Kettlewell S, Walker N L, Cobbe S M, Burton F L, Smith G L
Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow, G12 8QQ, Scotland, UK.
Exp Physiol. 2004 Mar;89(2):163-72. doi: 10.1113/expphysiol.2003.026732. Epub 2004 Feb 17.
Procedures that reduce contraction are used to facilitate optical measurements of membrane potential, but it is unclear to what extent they affect the excitability of the heart. This study has examined the electrophysiological consequences of a range of extracellular [Ca2+] (0.7-2.5 mmol l(-1)), 2,3-butane-dione monoxime (BDM; 1-20 mmol l(-1)) and cytochalasin-D (Cyto-D; 1-5 micromol l(-1)).
Monophasic action potentials (MAPs) were recorded from the basal epicardial surface of the left ventricle of isolated rabbit hearts. Conduction delay (CD) and time to 90% repolarisation of the monophasic action potential (MAPD90) were measured. The effects of BDM and Cyto-D on restitution were studied at a [Ca2+] of 1.9 mmol l(-1). Restitution curves for MAPD90 were generated using a standard S1-S2 protocol.
All manoeuvres decreased left ventricular developed pressure (LVDP): 0.7 mmol l(-1) Ca2+ to 74.0 +/- 6.1%, 20 mmol l(-1) BDM to 4.5 +/- 1.0%, and 5 micromol l(-1) Cyto-D to 12.8 +/- 3.5% of control value. CD decreased from a control value (33.3 +/- 1.0 ms, n= 16) to 93.0 +/- 2.2% in 0.7 mmol l(-1) Ca2+, but increased to 133.7 +/- 10.5% in 20 mmol l(-1) BDM and 127.4 +/- 10.6% in 5 micromol l(-1) Cyto-D. At 350 ms pacing cycle length, MAPD90 (control = 119.6 +/- 1.7 ms n= 16) was prolonged by reduced extracellular [Ca2+]. BDM had no effects on MAPD90 at control pacing rates. Cyto-D caused a significant prolongation (to 115.0 +/- 3.0% of control, n= 6) at the highest concentration studied (5 micromol l(-1)). Both BDM (20 mmol l(-1)) and Cyto-D (3 micromol l(-1)) flattened the restitution curves but neither agent altered maximum MAPD90.
Extracellular [Ca2+] of 1.9 mmol l(-1) in conjunction with a moderate dose of Cyto-D (3 micromol l(-1)) reduced contractility with minimal effects on action potential duration and conduction at a fixed pacing cycle length. However, both BDM and Cyto-D had pronounced effects on electrical restitution.
用于减少收缩的程序被用于促进膜电位的光学测量,但它们对心脏兴奋性的影响程度尚不清楚。本研究检测了一系列细胞外[Ca2+](0.7 - 2.5 mmol·l(-1))、2,3 - 丁二酮单肟(BDM;1 - 20 mmol·l(-1))和细胞松弛素 - D(细胞松弛素 - D;1 - 5 μmol·l(-1))的电生理后果。
从离体兔心脏左心室的心外膜基底面记录单相动作电位(MAPs)。测量传导延迟(CD)和单相动作电位90%复极化时间(MAPD90)。在[Ca2+]为1.9 mmol·l(-1)时研究BDM和细胞松弛素 - D对恢复的影响。使用标准的S1 - S2方案生成MAPD90的恢复曲线。
所有操作均降低了左心室舒张末压(LVDP):0.7 mmol·l(-1) Ca2+降至对照值的74.0±6.1%,20 mmol·l(-1) BDM降至4.5±1.0%,5 μmol·l(-1)细胞松弛素 - D降至12.8±3.5%。CD从对照值(33.3±1.0 ms,n = 16)在0.7 mmol·l(-1) Ca2+时降至93.0±2.2%,但在20 mmol·l(-1) BDM时升至133.7±10.5%,在5 μmol·l(-1)细胞松弛素 - D时升至127.4±10.6%。在350 ms起搏周期长度时,MAPD90(对照 = 119.6±1.7 ms,n = 16)因细胞外[Ca2+]降低而延长。在对照起搏频率下,BDM对MAPD90无影响。在研究的最高浓度(5 μmol·l(-1))时,细胞松弛素 - D导致显著延长(至对照值的115.0±3.0%,n = 6)。BDM(20 mmol·l(-1))和细胞松弛素 - D(3 μmol·l(-1))均使恢复曲线变平,但两种药物均未改变最大MAPD90。
1.9 mmol·l(-1)的细胞外[Ca2+]与中等剂量的细胞松弛素 - D(3 μmol·l(-1))联合使用可降低收缩性,在固定起搏周期长度时对动作电位持续时间和传导的影响最小。然而,BDM和细胞松弛素 - D对电恢复均有显著影响。