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Published on: May 29, 2019
42-Day Repeated Oral 6PPD-Quinone Exposure Is Associated with Splenic Injury, Reduced mtDNA Abundance, and
Yuyi Zhang1, Linlin Fu1, Shuqi Zhang1
1College of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, People's Republic of China.
Abstract:
6PPD-quinone (6PPD-Q), a tire rubber-derived contaminant, has raised concern because of its widespread occurrence and potential systemic toxicity. Here, we examined splenic injury and associated innate immune signaling changes after repeated oral 6PPD-Q exposure. Male C57BL/6 mice received 60μg/kg/day 6PPD-Q by oral gavage for 42 days. Exposure was associated with a reduced spleen index and histopathological disruption, together with increased MDA and 8-OHdG and altered antioxidant indices. qPCR targeting D-loop, CYTB, ND1, and ND4 showed reduced relative mtDNA abundance; these measurements do not directly establish structural mtDNA damage or cytosolic mtDNA release. Concurrently, cGAS-STING-related protein changes and increased phosphorylation ratios of STING, TBK1, and IRF3 were observed, accompanied by NF-κB-related signaling changes. NLRP3-, ASC-, GSDMD-, and inflammatory cytokine-related markers also changed, consistent with altered NLRP3- and pyroptosis-associated signaling. Because cytosolic mtDNA, pathway-specific intervention, and direct pyroptotic cell-death endpoints were not assessed, the observed molecular changes are interpreted as associations rather than evidence of a causal mtDNA-cGAS-STING-pyroptosis axis. These findings identify the spleen as a potential target of repeated 6PPD-Q exposure and provide evidence of splenic injury associated with altered redox status, reduced mtDNA abundance, and innate immune signaling changes.