Literature DB >> 25675906

The Role of the Two-Pore Domain Potassium Channel TREK-1 in the Therapeutic Effects of Escitalopram in a Rat Model of Poststroke Depression.

Dai-Hua Lin1, Xiang-Rong Zhang1, Dong-Qing Ye1, Guang-Jun Xi1, Jiao-Jie Hui1, Shan-Shan Liu1, Lin-Jiang Li2, Zhi-Jun Zhang1.   

Abstract

AIM: Poststroke depression (PSD) is one of the most common neuropsychiatric complications after stroke. TREK-1, a two-pore-domain potassium channel, has been implicated in the pathogenesis of stroke and depression. The aim of this study was to investigate whether TREK-1 plays a role in the therapeutic effects of the selective serotonin reuptake inhibitor (SSRI) escitalopram in a rat PSD model.
METHODS: The whole-cell patch-clamp technique was performed to assess the effect of escitalopram on recombinant TREK-1 currents in HEK293 cells. The expression of TREK-1 mRNA and protein was measured in the hippocampus and prefrontal cortex (PFC), and neural stem cell (NSC) proliferation was detected in the hippocampal dentate gyrus (DG) in PSD rats after 3 weeks of escitalopram administration.
RESULTS: Escitalopram reversibly inhibited TREK-1 currents in a concentration-dependent manner. Chronic treatment with escitalopram significantly reversed the reductions in weight gain, locomotor activity, and sucrose preference in PSD rats. The expressions of TREK-1 mRNA and protein were significantly increased in hippocampal CA1, CA3, DG, and PFC in PSD rats, with the exception of TREK-1 mRNA in hippocampal CA1. NSC proliferation was significantly decreased in hippocampal DG of PSD rats. Escitalopram significantly reversed the regional increases of TREK-1 expression and the reduction of hippocampal NSC proliferation in PSD rats.
CONCLUSION: TREK-1 plays an important role in the therapeutic effects of the SSRI escitalopram in PSD model, making TREK-1 an attractive candidate molecule for further understanding the pathophysiology and treatment of PSD.
© 2015 John Wiley & Sons Ltd.

Entities:  

Keywords:  Escitalopram; Poststroke depression; TREK-1 (TWIK-related potassium channel, type 1); Therapeutic effects

Mesh:

Substances:

Year:  2015        PMID: 25675906      PMCID: PMC6495393          DOI: 10.1111/cns.12384

Source DB:  PubMed          Journal:  CNS Neurosci Ther        ISSN: 1755-5930            Impact factor:   5.243


  50 in total

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  5 in total

1.  Over-expressed human TREK-1 inhibits CHO cell proliferation via inhibiting PKA and p38 MAPK pathways and subsequently inducing G1 arrest.

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Review 2.  Two-Pore Domain Potassium Channel in Neurological Disorders.

Authors:  Punita Aggarwal; Sanjiv Singh; V Ravichandiran
Journal:  J Membr Biol       Date:  2021-06-24       Impact factor: 1.843

3.  The Two-Pore Domain Potassium Channel TREK-1 Promotes Blood-Brain Barrier Breakdown and Exacerbates Neuronal Death After Focal Cerebral Ischemia in Mice.

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Journal:  Mol Neurobiol       Date:  2022-01-24       Impact factor: 5.590

4.  Electroacupuncture Ameliorates Depressive-Like Behaviors in Poststroke Rats via Activating the tPA/BDNF/TrkB Pathway.

Authors:  Hao Dong; Yan-Qiang Qin; Ying-Chun Sun; Hai-Jiang Yao; Xian-Kuan Cheng; Yan Yu; Shou-Si Lu
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5.  Comparing the Therapeutic Effects of Crocin, Escitalopram and Co-Administration of Escitalopram and Crocin on Learning and Memory in Rats with Stress-Induced Depression.

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  5 in total

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