Evidence map›Paper›PMID 42878420›Full record

ArticleArchives of endocrinology and metabolism2026

Tetraethylammonium-Sensitive ventricular repolarization in diabetic rat myocardium: effects of rosiglitazone.

Servet Kavak, Mehmet Ali Ijik, Mustafa Emre

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Article in Archives of endocrinology and metabolism, 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

3 authors.

Servet KavakDepartment of Biophysics, Faculty of Medicine, Izmir Bakircay University, Izmir, Türkiye.ORCID 0000-0003-4983-6071
Mehmet Ali IjikDepartment of Cardiology, Mardin State Hospital, Mardin, Türkiye.ORCID 0000-0001-8527-3769
Mustafa EmreDepartment of Biophysics, Faculty of Medicine, Çukurova University, Adana, Türkiye.ORCID 0000-0001-9897-6674

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo examine ventricular action-potential responses to tetraethylammonium (TEA), a non-selective potassium-channel blocker, in streptozotocin-induced diabetic rats and determine whether rosiglitazone modifies these responses. MATERIALS AND

methodsMale Wistar rats were assigned to Control (C), Control plus Rosiglitazone (C+RSG), Diabetic (D), or Diabetic plus Rosiglitazone (D+RSG) groups. Diabetes was induced with streptozotocin (45 mg/kg, intravenous). Resting membrane potential (RMP), action potential amplitude (APA), and half-repolarization time (½RT) were recorded from isolated left ventricular papillary muscles before and after TEA administration (2 mmol/L).

resultsAt week 8, blood glucose was 563 ± 29 mg/dL in diabetic rats and 98 ± 6 mg/dL in controls (p < 0.001). Rosiglitazone reduced the diabetic value to 336 ± 25 mg/dL (p < 0.05 vs. D). TEA increased ½RT from 18 ± 1 to 38 ± 2 ms in controls (+20 ms) and from 60 ± 3 to 65 ± 3 ms in diabetic myocardium (+5 ms). Diabetic preparations had higher post-TEA ½RT because repolarization was prolonged at baseline; however, the absolute TEA-associated increment was smaller than in controls. TEA also increased APA in untreated control and diabetic preparations.

conclusionDiabetes was associated with marked baseline prolongation of ventricular repolarization. The smaller absolute ½RT increment in diabetic myocardium does not support enhanced TEA responsiveness. Because TEA is non-selective, the findings reflect an integrated response to TEA-sensitive potassium conductances rather than dysfunction of a specific current subtype. Rosiglitazone modified selected electrophysiological responses without normalizing diabetic repolarization.

Indexed as

Action PotentialsDiabetes Mellitus, ExperimentalHeart VentriclesHypoglycemic AgentsPotassium Channel BlockersTetraethylammoniumThiazolidinedionesAnimalsBlood GlucoseMaleMembrane PotentialsMyocardiumPPAR-gamma AgonistsRatsRats, WistarRosiglitazoneBlood GlucoseHypoglycemic AgentsPotassium Channel BlockersPPAR-gamma AgonistsRosiglitazoneTetraethylammoniumThiazolidinedionescardiac electrophysiologyDiabetes mellitusdiabetic cardiomyopathypotassium channelsrosiglitazonetetraethylammoniumventricular repolarization

Identifiers

PMID42878420
PMCPMC13668016

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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.