Caplan R A, Su J Y
Anesth Analg. 1986 May;65(5):463-8.
The combined depressant effects of verapamil and halothane on myocardial contractility were studied using isolated papillary muscle from the rabbit. Verapamil alone (0.5 microM) significantly decreased peak developed tension (PDT) by 15 +/- 2%, time to peak tension (TPT) by 10 +/- 1%, and maximum rate of increase of tension (+dT/dt) by 5 +/- 1%, but not maximum rate of decrease of tension (-dT/dt). Halothane alone (0.8%) significantly decreased PDT by 56 +/- 2%, TPT by 11 +/- 2%, +dT/dt by 53 +/- 2%, and -dT/dt by 56 +/- 2%. During the exposure period, the combination of verapamil and halothane together produced a simple additive effect (no significant interaction effect by two-way analysis of variance), with PDT decreased by 68 +/- 2%, TPT by 20 +/- 3%, +dT/dt by 62 +/- 2%, and -dT/dt by 65 +/- 2%. The reversibility of halothane-induced depression was also studied. Peak developed tension showed complete reversibility 30 min after discontinuing halothane. In the presence of verapamil, however, the reversibility of halothane-induced depression was not complete, and significant residual depression of PDT (19 +/- 3%) was observed. We conclude that the acute depressant effect of verapamil plus halothane in isolated papillary muscle is additive, but reversibility of halothane-induced depression may be impaired or prolonged in the presence of verapamil.
利用兔离体乳头肌研究了维拉帕米和氟烷对心肌收缩力的联合抑制作用。单独使用维拉帕米(0.5微摩尔)可使峰值收缩张力(PDT)显著降低15±2%,张力峰值时间(TPT)降低10±1%,张力最大上升速率(+dT/dt)降低5±1%,但张力最大下降速率(-dT/dt)未受影响。单独使用氟烷(0.8%)可使PDT显著降低56±2%,TPT降低11±2%,+dT/dt降低53±2%,-dT/dt降低56±2%。在暴露期间,维拉帕米和氟烷联合使用产生简单的相加效应(经双向方差分析无显著交互作用),PDT降低68±2%,TPT降低20±3%,+dT/dt降低62±2%,-dT/dt降低65±2%。还研究了氟烷诱导的抑制作用的可逆性。停止使用氟烷30分钟后,峰值收缩张力显示出完全可逆性。然而,在存在维拉帕米的情况下,氟烷诱导的抑制作用的可逆性不完全,观察到PDT有显著的残余抑制(19±3%)。我们得出结论,维拉帕米加氟烷对离体乳头肌的急性抑制作用是相加的,但在存在维拉帕米的情况下,氟烷诱导的抑制作用的可逆性可能受损或延长。