Effect of renal sympathetic denervation on the inducibility of atrial fibrillation during rapid atrial pacing
Background Atrial fibrillation (AF) is associated with activity of renin–angiotensin–aldosterone system (RAAS). Reduction in renal noradrenaline spillover could be achieved after renal sympathetic denervation (RSD). The relationship between RSD and AF is unknown. Objective The objective of the study...
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Veröffentlicht in: | Journal of interventional cardiac electrophysiology 2012-11, Vol.35 (2), p.119-125 |
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Sprache: | eng |
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Zusammenfassung: | Background
Atrial fibrillation (AF) is associated with activity of renin–angiotensin–aldosterone system (RAAS). Reduction in renal noradrenaline spillover could be achieved after renal sympathetic denervation (RSD). The relationship between RSD and AF is unknown.
Objective
The objective of the study was to investigate the inducibility of AF during atrial rapid pacing after RSD.
Methods
Thirteen dogs were used for the study as follows: control group (seven dogs) and RSD group (six dogs). In the control group, dogs were subjected to atrial pacing at 800 beats/min for 7 h, and atrial effective refractory period (AERP) was measured every hour in the status of non-pacing. Subsequently, pacing was stopped and the burst pacing (500 bpm) was repeated to induce AF three times. In the RSD group, after each renal artery ablation, the procedure of pacing and electrophysiological measurement was exactly same as in the control group. Blood was collected before and after pacing to measure the levels of renin, angiotensin II and aldosterone.
Results
There was a persistent decrease in AERP in both groups. However, 7 h after cessation of pacing, the induced number of times and duration of AF were higher in the control group than that in the RSD group (1.0 ± 1.26 vs 3.14 ± 2.54,
P
= 0.03; 16.5 ± 25.1 vs 86.6 ± 116.4,
P
= 0.02). The plasma aldosterone concentration increased significantly 7 h after rapid pacing in control group (renin, 119.8 ± 31.1 vs 185.3 ± 103.5 pg/ml,
P
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ISSN: | 1383-875X 1572-8595 |
DOI: | 10.1007/s10840-012-9717-y |