4.7 Article

Ventricular fibrillation mechanism and global fibrillatory organization are determined by gap junction coupling and fibrosis pattern

期刊

CARDIOVASCULAR RESEARCH
卷 117, 期 4, 页码 1078-1090

出版社

OXFORD UNIV PRESS
DOI: 10.1093/cvr/cvaa141

关键词

Ventricular fibrillation; Fibrosis; Gap junctions; Rotational activity; Fibrillation; Mechanisms

资金

  1. British Heart Foundation [RG/16/3/32175, PG/16/17/32069]
  2. National Institute for Health Research (NIHR) Imperial Biomedical Research Centre
  3. NIHR Clinical Lectureship [CL-2011-21-001]
  4. Medical Research Council Skills Development Fellowship [MR/S015086/1]
  5. BHF Centre for Regenerative Medicine [RM/17/1/33377]
  6. MRC [MR/S015086/1] Funding Source: UKRI

向作者/读者索取更多资源

Conflicting data exist supporting differing mechanisms for sustaining ventricular fibrillation (VF), ranging from disorganized multiple-wavelet activation to organized rotational activities (RAs). The degree of gap junction (GJ) coupling and pattern of fibrosis influences the mechanism sustaining VF. There is a continuous spectrum of organization in VF, ranging between globally organized fibrillation sustained by stable RAs and disorganized, possibly multiple-wavelet driven fibrillation with no RAs.
Aims Conflicting data exist supporting differing mechanisms for sustaining ventricular fibrillation (VF), ranging from disorganized multiple-wavelet activation to organized rotational activities (RAs). Abnormal gap junction (GJ) coupling and fibrosis are important in initiation and maintenance of VF. We investigated whether differing ventricular fibrosis patterns and the degree of GJ coupling affected the underlying VF mechanism. Methods and results Optical mapping of 65 Langendorff-perfused rat hearts was performed to study VF mechanisms in control hearts with acute GJ modulation, and separately in three differing chronic ventricular fibrosis models; compact fibrosis (CF), diffuse fibrosis (DiF), and patchy fibrosis (PF). VF dynamics were quantified with phase mapping and frequency dominance index (FDI) analysis, a power ratio of the highest amplitude dominant frequency in the cardiac frequency spectrum. Enhanced GJ coupling with rotigaptide (n = 10) progressively organized fibrillation in a concentration-dependent manner; increasing FDI (0 nM: 0.53 +/- 0.04, 80 nM: 0.78 +/- 0.03, P< 0.001), increasing RA-sustained VF time (0 nM: 44 +/- 6%, 80 nM: 94 +/- 2%, P < 0.001), and stabilized RAs (maximum rotations for an RA; 0 nM: 5.4 +/- 0.5, 80 nM: 48.2 +/- 12.3, P<0.001). GJ uncoupling with carbenoxolone progressively disorganized VF; the FDI decreased (0 mu M: 0.60 +/- 0.05, 50 mu M: 0.17 +/- 0.03, P< 0.001) and RA-sustained VF time decreased (0 mu M: 61 +/- 9%, 50 mu M: 3 +/- 2%, P < 0.001). In CF, VF activity was disorganized and the RA-sustained VF time was the lowest (CF: 27 +/- 7% vs. PF: 75 +/- 5%, P < 0.001). Global fibrillatory organization measured by FDI was highest in PF (PF: 0.67 +/- 0.05 vs. CF: 0.33 +/- 0.03, P< 0.001). PF harboured the longest duration and most spatially stable RAs (patchy: 1411 +/- 266 ms vs. compact: 354 38ms, P < 0.001). DiF (n= 11) exhibited an intermediately organized VF pattern, sustained by a combination of multiple-wavelets and short-lived RAs. Conclusion The degree of GJ coupling and pattern of fibrosis influences the mechanism sustaining VF. There is a continuous spectrum of organization in VF, ranging between globally organized fibrillation sustained by stable RAs and disorganized, possibly multiple-wavelet driven fibrillation with no RAs. [GRAPHICS] .

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