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新型III类抗心律失常药物E-4031对犬无菌性心包炎模型心房扑动、心房不应期及传导延迟的电生理效应

Electrophysiologic effects of a new class III antiarrhythmic agent, E-4031, on atrial flutter, atrial refractoriness, and conduction delay in a canine sterile pericarditis model.

作者信息

Shimizu A, Kaibara M, Centurion O A, Kapuku G, Hirata T, Fukatani M, Yano K, Hashiba K

机构信息

Third Department of Internal Medicine, Nagasaki University School of Medicine, Japan.

出版信息

J Cardiovasc Pharmacol. 1993 Apr;21(4):656-62. doi: 10.1097/00005344-199304000-00021.

Abstract

Numerous studies have shown that E-4031 generally prolongs the atrial effective refractory period (AERP) without affecting cardiac conduction. The effects of E-4031 on AERP and cardiac conduction at short cycle lengths (CLs) close to the AERP were measured in 12 dogs with sterile pericarditis. Three pairs of electrodes were sutured at three sites in the atria 4 days after the model was created. We measured AERP and maximum conduction delay (MCD) after 8 beats train at CLs of 400, 300, 200 and 150 ms before and during continuous infusion of E-4031 (0.1 microgram/kg/min) that followed an initial dose of 10 micrograms/kg/min/5 min. E-4031 interrupted sustained atrial flutter (AF) (> or = 10 min) in 4 of 5 episodes and atrial fibrillation (> or = 10 min) in 4 of 4. The CL of AF defined as a rapid atrial rhythm (rate > or = 240 beats/min) in five episodes studied in the sterile pericarditis model was significantly (p < 0.005) prolonged from 120 +/- 8 to 160 +/- 17 ms. There were significant (p < 0.005) increases in AERP at each CL, and prolongation of AERP was 39 +/- 18, 31 +/- 14, 23 +/- 14, and 16 +/- 14 ms at CL 400, 300, 200, and 150 ms, respectively. E-4031 produced less prolongation of AERP at short pacing CLs and had no effect on conduction time during atrial rapid pacing at CLs > 150 ms. E-4031 did not prolong MCD at CL 400 ms, but did prolong MCD at CLs of 300, 200, and 150 ms, despite prolongation of AERP.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

大量研究表明,E - 4031通常会延长心房有效不应期(AERP),而不影响心脏传导。在12只患有无菌性心包炎的犬中,测量了E - 4031在接近AERP的短周期长度(CLs)时对AERP和心脏传导的影响。在创建模型4天后,在心房的三个部位缝合三对电极。在以10微克/千克/分钟/5分钟的初始剂量之后持续输注E - 4031(0.1微克/千克/分钟)之前和期间,我们在400、300、200和150毫秒的CLs下测量了8次搏动序列后的AERP和最大传导延迟(MCD)。E - 4031在5次发作中的4次中断了持续心房扑动(AF)(≥10分钟),在4次发作中的4次中断了心房颤动(≥10分钟)。在无菌性心包炎模型中研究的5次发作中,定义为快速心房节律(心率≥240次/分钟)的AF的CL从120±8显著延长至160±17毫秒(p < 0.005)。每个CL下的AERP均有显著增加(p < 0.005),在400、300、200和150毫秒的CL下,AERP的延长分别为39±18、31±14、23±14和16±14毫秒。E - 4031在短起搏CLs时对AERP的延长较少,并且在CL>150毫秒的心房快速起搏期间对传导时间没有影响。E - 4031在400毫秒的CL下未延长MCD,但在300、200和150毫秒的CL下确实延长了MCD,尽管AERP有所延长。(摘要截断于250字)

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