Evidence map›Paper›PMID 25539574›Full record

ArticleBMC neuroscience2014

Ability of naringenin, a bioflavonoid, to activate M-type potassium current in motor neuron-like cells and to increase BKCa-channel activity in HEK293T cells transfected with α-hSlo subunit.

Hung-Te Hsu, Yu-Ting Tseng, Yi-Ching Lo, Sheng-Nan Wu

Open access · goldAbstract read
In one paragraph

Article in BMC neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.3field-weighted citation impact, top 41% of its field
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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Review
  3. Evaluation of Small-Molecule Candidates as Modulators of M-Type KInternational journal of molecular sciences · 2025
    Review
  4. Naringenin modulates GABA mediated response in a sexdependent manner in substantia gelatinosa neurons of trigeminal subnucleus caudalis in immature mice.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2024
    Article
  5. Article
  6. Flavonoids as Modulators of Potassium Channels.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
  9. Evidence for Dual Activation ofInternational journal of molecular sciences · 2022
    Article
  10. Review
  11. The Effectiveness in Activating M-Type KInternational journal of molecular sciences · 2021
    Article
  12. Effective Activation of BKPharmaceuticals (Basel, Switzerland) · 2021
    Article
  13. Article
  14. Article
  15. Regulation of the Mitochondrial BKMolecules (Basel, Switzerland) · 2020
    Article
  16. Article
  17. Article
  18. Naringenin AmelioratesFrontiers in neuroscience · 2019
    Article
  19. Evidence for Effective Multiple KFrontiers in pharmacology · 2019
    Article
  20. Pioglitazone, a PPAR-γ Activator, Stimulates BKFrontiers in pharmacology · 2018
    Article
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

4 authors at 2 institutions in 1 country.

Hung-Te HsuGraduate Institute of Medicine, Kaohsiung Medical University, Kaohsiung, 80708, Taiwan. hdhsu1228@hotmail.com.
Yu-Ting TsengDepartment of Pharmacology, School of Medicine, Kaohsiung Medical University, Kaohsiung, 80708, Taiwan. mmship1112@yahoo.com.tw.
Yi-Ching LoGraduate Institute of Medicine, Kaohsiung Medical University, Kaohsiung, 80708, Taiwan. yichlo@kmu.edu.tw.
Sheng-Nan WuDepartment of Physiology, National Cheng Kung University Medical College, Tainan City, 70101, Taiwan. snwu@mail.ncku.edu.tw.
Kaohsiung Medical University · TWNational Cheng Kung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNaringenin (NGEN) is a citrus bioflavonoid known to have beneficial health properties; however, the ionic mechanism of its actions remains largely unclear. In this study, we attempted to evaluate the possible effects of NGEN on K(+) currents in NSC-34 neuronal cells and in HEK293T cells expressing α-hSlo.

resultsNGEN increased M-type K(+) current (I(K(M))) in a concentration-dependent manner with an EC50 value of 9.8 μM in NSC-34 cells. NGEN shifted the activation curve of I(K(M)) conductance to the more negative potentials. In cell-attached recordings, NGEN or flupirtine enhanced the activity of M-type K(+) (K(M)) channels with no changes in single-channel amplitude. NGEN (10 μM) had minimal effect on erg-mediated K(+) currents. Under cell-attached voltage-clamp recordings, NGEN decreased the frequency of spontaneous action currents and further application of linopirdine can reverse NGEN-induced inhibition of firing. In HEK293T cells expressing α-hSlo, this compound increased the amplitude of Ca(2+)-activated K(+) current (I(K(Ca))). Under inside-out recordings, NGEN applied to the intracellular side of the detached patch enhanced the activity of large-conductance Ca(2+)-activated K(+) (BK(Ca)) channels. Moreover, from the study of a modeled neuron, burst firing of simulated action potentials (APs) was reduced in the presence of the increased conductances of both K(M) and K(Ca) channels. Fast-slow analysis of AP bursting from this model also revealed that as the conductances of both K(M) and BK(Ca) channels were increased by two-fold, the voltage nullcline was shifted in an upward direction accompanied by the compression of burst trajectory.

conclusionsThe present results demonstrate that activation of both K(M) and BK(Ca) channels caused by NGEN might combine to influence neuronal activity if similar channels were functionally co-expressed in central neurons in vivo.

Indexed as

AminopyridinesAnimalsDose-Response Relationship, DrugFlavanonesHEK293 CellsHumansIndolesKCNQ Potassium ChannelsLarge-Conductance Calcium-Activated Potassium Channel alpha SubunitsMembrane PotentialsMiceMotor NeuronsNeurotransmitter AgentsPatch-Clamp TechniquesPotassiumPotassium Channel BlockersAminopyridinesFlavanonesflupirtineIndolesKCNMA1 protein, humanKCNQ Potassium ChannelsLarge-Conductance Calcium-Activated Potassium Channel alpha SubunitslinopirdinenaringeninNeurotransmitter AgentsPotassiumPotassium Channel BlockersPyridines

Identifiers

PMID25539574
PMCPMC4288500
OpenAlexW1984420438

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.