Early-Life Multiple Sevoflurane Exposures Alleviate Long-term Anxiety-Like Behaviors in Mice via the proBDNF/ERK Pathway

Mol Neurobiol. 2021 Jan;58(1):170-183. doi: 10.1007/s12035-020-02113-y. Epub 2020 Sep 10.

Abstract

Early-life multiple anesthetics exposure causes neurotoxicity and hence cognitive dysfunction on developing brain. However, the effects of early-life multiple sevoflurane exposures on emotional changes, especially upon stress, are far beyond understood. In young male C57BL6/J mice, the present study showed that 3% sevoflurane inhalation for 2 h in three consecutive days did not influence anxiety-like behaviors as measured by open field test, light dark transition, and elevated plus maze test. In addition, foot shocks stress induced both the short- and long-term anxiety-like behaviors. However, triple sevoflurane exposures ameliorated the long-term anxiety-like behaviors induced by the foot shocks. In parallel, foot shocks stress upregulated the expression of phosphorylated extracellular signal-regulated kinase (p-ERK) and brain-derived neurotrophic factor precursor (proBDNF) in the anterior cingulate cortex (ACC), which were significantly inhibited by triple sevoflurane exposures. Immunofluorescence further indicated that the increased p-ERK was mainly expressed in the proBDNF-positive staining cells. Intra-ACC injection of recombinant proBDNF protein upregulated the p-ERK expression and blocked the anxiolytic effect of sevoflurane exposure on long-term anxiety-like behaviors. Therefore, our study demonstrated that multiple sevoflurane exposures alleviate long-term anxiety-like behaviors upon acute stress in young mice by inhibiting proBDNF-ERK signaling in the ACC.

Keywords: Anterior cingulate cortex; Anxiety-like behaviors; Brain-derived neurotrophic factor precursor; Phosphorylated extracellular signal-regulated kinase; Sevoflurane; Stress.

MeSH terms

  • Acid-Base Imbalance / blood
  • Acid-Base Imbalance / complications
  • Animals
  • Anxiety / blood
  • Anxiety / complications
  • Anxiety / metabolism*
  • Anxiety / pathology*
  • Behavior, Animal*
  • Blood Gas Analysis
  • Brain-Derived Neurotrophic Factor / metabolism*
  • Gyrus Cinguli / drug effects
  • Gyrus Cinguli / metabolism
  • Hypoxia / blood
  • Hypoxia / complications
  • MAP Kinase Signaling System* / drug effects
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Phosphorylation / drug effects
  • Protein Precursors / metabolism*
  • Sevoflurane / pharmacology*
  • Stress, Physiological / drug effects
  • Time Factors
  • Up-Regulation / drug effects

Substances

  • Brain-Derived Neurotrophic Factor
  • Protein Precursors
  • brain-derived neurotrophic factor precursor
  • Sevoflurane