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  4. Upregulated 5-HT1A Receptors Regulate Lower Urinary Tract Function in Rats after Complete Spinal Cord Injury

Upregulated 5-HT1A Receptors Regulate Lower Urinary Tract Function in Rats after Complete Spinal Cord Injury

Journal of Neurotrauma, 2023 · DOI: 10.1089/neu.2022.0329 · Published: May 1, 2023

Spinal Cord InjuryUrologyNeurology

Simple Explanation

Spinal cord injuries can lead to bladder dysfunction, including detrusor hyperreflexia, which involves low bladder compliance and increased pressure. This study investigates the role of serotonin 1A (5-HT1A) receptors in this dysfunction. The research team examined how blocking 5-HT1A receptors affects bladder and urethral sphincter activity in rats with and without spinal cord injuries using pharmacological interventions. The findings suggest that 5-HT1A receptors play a significant role in regulating lower urinary tract function after spinal cord injury, indicating a potential therapeutic target.

Study Duration
2 months
Participants
42 adult female Sprague-Dawley rats
Evidence Level
Level II, Animal Study

Key Findings

  • 1
    The study identified significant upregulation of the 5-HT1A receptor in the T10-L2 and L6/S1 spinal segments after chronic complete SCI.
  • 2
    Blocking the 5-HT1A receptor resulted in inhibitory effects on non-voiding contractions (NVCs) in SCI rats, reducing their number and amplitude.
  • 3
    The reduction of NVCs observed by WAY100635 may be the result of blocking the constitutive activities of the 5-HT1A receptor but activating the beta-adrenergic sympathetic pathway, which in turn relaxes bladder activity.

Research Summary

This study investigates the role of the 5-HT1A receptor in regulating lower urinary tract (LUT) function after spinal cord injury (SCI) in rats. It examines the expression levels of the 5-HT1A receptor in segments both rostral and caudal to the injured site. The results showed a significant upregulation of the 5-HT1A receptor in the T10-L2 and L6/S1 segments after chronic complete SCI. Pharmacological blockade of the 5-HT1A receptor also altered detrusor and external urethral sphincter (EUS) activities. The findings suggest that the neuroplasticity of the 5-HT1A receptor can be a potential therapeutic target for the treatment of bladder dysfunction after SCI.

Practical Implications

Therapeutic Target

The 5-HT1A receptor can be a potential therapeutic target for treatment of bladder dysfunction after SCI.

Pharmacological Interventions

Pharmacological interventions targeting the 5-HT1A receptor may help manage neurogenic detrusor overactivity.

Bladder Relaxation

Blocking the constitutive activities of the 5-HT1A receptor may activate the beta-adrenergic sympathetic pathway, which in turn relaxes bladder activity.

Study Limitations

  • 1
    Species-dependent differences in the influence of the 5-HT1A receptor on micturition.
  • 2
    The study was performed on female rats only, and results may differ in males.
  • 3
    The interaction of WAY100635 with dopamine receptors was not fully explored.

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