Changes of the peripheral nerve excitability in vivo induced by the persistent Na⁺ current blocker ranolazine

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• 作者：Hiroyuki Nodera ; ^{hodera@bidmc.harvard.edu} ; ^{hnodera1@yahoo.co.jp} ; Seward B. Rutkove
• 关键词：HCN ; hyperpolarization-activated cyclic nucleotide-gated ; Ih ; hyperpolarization-activated current ; I/V ; current&ndash ; threshold relationship ; Nap ; persistent Na+ current ; RC ; recovery cycle ; SDTC ; strength-duration time constant ; SNAP ; sensory nerve actio
• 刊名：Neuroscience Letters
• 出版年：2012
• 期刊代码：52_03043940
• 类别：neu
• 出版时间：14 June, 2012
• 卷：518
• 期：1
• 页码：36-40
• 文件大小：517 K

摘要

Persistent Na⁺ current (Na_p) in the peripheral axons play an important functional role in controlling the axonal excitability. Abnormal Na_p is believed to contribute to neurodegeneration and neuropathic pain, and thus it is an attractive therapeutic target. To assess the behavior of selective Na_p blockade, axonal excitability testing was performed in vivo in 10 normal male mice exposed to ranolazine by recording the tail sensory nerve action potentials (SNAPs). Twenty minutes after administering ranolazine i.p. (50 mg/kg), the following changes were observed: lower SNAP amplitudes and the need for greater stimulus currents; greater threshold changes induced by long hyperpolarizing currents; reduced accommodation to long depolarizing current along with reduced late subexcitability; and reduced strength-duration time constant. These changes are explained by the suppression of Na_p leading to greater threshold currents, partial block of transient Na⁺ current, and suppression of slow K⁺ currents. The suppressed slow K⁺ currents appear to limit the modification of the membrane excitability by ranolazine. This study confirms the utility of axonal excitability testing as a useful treatment biomarker in neurological conditions in which Na_p function is being modified.