Evidence map›Paper›PMID 42238749›Full record

ArticleBasic and clinical neuroscience2025

A New Potassium Channel on the Endoplasmic Reticulum Membrane in a Rat Brain: Electropharmacology and Molecular Evidence.

Maryam Nazari, Afsaneh Eliassi, Reza Saghiri, Farnaz Nikbakht, Javad Fahanik-Babaei

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Article in Basic and clinical neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Maryam NazariDepartment of Physiology, School of Medicine, Arak University of Medical Sciences, Arak, Iran.
Afsaneh EliassiNeurophysiology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Reza SaghiriDepartment of Biochemistry, Pasteur Institute of Iran, Tehran, Iran.
Farnaz NikbakhtDepartment of Physiology, Cellular and Molecular Research Center, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.ORCID 0000-0002-1239-3388
Javad Fahanik-BabaeiElectrophysiology Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0001-6707-132X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Several types of ion channels found in the plasma membrane have also been identified in the membranes of intracellular organelles. These ion channels, including potassium channels, play a crucial role in regulating intracellular ion homeostasis. An ATP-sensitive potassium (KATP) channel with various functional roles has been identified in the endo/sarcoplasmic reticulum membranes of both excitable and non-excitable cells. Our previous studies investigated the electropharmacological and molecular properties of KATP and BKCa Methods: In this study, for the first time, we described the electropharmacological and molecular properties of the RER KATP channel in rat brain cells using an incorporated single-channel in a planar lipid bilayer and Western blotting. Results: The results of the study revealed the presence of a KATP channel with a conductance of 306 pS, and the open probability was found to be voltage-independent at holding potentials ranging from +40 to -60 in an asymmetric solution (200/50 mM KCl; cis/trans). Additionally, we observed that adding ATP (2.5 mM) to both positive and negative potentials, and 100 μM glibenclamide to the positive voltages inhibited channel activity. The addition of 100 mM 5-HD and 100 nM charybdotoxin to the cis side did not affect the channel behavior. Furthermore, a Western blot analysis provided evidence of the expression of Kir6.2, Kir6.1, sulfonylurea receptor (SUR)1, and/or SUR2B, but not SUR2A, in the RER of rat brain fractions. Conclusion: In this study, we provide strong evidence for the existence of a KATP channel on the RER membrane of rat brain cells, displaying pharmacological properties distinct from those classically described for the plasma membrane and other intracellular organelles.

Indexed as

ATP-sensitive potassium (KATP) channelBilayer lipid membranePotassium channelsRough endoplasmic reticulum (RER)Single channel recording

Identifiers

PMID42238749
PMCPMC13228105

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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.