Cholinergic stimulation with pyridostigmine reduces the QTc interval in coronary artery disease

被引:17
作者
Castro, RRT
Porphirio, G
Serra, SM
Nóbrega, ACL
机构
[1] Univ Fed Fluminense, Dept Fisiol & Farmacol, Niteroi, RJ, Brazil
[2] Univ Fed Fluminense, Programa Pos Graduacao Cardiol, Niteroi, RJ, Brazil
[3] Inst Estadual Cardiol Aluisio Castro, Rio De Janeiro, Brazil
关键词
pyridostigmine; QTc interval; stable angina; anticholinesterase;
D O I
10.1590/S0100-879X2002000600008
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Parasympathetic dysfunction is an independent risk factor in patients with coronary artery disease; thus, cholinergic stimulation is a potential therapeutic measure that may be protective by acting on ventricular repolarization. The purpose of the present study was to determine the effects of pyridostigmine bromide (PYR), a reversible anticholinesterase agent, on the electrocardiographic variables, particularly QTc interval, in patients with stable coronary artery disease. In a randomized double-blind crossover placebo-controlled study, simultaneous 12-lead electrocardiographic tracings were obtained at rest from 10 patients with exercise-induced myocardial ischemia before and 2 h after the oral administration of 45 mg PYR or placebo. PYR increased the RR intervals (pre: 921 +/- 27 ms vs post: 1127 +/- 37 ms; P<0.01) and, in**RR intervals (pre: 921 +/- 27 ms; P<0.01) and, in contrast with placebo, decreased the QTc interval (pre: 401 +/- 3 ms vs post: 382 +/- 3 ms; P<0.01). No other electrocardiographic variables were modified (PR segment, QT interval, QT and QTc dispersions). Cholinergic stimulation with PYR caused bradycardia and reduced the QTc interval without important side effects in patients with coronary disease. These effects, if confirmed in studies over longer periods of administration, may suggest a cardioprotection by cholinergic stimulation with PYR.
引用
收藏
页码:685 / 689
页数:5
相关论文
共 23 条
[1]  
AHNVE S, 1980, Clinical Cardiology, V3, P303
[2]  
Bazett HC, 1920, HEART-J STUD CIRC, V7, P353
[3]   HOW DO BETA-BLOCKERS PROTECT AFTER MYOCARDIAL-INFARCTION [J].
BIGGER, JT ;
COROMILAS, J .
ANNALS OF INTERNAL MEDICINE, 1984, 101 (02) :256-258
[4]   SYMPATHETIC AND VAGAL INFLUENCES ON RATE-DEPENDENT CHANGES OF QT INTERVAL IN HEALTHY-SUBJECTS [J].
CAPPATO, R ;
ALBONI, P ;
PEDRONI, P ;
GILLI, G ;
ANTONIOLI, G .
AMERICAN JOURNAL OF CARDIOLOGY, 1991, 68 (11) :1188-1193
[5]  
da N┬u┬Ebrega, 2000, ARQUIVOS BRASILEIROS, V75, P210
[6]   THE QT INTERVAL DURING REFLEX CARDIOVASCULAR ADAPTATION [J].
DAVIDOWSKI, TA ;
WOLF, S .
CIRCULATION, 1984, 69 (01) :22-25
[7]   TIME-RELATED CHANGES IN Q-T INTERVAL IN ACUTE MYOCARDIAL-INFARCTION - POSSIBLE RELATION TO LOCAL HYPOCALCEMIA [J].
DOROGHAZI, RM ;
CHILDERS, R .
AMERICAN JOURNAL OF CARDIOLOGY, 1978, 41 (04) :684-688
[8]   RATE-CORRECTED QT INTERVAL - TECHNIQUES AND LIMITATIONS [J].
FUNCKBRENTANO, C ;
JAILLON, P .
AMERICAN JOURNAL OF CARDIOLOGY, 1993, 72 (06) :B17-B22
[9]   Pyridostigmine blunts the increases in myocardial oxygen demand elicited by the stimulation of the central nervous system in anesthetized rats [J].
Grabe-Guimaraes, A ;
Alves, LM ;
Tibiriçá, E ;
Nóbrega, ACL .
CLINICAL AUTONOMIC RESEARCH, 1999, 9 (02) :83-89
[10]   The effects of reflex parasympathetic stimulation on the QT interval and QT dispersion [J].
Kautzner, J ;
Hartikainen, JEK ;
Heald, S ;
Camm, AJ ;
Malik, M .
AMERICAN JOURNAL OF CARDIOLOGY, 1997, 80 (09) :1229-&