Rolyan Harshvardhan, Liu Shujun, Hoeijmakers Janneke Gj, Faber Catharina G, Merkies Ingemar Sj, Lauria Giuseppe, Black Joel A, Waxman Stephen G
Department of Neurology, Yale University School of Medicine, New Haven, CT, USA.
Neuroscience and Regeneration Research Center, VA Connecticut Healthcare System, West Haven, CT, USA.
Mol Pain. 2016 Nov 7;12. doi: 10.1177/1744806916674472. Print 2016.
Small fiber neuropathy is a painful sensory nervous system disorder characterized by damage to unmyelinated C- and thinly myelinated Aδ- nerve fibers, clinically manifested by burning pain in the distal extremities and dysautonomia. The clinical onset in adulthood suggests a time-dependent process. The mechanisms that underlie nerve fiber injury in small fiber neuropathy are incompletely understood, although roles for energetic stress have been suggested. In the present study, we report time-dependent degeneration of neurites from dorsal root ganglia neurons in culture expressing small fiber neuropathy-associated G856D mutant Nav1.7 channels and demonstrate a time-dependent increase in intracellular calcium levels [Ca] and reactive oxygen species, together with a decrease in ATP levels. Together with a previous clinical report of burning pain in the feet and hands associated with reduced levels of Na/K-ATPase in humans with high altitude sickness, the present results link energetic stress and reactive oxygen species production with the development of a painful neuropathy that preferentially affects small-diameter axons.
小纤维神经病变是一种疼痛性感觉神经系统疾病,其特征是无髓鞘的C神经纤维和薄髓鞘的Aδ神经纤维受损,临床表现为远端肢体灼痛和自主神经功能障碍。成年期临床发病提示存在时间依赖性过程。尽管有研究表明能量应激在其中发挥作用,但小纤维神经病变中神经纤维损伤的潜在机制仍未完全明确。在本研究中,我们报告了表达与小纤维神经病变相关的G856D突变型Nav1.7通道的培养背根神经节神经元的神经突随时间发生变性,并证明细胞内钙水平[Ca]和活性氧随时间增加,同时ATP水平降低。结合之前一份关于高原病患者手足灼痛与Na/K-ATP酶水平降低相关的临床报告,目前的结果将能量应激和活性氧产生与优先影响小直径轴突的疼痛性神经病变的发展联系起来。