The impact of polar fraction of the fine particulate matter on redox responses in different rat tissues

Environ Sci Pollut Res Int. 2019 Nov;26(31):32476-32487. doi: 10.1007/s11356-019-06452-9. Epub 2019 Oct 15.

Abstract

Particulate matter (PM) contains different chemical substances that have been associated with health effects and an increased risk of mortality due to their toxicity. In this study, fine particulate matter (PM2.5) samples were collected in a region with rural characteristics (Seropédica (Se)) and another with some industries (Duque de Caxias (DC)) (Brazil, RJ). Rats were exposed to PM2.5 extracts daily for 25 days at different dilutions: 10×, 5×, and a concentrated solution (CS). Biochemical analyses were investigated for total antioxidant capacity (ACAP), lipid peroxidation (LPO) levels, reduced glutathione (GSH) concentration, activity of glutamate cysteine ligase (GCL), and activity of glutathione S-transferase (GST). The liver showed a significant increase in GCL (DC-5×, DC-CS and Se-CS) and GST activities (DC-CS and Se-CS) in both regions when compared to the control group. In the renal cortex, GCL activity decreased in most of the tested groups while GST activity increased only in the 5× groups of both regions (DC and Se). In the renal medulla, GCL activity decreased for Se-10× and DC-CS but increased for Se-5×, and GST activity increased in the Se-10×, DC-5×, and DC-CS groups. Lung GCL increased in all groups for both regions. Moreover, this organ also showed an increase in GST activity when higher metal concentrations were present (5× and CS). TBARS levels were increased for all tissues in most tested concentrations. These data indicate that soluble compounds (e.g., metals) from PM2.5 sampled in areas with different pollution indexes can change the redox status and cause damage to different tissues.

Keywords: Glutamate cysteine ligase; Glutathione; Glutathione S-transferase; Lipoperoxidation; Particulate matter.

MeSH terms

  • Animals
  • Antioxidants / metabolism*
  • Glutamate-Cysteine Ligase
  • Glutathione / metabolism*
  • Glutathione Transferase / metabolism
  • Lipid Peroxidation / drug effects*
  • Liver / drug effects*
  • Lung / drug effects*
  • Metals / chemistry
  • Oxidative Stress / drug effects*
  • Particulate Matter / chemistry
  • Particulate Matter / metabolism*
  • Rats
  • Thiobarbituric Acid Reactive Substances / chemistry
  • Thiobarbituric Acid Reactive Substances / metabolism*

Substances

  • Antioxidants
  • Metals
  • Particulate Matter
  • Thiobarbituric Acid Reactive Substances
  • Glutathione Transferase
  • GCLM protein, human
  • Glutamate-Cysteine Ligase
  • Glutathione