4.6 Review

Neurotransmitter CART as a New Therapeutic Candidate for Parkinson's Disease

Journal

PHARMACEUTICALS
Volume 6, Issue 1, Pages 108-123

Publisher

MDPI
DOI: 10.3390/ph6010108

Keywords

cocaine- and amphetamine- regulated transcript; mitochondria; antioxidant; dopamine; oxidative stress; neuroprotection

Funding

  1. American Heart Association [0565527Z]
  2. Department of Veterans Affair Merit Review Program
  3. National Institutes of Health (NIH) [AG028072, AG042178]
  4. National Center for Research Resources of NIH [RR000163]
  5. Office of Research Infrastructure Pro-grams (ORIP) of NIH [RR000163]
  6. NATIONAL CENTER FOR RESEARCH RESOURCES [K01RR000163, P51RR000163] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE ON AGING [R01AG042178, R01AG028072] Funding Source: NIH RePORTER

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Parkinson's disease (PD) is one of the most common neurodegenerative diseases. To date, there is no effective treatment that halts its progression. Increasing evidence indicates that mitochondria play an important role in the development of PD. Hence mitochondria-targeted approaches or agents may have therapeutic promise for treatment of the disease. Neuropeptide CART (cocaine-amphetamine-regulated transcript), a hypothalamus and midbrain enriched neurotransmitter with an antioxidant property, can be found in mitochondria, which is the main source of reactive oxygen species. Systemic administration of CART has been found to ameliorate dopaminergic neuronal loss and improve motor functions in a mouse model of PD. In this article, we summarize recent progress in studies investigating the relationship between CART, dopamine, and the pathophysiology of PD, with a focus on mitochondria-related topics.

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