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[在sns基因敲除小鼠上研究河豚毒素抗性钠通道在痛觉中的作用]

[The role of tetrodotoxin-resistant sodium channels in pain sensation studied on sns-knockout mice].

作者信息

Ogata N, Yamamoto M, Maruyama H

机构信息

Department of Physiology, Faculty of Medicine, Hiroshima University.

出版信息

Nihon Rinsho. 2001 Sep;59(9):1688-97.

Abstract

Nociceptive dorsal root ganglion neurons express sensory neuron-specific tetrodotoxin (TTX)-resistant voltage-gated sodium channel(SNS). The role of SNS in nociception has been studied by constructing sns-knockout mice. The sns-knockout mice expressed only TTX-sensitive sodium currents on step depolarizations from normal resting potentials, demonstrating that the slow TTX-resistant currents are mediated by the sns gene. The mutant mice were viable, fertile and apparently normal, although lowered thresholds of electrical activation of C-fibers and increased current densities of TTX-sensitive sodium channels demonstrated compensatory up-regulation of TTX-sensitive currents in DRG neurons. Behavioral studies demonstrated a pronounced analgesia to noxious mechanical stimuli, small deficits in noxious thermoreception and delayed development of inflammatory hyperalgesia. These data show that SNS is involved in pain sensation.

摘要

伤害性背根神经节神经元表达感觉神经元特异性河豚毒素(TTX)抗性电压门控钠通道(SNS)。通过构建sns基因敲除小鼠研究了SNS在痛觉中的作用。sns基因敲除小鼠在从正常静息电位进行阶跃去极化时仅表达TTX敏感的钠电流,表明缓慢的TTX抗性电流由sns基因介导。尽管C纤维电激活阈值降低以及TTX敏感钠通道电流密度增加表明DRG神经元中TTX敏感电流出现代偿性上调,但突变小鼠仍存活、可育且外观正常。行为学研究表明,突变小鼠对有害机械刺激有明显的镇痛作用,对有害温度感受有轻微缺陷,并且炎症性痛觉过敏的发展延迟。这些数据表明SNS参与痛觉感受。

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