An implantable system for long-term assessment of atrial fibrillation substrate in unanesthetized rats exposed to underlying pathological conditions.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
17 01 2020
Historique:
received: 07 08 2019
accepted: 16 12 2019
entrez: 19 1 2020
pubmed: 19 1 2020
medline: 11 11 2020
Statut: epublish

Résumé

Atrial fibrillation (AF) is a progressive arrhythmia with underlying mechanisms that are not fully elucidated, partially due to lack of reliable and affordable animal models. Here, we introduce a system for long-term assessment of AF susceptibility (substrate) in ambulatory rats implanted with miniature electrodes on the atrium. Rats were subjected to excessive aldosterone (Aldo) or solvent only (Sham). An additional group was exposed to myocardial infarction (MI). AF substrate was tested two- and four-weeks post implantation and was also compared with implanted rats early post-implantation (Base). Aldo and MI increased the AF substrate and atrial fibrosis. In the MI group only, AF duration was correlated with the level of atrial fibrosis and was inversely correlated with systolic function. Unexpectedly, Shams also developed progressive AF substrate relative to Base individuals. Further studies indicated that serum inflammatory markers (IL-6, TNF-alpha) were not elevated in the shams. In addition, we excluded anxiety\depression due to social-isolation as an AF promoting factor. Finally, enhanced biocompatibility of the atrial electrode did not inhibit the gradual development of AF substrate over a testing period of up to 8 weeks. Overall, we successfully validated the first system for long-term AF substrate testing in ambulatory rats.

Identifiants

pubmed: 31953473
doi: 10.1038/s41598-020-57528-3
pii: 10.1038/s41598-020-57528-3
pmc: PMC6969190
doi:

Substances chimiques

Il6 protein, rat 0
Interleukin-6 0
Tumor Necrosis Factor-alpha 0
Aldosterone 4964P6T9RB

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

553

Références

Heeringa, J. et al. Prevalence, incidence and lifetime risk of atrial fibrillation: the Rotterdam study. Eur Heart J 27, 949–953, https://doi.org/10.1093/eurheartj/ehi825 (2006).
doi: 10.1093/eurheartj/ehi825 pubmed: 16527828
Chugh, S. S. et al. Worldwide epidemiology of atrial fibrillation: a Global Burden of Disease 2010 Study. Circulation 129, 837–847, https://doi.org/10.1161/circulationaha.113.005119 (2014).
doi: 10.1161/circulationaha.113.005119 pubmed: 24345399
Haissaguerre, M. et al. Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins. N Engl J Med 339, 659–666, https://doi.org/10.1056/NEJM199809033391003 (1998).
doi: 10.1056/NEJM199809033391003 pubmed: 9725923
Brundel, B. J., Henning, R. H., Kampinga, H. H., Van Gelder, I. C. & Crijns, H. J. Molecular mechanisms of remodeling in human atrial fibrillation. Cardiovasc Res 54, 315–324 (2002).
doi: 10.1016/S0008-6363(02)00222-5
Wakili, R., Voigt, N., Kaab, S., Dobrev, D. & Nattel, S. Recent advances in the molecular pathophysiology of atrial fibrillation. J Clin Invest 121, 2955–2968 (2011).
doi: 10.1172/JCI46315
Heijman, J. et al. The value of basic research insights into atrial fibrillation mechanisms as a guide to therapeutic innovation: a critical analysis. Cardiovasc Res 109, 467–479, https://doi.org/10.1093/cvr/cvv275 (2016).
doi: 10.1093/cvr/cvv275 pubmed: 26705366
Lau, D. H., Nattel, S., Kalman, J. M. & Sanders, P. Modifiable Risk Factors and Atrial Fibrillation. Circulation 136, 583–596, https://doi.org/10.1161/circulationaha.116.023163 (2017).
doi: 10.1161/circulationaha.116.023163 pubmed: 28784826
Dzeshka, M. S., Lip, G. Y., Snezhitskiy, V. & Shantsila, E. Cardiac Fibrosis in Patients With Atrial Fibrillation: Mechanisms and Clinical Implications. J Am Coll Cardiol 66, 943–959, https://doi.org/10.1016/j.jacc.2015.06.1313 (2015).
doi: 10.1016/j.jacc.2015.06.1313 pubmed: 26293766
Dobrev, D., Carlsson, L. & Nattel, S. Novel molecular targets for atrial fibrillation therapy. Nat Rev Drug Discov 11, 275–291, https://doi.org/10.1038/nrd3682 (2012).
doi: 10.1038/nrd3682 pubmed: 22460122
Wijesurendra, R. S. et al. Lone Atrial Fibrillation Is Associated With Impaired Left Ventricular Energetics That Persists Despite Successful Catheter Ablation. Circulation 134, 1068–1081, https://doi.org/10.1161/circulationaha.116.022931 (2016).
doi: 10.1161/circulationaha.116.022931 pubmed: 27630135 pmcid: 5054971
Nattel, S., Shiroshita-Takeshita, A., Brundel, B. J. & Rivard, L. Mechanisms of atrial fibrillation: lessons from animal models. Prog Cardiovasc Dis 48, 9–28, https://doi.org/10.1016/j.pcad.2005.06.002 (2005).
doi: 10.1016/j.pcad.2005.06.002 pubmed: 16194689
Choisy, S. C. M., Arberry, L. A., Hancox, J. C. & James, A. F. Increased Susceptibility to Atrial Tachyarrhythmia in Spontaneously Hypertensive Rat Hearts. Hypertension 49, 498–505, https://doi.org/10.1161/01.HYP.0000257123.95372.ab (2007).
doi: 10.1161/01.HYP.0000257123.95372.ab pubmed: 17242301
Kirchhof, P. et al. PITX2c is expressed in the adult left atrium, and reducing Pitx2c expression promotes atrial fibrillation inducibility and complex changes in gene expression. Circ Cardiovasc Genet 4, 123–133, https://doi.org/10.1161/CIRCGENETICS.110.958058 (2011).
doi: 10.1161/CIRCGENETICS.110.958058 pubmed: 21282332
Shan, J. et al. Calcium leak through ryanodine receptors leads to atrial fibrillation in 3 mouse models of catecholaminergic polymorphic ventricular tachycardia. Circ Res 111, 708–717, https://doi.org/10.1161/CIRCRESAHA.112.273342 (2012).
doi: 10.1161/CIRCRESAHA.112.273342 pubmed: 22828895 pmcid: 3734386
Riley, G., Syeda, F., Kirchhof, P. & Fabritz, L. An introduction to murine models of atrial fibrillation. Front Physiol 3, 296 (2012).
pubmed: 22934047 pmcid: 3429067
Skibsbye, L. et al. Inhibition of Small Conductance Calcium-Activated Potassium (SK) Channels Prevents Arrhythmias in Rat Atria During beta-Adrenergic and Muscarinic Receptor Activation. Front Physiol 9, 510, https://doi.org/10.3389/fphys.2018.00510 (2018).
doi: 10.3389/fphys.2018.00510 pubmed: 29922167 pmcid: 5996028
Cheng, C. et al. Mutation in NPPA causes atrial fibrillation by activating inflammation and cardiac fibrosis in a knock-in rat model. FASEB J, fj201802455RRR. https://doi.org/10.1096/fj.201802455RRR (2019).
doi: 10.1096/fj.201802455RRR
Geng, L. et al. SNX17 (Sorting Nexin 17) Mediates Atrial Fibrillation Onset Through Endocytic Trafficking of the Kv1.5 (Potassium Voltage-Gated Channel Subfamily A Member 5) Channel. Circ Arrhythm Electrophysiol 12, e007097, https://doi.org/10.1161/circep.118.007097 (2019).
doi: 10.1161/circep.118.007097 pubmed: 30939909
Hulsmans, M. et al. A Miniaturized, Programmable Pacemaker for Long-Term Studies in the Mouse. Circ Res 123, 1208–1219, https://doi.org/10.1161/circresaha.118.313429 (2018).
doi: 10.1161/circresaha.118.313429 pubmed: 30571465 pmcid: 6309285
Etzion, Y. et al. New insights into the atrial electrophysiology of rodents using a novel modality: the miniature-bipolar hook electrode. Am J Physiol Heart Circ Physiol 295, H1460–1469, https://doi.org/10.1152/ajpheart.00414.2008 (2008).
doi: 10.1152/ajpheart.00414.2008 pubmed: 18660446
Mor, M. et al. INO-8875, a Highly-Selective A1 Adenosine Receptor Agonist: Evaluation of Chronotropic, Dromotropic and Hemodynamic Effects in Rats. J Pharmacol Exp Ther. https://doi.org/10.1124/jpet.112.200873 (2012).
doi: 10.1124/jpet.112.200873 pubmed: 23055540
Mor, M. et al. Speckle-tracking echocardiography elucidates the effect of pacing site on left ventricular synchronization in the normal and infarcted rat myocardium. PLoS One 9, e99191 (2014).
doi: 10.1371/journal.pone.0099191
Mulla, W. et al. Prominent differences in left ventricular performance and myocardial properties between right ventricular and left ventricular-based pacing modes in rats. Sci Rep 7, 5931 (2017).
doi: 10.1038/s41598-017-06197-w
Mulla, W. et al. Unanesthetized Rodents Demonstrate Insensitivity of QT Interval and Ventricular Refractory Period to Pacing Cycle Length. Front Physiol 9, 897, https://doi.org/10.3389/fphys.2018.00897 (2018).
doi: 10.3389/fphys.2018.00897 pubmed: 30050462 pmcid: 6050393
Mulla, W. et al. Rapid Atrial Pacing Promotes Atrial Fibrillation Substrate in Unanesthetized Instrumented Rats. Front Physiol 10, 1218, https://doi.org/10.3389/fphys.2019.01218 (2019).
doi: 10.3389/fphys.2019.01218 pubmed: 31616316 pmcid: 6763969
Reil, J. C. et al. Aldosterone promotes atrial fibrillation. Eur Heart J 33, 2098–2108, https://doi.org/10.1093/eurheartj/ehr266 (2012).
doi: 10.1093/eurheartj/ehr266 pubmed: 21816854
Miyauchi, Y. et al. Altered Atrial Electrical Restitution and Heterogeneous Sympathetic Hyperinnervation in Hearts With Chronic Left Ventricular Myocardial Infarction: Implications for Atrial Fibrillation. Circulation 108, 360–366 (2003).
doi: 10.1161/01.CIR.0000080327.32573.7C
Bejerano, T., Etzion, S., Elyagon, S., Etzion, Y. & Cohen, S. Nanoparticle Delivery of miRNA-21 Mimic to Cardiac Macrophages Improves Myocardial Remodeling after Myocardial Infarction. Nano letters 18, 5885–5891, https://doi.org/10.1021/acs.nanolett.8b02578 (2018).
doi: 10.1021/acs.nanolett.8b02578 pubmed: 30141949
Lammers, C. et al. Spironolactone prevents aldosterone induced increased duration of atrial fibrillation in rat. Cell Physiol Biochem 29, 833–840, https://doi.org/10.1159/000178483 (2012).
doi: 10.1159/000178483 pubmed: 22613983
Cardin, S. et al. Role for MicroRNA-21 in atrial profibrillatory fibrotic remodeling associated with experimental postinfarction heart failure. Circ Arrhythm Electrophysiol 5, 1027–1035, https://doi.org/10.1161/circep.112.973214 (2012).
doi: 10.1161/circep.112.973214 pubmed: 22923342
Dai, H. et al. Atrial Fibrillation Promotion in a Rat Model of Rheumatoid Arthritis. J Am Heart Assoc 6, https://doi.org/10.1161/jaha.117.007320 (2017).
Yao, C. et al. Enhanced Cardiomyocyte NLRP3 Inflammasome Signaling Promotes Atrial Fibrillation. Circulation 138, 2227–2242, https://doi.org/10.1161/circulationaha.118.035202 (2018).
doi: 10.1161/circulationaha.118.035202 pubmed: 29802206 pmcid: 6252285
Rygula, R. et al. Anhedonia and motivational deficits in rats: impact of chronic social stress. Behavioural brain research 162, 127–134, https://doi.org/10.1016/j.bbr.2005.03.009 (2005).
doi: 10.1016/j.bbr.2005.03.009 pubmed: 15922073
Peartree, N. A. et al. Limited physical contact through a mesh barrier is sufficient for social reward-conditioned place preference in adolescent male rats. Physiol Behav 105, 749–756, https://doi.org/10.1016/j.physbeh.2011.10.001 (2012).
doi: 10.1016/j.physbeh.2011.10.001 pubmed: 22008744
Shah Idil, A. & Donaldson, N. The use of tungsten as a chronically implanted material. Journal of neural engineering 15, 021006, https://doi.org/10.1088/1741-2552/aaa502 (2018).
doi: 10.1088/1741-2552/aaa502 pubmed: 29300000
Everett, T. H. & Olgin, J. E. Atrial fibrosis and the mechanisms of atrial fibrillation. Heart Rhythm 4, S24–27 (2007).
doi: 10.1016/j.hrthm.2006.12.040
Budzikowski, A. S. Aldosterone pathway in atrial fibrillation. Cardiology 118, 238, https://doi.org/10.1159/000329505 (2011).
doi: 10.1159/000329505 pubmed: 21734374
Hung, C. S. et al. Aldosterone Induces Tissue Inhibitor of Metalloproteinases-1 Expression and Further Contributes to Collagen Accumulation: From Clinical to Bench Studies. Hypertension 67, 1309–1320, https://doi.org/10.1161/hypertensionaha.115.06768 (2016).
doi: 10.1161/hypertensionaha.115.06768 pubmed: 27113051
Lendeckel, U., Dobrev, D. & Goette, A. Aldosterone-receptor antagonism as a potential therapeutic option for atrial fibrillation. Br J Pharmacol 159, 1581–1583 (2010).
doi: 10.1111/j.1476-5381.2010.00675.x
Zhao, J. et al. Effects of spironolactone on atrial structural remodelling in a canine model of atrial fibrillation produced by prolonged atrial pacing. Br J Pharmacol 159, 1584–1594 (2010).
doi: 10.1111/j.1476-5381.2009.00551.x
Ito, Y. et al. Effect of eplerenone on maintenance of sinus rhythm after catheter ablation in patients with long-standing persistent atrial fibrillation. Am J Cardiol 111, 1012–1018, https://doi.org/10.1016/j.amjcard.2012.12.020 (2013).
doi: 10.1016/j.amjcard.2012.12.020 pubmed: 23340033
Kritis, A. A., Gouta, C. P., Liaretidou, E. I. & Kallaras, K. I. Latest aspects of aldosterone actions on the heart muscle. J Physiol Pharmacol 67, 21–30 (2016).
pubmed: 27010892
Jalife, J. Novel upstream approaches to prevent atrial fibrillation perpetuation. Cardiol Clin 32, 637–650, https://doi.org/10.1016/j.ccl.2014.07.004 (2014).
doi: 10.1016/j.ccl.2014.07.004 pubmed: 25443242
Mummidi, S. et al. Metformin inhibits aldosterone-induced cardiac fibroblast activation, migration and proliferation in vitro, and reverses aldosterone+salt-induced cardiac fibrosis in vivo. J Mol Cell Cardiol 98, 95–102, https://doi.org/10.1016/j.yjmcc.2016.07.006 (2016).
doi: 10.1016/j.yjmcc.2016.07.006 pubmed: 27423273
Whaley-Connell, A., Johnson, M. S. & Sowers, J. R. Aldosterone: role in the cardiometabolic syndrome and resistant hypertension. Prog Cardiovasc Dis 52, 401–409, https://doi.org/10.1016/j.pcad.2009.12.004 (2010).
doi: 10.1016/j.pcad.2009.12.004 pubmed: 20226958 pmcid: 2841057
Lakin, R. et al. Inhibition of soluble TNFalpha prevents adverse atrial remodeling and atrial arrhythmia susceptibility induced in mice by endurance exercise. J Mol Cell Cardiol 129, 165–173, https://doi.org/10.1016/j.yjmcc.2019.01.012 (2019).
doi: 10.1016/j.yjmcc.2019.01.012 pubmed: 30796945
Dobrev, D., Aguilar, M., Heijman, J., Guichard, J. B. & Nattel, S. Postoperative atrial fibrillation: mechanisms, manifestations and management. Nat Rev Cardiol 16, 417–436, https://doi.org/10.1038/s41569-019-0166-5 (2019).
doi: 10.1038/s41569-019-0166-5 pubmed: 30792496
Fenger-Gron, M. et al. Depression, antidepressants, and the risk of non-valvular atrial fibrillation: A nationwide Danish matched cohort study. European journal of preventive cardiology 26, 187–195, https://doi.org/10.1177/2047487318811184 (2019).
doi: 10.1177/2047487318811184 pubmed: 30452291
Hatch, A. M. et al. Isolation syndrome in the rat. Toxicol Appl Pharmacol 7, 737–745 (1965).
doi: 10.1016/0041-008X(65)90132-8
Thanigaimani, S. et al. Progression and reversibility of stretch induced atrial remodeling: Characterization and clinical implications. Prog Biophys Mol Biol 130, 376–386, https://doi.org/10.1016/j.pbiomolbio.2017.07.010 (2017).
doi: 10.1016/j.pbiomolbio.2017.07.010 pubmed: 28734850

Auteurs

Hadar Klapper-Goldstein (H)

Cardiac Arrhythmia Research Laboratory, Department of Physiology and Cell Biology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel. hadarklapperp@gmail.com.
Regenerative Medicine & Stem Cell Research Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel. hadarklapperp@gmail.com.

Michael Murninkas (M)

Cardiac Arrhythmia Research Laboratory, Department of Physiology and Cell Biology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Regenerative Medicine & Stem Cell Research Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

Roni Gillis (R)

Cardiac Arrhythmia Research Laboratory, Department of Physiology and Cell Biology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Regenerative Medicine & Stem Cell Research Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

Wesam Mulla (W)

Cardiac Arrhythmia Research Laboratory, Department of Physiology and Cell Biology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Regenerative Medicine & Stem Cell Research Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

Eran Levanon (E)

Cardiac Arrhythmia Research Laboratory, Department of Physiology and Cell Biology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Regenerative Medicine & Stem Cell Research Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

Sigal Elyagon (S)

Cardiac Arrhythmia Research Laboratory, Department of Physiology and Cell Biology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Regenerative Medicine & Stem Cell Research Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

Ronen Schuster (R)

Department of Clinical Biochemistry & Pharmacology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

Dor Danan (D)

Beer-Sheva Mental Health Center, Ministry of Health, Anxiety and Stress Research Unit, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

Hagit Cohen (H)

Beer-Sheva Mental Health Center, Ministry of Health, Anxiety and Stress Research Unit, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

Yoram Etzion (Y)

Cardiac Arrhythmia Research Laboratory, Department of Physiology and Cell Biology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel. tzion@bgu.ac.il.
Regenerative Medicine & Stem Cell Research Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel. tzion@bgu.ac.il.

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