Evidence map›Paper›PMID 41874121›Full record

ArticleJournal of xenobiotics2026

Auxiliary TARP Subunits Define AMPA Receptor Pharmacology and Function.

Sosana Bdir, İrfan Çapan, Mohammed Hawash, Süleyman Servi, Mohammad Qneibi

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Article in Journal of xenobiotics, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Sosana BdirDepartment of Medicine, Faculty of Medicine and Allied Medical Sciences, An-Najah National University, Nablus P400, Palestine.
İrfan ÇapanDepartment of Pharmaceutical Basic Sciences, Faculty of Pharmacy, Gazi University, 06560 Ankara, Turkey.
Mohammed HawashDepartment of Pharmaceutical Chemistry and Technology, Faculty of Pharmacy, An-Najah National University, Nablus P400, Palestine.ORCID 0000-0001-5640-9700
Süleyman ServiDepartment of Chemistry, Faculty of Science, Fırat University, 23200 Elazığ, Turkey.ORCID 0000-0003-0827-8624
Mohammad QneibiDepartment of Biomedical Sciences and Basic Clinical Skills, Faculty of Medicine and Allied Health Sciences, An-Najah National University, Nablus P400, Palestine.ORCID 0000-0002-0702-7834

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFast excitatory transmission in the central nervous system is carried out by AMPA-type glutamate receptors. Neuronal hyperexcitability and epilepsy have been associated with the dysregulation of AMPA receptor function. Modulation of the gating kinetics of AMPA receptor function has been proposed to be a desirable target for therapy, especially when the modulation is transmembrane AMPA receptor regulatory protein (TARP)-dependent and AMPA receptor subunit composition-dependent.

methodsEight dibenzobarrelene-based heterocycles were characterized for their effects on the human embryonic kidney cells expressing homomeric GluA1 and heteromeric GluA1/2 AMPA receptors, either alone or co-expressed with the TARPγ8 auxiliary subunit, using whole-cell patch-clamp electrophysiological recordings, and the current amplitude and kinetics of desensitization and deactivation were measured after rapid glutamate application.

resultsEach chemical evaluated suppressed glutamate-induced currents via AMPA receptors and augmented both desensitization and deactivation, indicating a negative allosteric modulatory effect. The co-expression of TARPγ8 diminished, but did not eradicate, the inhibition and acceleration induced by the compounds. The observations indicate that the chemicals diminish agonist-bound open states and facilitate transitions to non-conducting states while maintaining effectiveness.

conclusionsThe present study describes a specific kinetic mechanism by which dibenzobarrelene derivatives impair the function of the AMPA receptor and its dependence on auxiliary proteins. The present study provides a mechanistic understanding of AMPA receptor gating modulation and establishes a pharmacological framework for future investigations in more physiologically relevant systems.

Indexed as

AMPA receptordibenzobarreleneGluA1GluA1/2TARPγ8

Identifiers

PMID41874121
PMCPMC13010758

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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 OpenQuestion graph.