<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zgierski-Johnston CM</submitter><funding>European Research Council</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>European Commission</funding><pagination>51-61</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7322525</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>154</volume><pubmed_abstract>Optogenetics enables cell-type specific monitoring and actuation via light-activated proteins. In cardiac research, expressing light-activated depolarising ion channels in cardiomyocytes allows optical pacing and defibrillation. Previous studies largely relied on epicardial illumination. Light penetration through the myocardium is however problematic when moving to larger animals and humans. To overcome this limitation, we assessed the utility of an implantable multi light-emitting diode (LED) optical probe (IMLOP) for intramural pacing of mouse hearts expressing cardiac-specific channelrhodopsin-2 (ChR2). Here we demonstrated that IMLOP insertion needs approximately 20 mN of force, limiting possible damage from excessive loads applied during implantation. Histological sections confirmed t</pubmed_abstract><journal>Progress in biophysics and molecular biology</journal><pubmed_title>Cardiac pacing using transmural multi-LED probes in channelrhodopsin-expressing mouse hearts.</pubmed_title><pmcid>PMC7322525</pmcid><funding_grant_id>323099</funding_grant_id><pubmed_authors>Fernandez MC</pubmed_authors><pubmed_authors>Kohl P</pubmed_authors><pubmed_authors>Ruther P</pubmed_authors><pubmed_authors>Rog-Zielinska EA</pubmed_authors><pubmed_authors>Barz F</pubmed_authors><pubmed_authors>Ayub S</pubmed_authors><pubmed_authors>Paul O</pubmed_authors><pubmed_authors>Zgierski-Johnston CM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cardiac pacing using transmural multi-LED probes in channelrhodopsin-expressing mouse hearts.</name><description>Optogenetics enables cell-type specific monitoring and actuation via light-activated proteins. In cardiac research, expressing light-activated depolarising ion channels in cardiomyocytes allows optical pacing and defibrillation. Previous studies largely relied on epicardial illumination. Light penetration through the myocardium is however problematic when moving to larger animals and humans. To overcome this limitation, we assessed the utility of an implantable multi light-emitting diode (LED) optical probe (IMLOP) for intramural pacing of mouse hearts expressing cardiac-specific channelrhodopsin-2 (ChR2). Here we demonstrated that IMLOP insertion needs approximately 20 mN of force, limiting possible damage from excessive loads applied during implantation. Histological sections confirmed t</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Aug</publication><modification>2025-04-19T00:59:56.639Z</modification><creation>2025-04-07T11:56:30.643Z</creation></dates><accession>S-EPMC7322525</accession><cross_references><pubmed>31738979</pubmed><doi>10.1016/j.pbiomolbio.2019.11.004</doi></cross_references></HashMap>