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局部麻醉药物在低刺激频率和高刺激频率下的抑制作用。大鼠离体膈神经与膈神经-膈肌标本的比较。

Inhibition by local anaesthetic drugs at low and high stimulation frequencies. A comparison between the isolated phrenic nerve of the rat and the phrenic nerve-diaphragm preparation.

作者信息

Brodin P, Røed A

出版信息

Neuropharmacology. 1984 Jan;23(1):83-8. doi: 10.1016/0028-3908(84)90221-1.

Abstract

The effects of lidocaine (0.25 mM), prilocaine (0.3 mM), diphenylhydantoin (0.24 mM), tetracaine (0.005 mM) and dibucaine (0.002 mM) on the isolated rat phrenic nerve, neuromuscular transmission and the directly stimulated rat diaphragm, were observed at low (twitch) and high (tetanic) stimulation frequency. The phrenic nerve compound action potential and muscle tension during indirect and direct stimulation were compared. At high frequency stimulation all drugs caused high frequency inhibition of both nerve and muscle. The high frequency inhibition was usually biphasic with an initial decrease in the amplitude of compound action potential and tetanic tension and a subsequent stabilization at a reduced plateau level. The duration of the initial phase increased with the potency of the drugs and was similar for nerve and muscle. A specific high frequency inhibition during indirect stimulation was found with diphenylhydantoin and prilocaine, indicating pre- and post-synaptic inhibition of neuromuscular transmission. At low frequency stimulation, the drugs induced a basal inhibition of the nerve compound action potential. In spite of that, the twitches were not depressed during indirect stimulation of the muscle, illustrating the margin of safety with neuromuscular transmission. These results indicate that the action of the drug was similar at the excitable nerve and muscle membranes when stimulated at high frequency, but different at low frequency stimulation.

摘要

观察了利多卡因(0.25 mM)、丙胺卡因(0.3 mM)、苯妥英(0.24 mM)、丁卡因(0.005 mM)和布比卡因(0.002 mM)在低(单收缩)和高(强直)刺激频率下对离体大鼠膈神经、神经肌肉传递以及直接刺激的大鼠膈肌的影响。比较了间接和直接刺激期间膈神经复合动作电位和肌肉张力。在高频刺激时,所有药物均引起神经和肌肉的高频抑制。高频抑制通常呈双相性,最初复合动作电位幅度和强直张力降低,随后在降低的平台水平稳定。初始阶段的持续时间随药物效力增加,神经和肌肉相似。苯妥英和丙胺卡因在间接刺激时出现特异性高频抑制,表明对神经肌肉传递有突触前和突触后抑制。在低频刺激时,药物诱导神经复合动作电位的基础抑制。尽管如此,在间接刺激肌肉时单收缩并未受到抑制,说明了神经肌肉传递的安全边际。这些结果表明,高频刺激时药物在可兴奋神经和肌肉膜上的作用相似,但低频刺激时不同。

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