2,5-hexanedione-induced deregulation of axon-related microRNA expression in rat nerve tissues

Toxicol Lett. 2020 Mar 1:320:95-102. doi: 10.1016/j.toxlet.2019.11.019. Epub 2019 Nov 21.

Abstract

Exposure to organic solvent in industry, including n-hexane is correlated with central-peripheral axonopathy, which is mediated by its active metabolite, 2,5-hexanedione (HD). However, the underlying mechanism is still largely unknown. Recently identified microRNAs (miRNAs) may play important roles in toxicant exposure and in the process of toxicant-induced neuropathys. To examine the role of miRNAs in HD-induced toxicity, neuropathic animal model was successfully built. miRNA microarray analysis revealed 105 differentially expressed miRNAs after HD exposure. Bioinformatics analysis showed that "Axon" and "Neurotrophin Signaling Pathway" was the top significant GO term and pathway, respectively. 7 miRNAs both related to "Axon" and "Neurotrophin Signaling Pathway" were screened out and further confirmed by Real-Time PCR. Correspondingly, the deregulation expression levels of proteins of four target genes (GSK3β, Map3k1, BDNF and MAP1B) were further confirmed via western blot, verifying the results of gene target analysis. Taken together, our results showed that the axon-related miRNAs to be associated with MAP1B or neurotrophin signal pathways changed in nerve tissues following HD exposure. These miRNAs may play important roles in HD-induced neurotoxicity.

Keywords: 2,5-Hexanedione; Neuropathy; Sciatic nerve; Spinal cord; miRNA; n-Hexane.

MeSH terms

  • Animals
  • Axons / drug effects*
  • Axons / metabolism
  • Brain-Derived Neurotrophic Factor / genetics
  • Brain-Derived Neurotrophic Factor / metabolism
  • Databases, Genetic
  • Gene Expression Regulation
  • Glycogen Synthase Kinase 3 beta / genetics
  • Glycogen Synthase Kinase 3 beta / metabolism
  • Hexanones / toxicity*
  • MAP Kinase Kinase Kinase 1 / genetics
  • MAP Kinase Kinase Kinase 1 / metabolism
  • Male
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism
  • Neurotoxicity Syndromes / etiology*
  • Neurotoxicity Syndromes / genetics
  • Neurotoxicity Syndromes / metabolism
  • Rats, Sprague-Dawley
  • Sciatic Nerve / drug effects*
  • Sciatic Nerve / metabolism
  • Signal Transduction
  • Solvents / toxicity*
  • Spinal Cord / drug effects*
  • Spinal Cord / metabolism
  • Transcriptome

Substances

  • Bdnf protein, rat
  • Brain-Derived Neurotrophic Factor
  • Hexanones
  • MicroRNAs
  • Microtubule-Associated Proteins
  • Solvents
  • microtubule-associated protein 1B
  • 2,5-hexanedione
  • Glycogen Synthase Kinase 3 beta
  • Gsk3b protein, rat
  • MAP Kinase Kinase Kinase 1