Department of Neuroscience, Max-Delbrück Center for Molecular Medicine, Berlin-Buch, Germany.
Science. 2011 Dec 16;334(6062):1557-60. doi: 10.1126/science.1213760.
Acid evokes pain by exciting nociceptors; the acid sensors are proton-gated ion channels that depolarize neurons. The naked mole-rat (Heterocephalus glaber) is exceptional in its acid insensitivity, but acid sensors (acid-sensing ion channels and the transient receptor potential vanilloid-1 ion channel) in naked mole-rat nociceptors are similar to those in other vertebrates. Acid inhibition of voltage-gated sodium currents is more profound in naked mole-rat nociceptors than in mouse nociceptors, however, which effectively prevents acid-induced action potential initiation. We describe a species-specific variant of the nociceptor sodium channel Na(V)1.7, which is potently blocked by protons and can account for acid insensitivity in this species. Thus, evolutionary pressure has selected for an Na(V)1.7 gene variant that tips the balance from proton-induced excitation to inhibition of action potential initiation to abolish acid nociception.
酸通过兴奋伤害感受器引起疼痛;酸传感器是质子门控离子通道,可使神经元去极化。裸鼹鼠(Heterocephalus glaber)在酸不敏感方面表现异常,但裸鼹鼠伤害感受器中的酸传感器(酸感应离子通道和瞬时受体电位香草醛 1 离子通道)与其他脊椎动物相似。然而,裸鼹鼠伤害感受器中的电压门控钠离子电流对酸的抑制作用比小鼠伤害感受器更为明显,这有效地阻止了酸诱导的动作电位起始。我们描述了一种伤害感受器钠通道 Na(V)1.7 的种特异性变体,该变体可被质子强烈阻断,并可解释该物种的酸不敏感性。因此,进化压力选择了一种 Na(V)1.7 基因变体,该变体使质子诱导的兴奋与动作电位起始抑制之间的平衡偏向后者,从而消除了酸伤害感受。