AI Article Synopsis

  • Paraoxonase-2 plays a key role in controlling reactive oxygen species in mitochondria, suggesting it is a target for therapies aimed at diseases linked to oxidative stress.
  • The anti-diabetic medication pioglitazone may offer protective benefits for neurodegenerative diseases and brain injuries, although the exact mechanisms behind this effect are not fully understood.
  • Research shows that administering pioglitazone at a specific dose for five days significantly boosts paraoxonase-2 levels in the mouse striatum, indicating its potential utility in exploring neuroprotection in the brain.

Article Abstract

Paraoxonase-2 regulates reactive oxygen species production in mitochondria. Stimulating its expression has therapeutic potential for diseases where oxidative stress plays a significant role in the pathology. Evidence suggests that the anti-diabetic drug pioglitazone may provide neuroprotection in Parkinson's disease, Alzheimer's disease, brain trauma and ischemia, but the biochemical pathway(s) responsible has not been fully elucidated. Here we report that pioglitazone (10 mg/kg/day) for 5 days significantly increased paraoxonase-2 expression in mouse striatum. Thus, this result highlights paraoxonase-2 as a target for neuroprotective strategies and identifies pioglitazone as a tool to study the role of paraoxonase-2 in brain.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089823PMC
http://dx.doi.org/10.1016/j.expneurol.2020.113234DOI Listing

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