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Application of Multielectrode Mapping to Assess the Effect of Mechanical Right Atrium Distension on the Work of the Isolated Rat Heart

Application of Multielectrode Mapping to Assess the Effect of Mechanical Right Atrium Distension on the Work of the Isolated Rat Heart

Kharkovskaia E.E., Kulikova A.A., Kataev R.D., Drugova O.V., Kostin V.А., Mukhina I.V., Osipov G.V.
Key words: isolated heart; multielectrode mapping; right atrium distension; heart rate variability; excitation wave propagation in myocardium.
2018, volume 10, issue 4, page 113.

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The aim of the study was to assess the effect of mechanical right atrium distension of the isolated rat heart on the heart rate and heart rate variability, and the velocity of excitation wave propagation in the left ventricular myocardium using multielectrode mapping with flexible arrays.

Materials and Methods. Experimental studies have been performed on the isolated rat heart in compliance with the Langendorff technique. Electrical heart activity was recorded using a flexible multielectrode array system.

Results. Characteristic electrophysiological parameter changes of the isolated heart with the right atrium distension were detected using multielectrode mapping with flexible arrays. The flexible array design allowed registration of electrical potentials from the left ventricular surface of the actively contracting rat heart perfused according to the Langendorff technique and assessment of interconnection in the work of different parts of the heart: the right atrium in which the sinus node regulating the heart rate is located and the left ventricle. Application of multiple electrodes arranged in a specific way in the array made it possible to analyze spatio-temporal characteristics of electrical activity on the heart surface and to establish both the increase of the sinus node excitation frequency and excitation wave propagation velocity in the left ventricle.

Conclusion. The growth of heart rate variability may suggest the existence of additional mechano-induced processes generating electrical instability in the distended atrium. The effects detected in the left ventricle with the given method may be caused by triggering intracardial regulation mechanisms.

  1. Bainbridge F.A. The influence of venous filling upon the rate of the heart. J Physiol 1915; 50(2): 65–84, https://doi.org/10.1113/jphysiol.1915.sp001736.
  2. Kositsky G.I. Afferentnye sistemy serdtsa [The afferent systems of the heart]. Moscow: Meditsina; 1975; 207 p.
  3. Frank O. Zur Dynamik des Herzmuskels. Z Biol 1895; 32: 370–447.
  4. Patterson S.W., Starling E.H. On the mechanical factors which determine the output of the ventricles. Physiol 1914; 48(5): 357–379.
  5. Kamkin A.G., Yarygin V.N., Kiseleva I.S. Mekhanoelekgricheskaya obratnaya svyaz’ v serdtse [Mechano-electric feedback in the heart]. Moscow: Natyurmort; 2003; 352 p.
  6. Teng J., Loukin S., Kung C. Mechanosensitive ion channels in cardiovascular physiology. Exp Clin Cardiol 2014; 20(10): 6550–6560.
  7. Inoue R., Jian Z., Kawarabayashi Y. Mechanosensitive TRP channels in cardiovascular pathophysiology. Pharmacol Ther 2009; 123(3): 371–385, https://doi.org/10.1016/j.pharmthera.2009.05.009.
  8. McCain M.L., Parker K.K. Mechanotransduction: the role of mechanical stress, myocyte shape, and cytoskeletal architecture on cardiac function. Pflugers Arch 2011; 462(1): 89–104, https://doi.org/10.1007/s00424-011-0951-4.
  9. Young J.L., Kretchmer K., Ondeck M.G., Zambon A.C., Engler A.J. Mechanosensitive kinases regulate stiffness-induced cardiomyocyte maturation. Sci Rep 2014; 4(1): 6425, https://doi.org/10.1038/srep06425.
  10. Schlomka G. Commotio cordis und ihre Folgen. (Die Einwirkung stumpfer Brustwandtraumen auf das Herz). In: Czerny A., Kraus F., Müller F., v. Pfaundler M., Schittenhelm A. (editors). Ergebnisse der Inneren Medizin und Kinderheilkunde. Springer, Berlin, Heidelberg; 1934; p. 1–91, https://doi.org/10.1007/978-3-642-90672-5_1.
  11. Michel J., Johnson A.D., Bridges W.C. Arrhythmias during intracardiac catheterization. Circulation 1950; 2(2): 240–250, https://doi.org/10.1161/01.cir.2.2.240.
  12. Brohawn S.G., Su Z., MacKinnon R. Mechanosensitivity is mediated directly by the lipid membrane in TRAAK and TREK1 K+ channels. Proc Natl Acad Sci USA 2014; 111(9): 3614–3619, https://doi.org/10.1073/pnas.1320768111.
  13. Thompson S.A., Copeland C.R., Reich D.H., Tung L. Mechanical coupling between myofibroblasts and cardiomyocytes slows electrical conduction in fibrotic cell monolayers. Circulation 2011; 123(19): 2083–2093, https://doi.org/10.1161/circulationaha.110.015057.
  14. Vandebrouck C., Martin D., Colson-Van Schoor M., Debaix H., Gailly P. Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers. J Cell Biol 2002; 158(6): 1089–1096, https://doi.org/10.1083/jcb.200203091.
  15. Wang K., Terrar D., Gavaghan D.J., Mu-u-min R., Kohl P., Bollensdorff C. Living cardiac tissue slices: an organotypic pseudo two-dimensional model for cardiac biophysics research. Prog Biophys Mol Biol 2014; 115 (2–3): 314–327, https://doi.org/10.1016/j.pbiomolbio.2014.08.006.
  16. Filgueiras-Rama D., Martins R.P., Ennis S.R., Mironov S., Jiang J., Yamazaki M., Kalifa J., Jalife J., Berenfeld O. High-resolution endocardial and epicardial optical mapping in a sheep model of stretch-induced atrial fibrillation. J Vis Exp 2011; 53: 3103, https://doi.org/10.3791/3103.
  17. Nazir S.A., Lab M.J. Mechanoelectric feedback in the atrium of the isolated guinea-pig heart. Cardiovasc Res 1996; 32(1): 112–119, https://doi.org/10.1016/s0008-6363(96)00077-6.
  18. Franz M.R. Mechano-electrical feedback in ventricular myocardium. Cardiovasc Res 1996; 32(1): 15–24, https://doi.org/10.1016/s0008-6363(96)00074-0.
  19. Quinn T.A., Kohl P. Mechano-sensitivity of cardiac pacemaker function: pathophysiological relevance, experimental implications, and conceptual integration with other mechanisms of rhythmicity. Prog Biophys Mol Biol 2012; 110(2–3): 257–268, https://doi.org/10.1016/j.pbiomolbio.2012.08.008.
  20. Bokeriya L.A., Filatov A.G. Mapping of arrhythmias. Annaly aritmologii 2012; 9(1): 5–13.
  21. Vigmond E.J., Efimov I.R., Rentschler S.L., Coronel R., Boukens B.J. Fractionated electrograms with ST-segment elevation recorded from the human right ventricular outflow tract. HeartRhythm Case Rep 2017; 3(11): 546–550, https://doi.org/10.1016/j.hrcr.2017.08.010.
  22. Linnenbank A.C., de Bakker J.M.T., Coronel R. How to measure propagation velocity in cardiac tissue: a simulation study. Front Physiol 2014; 5: 267, https://doi.org/10.3389/fphys.2014.00267.
  23. Baevskiy R.M., Ivanov G.G., Chireykin L.V., Gavrilushkin A.P., Dovgalevskiy P.Ya., Kukushkin Yu.A., Mironova T.F., Prilutskiy D.A., Semenov A.V., Fedorov V.F., Fleyshman A.N., Medvedev M.M. Analysis of heart rate variability using different electrocardiographic systems: methodical recommendations. Vestnik aritmologii 2001; 24: 65–86.
  24. Hooks D.A., Tomlinson K.A., Marsden S.G., LeGrice I.J., Smaill B.H., Pullan A.J., Hunter P.J. Cardiac microstructure: implications for electrical propagation and defibrillation in the heart. Circ Res 2002; 91(4): 331–338, https://doi.org/10.1161/01.res.0000031957.70034.89.
  25. Tiitso M. Chronotrope Wirkungen der Spannungsänderungen des rechten Vorhofes. Pflugers Arch Gesamte Physiol Menschen Tiere 1937; 238(1): 738–748, https://doi.org/10.1007/bf01767681.
  26. Blinks J.R. Positive chronotropic effect of increasing right atrial pressure in the isolated mammalian heart. Am J Physiol 1956; 186(2): 299–303, https://doi.org/10.1152/ajplegacy.1956.186.2.299.
  27. Deck K.A. Effects of stretch on the spontaneously beating, isolated sinus node. Pflugers Arch Gesamte Physiol Menschen Tiere 1964; 280: 120–130.
Kharkovskaia E.E., Kulikova A.A., Kataev R.D., Drugova O.V., Kostin V.А., Mukhina I.V., Osipov G.V. Application of Multielectrode Mapping to Assess the Effect of Mechanical Right Atrium Distension on the Work of the Isolated Rat Heart. Sovremennye tehnologii v medicine 2018; 10(4): 113, https://doi.org/10.17691/stm2018.10.4.13


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