Additive neuroprotective effects of creatine and cyclooxygenase 2 inhibitors in a transgenic mouse model of amyotrophic lateral sclerosis

Peter Klivenyi, Mahmoud Kiaei, Gabrielle Gardian, Noel Y. Calingasan, M. Flint Beal

Research output: Contribution to journalArticle

148 Citations (Scopus)

Abstract

There is substantial evidence implicating both inflammation and mitochondrial dysfunction in amyotrophic lateral sclerosis (ALS) pathogenesis. We investigated the therapeutic effects of cyclooxygenase 2 (COX-2) inhibitors both alone and in combination with creatine in the G93A transgenic mouse model of ALS, Oral administration of either celecoxib or rofecoxib significantly improved motor performance, attenuated weight loss and extended survival. The administration of COX-2 inhibitors significantly reduced prostaglandin E2 levels at 110 days of age. The combination of creatine with COX-2 inhibitors produced additive neuroprotective effects and extended survival by approximately 30%. The COX-2 inhibitors significantly protected against depletion of anterior horn motor neurons and creatine with COX-2 inhibitors showed greater protection than COX-2 inhibitors alone. These results suggest that combinations of therapies targeting different disease mechanisms may be a useful strategy in the treatment of ALS.

Original languageEnglish
Pages (from-to)576-582
Number of pages7
JournalJournal of neurochemistry
Volume88
Issue number3
DOIs
Publication statusPublished - Feb 1 2004

Keywords

  • Creatine
  • Cyclooxygenase
  • Free radicals
  • Mitochondria
  • Prostaglandin E2
  • Superoxide dismutase

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience

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