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. 2019 Apr 11;10:379. doi: 10.3389/fphar.2019.00379

Table 3.

TREK-1 in CNS pathologies.

Pathology TREK-1 expression Potential treatment References

Immunofluorescence mRNA Protein
Depression nd nd ↑ in the frontal cortex 3 weeks after CMS in rat No change in the hippocampus TREK-1 blockers as potential treatment in depression Chen et al., 2015
Fluoxetine per os daily for 3 weeks
Reverse TREK-1 overexpression in the frontal cortex
Ischemia Broad distribution in the cortex and CA1 (glia and neurons) ↑ in the hippocampus at 3 and 30 days after BCAL In situ hybridization: ↑ in the cortex and hippocampus 7 and 30 days after BCAL (Xu et al., 2004) in the hippocampus 7 and 30 days after MCAO TREK-1 openers as potential treatment in ischemia Wang et al., 2012
↑ in the cortex and the hippocampus after 3, 7, and 30 days after MCAO
Pain perception TREK-1 expression in DRG sensory neurons ↑ in DRG of CCI mice ↑ in DRG of CCI mice TREK-1 openers as potential analgesics Alloui et al., 2006; Han et al., 2016
Post-stroke depression Broad distribution in PFC, CA1, CA3, and DG No treatment, after 31 days of MMCAO Lin et al., 2015
↑ in PFC, CA3 and DG ↑ in PFC, CA1, CA3 and DG TREK-1 blockers as potential treatment in PSD
Escitalopram (3 weeks)
↓ in PFC, CA3 and DG ↓ in PFC, CA1,CA3 and DG