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    Home > Biochemistry News > Biotechnology News > Exercise may be key to developing treatments for rare movement disorders

    Exercise may be key to developing treatments for rare movement disorders

    • Last Update: 2022-10-03
    • Source: Internet
    • Author: User
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    Spinal cerebellar ataxia (SCA6) is an inherited neurological disorder that has a debilitating effect


    Now, a research team at McGill University that specializes in SCA6 and other forms of ataxia has published a study that not only offers hope for SCA6 patients, but may also open the way


    Exercise with tablets

    A team of researchers led by Alanna Watt, a professor of biology at McGill University, found that in mice affected by SCA6, exercise restored the health of cerebellum cells, the part of


    Early intervention is essential

    The researchers also found that BDNF levels in SCA6 mice declined before mobility difficulties began to appear


    "It's not something we really know about SCA6," said


    Activation of TrkB - Akt signaling rescues deficits in a mouse model of SCA6

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