Evidence map›Paper›PMID 31091801›Full record

ArticleCells2019

Involvement of TREK-1 Channel in Cell Viability of H9c2 Rat Cardiomyoblasts Affected by Bupivacaine and Lipid Emulsion.

Jun Ho Yang, Adrian S Siregar, Eun-Jin Kim, Marie Merci Nyiramana, Eui-Jung Shin, Jaehee Han, Ju-Tae Sohn, Jong Woo Kim, Dawon Kang

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Jun Ho YangDepartments of Medicine and Thoracic and Cardiovascular Surgery, College of Medicine, Gyeongsang National University, Jinju 52727, Korea. junhoyah@hanmail.net.
Adrian S SiregarDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. adriansiregar46@gmail.com.
Eun-Jin KimDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. eunjin1981@hanmail.net.
Marie Merci NyiramanaDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. mariemerci0222@gmail.com.
Eui-Jung ShinDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. eui-jung@naver.com.
Jaehee HanDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. jheehan@gnu.ac.kr.
Ju-Tae SohnDepartment of Anesthesiology and Pain Medicine, College of Medicine, Gyeongsang National University, Jinju 52727, Korea. jtsohn@gnu.ac.kr.
Jong Woo KimDepartments of Medicine and Thoracic and Cardiovascular Surgery, College of Medicine, Gyeongsang National University, Jinju 52727, Korea. junhoyah@hanmail.net.
Dawon KangDepartment of Physiology, College of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju 52727, Korea. dawon@gnu.ac.kr.
Gyeongsang National University · KRChangwon National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipid emulsion (LE) therapy has been used to reduce overdose of bupivacaine (BPV)-induced cardiotoxicity. The TWIK-related potassium channel-1 (TREK-1) is inhibited by BPV and activated by polyunsaturated fatty acids, which are the main component in LE. These pharmacological properties inspired us to investigate whether the TREK-1 channel is associated with cell viability of H9c2 cardiomyoblasts affected by BPV and LE. Consistent with previous studies, BPV-induced cell death was reduced by LE treatment. The reduction in the TREK-1 expression level by BPV was alleviated by LE. The BPV cytotoxicity highly decreased in TREK-1 overexpressed cells but was the opposite in TREK-1 knocked-down cells. TREK-1 channel activators and inhibitors increased and decreased cell viability, respectively. BPV-induced depolarization of the plasma and mitochondrial membrane potential and increase in intracellular Ca

Indexed as

AnimalsBupivacaineCardiotoxicityCell LineCell SurvivalHumansLipidsMembrane Potential, MitochondrialMyoblasts, CardiacPotassium Channels, Tandem Pore DomainBupivacaineLipidspotassium channel protein TREK-1Potassium Channels, Tandem Pore Domainbupivacainecardiomyoblastlipid emulsionmembrane potentialTREK-1

Identifiers

PMID31091801
PMCPMC6563050
OpenAlexW2945470974

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.