Inhibition of EPAC2 Attenuates Intracerebral Hemorrhage-Induced Secondary Brain Injury via the p38/BIM/Caspase-3 Pathway

J Mol Neurosci. 2019 Mar;67(3):353-363. doi: 10.1007/s12031-018-1215-y. Epub 2019 Jan 3.

Abstract

Exchange proteins directly activated by cAMP (EPACs) are critical cAMP-dependent signaling pathway intermediaries that have been implicated in the pathogenesis of several human diseases, particularly neurological disorders. However, their pathogenic role in secondary brain injury (SBI) induced by intracranial hemorrhage (ICH) is unknown. The aim of this study was to examine the effects of EPAC2 on ICH-induced SBI and its underlying mechanisms. An in vivo ICH model was established in Sprague-Dawley rats by autologous blood injection. In addition, rat primary cortical neuronal cultures were exposed to oxyhemoglobin to simulate ICH in vitro. The function of EPAC2 in SBI induced by ICH was studied using the EPAC2-specific inhibitor ESI-05. In this study, we found that EPAC2 protein expression was significantly increased in the ICH models in vitro and in vivo. Furthermore, EPAC2 activation was inhibited by ESI-05 under ICH conditions. Inhibition of EPAC2 decreased the apoptosis rate of nerve cells in the cortex accompanied by a corresponding decrease in the protein expression of phosphorylated p38, Bcl-2-like protein 11 (BIM), and caspase-3. In summary, this study showed that inhibition of EPAC2 activation by ESI-05 suppressed SBI induced by ICH via the p38/BIM/caspase-3 signaling pathway.

Keywords: Apoptosis; BIM; EPAC2; Intracranial hemorrhage; Secondary brain injury; p38.

MeSH terms

  • Animals
  • Apoptosis
  • Bcl-2-Like Protein 11 / metabolism
  • Benzene Derivatives / pharmacology
  • Brain / drug effects*
  • Brain / metabolism
  • Caspase 3 / metabolism
  • Cells, Cultured
  • Guanine Nucleotide Exchange Factors / antagonists & inhibitors*
  • Guanine Nucleotide Exchange Factors / genetics
  • Guanine Nucleotide Exchange Factors / metabolism
  • Intracranial Hemorrhages / metabolism*
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction*
  • Sulfones / pharmacology
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Bcl-2-Like Protein 11
  • Bcl2l11 protein, rat
  • Benzene Derivatives
  • ESI-05
  • Guanine Nucleotide Exchange Factors
  • Rapgef4 protein, rat
  • Sulfones
  • p38 Mitogen-Activated Protein Kinases
  • Caspase 3