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 |
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Fluoxetine per os daily for 3 weeks |
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Reverse TREK-1 overexpression in the frontal cortex |
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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 |
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↑ in the cortex and the hippocampus after 3, 7, and 30 days after MCAO |
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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 |
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↑ in PFC, CA3 and DG |
↑ in PFC, CA1, CA3 and DG |
TREK-1 blockers as potential treatment in PSD |
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Escitalopram (3 weeks) |
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↓ in PFC, CA3 and DG |
↓ in PFC, CA1,CA3 and DG |
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