Literature DB >> 35286678

Optogenetic Control of Heart Rhythm: Lightly Guiding the Cardiac Pace.

Lolita Dokshokova1,2, Nicola Pianca1,2, Tania Zaglia3,4, Marco Mongillo5,6.   

Abstract

It is well appreciated that, differently from skeletal muscles, the heart contracts independently from neurogenic inputs. However, the speed and force of heartbeats are finely modulated during stresses, emotions, and daily activities, by the autonomic neurons (both parasympathetic and sympathetic) which highly innervate the myocardium. Despite this aspect of cardiac physiology has been known for long, research has only recently shed light on the biophysical mechanisms underlying the meticulous adaptation of heart activity to the needs of the organism. A conceptual advancement in this regard has come from the use of optogenetics, a revolutionary methodology which allows to control the activity of a given excitable cell type, with high specificity, temporal and spatial resolution, within intact tissues and organisms. The method, widely affirmed in the field of neuroscience, has more recently been exploited also in research on heart physiology and pathology, including the study of the mechanisms regulating heart rhythm. The last point is the object of this book chapter which, starting from the description of the physiology of heart rhythm automaticity and the neurogenic modulation of heart rate, makes an excursus on the theoretical basis of such biotechnology (with its advantages and limitations), and presents a series of examples in cardiac and neuro-cardiac optogenetics.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Cardiomyocytes; Channelrhodopsin-2; Heart rhythm; Optogenetics; Sino-atrial node; Sympathetic neurons

Mesh:

Year:  2022        PMID: 35286678     DOI: 10.1007/978-1-0716-2245-2_13

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  51 in total

1.  Optogenetic control of heart muscle in vitro and in vivo.

Authors:  Tobias Bruegmann; Daniela Malan; Michael Hesse; Thomas Beiert; Christopher J Fuegemann; Bernd K Fleischmann; Philipp Sasse
Journal:  Nat Methods       Date:  2010-10-03       Impact factor: 28.547

2.  Millisecond-timescale, genetically targeted optical control of neural activity.

Authors:  Edward S Boyden; Feng Zhang; Ernst Bamberg; Georg Nagel; Karl Deisseroth
Journal:  Nat Neurosci       Date:  2005-08-14       Impact factor: 24.884

Review 3.  Next-generation optical technologies for illuminating genetically targeted brain circuits.

Authors:  Karl Deisseroth; Guoping Feng; Ania K Majewska; Gero Miesenböck; Alice Ting; Mark J Schnitzer
Journal:  J Neurosci       Date:  2006-10-11       Impact factor: 6.167

Review 4.  Cardiac sympathetic innervation, from a different point of (re)view.

Authors:  Tania Zaglia; Marco Mongillo
Journal:  J Physiol       Date:  2017-06-15       Impact factor: 5.182

Review 5.  Will cardiac optogenetics find the way through the obscure angles of heart physiology?

Authors:  Nicola Pianca; Tania Zaglia; Marco Mongillo
Journal:  Biochem Biophys Res Commun       Date:  2016-11-18       Impact factor: 3.575

Review 6.  Optogenetic tools for analyzing the neural circuits of behavior.

Authors:  Jacob G Bernstein; Edward S Boyden
Journal:  Trends Cogn Sci       Date:  2011-11-04       Impact factor: 20.229

7.  Dynamics of neuroeffector coupling at cardiac sympathetic synapses.

Authors:  Valentina Prando; Francesca Da Broi; Mauro Franzoso; Anna Pia Plazzo; Nicola Pianca; Maura Francolini; Cristina Basso; Matthew W Kay; Tania Zaglia; Marco Mongillo
Journal:  J Physiol       Date:  2018-04-17       Impact factor: 5.182

8.  Optogenetic release of norepinephrine from cardiac sympathetic neurons alters mechanical and electrical function.

Authors:  Anastasia M Wengrowski; Xin Wang; Srinivas Tapa; Nikki Gillum Posnack; David Mendelowitz; Matthew W Kay
Journal:  Cardiovasc Res       Date:  2014-12-16       Impact factor: 10.787

9.  Optogenetic determination of the myocardial requirements for extrasystoles by cell type-specific targeting of ChannelRhodopsin-2.

Authors:  Tania Zaglia; Nicola Pianca; Giulia Borile; Francesca Da Broi; Claudia Richter; Marina Campione; Stephan E Lehnart; Stefan Luther; Domenico Corrado; Lucile Miquerol; Marco Mongillo
Journal:  Proc Natl Acad Sci U S A       Date:  2015-07-23       Impact factor: 11.205

10.  Sudden Heart Rate Reduction Upon Optogenetic Release of Acetylcholine From Cardiac Parasympathetic Neurons in Perfused Hearts.

Authors:  Angel Moreno; Kendal Endicott; Matthew Skancke; Mary Kate Dwyer; Jaclyn Brennan; Igor R Efimov; Gregory Trachiotis; David Mendelowitz; Matthew W Kay
Journal:  Front Physiol       Date:  2019-01-28       Impact factor: 4.566

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