Full text is available at the source.
Abstract
Environmentally relevant concentrations of DCOIT (37, 370, and 3700 ng/L) significantly impaired both lifespan and healthspan in Caenorhabditis elegans.
- DCOIT exposure led to upregulation of comt-4, a gene involved in dopamine metabolism.
- Increased comt-4 activity resulted in dopamine depletion and higher oxidative stress levels.
- This oxidative stress is associated with accelerated aging phenotypes in the organism.
- Genetic and pharmacological interventions that targeted comt-4 restored dopamine levels and reduced oxidative stress.
- Restoring dopamine levels reversed the aging deficits caused by DCOIT exposure.
Simplified