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001-es BibID:BIBFORM091600
035-os BibID:(WoS)000635517300013 (Scopus)85099368265 (PubMed)33383036
Első szerző:Szlovák Jozefina
Cím:Blockade of sodium-calcium exchanger via ORM-10962 attenuates cardiac alternans / Szlovák Jozefina, Tomek Jakub, Zhou Xin, Tóth Noémi, Veress Roland, Horváth Balázs, Szentandrássy Norbert, Levijoki Jouko, Papp Julius Gy., Herring Neil, Varró András, Eisner David A., Rodriguez Blanca, Nagy Norbert
Dátum:2021
ISSN:0022-2828
Megjegyzések:Repolarization alternans, a periodic oscillation of long-short action potential duration, is an important source of arrhythmogenic substrate, although the mechanisms driving it are insufficiently understood. Despite its relevance as an arrhythmia precursor, there are no successful therapies able to target it specifically. We hypothesized that blockade of the sodium?calcium exchanger (NCX) could inhibit alternans. The effects of the selective NCX blocker ORM-10962 were evaluated on action potentials measured with microelectrodes from canine papillary muscle preparations, and calcium transients measured using Fluo4-AM from isolated ventricular myocytes paced to evoke alternans. Computer simulations were used to obtain insight into the drug's mechanisms of action. ORM-10962 attenuated cardiac alternans, both in action potential duration and calcium transient amplitude. Three morphological types of alternans were observed, with differential response to ORM-10962 with regards to APD alternans attenuation. Analysis of APD restitution indicates that calcium oscillations underlie alternans formation. Furthermore, ORM-10962 did not markedly alter APD restitution, but increased post-repolarization refractoriness, which may be mediated by indirectly reduced L-type calcium current. Computer simulations reproduced alternans attenuation via ORM-10962, suggesting that it is acts by reducing sarcoplasmic reticulum release refractoriness. This results from the ORM-10962-induced sodium?calcium exchanger block accompanied by an indirect reduction in L-type calcium current. Using a computer model of a heart failure cell, we furthermore demonstrate that the anti-alternans effect holds also for this disease, in which the risk of alternans is elevated. Targeting NCX may therefore be a useful anti-arrhythmic strategy to specifically prevent calcium driven alternans.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Alternans
Sodium-calcium exchanger
Sodium-calcium exchanger inhibition
Canine myocytes
Cardiac simulation
Megjelenés:Journal Of Molecular And Cellular Cardiology. - 153 (2021), p. 111-122. -
További szerzők:Tomek, Jakub Zhou, Xin Tóth Noémi Veress Roland (1992-) (molekuláris biológus) Horváth Balázs (1981-) (élettanász) Szentandrássy Norbert (1976-) (élettanász) Levijoki, Jouko Papp Gy. Julius (Szeged) Herring, Neil Varró András (1954-) (farmakológus, klinikai farmakológus) Eisner, David A. Rodríguez, Blanca Nagy Norbert (1977-) (kísérletes farmakológus)
Pályázati támogatás:PD-125402
OTKA
FK-129117
OTKA
GINOP-2.3.2-15-2016-00006
GINOP
GINOP-2.3.2-15-2016-00012
GINOP
EFOP-3.6.2-16-2017-00006
EFOP
EFOP-3.6.3-VEKOP-16-2017-00009
EFOP
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DOI
Intézményi repozitóriumban (DEA) tárolt változat
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2.

001-es BibID:BIBFORM096080
035-os BibID:(cikkazonosító)16652 (WOS)000686690900023 (Scopus)85113167051 (PMID)34404848
Első szerző:Tóth Noémi
Cím:The development of L-type Ca2+ current mediated alternans does not depend on the restitution slope in canine ventricular myocardium / Tóth Noémi, Szlovák Jozefina, Kohajda Zsófia, Bitay Gergő, Veress Roland, Horváth Balázs, Papp Julius Gy., Varró András, Nagy Norbert
Dátum:2021
ISSN:2045-2322
Megjegyzések:Cardiac alternans have crucial importance in the onset of ventricular fibrillation. The early explanation for alternans development was the voltage-driven mechanism, where the action potential (AP) restitution steepness was considered as crucial determining factor. Recent results suggest that restitution slope is an inadequate predictor for alternans development, but several studies still claim the role of membrane potential as underlying mechanism of alternans. These controversial data indicate that the relationship of restitution and alternans development is not completely understood. APs were measured by conventional microelectrode technique from canine right ventricular papillary muscles. Ionic currents combined with fluorescent measurements were recorded by patch-clamp technique. APs combined with fluorescent measurements were monitored by sharp microelectrodes. Rapid pacing evoked restitution-independent AP duration (APD) alternans. When non-alternating AP voltage command was used, Ca2+i-transient (CaT) alternans were not observed. When alternating rectangular voltage pulses were applied, CaT alternans were proportional to ICaL amplitude alternans. Selective ICaL inhibition did not influence the fast phase of APD restitution. In this study we found that ICaL has minor contribution in shaping the fast phase of restitution curve suggesting that ICaL?if it plays important role in the alternans mechanism?could be an additional factor that attenuates the reliability of APD restitution slope to predict alternans.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Scientific Reports. - 11 : 1 (2021), p. 16652. -
További szerzők:Szlovák Jozefina Kohajda Zsófia Bitay Gergő Veress Roland (1992-) (molekuláris biológus) Horváth Balázs (1981-) (élettanász) Papp Gy. Julius (Szeged) Varró András (1954-) (farmakológus, klinikai farmakológus) Nagy Norbert (1977-) (kísérletes farmakológus)
Pályázati támogatás:FK128116
OTKA
ÚNKP-20-5-SZTE-165
Egyéb
ÚNKP-20-3-SZTE-126
Egyéb
GINOP-2.3.2-15-2016-00006
GINOP
EFOP-3.6.2-16-2017-0006
EFOP
Internet cím:Szerző által megadott URL
DOI
Intézményi repozitóriumban (DEA) tárolt változat
Borító:
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