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Author Notes:

Corresponding author: Jeffrey H. Boatright, PhD, Room B5511, Emory Eye Center, 1365B Clifton Road, NE, Atlanta, GA, 30322, jboatri@emory.edu

Subjects:

Research Funding:

We are grateful for support provided by the Abraham J. & Phyllis Katz Foundation (J.H.B.), NIH R01EY014026 (J.H.B.), R01EY021592 (J.M.N.), R01EY016470 (J.M.N.), VA RR&D C1924P I21RX001924 (J.H.B.), VA RR&D C9246C (Atlanta VA Center of Excellence in Visual and Neurocognitive Rehabilitation), P30EY006360, and an unrestricted grant to the Department of Ophthalmology at Emory University from Research to Prevent Blindness, Inc.

Keywords:

  • Animals
  • Brain-Derived Neurotrophic Factor
  • Clinical Studies as Topic
  • DNA Damage
  • DNA Repair
  • Exercise
  • Gene Editing
  • Humans
  • Neurodegenerative Diseases
  • Oxidative Stress

Exercise as Gene Therapy: BDNF and DNA Damage Repair

Tools:

Journal Title:

Asia-Pacific Journal of Ophthalmology

Volume:

Volume 5, Number 4

Publisher:

, Pages 309-311

Type of Work:

Article | Post-print: After Peer Review

Abstract:

DNA damage is a common feature of neurodegenerative illnesses, and the ability to repair DNA strand breaks and lesions is crucial for neuronal survival, reported by Jeppesen et al (Prog Neurobiol. 2011;94:166-200) and Shiwaku et al (Curr Mol Med. 2015;15:119-128). Interventions aimed at repairing these lesions, therefore, could be useful for preventing or delaying the progression of disease. One potential strategy for promoting DNA damage repair (DDR) is exercise. Although the role of exercise in DDR is not understood, there is increasing evidence that simple physical activity may impact clinical outcomes for neurodegeneration. Here, we discuss what is currently known about the molecular mechanisms of brain-derived neurotrophic factor and how these mechanisms might influence the DDR process.

Copyright information:

© 2006 Lippincott Williams & Wilkins.

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