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哌替啶可抑制脊髓背角神经元的兴奋性。

Meperidine suppresses the excitability of spinal dorsal horn neurons.

作者信息

Wolff Matthias, Olschewski Andrea, Vogel Werner, Hempelmann Gunter

机构信息

Department of Anesthesiology, Intensive Care Medicine, Pain Therapy, Justus-Liebig-University, Giessen, Germany.

出版信息

Anesthesiology. 2004 Apr;100(4):947-55. doi: 10.1097/00000542-200404000-00027.

DOI:10.1097/00000542-200404000-00027
PMID:15087632
Abstract

BACKGROUND

In addition to local anesthetics, meperidine has been successfully used for local anesthesia. When applied intrathecally, the dorsal horn neurons of the superficial laminae are exposed to high concentrations of meperidine. These cells represent an important point for the transmission of pain information. This study investigated the blocking effects of meperidine on different ionic currents of spinal dorsal horn neurons and, in particular, its impact on the generation of action potentials.

METHODS

Using a combination of the patch clamp technique and the entire soma isolation method, the action of meperidine on voltage-gated Na+ and K+ currents in spinal dorsal horn neurons of rats was described. Current clamp recordings from intact neurons showed the functional relevance of the ion current blockade for the generation of action potentials.

RESULTS

Externally applied meperidine reversibly blocked voltage-gated Na+ currents with a half-maximum inhibiting concentration (IC50) of 112 microM. During repetitive stimulation, a slight phasic block occurred. In addition, A-type K+ currents and delayed-rectifier K+ currents were affected in a dose-dependent manner, with IC50 values of 102 and 52 microM, respectively. In the current clamp mode, single action potentials were suppressed by meperidine. The firing frequency was lowered to 54% at concentrations (100 microM) insufficient for the suppression of a single action potential.

CONCLUSIONS

Meperidine inhibits the complex mechanism of generating action potentials in spinal dorsal horn neurons by the blockade of voltage-gated Na+ and K+ channels. This can contribute to the local anesthetic effect of meperidine during spinal anesthesia.

摘要

背景

除局部麻醉药外,哌替啶已成功用于局部麻醉。鞘内给药时,浅层层的背角神经元会暴露于高浓度的哌替啶中。这些细胞是疼痛信息传递的重要节点。本研究调查了哌替啶对脊髓背角神经元不同离子电流的阻断作用,尤其是其对动作电位产生的影响。

方法

采用膜片钳技术与全细胞分离方法相结合,描述了哌替啶对大鼠脊髓背角神经元电压门控性钠电流和钾电流的作用。完整神经元的电流钳记录显示了离子电流阻断对动作电位产生的功能相关性。

结果

外部施加的哌替啶可逆性阻断电压门控性钠电流,半数最大抑制浓度(IC50)为112微摩尔。在重复刺激期间,出现轻微的时相性阻断。此外,A型钾电流和延迟整流钾电流受到剂量依赖性影响,IC50值分别为102和52微摩尔。在电流钳模式下,哌替啶抑制单个动作电位。在浓度(100微摩尔)不足以抑制单个动作电位时,放电频率降低至54%。

结论

哌替啶通过阻断电压门控性钠通道和钾通道来抑制脊髓背角神经元产生动作电位的复杂机制。这有助于哌替啶在脊髓麻醉期间的局部麻醉作用。

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