Effect of simvastatin and antioxidant vitamins on atrial fibrillation promotion by atrial-tachycardia remodeling in dogs

被引:300
作者
Shiroshita-Takeshita, A
Schram, G
Lavoie, J
Nattel, S
机构
[1] Montreal Heart Inst, Dept Med, Montreal, PQ H1T 1C8, Canada
[2] Montreal Heart Inst, Res Ctr, Montreal, PQ H1T 1C8, Canada
[3] Univ Montreal, Montreal, PQ, Canada
关键词
antioxidants; antiarrhythmia agents; electrophysiology;
D O I
10.1161/01.CIR.0000145163.56529.D1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - There is evidence for a role of oxidant stress and inflammation in atrial fibrillation (AF). Statins have both antioxidant and antiinflammatory properties. We compared the effects of simvastatin with those of antioxidant vitamins on AF promotion by atrial tachycardia in dogs. Methods and Results - We studied dogs subjected to atrial tachypacing (ATP) at 400 bpm in the absence and presence of treatment with simvastatin, vitamin C, and combined vitamins C and E. Serial closed-chest electrophysiological studies were performed in each dog at baseline and 2, 4, and 7 days after tachypacing onset. Atrioventricular block was performed to control ventricular rate. Mean duration of induced AF was increased from 42 +/- 18 to 1079 +/- 341 seconds at terminal open-chest study after tachypacing alone ( P < 0.01), and atrial effective refractory period (ERP) at a cycle length of 300 ms was decreased from 117 +/- 5 to 76 +/- 6 ms ( P < 0.01). Tachypacing-induced ERP shortening and AF promotion were unaffected by vitamin C or vitamins C and E; however, simvastatin suppressed tachypacing-induced remodeling effects significantly, with AF duration and ERP averaging 41 +/- 15 seconds and 103 +/- 4 ms, respectively, after tachypacing with simvastatin therapy. Tachypacing downregulated L-type Ca2+-channel alpha-subunit expression (Western blot), an effect that was unaltered by antioxidant vitamins but greatly attenuated by simvastatin. Conclusions - Simvastatin attenuates AF promotion by atrial tachycardia in dogs, an effect not shared by antioxidant vitamins, and constitutes a potentially interesting new pharmacological approach to preventing the consequences of atrial tachycardia remodeling.
引用
收藏
页码:2313 / 2319
页数:7
相关论文
共 37 条
[11]   Importance of refractoriness heterogeneity in the enhanced vulnerability to atrial fibrillation induction caused by tachycardia-induced atrial electrical remodeling [J].
Fareh, S ;
Villemaire, C ;
Nattel, S .
CIRCULATION, 1998, 98 (20) :2202-2209
[12]   ASCORBATE IS AN OUTSTANDING ANTIOXIDANT IN HUMAN-BLOOD PLASMA [J].
FREI, B ;
ENGLAND, L ;
AMES, BN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (16) :6377-6381
[13]  
Gaspo R, 1997, CIRCULATION, V96, P4027
[14]   Electrical remodeling in atrial fibrillation - Time course and mechanisms [J].
Goette, A ;
Honeycutt, C ;
Langberg, JJ .
CIRCULATION, 1996, 94 (11) :2968-2974
[15]   Role of the Na+/H+ exchanger in short-term atrial electrophysiological remodeling [J].
Jayachandran, JV ;
Zipes, DP ;
Weksler, J ;
Olgin, JE .
CIRCULATION, 2000, 101 (15) :1861-1866
[16]   The HMG-CoA reductase inhibitor simvastatin activates the protein kinase Akt and promotes angiogenesis in normocholesterolemic animals. [J].
Kureishi, Y ;
Luo, ZY ;
Shiojima, I ;
Bialik, A ;
Fulton, D ;
Lefer, DJ ;
Sessa, WC ;
Walsh, K .
NATURE MEDICINE, 2000, 6 (09) :1004-1010
[17]   Upregulation of endothelial nitric oxide synthase by HMG CoA reductase inhibitors [J].
Laufs, U ;
La Fata, V ;
Plutzky, J ;
Liao, JK .
CIRCULATION, 1998, 97 (12) :1129-1135
[18]   Effect of verapamil on long-term tachycardia-induced atrial electrical remodeling [J].
Lee, SH ;
Yu, WC ;
Cheng, JJ ;
Hung, CR ;
Ding, YA ;
Chang, MS ;
Chen, SA .
CIRCULATION, 2000, 101 (02) :200-206
[19]   Atrial contractile dysfunction after short-term atrial fibrillation is reduced by verapamil but increased by BAY K8644 [J].
Leistad, E ;
Aksnes, G ;
Verburg, E ;
Christensen, G .
CIRCULATION, 1996, 93 (09) :1747-1754
[20]  
Luo JD, 2002, ACTA PHARMACOL SIN, V23, P124