4.6 Review

From Mitochondrial Function to Neuroprotection-an Emerging Role for Methylene Blue

期刊

MOLECULAR NEUROBIOLOGY
卷 55, 期 6, 页码 5137-5153

出版社

SPRINGER
DOI: 10.1007/s12035-017-0712-2

关键词

Methylene blue; Neuroprotection; Neurogenesis; Neurodegenerative disorders; Cognitive enhancement

资金

  1. National Institute of Neurological Disorders and Stroke, National Institutes of Health, USA [NS086929]
  2. American Heart Association [15GRNT25240004]

向作者/读者索取更多资源

Methylene blue (MB) is a well-established drug with a long history of use, owing to its diverse range of use and its minimal side effect profile. MB has been used classically for the treatment of malaria, methemoglobinemia, and carbon monoxide poisoning, as well as a histological dye. Its role in the mitochondria, however, has elicited much of its renewed interest in recent years. MB can reroute electrons in the mitochondrial electron transfer chain directly from NADH to cytochrome c, increasing the activity of complex IV and effectively promoting mitochondrial activity while mitigating oxidative stress. In addition to its beneficial effect on mitochondrial protection, MB is also known to have robust effects in mitigating neuroinflammation. Mitochondrial dysfunction has been identified as a seemingly unifying pathological phenomenon across a wide range of neurodegenerative disorders, which thus positions methylene blue as a promising therapeutic. In both in vitro and in vivo studies, MB has shown impressive efficacy in mitigating neurodegeneration and the accompanying behavioral phenotypes in animal models for such conditions as stroke, global cerebral ischemia, Alzheimer's disease, Parkinson's disease, and traumatic brain injury. This review summarizes recent work establishing MB as a promising candidate for neuroprotection, with particular emphasis on the contribution of mitochondrial function to neural health. Furthermore, this review will briefly examine the link between MB, neurogenesis, and improved cognition in respect to age-related cognitive decline.

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