10.3389/fphys.2018.01454.s001 Iffath A. Ghouri Iffath A. Ghouri Allen Kelly Allen Kelly Simona Salerno Simona Salerno Karin Garten Karin Garten Tomas Stølen Tomas Stølen Ole-Johan Kemi1 Ole-Johan Kemi1 Godfrey L. Smith Godfrey L. Smith Table_1_Characterization of Electrical Activity in Post-myocardial Infarction Scar Tissue in Rat Hearts Using Multiphoton Microscopy.pdf Frontiers 2019 myocardial infarction optical mapping two-photon microscopy intracellular calcium border zone 2019-04-05 14:43:24 Dataset https://frontiersin.figshare.com/articles/dataset/Table_1_Characterization_of_Electrical_Activity_in_Post-myocardial_Infarction_Scar_Tissue_in_Rat_Hearts_Using_Multiphoton_Microscopy_pdf/7959107 <p>Background: The origin of electrical behavior in post-myocardial infarction scar tissue is still under debate. This study aims to examine the extent and nature of the residual electrical activity within a stabilized ventricular infarct scar.</p><p>Methods and Results: An apical infarct was induced in the left ventricle of Wistar rats by coronary artery occlusion. Five weeks post-procedure, hearts were Langendorff-perfused, and optically mapped using di-4-ANEPPS. Widefield imaging of optical action potentials (APs) on the left ventricular epicardial surface revealed uniform areas of electrical activity in both normal zone (NZ) and infarct border zone (BZ), but only limited areas of low-amplitude signals in the infarct zone (IZ). 2-photon (2P) excitation of di-4-ANEPPS and Fura-2/AM at discrete layers in the NZ revealed APs and Ca<sup>2+</sup> transients (CaTs) to 500–600 μm below the epicardial surface. 2P imaging in the BZ revealed superficial connective tissue structures lacking APs or CaTs. At depths greater than approximately 300 μm, myocardial structures were evident that supported normal APs and CaTs. In the IZ, although 2P imaging did not reveal clear myocardial structures, low-amplitude AP signals were recorded at discrete layers. No discernible Ca<sup>2+</sup> signals could be detected in the IZ. AP rise times in BZ were slower than NZ (3.50 ± 0.50 ms vs. 2.23 ± 0.28 ms) and further slowed in IZ (9.13 ± 0.56 ms). Widefield measurements of activation delay between NZ and BZ showed negligible difference (3.37 ± 1.55 ms), while delay values in IZ showed large variation (11.88 ± 9.43 ms).</p><p>Conclusion: These AP measurements indicate that BZ consists of an electrically inert scar above relatively normal myocardium. Discrete areas/layers of IZ displayed entrained APs with altered electrophysiology, but the structure of this tissue remains to be elucidated.</p>