Evidence map›Paper›PMID 26417322›Full record

ArticleEXCLI journal2014

Endoplasmic reticulum membrane potassium channel dysfunction in high fat diet induced stress in rat hepatocytes.

Naser Khodaee, Maedeh Ghasemi, Reza Saghiri, Afsaneh Eliassi

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In one paragraph

Article in EXCLI journal, 2014. 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
–field-weighted citation impact, top 80% 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, 7 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

4 authors at 1 institution in 1 country.

Naser KhodaeeNeurophysiology Research Center, Shahid Beheshti University of Medical Sciences, Evin, Tehran 19857, Iran ; Department of Physiology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Evin, Tehran 19857, Iran.
Maedeh GhasemiNeurophysiology Research Center, Shahid Beheshti University of Medical Sciences, Evin, Tehran 19857, Iran ; Department of Physiology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Evin, Tehran 19857, Iran.
Reza SaghiriDepartment of Biochemistry, Pasteur Institute of Iran, Tehran, Iran.
Afsaneh EliassiNeurophysiology Research Center, Shahid Beheshti University of Medical Sciences, Evin, Tehran 19857, Iran ; Department of Physiology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Evin, Tehran 19857, Iran.
Pasteur Institute of Iran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In a previous study we reported the presence of a large conductance K(+) channel in the membrane of endoplasmic reticulum (ER) from rat hepatocytes. The channel open probability (Po) appeared voltage dependent and reached to a minimum 0.2 at +50 mV. Channel activity in this case was found to be totally inhibited at ATP concentration 2.5 mM, glibenclamide 100 µM and tolbutamide 400 µM. Existing evidence indicates an impairment of endoplasmic reticulum functions in ER stress condition. Because ER potassium channels have been involved in several ER functions including cytoprotection, apoptosis and calcium homeostasis, a study was carried out to consider whether the ER potassium channel function is altered in a high fat diet model of ER stress. Male Wistar rats were made ER stress for 2 weeks with a high fat diet. Ion channel incorporation of ER stress model into the bilayer lipid membrane allowed the characterization of K(+) channel. Our results indicate that the channel Po was significantly increased at voltages above +30 mV. Interestingly, addition of ATP 7.5 mM, glibenclamide 400 µM and tolbutamide 2400 µM totally inhibited the channel activities, 3-fold, 4-fold and 6-fold higher than that in the control groups, respectively. Our results thus demonstrate a modification in the ER K(+) channel gating properties and decreased sensitivity to drugs in membrane preparations coming from ER high fat model of ER stress, an effect potentially linked to a change in ER K(+) channel subunits in ER stress condition. Our results may provide new insights into the cellular mechanisms underlying ER dysfunctions in ER stress.

Indexed as

bilayer lipid membraneendoplasmic reticulumER stresshepatocytespotassium channel

Identifiers

PMID26417322
PMCPMC4464507
OpenAlexW2339371086

What OpenQuestion holds

Textmetadata
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.