Riccioppo Neto F
Eur J Pharmacol. 1979 Mar 1;54(3):203-7. doi: 10.1016/0014-2999(79)90078-5.
The local anesthetic effect of cyproheptadine on nerve fibres in the rabbit's cervical vagus and sciatic nerve was studied by the single sucrose-gap technique. Local anesthetics such as procaine and tetracaine, and an antihistaminic with local anesthetic activity, diphenhydramine, were studied for comparison. Increasing concentrations of cypropheptadine, starting from 5 x 10(-5) M, produced a dose-related fall in the amplitude of the compound action potential of the vagus nerve without significant change in the resting membrane potential. A complete reversibility of the local anesthetic effect was difficult or impossible to obtain when doses greater than 1 x 10(-4) M were used. Cyproheptadine was more potent than procaine and diphenhydramine, and less potent than tetracaine in producing nerve conduction block. Frequency-dependent block was observed with cyproheptadine and the other agents at frequencies that can be considered low (1--5 Hz). Myelinated fibres of the sciatic nerves were also blocked by cyproheptadine within the same range of concentrations (1 x 10(-4) to 1 x 10(-3) M). Our results provide an additional explanation for the mechanism underlying the actions of cyproheptadine as an antiarrhythmic and an antipruritic agent.
采用单蔗糖间隙技术研究了赛庚啶对家兔颈迷走神经和坐骨神经纤维的局部麻醉作用。为作比较,还研究了局部麻醉药如普鲁卡因和丁卡因,以及具有局部麻醉活性的抗组胺药苯海拉明。从5×10⁻⁵M开始增加赛庚啶浓度,可使迷走神经复合动作电位的幅度呈剂量依赖性下降,而静息膜电位无明显变化。当使用大于1×10⁻⁴M的剂量时,局部麻醉作用很难或无法完全逆转。在产生神经传导阻滞方面,赛庚啶比普鲁卡因和苯海拉明更有效,比丁卡因效力稍弱。在可认为是低频率(1 - 5Hz)时,观察到赛庚啶和其他药物存在频率依赖性阻滞。在相同浓度范围(1×10⁻⁴至1×10⁻³M)内,赛庚啶也可阻断坐骨神经的有髓纤维。我们的结果为赛庚啶作为抗心律失常药和止痒药的作用机制提供了额外的解释。