摘要
用乙酰毒毛旋花子成元0.2μmol/L诱发绵羊心脏浦肯野纤维产生延迟后除极(DAD),采用细胞内微电极记录。在用普奈洛尔1.0μmol/L阻断β受体条件下,苯肾上腺素1.0μmol/L使DAD幅值由8.1±2.2mV增至9.5±2.8mV,时程由240±47ms延长到273±47ms(n=13,PM<0.01),DAD上升速率由0.039±0.023V/s增至0.051±0.026V/s(n=13,P<0.05),DAD在动作电位后出现的时间提前了30±47ms(n=13,P<0.05)。用去甲肾上腺素1.0μmol/L增强DAD引起触发活动时,酚妥0拉明1.8μmol/L不能抑制触发活动,普奈洛尔1.0μmol/L能抑制之。上述结果表明α受体激动对DAD有轻度增强作用,但由DAD引起的触发活动,α受体阻滞剂的抑制作用不如β受体阻滞剂有效。
By using acetyl strophanthidin (AS)0.2μmol/L,the delayed after-deplarization(DAD)was induced in sheep cardiac Purkinje fibers and recorded with intra-cellular microelectrode.When bead-adrenoceptor was blocked by proptanolol 1.0μmol/L,phenylephrine 1.0μmol/L increased the amplitude of DAD from 8.1±2.2 mV to9.5±2.8 mV,prolonged the duration of DAD from 240±47 ms to 273±47 ms(n=13,P<0.01)and increased the up rising velocity of DAD from of 0.39±0.023V/s to 0.051±0.026 V/s(n=13, P<0.05).The DAD occured earlier for 30±47 ms to preceding action potential (n= 13,P<0.05).When triggered acting potentials were induced by norepinephrine 1.0 μmol/L on the basis of DAD,proptanolol1.0 μmol/L could suppress the triggered.beats while phentolamine 1.μmol/L showedlittle effect.The above results indicate that excitation of alpha-receptor had only slightaugmentation effect on DAD.However,for the triggered activity induced by DAD,the inhibitory effect of bead-blockers are stronger than that of alpha-blockers.
出处
《生理学报》
CAS
CSCD
北大核心
1994年第2期181-186,共6页
Acta Physiologica Sinica
基金
国家自然科学基金
关键词
延迟后除极
心脏
浦肯野纤维
受体
delayed aftsr-depolarization
cardiac Purkinje fibers
acetyl strophanthidin
α-adrenoceptor