4.3 Article

Effects of real-ambient PM2.5 exposure plus lipopolysaccharide on multiple organ damage in mice

Journal

HUMAN & EXPERIMENTAL TOXICOLOGY
Volume 41, Issue -, Pages -

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/09603271211061505

Keywords

PM2.5; lipopolysaccharide; multi-organ injury; pathology; mice

Categories

Funding

  1. National Natural Science Foundation of China [91843301]
  2. Project on Social Development by the Shanxi Science and Technology Department [201903D321079]

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This study explored the toxicological effects of co-exposure of PM2.5 and LPS on different organs of mice. The results showed that co-exposure led to pathological tissue injury in multiple organs, with the spleen and kidney being more sensitive.
Background: The toxicological effects of fine particulate matter (PM2.5) on the cardiopulmonary and nervous systems have been studied widely, whereas the study of PM2.5 on systemic toxicity is not in-depth enough. Lipopolysaccharide (LPS) can cause multiple organ damage. The combined effects of co-exposure of PM2.5 plus LPS on the stomach, spleen, intestine, and kidney are still unclear. Purpose: This study was aimed to explore the toxicological effects of co-exposure of PM2.5 and LPS on the different organs of mice. Research Design and Study Sample Using a real-ambient PM2.5 exposure system and an intraperitoneal LPS injection mouse model, we investigated multiple organ damage effects on male BALB/c mice after co-exposure of PM2.5 plus LPS for 23 weeks in Linfen, a city with a high PM2.5 concentration in China. Data Collection: Eosin-hematoxylin staining, ELISA and the biochemical assay analysed the toxicological effects. Results: The pathological tissue injury on the four organs above appeared in mice co-exposed to PM2.5 plus LPS, accompanied by the body weight and stomach organ coefficient abnormality, and significant elevation of pro-inflammatory cytokines levels, oxidative stress in the spleen and kidney, and levels of kidney injury molecule (KIM-1) increase in the kidney. There were tissue differences in the pathological damage and toxicological effects on mice after co-exposure, in which the spleen and kidney were more sensitive to pollutants. In the PM2.5 + LPS group, the superoxide dismutase inhibition and catalase (CAT) activity promotion in the kidney or spleen of mice were significant relative to the PM2.5 group; the CAT and interleukin-6 (IL-6) levels in the spleen were raised considerably compared with the LPS group. Conclusions: These findings suggested the severity and sensitivity of multiple organ injuries in mice in response to PM2.5 plus LPS.

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