Evidence map›Paper›PMID 40175331›Full record

ArticleTranslational psychiatry2025

A novel role of the antidepressant paroxetine in inhibiting neuronal Kv7/M channels to enhance neuronal excitability.

Huan Shi, Qinqin Li, Fang Hu, Yani Liu, KeWei Wang

Abstract read
In one paragraph

Article in Translational psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Huan Shi *Department of Pharmacology, School of Pharmacy, Qingdao University Medical college, Qingdao, China.
Qinqin Li *Department of Pharmacology, School of Pharmacy, Qingdao University Medical college, Qingdao, China.
Fang HuDepartment of Pharmacology, School of Pharmacy, Qingdao University Medical college, Qingdao, China.
Yani LiuDepartment of Pharmacology, School of Pharmacy, Qingdao University Medical college, Qingdao, China. liuyani@qdu.edu.cn.
KeWei WangDepartment of Pharmacology, School of Pharmacy, Qingdao University Medical college, Qingdao, China. wangkw@qdu.edu.cn.ORCID http://orcid.org/0000-0001-7023-9998

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81973299National Natural Science Foundation of China (National Science Foundation of China) 82104149
6 · The paper itself

Abstract

The voltage-gated Kv7/KCNQ/M potassium channels exert inhibitory control over neuronal membrane excitability. The reduction of Kv7 channel function can improve neuronal excitability that defines the fundamental mechanism of learning and memory. This suggests that pharmacological inhibition of Kv7 channels may present a therapeutic strategy for cognitive improvement. Paroxetine, a selective serotonin reuptake inhibitor, is widely used in the treatment of various types of depression with reported improvements in memory and attention. However, the exact mechanism underlying cognitive improvement by paroxetine remains poorly understood. In this study, we demonstrate that paroxetine inhibits whole-cell Kv7.2/Kv7.3 channel currents in a concentration-dependent manner with an IC

Indexed as

Antidepressive Agents, Second-GenerationKCNQ2 Potassium ChannelKCNQ3 Potassium ChannelNeuronsParoxetineSelective Serotonin Reuptake InhibitorsAction PotentialsAnimalsHippocampusHumansPatch-Clamp TechniquesRatsAntidepressive Agents, Second-GenerationKCNQ2 Potassium ChannelKCNQ3 Potassium ChannelParoxetineSelective Serotonin Reuptake Inhibitors

Identifiers

PMID40175331
PMCPMC11965407

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.