{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T23:52:07Z","timestamp":1791330727525,"version":"4.3.1"},"reference-count":43,"publisher":"Korean Continence Society","issue":"3","license":[{"start":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T00:00:00Z","timestamp":1790726400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"funder":[{"DOI":"10.13039\/100008191","name":"Wings for Life","doi-asserted-by":"publisher","award":["198"],"award-info":[{"award-number":["198"]}],"id":[{"id":"10.13039\/100008191","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["einj.org"],"crossmark-restriction":true},"short-container-title":["Int Neurourol J"],"published-print":{"date-parts":[[2026,9,30]]},"abstract":"<jats:p>Purpose: Neurogenic lower urinary tract dysfunction (nLUTD) develops in nearly all patients after spinal cord injury (SCI). Evolving neuroinflammation is considered a key driver of secondary injury and is associated with worsening outcomes. However, few studies have examined treatments for nLUTD after SCI that specifically target these processes. This study investigated whether early montelukast therapy targeting proinflammatory leukotrienes improves long-term urological function and reduces pathological bladder remodeling.Methods: Female Lewis rats received a permanently implanted urinary catheter and underwent contusion SCI (Th8\/Th9) or sham surgery. Daily montelukast treatment began 1 day after injury and continued throughout the 2- or 6-month follow-up period. Injury severity and regeneration were evaluated using the Basso-Beattie-Bresnahan locomotor score and microcomputed tomography of the spinal cord. Bladder function was assessed through weekly urodynamic recordings in awake animals, and bladder structure was assessed by histological measurement of wall thickness. Transcriptomic and proteomic analyses were used to characterize the molecular processes underlying bladder remodeling.Results: Spinal cord tissue damage and functional impairment were comparable across animals, regardless of treatment. Montelukast did not improve urodynamic outcomes and was associated with transiently poorer functional scores during early recovery. Bladder wall thickness increased after SCI and was greatest in the treated groups, suggesting ongoing remodeling. Transcriptomic and proteomic analyses demonstrated marked activation of immune and contractility-related pathways in treated animals at 2 months. Animals followed for the longer period showed intensified immune signaling, indicating sustained inflammatory activity.Conclusions: Early montelukast treatment did not improve functional or structural urological outcomes after contusion SCI. The unfavorable functional trends and intensified inflammatory and injury-related pathways suggested adverse effects rather than therapeutic benefit under the conditions studied. These findings may indicate the importance of injury model-specific mechanisms and of dose and timing when developing anti-inflammatory strategies for SCI-induced nLUTD.<\/jats:p>","DOI":"10.5213\/inj.2652074.037","type":"journal-article","created":{"date-parts":[[2026,9,29]],"date-time":"2026-09-29T04:26:12Z","timestamp":1790655972000},"page":"254-265","update-policy":"https:\/\/doi.org\/10.5213\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Modulating Secondary Inflammation After Spinal Cord Injury Affects Pathological Bladder Remodeling"],"prefix":"10.5213","volume":"30","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-4057-0246","authenticated-orcid":true,"given":"Michael","family":"Kleindorfer","sequence":"first","affiliation":[{"name":"Institute of Molecular Regenerative Medicine, Paracelsus Medical Private University, Salzburg, Austria"},{"name":"Department of Urology and Andrology, Landeskrankenhaus\u2014University Clinic, Paracelsus Medical University, Salzburg, Austria"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0007-2792-3904","authenticated-orcid":true,"given":"Karin","family":"Roider","sequence":"additional","affiliation":[{"name":"Institute of Molecular Regenerative Medicine, Paracelsus Medical Private University, Salzburg, Austria"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2042-1139","authenticated-orcid":true,"given":"Katia","family":"Monastyrskaia","sequence":"additional","affiliation":[{"name":"Functional Urology Research Lab, DBMR and Department of Urology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3186-7478","authenticated-orcid":true,"given":"Akshay","family":"Akshay","sequence":"additional","affiliation":[{"name":"Functional Urology Research Lab, DBMR and Department of Urology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland"},{"name":"European Molecular Biology Laboratory (EMBL), Gene Biology Unit, Heidelberg, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2499-325X","authenticated-orcid":true,"given":"Patrick","family":"Heimel","sequence":"additional","affiliation":[{"name":"Core Facility Hard Tissue and Biomaterial Research, Karl Donath Laboratory, University Clinic of Dentistry, Medical University Vienna, Wien, Austria"},{"name":"Ludwig Boltzmann Institute for Traumatology, The Research Center in Cooperation with AUVA, Vienna, Austria"},{"name":"Austrian Cluster for Tissue Regeneration, Vienna, Austria"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5928-9492","authenticated-orcid":true,"given":"David","family":"Hercher","sequence":"additional","affiliation":[{"name":"Ludwig Boltzmann Institute for Traumatology, The 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