Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Cardiovasc Res ; 113(3): 354-366, 2017 03 01.
Artigo em Inglês | MEDLINE | ID: mdl-28395022

RESUMO

Aims: Anatomical re-entry is an important mechanism of ventricular tachycardia, characterized by circular electrical propagation in a fixed pathway. It's current investigative and therapeutic approaches are non-biological, rather unspecific (drugs), traumatizing (electrical shocks), or irreversible (ablation). Optogenetics is a new biological technique that allows reversible modulation of electrical function with unmatched spatiotemporal precision using light-gated ion channels. We therefore investigated optogenetic manipulation of anatomical re-entry in ventricular cardiac tissue. Methods and results: Transverse, 150-µm-thick ventricular slices, obtained from neonatal rat hearts, were genetically modified with lentiviral vectors encoding Ca2+-translocating channelrhodopsin (CatCh), a light-gated depolarizing ion channel, or enhanced yellow fluorescent protein (eYFP) as control. Stable anatomical re-entry was induced in both experimental groups. Activation of CatCh was precisely controlled by 470-nm patterned illumination, while the effects on anatomical re-entry were studied by optical voltage mapping. Regional illumination in the pathway of anatomical re-entry resulted in termination of arrhythmic activity only in CatCh-expressing slices by establishing a local and reversible, depolarization-induced conduction block in the illuminated area. Systematic adjustment of the size of the light-exposed area in the re-entrant pathway revealed that re-entry could be terminated by either wave collision or extinction, depending on the depth (transmurality) of illumination. In silico studies implicated source-sink mismatches at the site of subtransmural conduction block as an important factor in re-entry termination. Conclusions: Anatomical re-entry in ventricular tissue can be manipulated by optogenetic induction of a local and reversible conduction block in the re-entrant pathway, allowing effective re-entry termination. These results provide distinctively new mechanistic insight into re-entry termination and a novel perspective for cardiac arrhythmia management.


Assuntos
Arritmias Cardíacas/prevenção & controle , Canais de Cálcio/efeitos da radiação , Luz , Miócitos Cardíacos/efeitos da radiação , Optogenética , Rodopsina/efeitos da radiação , Potenciais de Ação , Animais , Animais Recém-Nascidos , Arritmias Cardíacas/genética , Arritmias Cardíacas/metabolismo , Arritmias Cardíacas/fisiopatologia , Proteínas de Bactérias/biossíntese , Proteínas de Bactérias/genética , Canais de Cálcio/biossíntese , Canais de Cálcio/genética , Simulação por Computador , Vetores Genéticos , Lentivirus/genética , Proteínas Luminescentes/biossíntese , Proteínas Luminescentes/genética , Modelos Cardiovasculares , Miócitos Cardíacos/metabolismo , Ratos Wistar , Rodopsina/biossíntese , Rodopsina/genética , Fatores de Tempo , Técnicas de Cultura de Tecidos , Transfecção , Imagens com Corantes Sensíveis à Voltagem
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA