Tauroursodeoxycholic Acid Reduces Neuroinflammation but Does Not Support Long Term Functional Recovery of Rats with Spinal Cord Injury

S.Y. Wu, C. Garcia-Rama, L. Romero-Ramirez, J.P.J.M. de Munter, E.C. Wolters, B.W. Kramer, J. Mey*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

The bile acid tauroursodeoxycholic acid (TUDCA) reduces cell death under oxidative stress and inflammation. Implants of bone marrow-derived stromal cells (bmSC) are currently under investigation in clinical trials of spinal cord injury (SCI). Since cell death of injected bmSC limits the efficacy of this treatment, the cytoprotective effect of TUDCA may enhance its benefit. We therefore studied the therapeutic effect of TUDCA and its use as a combinatorial treatment with human bmSC in a rat model of SCI. A spinal cord contusion injury was induced at thoracic level T9. Treatment consisted of i.p. injections of TUDCA alone or in combination with one injection of human bmSC into the cistern magna. The recovery of motor functions was assessed during a surveillance period of six weeks. Biochemical and histological analysis of spinal cord tissue confirmed the anti-inflammatory activity of TUDCA. Treatment improved the recovery of autonomic bladder control and had a positive effect on motor functions in the subacute phase, however, benefits were only transient, such that no significant differences between vehicle and TUDCA-treated animals were observed 1-6 weeks after the lesion. Combinatorial treatment with TUDCA and bmSC failed to have an additional effect compared to treatment with bmSC only. Our data do not support the use of TUDCA as a treatment of SCI.
Original languageEnglish
Article number1501
Number of pages25
JournalBiomedicines
Volume10
Issue number7
DOIs
Publication statusPublished - 1 Jul 2022

Keywords

  • bile acid
  • spinal cord injury
  • bone marrow-derived stromal cells
  • rat
  • neuroinflammation
  • RECEPTOR TGR5
  • BLADDER
  • PATHOPHYSIOLOGY
  • INFLAMMATION
  • AGONIST
  • CELLS

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