Experimental and Molecular Medicine (Jun 2019)

Metformin treatment reduces motor and neuropsychiatric phenotypes in the zQ175 mouse model of Huntington disease

  • Ana Sanchis,
  • María Adelaida García-Gimeno,
  • Antonio José Cañada-Martínez,
  • María Dolores Sequedo,
  • José María Millán,
  • Pascual Sanz,
  • Rafael P. Vázquez-Manrique

DOI
https://doi.org/10.1038/s12276-019-0264-9
Journal volume & issue
Vol. 51, no. 6
pp. 1 – 16

Abstract

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Huntington’s disease: Diabetes drug limits disease-related degeneration in mice Metformin, an existing drug for diabetes, shows promise in alleviating symptoms of early Huntington’s disease in mouse models. Huntington’s disease is a genetic disorder that results in the gradual deterioration of motor skills and cognitive ability. It is caused by a defect in a single gene that then encodes a mutant huntingtin protein, which aggregates and kills brain cells. Growing observational evidence suggests that patients undergoing metformin treatment for diabetes type II exhibit fewer symptoms of age-related disease, as well as Huntington’s disease. Rafael Vázquez-Manrique at Hospital Universitario y Politécnico La Fe, València and Pascual Sanz at IBV-CSIC and CIBERER, València, and scientists across Spain used metformin to treat motor and neuropsychiatric symptoms in a Huntington’s mouse model. They found that metformin alleviated symptoms by actively reducing huntingtin levels, dispersing aggregations and limiting brain inflammation.