Effects and mechanisms of sub-chronic exposure to copper nanoparticles on renal cytochrome P450 enzymes in rats

Environ Toxicol Pharmacol. 2018 Oct:63:135-146. doi: 10.1016/j.etap.2018.08.004. Epub 2018 Aug 7.

Abstract

Copper nanoparticles (Cu NPs) have widespread application because of their special physicochemical characteristics, however we need to more clearly study the toxicity mechanism of Cu NPs to ensure its safe use in pharmaceutical and animal feed. Thus, the aim of this study was to evaluate the effects and mechanisms of sub-chronic exposure to Cu NPs on renal CYP450 s of rats. In this study, we investigated the effects of Cu NPs on renal oxidative stress, cytokines and histopathology of rats. We found that Cu NPs (200 mg/kg) significantly disordered the function and structure of the kidney and caused a dose-dependent increase in oxidative stress and cytokines, which significantly decreased the levels of mRNA, protein, and activity of CYP450 s. Micro-coppers (Cu MPs) and Cu ions have similar effects, but their effects on CYP450 s were weaker than Cu NPs. The expression of nuclear receptors were inhibited and the expression of Akt, STAT3/5, CREB, p70S6K, NF-κB, P38 and ERK1/2 were activated when the inhibition effects of CYP450 s activity were observed in renal of rats. Therefore, we believe that Cu NPs can activate the STAT, NF-κB and MAPK signaling pathways to down-regulate the expression and activity of CYP450 s by inducing oxidative stress and inflammatory response in rat kidney.

Keywords: Copper nanoparticles; Inflammation; Oxidative stress; Renal cytochrome P450s; Signaling pathway.

MeSH terms

  • Animal Feed / toxicity
  • Animals
  • Copper / toxicity*
  • Cytochrome P-450 Enzyme System / genetics*
  • Cytochrome P-450 Enzyme System / metabolism*
  • Cytokines / metabolism
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation / drug effects
  • Kidney / drug effects*
  • Kidney / enzymology
  • Kidney / immunology
  • Male
  • Metal Nanoparticles / chemistry*
  • Metal Nanoparticles / toxicity
  • Oxidative Stress
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / drug effects
  • Toxicity Tests, Subchronic

Substances

  • Cytokines
  • Copper
  • Cytochrome P-450 Enzyme System