Kraynack B J, Lawson N W, Gintautas J
Anesthesiology Research Laboratories, Texas Tech University Health Science Center, School of Medicine, Lubbock.
Can Anaesth Soc J. 1983 May;30(3 Pt 1):242-7. doi: 10.1007/BF03013802.
The effects of the calcium (slow) channel blocker verapamil, on non-cardiac excitable membranes were examined in vivo. In barbiturate anaesthetized cats, the effect of intravenously administered verapamil (0.1, 0.2, and 0.4 mg.kg-1) on isometric twitch amplitude of the flexor carpi radialis muscle, elicited by indirect and direct electrical stimulation, was determined. At all doses tested, verapamil significantly reduced muscle twitch amplitude from control values. The effect of dosage on twitch reduction was far more pronounced for indirect than direct stimulation. Full recovery to control was observed by 90 minutes only with the lowest dose (0.1 mg.kg-1 IV). Reduction of twitch amplitude (direct and indirect) lasted the duration of the experiment (180 minutes) for the two higher doses of verapamil. No significant changes in blood pressure, cardiac rate or rhythm were observed. The specific site and mechanism of verapamil's neuromuscular blocking action remains unclear. In clinical situations where potent inhalation agents, adjuncts or neuromuscular blocking agents may be used, therapeutic doses of verapamil may interact to promote muscle weakness.
在体内研究了钙(慢)通道阻滞剂维拉帕米对非心脏可兴奋膜的作用。在巴比妥类麻醉的猫中,测定静脉注射维拉帕米(0.1、0.2和0.4mg·kg-1)对由间接和直接电刺激引起的桡侧腕屈肌等长收缩幅度的影响。在所有测试剂量下,维拉帕米均使肌肉收缩幅度显著低于对照值。与直接刺激相比,剂量对间接刺激引起的收缩幅度降低的影响更为明显。仅最低剂量(0.1mg·kg-1静脉注射)在90分钟时观察到完全恢复至对照水平。对于较高剂量的维拉帕米,收缩幅度(直接和间接)的降低持续整个实验过程(180分钟)。未观察到血压、心率或心律有显著变化。维拉帕米神经肌肉阻滞作用的具体部位和机制尚不清楚。在可能使用强效吸入剂、辅助药物或神经肌肉阻滞剂的临床情况下,治疗剂量的维拉帕米可能相互作用导致肌无力。