| Literature DB >> 26840736 |
Irma Martišienė1, Regina Mačianskienė2, Rimantas Treinys1, Antanas Navalinskas1, Mantė Almanaitytė1, Dainius Karčiauskas1, Audrius Kučinskas1, Ramunė Grigalevičiūtė1, Vilma Zigmantaitė1, Rimantas Benetis1, Jonas Jurevičius1.
Abstract
So far, the optical mapping of cardiac electrical signals using voltage-sensitive fluorescent dyes has only been performed in experimental studies because these dyes are not yet approved for clinical use. It was recently reported that the well-known and widely used fluorescent dye indocyanine green (ICG), which has FDA approval, exhibits voltage sensitivity in various tissues, thus raising hopes that electrical activity could be optically mapped in the clinic. The aim of this study was to explore the possibility of using ICG to monitor cardiac electrical activity. Optical mapping experiments were performed on Langendorff rabbit hearts stained with ICG and perfused with electromechanical uncouplers. The residual contraction force and electrical action potentials were recorded simultaneously. Our research confirms that ICG is a voltage-sensitive dye with a dual-component (fast and slow) response to membrane potential changes. The fast component of the optical signal (OS) can have opposite polarities in different parts of the fluorescence spectrum. In contrast, the polarity of the slow component remains the same throughout the entire spectrum. Separating the OS into these components revealed two different voltage-sensitivity mechanisms for ICG. The fast component of the OS appears to be electrochromic in nature, whereas the slow component may arise from the redistribution of the dye molecules within or around the membrane. Both components quite accurately track the time of electrical signal propagation, but only the fast component is suitable for estimating the shape and duration of action potentials. Because ICG has voltage-sensitive properties in the entire heart, we suggest that it can be used to monitor cardiac electrical behavior in the clinic.Entities:
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Year: 2016 PMID: 26840736 PMCID: PMC4744163 DOI: 10.1016/j.bpj.2015.12.021
Source DB: PubMed Journal: Biophys J ISSN: 0006-3495 Impact factor: 4.033