Your browser doesn't support javascript.
loading
Bladder pain in an LL-37 interstitial cystitis and painful bladder syndrome model.
Jia, Wanjian; Schults, Austin J; Jensen, Mark Martin; Ye, Xiangyang; Alt, Jeremiah A; Prestwich, Glenn D; Oottamasathien, Siam.
Afiliación
  • Jia W; Division of Urology, Section of Pediatric Urology, University of UtahSalt Lake City, UT.
  • Schults AJ; Division of Urology, Section of Pediatric Urology, University of UtahSalt Lake City, UT.
  • Jensen MM; Department of Bioengineering, University of UtahSalt Lake City, UT.
  • Ye X; Department of Pharmacotherapy, University of UtahSalt Lake City, UT.
  • Alt JA; Center for Therapeutic Biomaterials, Department of Medicinal Chemistry, University of UtahSalt Lake City, UT.
  • Prestwich GD; Center for Therapeutic Biomaterials, Department of Medicinal Chemistry, University of UtahSalt Lake City, UT.
  • Oottamasathien S; Department of Surgery and Division of OtolaryngologySalt Lake City, UT.
Am J Clin Exp Urol ; 5(2): 10-17, 2017.
Article en En | MEDLINE | ID: mdl-29034266
ABSTRACT
Our goal was to evaluate the pain response in an LL-37 induced murine model for interstitial cystitis/painful bladder syndrome (IC/PBS). In particular, we sought to characterize the dose dependence, time-course, and relationship of LL-37 induced bladder inflammation and pain. The IC/PBS model was induced in C57Bl/6 mice by instilling 50 µL of LL-37, an immunomodulatory human cathelicidin (anti-microbial peptide), in the bladder for 1 hr. Pain responses were measured using von Frey filaments (0.04 gm to 4.0 gm) before and after LL-37 instillation. Inflammation was evaluated using tissue myeloperoxidase (MPO) assay, gross inspection, and microscopic histologic examination. The dose response experiment demonstrated a graded pain response, with higher concentrations of LL-37 challenge yielding higher pain responses across all stimuli tested. Statistical significance was seen when comparing 1.0 gm von Frey filament results at 320 µM (68 ± 8% response) vs. 0 µM (38 ± 6% response). Interestingly, pain responses did not attenuate across time but increased significantly after 5 (p=0.0012) and 7 days (p=0.0096). Comparison with MPO data suggested that pain responses could be independent of inflammation. We demonstrated within our LL-37 induced IC/PBS model pain occurs in a dose-dependent fashion, pain responses persist beyond the initial point of insult, and our dose response and time course experiments demonstrated that pain was independent of inflammation.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Am J Clin Exp Urol Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Am J Clin Exp Urol Año: 2017 Tipo del documento: Article
...