摘要
目的与方法:采用常规玻璃微电极技术研究丹皮酚对离体心肌细胞自律性(AM)、延迟后除极(DAD) 及触发活动(TA)的影响。结果:1.8×10-4mol/L丹皮酚灌流组,肾上腺素(Adr)的阈浓度空白对照组为(1.28±0.57)μmol/L,药后为(1.56±0.53)μmol/L(n=9,P>0.05);用(1.8×10- 3) mol/L丹皮酚(Pae)灌流组,Adr 浓度由空白对照组的(1.22 ±0.62)μmol/L升高到(6.22±2.11)μmol/L(n=9,P<0.01)。1.8×10-3mol/L的Pae 能明显抑制哇巴因(Oua)诱发的DAD的幅值,当基本刺激周长为500,400,300 和200 ms 时,其DAD幅值从(5.5±2.0)mV,(7.3±2.1)mV,(8.0 ±2.4)mV和(9.2±1.9)mV减小到(3.0±1.1)mV、(3.6±1.7)mV,(4.3±2.0) mV和(5.9 ±1.6) mV,P<0.01。当基本刺激周长为200 ms时,TA 数目由5.5±1.0 降至0.7±0.3(P<0.01)。结论:丹皮酚能抑制心肌细胞AM、DAD及TA。
Aim and Methods: Standard microelectrode technique was used to study the effects of paeonal on the automaticity induced by epinephrine, ouabain induced delayed afterdepolarization (DAD) and triggered activity (TA) of isolated guinea pig right ventricular papillary muscle. Results: Paeonal 1.8×10 -3 mol/L could inhibit the automaticity, concentration of epinephrine from (1.22± 0.62 ) μmol/L to (6.22±2.11)μmol/L ( n =9, P <0.01), but paeonal 1.8×10 -4 mol/L exected no influence on the automaticity, concentration of epinephrine from 1.28±0.57 μmol/L to 1.56±0.53μmol/L ( n =9, P >0.05). In additional presence of paeonal 1.8×10 -3 mol/L, the DAD amplitude at 500 ms, 400 ms, 300 ms and 200 ms were decreased from 5.5±2.0, 7.3±2.1, 8.0± 2.4 and 9.2±1.9 to 3.0±1.1, 3.6±1.7,4.3±2.0 and 5.9±1.6(mV) respectively, all P <0.01. The number of TA induced at BCL 200 ms was decreased from 5.5±1.0 to 0.7±0.3( P <0.01). Conclution:Paeonal could inhibit automaticity, DAD and TA, which contributes to its anti arrhythmic effect.
出处
《中国应用生理学杂志》
CAS
CSCD
1999年第4期332-334,共3页
Chinese Journal of Applied Physiology