Pereira Vanessa, Busserolles Jérôme, Christin Marine, Devilliers Maïly, Poupon Laura, Legha Wassim, Alloui Abdelkrim, Aissouni Youssef, Bourinet Emmanuel, Lesage Florian, Eschalier Alain, Lazdunski Michel, Noël Jacques
Clermont Université, Université d'Auvergne, Pharmacologie fondamentale et clinique de la douleur, Clermont-Ferrand, France Inserm, U 1107, Neuro-Dol, Clermont-Ferrand, France CHU Clermont-Ferrand, Service de pharmacologie, Clermont-Ferrand, France Université de Nice Sophia Antipolis, Nice, France CNRS, Institut de Pharmacologie Moléculaire et Cellulaire, UMR 7275, Valbonne, France Universités de Montpellier 1 et 2, Montpellier, France CNRS, Institut de Génomique Fonctionnelle, UMR-5203, Département de Physiologie, Montpellier, France LabEx Ion Channel Science and Therapeutics, Valbonne, France.
Pain. 2014 Dec;155(12):2534-2544. doi: 10.1016/j.pain.2014.09.013. Epub 2014 Sep 18.
Two-pore domain background K(+) channels (K2p or KCNK) produce hyperpolarizing currents that control cell membrane polarity and neuronal excitability throughout the nervous system. The TREK2 channel as well as the related TREK1 and TRAAK channels are mechanical-, thermal- and lipid-gated channels that share many regulatory properties. TREK2 is one of the major background channels expressed in rodent nociceptive neurons of the dorsal root ganglia that innervate the skin and deep body tissues, but its role in somatosensory perception and nociception has remained poorly understood. We now report that TREK2 is a regulatory channel that controls the perception of non aversive warm, between 40°C and 46°C, and moderate ambient cool temperatures, between 20°C and 25°C, in mice. TREK2 controls the firing activity of peripheral sensory C-fibers in response to changes in temperature. The role of TREK2 in thermosensation is different from that of TREK1 and TRAAK channels; rather, TREK2, TREK1, and TRAAK channels appear to have complementary roles in thermosensation. TREK2 is also involved in mechanical pain perception and in osmotic pain after sensitization by prostaglandin E2. TREK2 is involved in the cold allodynia that characterizes the neuropathy commonly associated with treatments with the anticancer drug oxaliplatin. These results suggest that positive modulation of the TREK2 channel may have beneficial analgesic effects in these neuropathic conditions.
双孔结构域背景钾离子通道(K2p或KCNK)产生超极化电流,在整个神经系统中控制细胞膜极性和神经元兴奋性。TREK2通道以及相关的TREK1和TRAAK通道是机械门控、温度门控和脂质门控通道,具有许多共同的调节特性。TREK2是表达于支配皮肤和身体深部组织的背根神经节啮齿动物伤害性神经元中的主要背景通道之一,但其在体感和痛觉中的作用仍知之甚少。我们现在报告,TREK2是一种调节通道,可控制小鼠对40℃至46℃之间的非厌恶性温暖以及20℃至25℃之间的适度环境低温的感知。TREK2响应温度变化控制外周感觉C纤维的放电活动。TREK2在温度感觉中的作用不同于TREK1和TRAAK通道;相反,TREK2、TREK1和TRAAK通道在温度感觉中似乎具有互补作用。TREK2还参与机械性疼痛感知以及前列腺素E2致敏后的渗透压性疼痛。TREK2参与了以抗癌药物奥沙利铂治疗常见的神经病变为特征的冷觉异常。这些结果表明,TREK2通道的正向调节在这些神经病变情况下可能具有有益的镇痛作用。