Kim Kyeongmin, Nan Guanghai, Kim Hee Young, Cha Myeounghoon, Lee Bae Hwan
Department of Physiology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Department of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul, Republic of Korea.
FASEB J. 2025 Jan 31;39(2):e70285. doi: 10.1096/fj.202402381R.
Neuropathic pain, caused by nerve damage, greatly affects quality of life. Recent research proposes modulating brain activity, particularly through electrical stimulation of the insular cortex (IC), as a treatment option. This study aimed to understand how IC stimulation (ICS) affects pain modulation. In a rat neuropathy model, researchers used optogenetic and ICS techniques to evaluate changes in mechanical allodynia and synaptic changes, focusing on glutamate receptors (AMPAR, NR2A, NR2B). Optogenetic inhibition of IC neurons relieved pain without altering synaptic plasticity. However, repetitive ICS combined with optogenetic activation diminished the pain-relieving effects of ICS and increased AMPAR and NR2B receptor levels. Additionally, activating inhibitory neurons also reduced pain, while repetitive activation of excitatory neurons lessened the effectiveness of ICS and was associated with heightened receptor expression. These findings suggest that inhibiting excitatory neurons or activating inhibitory neurons in the IC could help modulate pain in neuropathic conditions, shedding light on how ICS can influence pain management through changes in synaptic plasticity.
由神经损伤引起的神经性疼痛极大地影响生活质量。最近的研究提出调节大脑活动,特别是通过对岛叶皮质(IC)进行电刺激,作为一种治疗选择。本研究旨在了解IC刺激(ICS)如何影响疼痛调节。在大鼠神经病变模型中,研究人员使用光遗传学和ICS技术来评估机械性异常性疼痛的变化和突触变化,重点关注谷氨酸受体(AMPAR、NR2A、NR2B)。对IC神经元的光遗传学抑制可缓解疼痛,而不改变突触可塑性。然而,重复性ICS与光遗传学激活相结合会降低ICS的止痛效果,并增加AMPAR和NR2B受体水平。此外,激活抑制性神经元也可减轻疼痛,而重复性激活兴奋性神经元则会降低ICS的有效性,并与受体表达升高有关。这些发现表明,抑制IC中的兴奋性神经元或激活抑制性神经元可能有助于调节神经性疾病中的疼痛,揭示了ICS如何通过突触可塑性的变化影响疼痛管理。