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Montelukast Improves Urinary Bladder Function After Complete Spinal Cord Injury in Rats
Elena E Keller1, Sophina Bauer2, Karin Roider1
1Institute of Molecular and Regenerative Medicine, Paracelsus Medical University, Strubergasse 21, 5020 Salzburg, Austria.
Early montelukast (MLK) treatment in rats with spinal cord injury (SCI) preserved bladder function. This pilot study suggests MLK may improve lower urinary tract (LUT) integrity after SCI.
Area of Science:
- Neuroscience
- Urology
- Pharmacology
Background:
- Spinal cord injury (SCI) frequently causes severe bladder dysfunction, impacting quality of life.
- Neuroinflammation in the lower urinary tract (LUT) is a suspected driver of neurogenic bladder dysfunction and fibrosis post-SCI.
- Leukotrienes are potent inflammatory mediators implicated in SCI-related LUT pathology.
Purpose of the Study:
- To investigate the therapeutic potential of early montelukast (MLK) administration.
- To assess MLK's effects on LUT function and structure following severe SCI in a rat model.
- To determine if MLK can mitigate SCI-induced bladder dysfunction.
Main Methods:
- Lewis rats (female, n=50) underwent T9 spinal cord transection and received a bladder catheter.
- Daily oral montelukast (MLK) treatment commenced on day one post-injury.
- Bladder and locomotor function were monitored, with subsequent histological and immunohistochemical analysis of bladder tissue.
Main Results:
- Clinically relevant MLK concentrations were achieved in plasma and cerebrospinal fluid post-SCI.
- Montelukast administration significantly improved bladder functionality in SCI rats.
- No significant impact of MLK on smooth muscle alignment or uroepithelial integrity was observed at this early time point.
Conclusions:
- Early, continuous oral MLK treatment shows promise in preserving LUT function after SCI.
- This pilot study provides initial evidence for MLK's potential in improving tissue integrity post-SCI.
- Further research is warranted to explore the long-term effects and mechanisms of MLK in SCI-related bladder dysfunction.
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