1. Academic Validation
  2. Beneficial effects of glatiramer acetate in Huntington's disease mouse models: Evidence for BDNF-elevating and immunomodulatory mechanisms

Beneficial effects of glatiramer acetate in Huntington's disease mouse models: Evidence for BDNF-elevating and immunomodulatory mechanisms

  • Brain Res. 2017 Oct 15;1673:102-110. doi: 10.1016/j.brainres.2017.08.013.
Jody Corey-Bloom 1 Alaina M Aikin 2 Ashley M Gutierrez 2 Jwan S Nadhem 2 Taylor L Howell 2 Elizabeth A Thomas 3
Affiliations

Affiliations

  • 1 Department of Neurosciences, University of California, San Diego, CA, USA.
  • 2 Department of Neuroscience, The Scripps Research Institute, La Jolla, CA, USA.
  • 3 Department of Neuroscience, The Scripps Research Institute, La Jolla, CA, USA. Electronic address: [email protected].
Abstract

Huntington's disease (HD) is a fatal, neurodegenerative movement disorder that has no cure and few treatment options. In these preclinical studies, we tested the effects of chronic treatment of glatiramer acetate (GA; Copaxone®), an FDA-approved drug used as first-line therapy for MS, in two different HD mouse models, and explored potential mechanisms of action of drug efficacy. Groups of CAG140 knock-in and N171-82Q transgenic mice were treated with GA for up to 1year of age (CAG140 knock-in mice) or 20weeks (N171-82Q mice). Various behavioral assays were measured over the course of drug treatment whereby GA treatment delayed the onset and reduced the severity of HD behavioral symptoms in both mouse models. The beneficial actions of GA were associated with elevated levels of promoter I- and IV-driven brain-derived neurotrophic factor (Bdnf) expression and reduced levels of cytokines, in particular, interleukins IL4 and IL12, in the brains of HD mice. In addition, the GA-induced effects on BDNF, IL4 and IL12 levels were detected in plasma from drug-treated mice and rats, suggesting utility as a peripheral biomarker of treatment effectiveness. These preclinical studies support the use of GA as a relevant clinical therapy for HD patients.

Keywords

Huntingtin; Striatum; Therapeutic.

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