechanisms, and have therapeutic potential in SCI patients.