Evidence map›Paper›PMID 31500374›Full record

ArticleInternational journal of molecular sciences2019

Ethanol Elevates Excitability of Superior Cervical Ganglion Neurons by Inhibiting Kv7 Channels in a Cell Type-Specific and PI(4,5)P

Kwon-Woo Kim, Keetae Kim, Hyosang Lee, Byung-Chang Suh

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. PI4KIIIβ-Mediated Phosphoinositides Metabolism Regulates Function of the VTA Dopaminergic Neurons and Depression-Like Behavior.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Pharmacological Manipulation of KFrontiers in physiology · 2020
    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

4 authors at 1 institution in 1 country.

Kwon-Woo KimDepartment of Brain and cognitive sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Korea. kwkim@dgist.ac.kr.
Keetae KimDepartment of New biology, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Korea. keetae@dgist.ac.kr.
Hyosang LeeDepartment of Brain and cognitive sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Korea. hyosang22@dgist.ac.kr.
Byung-Chang SuhDepartment of Brain and cognitive sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Korea. bcsuh@dgist.ac.kr.
Daegu Gyeongbuk Institute of Science and Technology · KR

Funding

Basic Science Research Program 2017R1A2B4003351Basic Science Research Program 2019R1A2B5B01070546Brain Research Program 2017R1A2B4003351Brain Research Program NRF-2017R1A2B4003351KBRI basic research program 19-BR-04-01KBRI basic research program 19-BR-04-03
6 · The paper itself

Abstract

Alcohol causes diverse acute and chronic symptoms that often lead to critical health problems. Exposure to ethanol alters the activities of sympathetic neurons that control the muscles, eyes, and blood vessels in the brain. Although recent studies have revealed the cellular targets of ethanol, such as ion channels, the molecular mechanism by which alcohol modulates the excitability of sympathetic neurons has not been determined. Here, we demonstrated that ethanol increased the discharge of membrane potentials in sympathetic neurons by inhibiting the M-type or Kv7 channel consisting of the Kv7.2/7.3 subunits, which were involved in determining the membrane potential and excitability of neurons. Three types of sympathetic neurons, classified by their threshold of activation and firing patterns, displayed distinct sensitivities to ethanol, which were negatively correlated with the size of the Kv7 current that differs depending on the type of neuron. Using a heterologous expression system, we further revealed that the inhibitory effects of ethanol on Kv7.2/7.3 currents were facilitated or diminished by adjusting the amount of plasma membrane phosphatidylinositol 4,5-bisphosphate (PI(4,5)P

Indexed as

Action PotentialsBiomarkersCell MembraneCells, CulturedEthanolGene ExpressionKCNQ Potassium ChannelsNeuronsPhosphatidylinositol 4,5-DiphosphateSuperior Cervical GanglionBiomarkersEthanolKCNQ Potassium ChannelsPhosphatidylinositol 4,5-DiphosphateethanolKv7.2/7.3 currentKv7 channelPI(4,5)P2SCG neuron

Identifiers

PMID31500374
PMCPMC6770022
OpenAlexW2971970091

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.