Apfel H, Vassalle M
Department of Physiology, State University of New York, Brooklyn 11203.
Cardiovasc Res. 1988 Jun;22(6):425-38. doi: 10.1093/cvr/22.6.425.
The hypothesis that in the presence of acetylcholine overdrive may induce spontaneous repetitive activity (overdrive excitation) was tested by recording the transmembrane potentials and contractile force in sheep cardiac Purkinje fibres perfused in vitro. The results were: (a) acetylcholine 10(-8) to 10(-4) mol.litre-1 increased the action potential duration, the diastolic depolarisation slope and amplitude, and the twitch amplitude in a dose dependent manner; (b) at concentrations of 10(-5) to 10(-4) mol.litre-1 the interruption of a 60 beat.min-1 drive often induced repetitive spontaneous activity which was fastest immediately after the drive, slowed gradually, and ceased abruptly when an oscillatory potential failed to attain the threshold; (c) in the presence of acetylcholine, in quiescent preparations, applying drives of different durations and at different frequencies resulted in a steeper and larger diastolic depolarisation, oscillatory potentials, and a prolonged afterdepolarisation; (d) when overdrive excitation was induced it was faster and longer after faster or longer overdrives; (e) the cessation of overdrive was often associated with an aftercontraction; (f) in the presence of acetylcholine and a high extracellular calcium concentration (10.8 mmol.litre-1) overdrive excitation was preceded by a short period of inhibition; (g) strophanthidin (5 x 10(-8) mol.litre-1) facilitated acetylcholine induced overdrive excitation (without an initial inhibition); (h) lowering the extracellular sodium concentration (-50% NaCl) antagonised overdrive excitation; and (i) atropine 10(-5) mol.litre-1 prevented acetylcholine induced overdrive excitation. It is concluded that acetylcholine induces overdrive excitation by causing a larger diastolic depolarisation, oscillatory potentials, and a transient prolonged afterdepolarisation; that overdrive excitation requires sodium as a charge carrier underlying the electrical events leading to the attainment of the threshold; and that acetylcholine induces excitation by acting on a muscarinic receptor.
通过记录体外灌注的绵羊心脏浦肯野纤维的跨膜电位和收缩力,对乙酰胆碱过量存在时可能诱发自发重复活动(超速兴奋)这一假说进行了检验。结果如下:(a) 10(-8)至10(-4)mol·L-1的乙酰胆碱以剂量依赖方式增加动作电位持续时间、舒张期去极化斜率和幅度以及抽搐幅度;(b) 在10(-5)至10(-4)mol·L-1浓度下,中断60次/分钟的驱动常诱发重复自发活动,该活动在驱动后即刻最快,随后逐渐减慢,当振荡电位未达到阈值时突然停止;(c) 在乙酰胆碱存在下,在静息标本中,施加不同持续时间和不同频率的驱动会导致更陡峭、更大的舒张期去极化、振荡电位以及延长的后去极化;(d) 当诱发超速兴奋时,更快或更长时间的超速驱动后其速度更快、持续时间更长;(e) 超速驱动的停止常伴有后收缩;(f) 在乙酰胆碱和高细胞外钙浓度(10.8mmol·L-1)存在下,超速兴奋之前有一段短暂的抑制期;(g) 毒毛花苷(5×10(-8)mol·L-1)促进乙酰胆碱诱发的超速兴奋(无初始抑制);(h) 降低细胞外钠浓度(-50%NaCl)拮抗超速兴奋;(i) 10(-5)mol·L-1的阿托品可预防乙酰胆碱诱发的超速兴奋。得出的结论是,乙酰胆碱通过引起更大的舒张期去极化、振荡电位和短暂的延长后去极化来诱发超速兴奋;超速兴奋需要钠作为导致达到阈值的电活动的电荷载体;并且乙酰胆碱通过作用于毒蕈碱受体来诱发兴奋。