Effects of verapamil and procainamide on acute atrial electrical remodeling induced by short-term rapid atrial pacing in humans
- PMID: 18192095
- PMCID: PMC11918004
- DOI: 10.1016/S1607-551X(08)70058-5
Effects of verapamil and procainamide on acute atrial electrical remodeling induced by short-term rapid atrial pacing in humans
Abstract
Atrial electrical remodeling (ER) after spontaneous or pacing-induced atrial fibrillation has been previously described in humans. We investigated atrial ER induced by a 5-minute period of rapid atrial pacing and the pharmacologic effects of verapamil and procainamide on this atrial ER phenomenon. The atrial effective refractory periods (ERPs) at drive cycle lengths of 400 (ERP 400 ) and 600 (ERP 600 ) ms, at five representative atrial sites (high right atrium [HRA]; proximal, middle and distal coronary sinus; interatrial septum), were determined in 20 patients at baseline and immediately after cessation of a 5-minute period of rapid pacing from the HRA at a rate of 150 bpm. The degrees of atrial ERP 400 and ERP 600 shortening after pacing were calculated as acute atrial ER. The same protocol was repeated in another 15 patients after intravenous administration of verapamil (0.15 mg/kg) and in another 15 patients after intravenous administration of procainamide (15 mg/kg). The results demonstrated that, in the control state acute atrial ER can be significantly demonstrated at each atrial representative site ( p < 0.001). The mean ERP 400 and ERP 600 shortenings were 9 +/- 4% and 8 +/- 4%, respectively. After procainamide infusion, but not after verapamil, baseline ERP 400 and ERP 600 values were significantly prolonged at the five representative atrial sites ( p < 0.01). Acute atrial ER could still be demonstrated at each atrial site after procainamide or verapamil infusion ( p < 0.001). In conclusion, acute atrial ER can be demonstrated after only a 5-minute period of rapid atrial pacing in humans. Intravenous verapamil or procainamide does not abolish this ER process.
Similar articles
-
Effect of verapamil and procainamide on atrial fibrillation-induced electrical remodeling in humans.Circulation. 1997 Sep 2;96(5):1542-50. doi: 10.1161/01.cir.96.5.1542. Circulation. 1997. PMID: 9315545
-
Effects of verapamil on superior vena cava electrical remodeling induced by short-term pacing from right atrium and superior vena cava in human.Int J Cardiol. 2007 Sep 3;120(3):380-6. doi: 10.1016/j.ijcard.2006.10.015. Epub 2006 Dec 18. Int J Cardiol. 2007. PMID: 17175044
-
Verapamil reduces tachycardia-induced electrical remodeling of the atria.Circulation. 1997 Apr 1;95(7):1945-53. doi: 10.1161/01.cir.95.7.1945. Circulation. 1997. PMID: 9107184
-
Tachycardia-induced change of atrial refractory period in humans: rate dependency and effects of antiarrhythmic drugs.Circulation. 1998 Jun 16;97(23):2331-7. doi: 10.1161/01.cir.97.23.2331. Circulation. 1998. PMID: 9639377 Clinical Trial.
-
Verapamil suppresses the inhomogeneity of electrical remodeling in a canine long-term rapid atrial stimulation model.Pacing Clin Electrophysiol. 2003 Nov;26(11):2072-82. doi: 10.1046/j.1460-9592.2003.00323.x. Pacing Clin Electrophysiol. 2003. PMID: 14622307
References
-
- Nattel S. New ideas about atrial fibrillation 50 years on. Nature. 2002; 415: 219–226. - PubMed
-
- Allessie M, Ausma J, Schotten U. Electrical, contractile and structural remodeling during atrial fibrillation. Cardiovasc Res. 2002; 54: 230–246. - PubMed
-
- Goette A, Honeycutt C, Langberg JJ. Electrical remodeling in atrial fibrillation. Time course and mechanisms. Circulation. 1996; 94: 2968–2974. - PubMed
-
- Wijffels MC, Kirchhof CJ, Dorland R, et al. Electrical remodeling due to atrial fibrillation in chronically instrumented conscious goats: roles of neurohumoral changes, ischemia, atrial stretch, and high rate of electrical activation. Circulation. 1997; 96: 3710–3720. - PubMed
-
- Everett TH 4th, Li H, Mangrum JM, et al. Electrical, morphological, and ultrastructural remodeling and reverse remodeling in a canine model of chronic atrial fibrillation. Circulation. 2000; 102: 1454–1460. - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources