Khan A R, Edman K A
Acta Physiol Scand. 1979 Apr;105(4):443-52. doi: 10.1111/j.1748-1716.1979.tb00109.x.
The effects of 4-aminopyridine (4-AP) were studied on isolated single muscle fibres of the frog and toe muscles of the rat. In both muscle preparations, 4-AP potentiated the twitch amplitude without significantly affecting the tetanus response. There was an increase of the time to peak tension and, in frog muscle, an increased time to half relaxation. 4-AP produced no change of the resting membrane potential. The rate of decay and, hence, the total duration of the action potential were markedly prolonged. 4-AP did not induce contractures by itself nor did it affect the contracture induced by caffeine. The mechanical threshold was determined by measuring the contracture response to various degrees of depolarization by potassium. This threshold was not affected by 4-AP. Twitch potentiation by 4-AP was independent of the extracellular calcium concentration. It is concluded that 4-AP potentiates the twitch response by increasing the release of activator calcium into the myofibrillar space by prolongation of the action potential. In addition, there may be a more direct inhibitory action of 4-AP on the calcium re-uptake by the sarcoplasmic reticulum in frog muscle.
研究了4-氨基吡啶(4-AP)对青蛙离体单肌纤维和大鼠趾肌的作用。在这两种肌肉标本中,4-AP增强了单收缩幅度,而对强直收缩反应无明显影响。达到峰值张力的时间增加,在青蛙肌肉中,达到半松弛的时间也增加。4-AP对静息膜电位无影响。动作电位的衰减速率以及因此动作电位的总持续时间显著延长。4-AP本身不诱导挛缩,也不影响咖啡因诱导的挛缩。通过测量对不同程度钾去极化的挛缩反应来确定机械阈值。该阈值不受4-AP影响。4-AP引起的单收缩增强与细胞外钙浓度无关。得出的结论是,4-AP通过延长动作电位增加激活钙释放到肌原纤维空间来增强单收缩反应。此外,4-AP对青蛙肌肉肌浆网钙再摄取可能有更直接的抑制作用。