Yang Shu-sen, Han Wei, Zhou Hong-yan, Dong Guo, Wang Bai-chun, Huo Hong, Wei Na, Cao Yong, Zhou Guo, Xiu Chun-hong, Li Wei-min
Department of Cardiology, First Clinical College of Harbin Medical University, Harbin, Heilongjiang 150001, China.
Chin Med J (Engl). 2008 Jan 5;121(1):38-42.
Renin-angiotensin-aldosterone system has been demonstrated to be associated with both congestive heart failure (CHF) and atrial fibrillation (AF). This study investigated the effects of spironolactone, a kind of aldosterone antagonist, on atrial electrical remodeling and fibrosis in CHF dogs induced by chronic rapid ventricular pacing.
Twenty one dogs were randomly divided into sham-operated group, control group, and spironolactone group. In control group and spironolactone group, dogs were ventricular paced at 220 beats per minute for 6 weeks. Additionally, spironolactone at 15 mg x kg(-1) x d(-1) was given to dogs 1 week before rapid ventricular pacing until pacing stopped. Transthoracic and transoesophageal echocardiographic examinations were performed to detect structural and functional changes of the atrium. Swan2 Ganz floating catheters were used to measure hemadynamics variances. Atrial effective refractory period (AERP), AERP dispersion (AERPd), intra- and inter-atrium conduction time (CT) and intra-atrium conduction velocity (CV) were determined. The inducibility and duration of AF were also measured in all groups. Finally, atrial fibrosis was quantified with Masson staining.
AERP did not change significantly after dogs were ventricular paced for 6 weeks. However, AERPd, intra- and inter-atrium CT increased significantly, and CV decreased apparently, which was negatively correlated to the atrial fibrosis (r = -0.74, P < 0.05). Simultaneously, left atriums were enlarged and cardiac hemadynamics worsened in pacing dogs. Although spironolactone could not affect cardiac hemadynamics effectively, it can obviously improve left atrial ejection fraction (P < 0.05). Spironolactone treatment did not alter AERP duration, but this medicine dramatically decreased AERPd (P < 0.05), shortened intra- and inter-atrium conduction time (P < 0.05), and increased atrium CV. Moreover, spironolactone decreased the inducibility and duration of AF (P < 0.05), as well as atrial fibrosis (P < 0.01) induced by chronic rapid ventricular pacing.
Spironolactone contributes to AF prevention in congestive heart failure dogs induced by chronic rapid ventricular pacing, which is related to atrial fibrosis reduction and independent of hemadynamics.
肾素 - 血管紧张素 - 醛固酮系统已被证明与充血性心力衰竭(CHF)和心房颤动(AF)均有关联。本研究调查了醛固酮拮抗剂螺内酯对慢性快速心室起搏诱导的CHF犬心房电重构和纤维化的影响。
21只犬随机分为假手术组、对照组和螺内酯组。对照组和螺内酯组犬以每分钟220次的频率进行心室起搏,持续6周。此外,在快速心室起搏前1周开始,给予犬15mg·kg⁻¹·d⁻¹的螺内酯,直至起搏停止。进行经胸和经食管超声心动图检查以检测心房的结构和功能变化。使用Swan - Ganz漂浮导管测量血流动力学变化。测定心房有效不应期(AERP)、AERP离散度(AERPd)、房内和房间传导时间(CT)以及房内传导速度(CV)。还测量了所有组中AF的诱发率和持续时间。最后,用Masson染色对心房纤维化进行定量分析。
犬心室起搏6周后,AERP无明显变化。然而,AERPd、房内和房间CT显著增加,CV明显降低,且与心房纤维化呈负相关(r = -0.74,P < 0.05)。同时,起搏犬的左心房扩大,心脏血流动力学恶化。虽然螺内酯不能有效影响心脏血流动力学,但它能明显改善左心房射血分数(P < 0.05)。螺内酯治疗未改变AERP持续时间,但该药物显著降低了AERPd(P < 0.05),缩短了房内和房间传导时间(P < 0.05),并增加了心房CV。此外,螺内酯降低了慢性快速心室起搏诱导的AF的诱发率和持续时间(P < 0.05),以及心房纤维化(P < 0.01)。
螺内酯有助于预防慢性快速心室起搏诱导的充血性心力衰竭犬的AF,这与减少心房纤维化有关,且与血流动力学无关。