Exposure to 6-PPD Quinone at Environmentally Relevant Concentrations Inhibits Both Lifespan and Healthspan in C. elegans .
Xin HuaDayong WangPublished in: Environmental science & technology (2023)
N -(1,3-Dimethylbutyl)- N '-phenyl- p -phenylenediamine (6-PPD), one of the most common additives used in rubber, enters the environment due to significant emissions of tire wear particles. 6-PPD quinone (6-PPDQ) is an important derivative of 6-PPD after ozonization. With concentrations ranging from nanograms per liter to μg/L, 6-PPDQ has so far been identified in a series of water samples. Acute lethality of 6-PPDQ in coho salmon (LC 50 < 1 μg/L) was lower than environmental concentrations of 6-PPDQ, highlighting the environment exposure risks of 6-PPDQ. It is becoming increasingly necessary to investigate the potential toxicity of 6-PPDQ at environmental concentrations. Here, we examined the effect of 6-PPDQ exposure on lifespan and healthspan and the underlying mechanism in Caenorhabditis elegans . Exposure to 6-PPDQ (1 and 10 μg/L) shortened the lifespan. Meanwhile, during the aging process, 6-PPDQ (0.1-10 μg/L) could decrease both pumping rate and locomotion behavior, suggesting the 6-PPDQ toxicity on healthspan. For the underlying molecular mechanism, the dysregulation in the insulin signaling pathway was linked to toxicity of 6-PPDQ on lifespan and healthspan. In the insulin signaling pathway, DAF-2 restricted the function of DAF-16 to activate downstream targets (SOD-3 and HSP-6), which in turn controlled the toxicity of 6-PPDQ on lifespan and healthspan. Additionally, in response to 6-PPDQ toxicity, insulin peptides (INS-6, INS-7, and DAF-28) could activate the corresponding receptor DAF-2. Therefore, exposure to 6-PPDQ at environmentally relevant concentrations potentially causes damage to both lifespan and healthspan by activating insulin signaling in organisms.
Keyphrases
- signaling pathway
- type diabetes
- oxidative stress
- human health
- glycemic control
- pi k akt
- risk assessment
- induced apoptosis
- liver failure
- oxide nanoparticles
- metabolic syndrome
- heat shock protein
- intensive care unit
- skeletal muscle
- high resolution
- cell proliferation
- adipose tissue
- drug induced
- hepatitis b virus
- heat stress
- fluorescent probe
- heavy metals
- endoplasmic reticulum stress
- simultaneous determination