Activating the vlPAG-LC neural pathway alleviates neuropathic pain and comorbid anxiety-like behaviors through distinct projections

蓝斑 SNi公司 神经病理性疼痛 神经科学 医学 止痛药 导水管周围灰质 伤害 抗焦虑药 药理学 直接运动途径 神经损伤 延髓头端腹内侧区 慢性疼痛 间接运动途径 中枢神经系统 麻醉 痛阈 微量注射
作者
Liang Zhang,Fei Li,Han-Xue Sun,Hui Li,Fen-Sheng Huang,Jun-Bin Yin,Yun-Qing Li
出处
期刊:Neurobiology of Disease [Elsevier BV]
卷期号:220: 107298-107298
标识
DOI:10.1016/j.nbd.2026.107298
摘要

The ventrolateral periaqueductal gray (vlPAG) functions as a critical hub in the descending pain modulatory system. The vlPAG receives and processes upstream pain information, which is involved in descending pain modulation through projecting downstream to rostroventral medulla (RVM) or locus coeruleus (LC). Although the modulatory roles of the upstream pathways and the vlPAG-RVM connection in neuropathic pain have been extensively studied, but the involvement of the vlPAG-LC neural pathway in regulating neuropathic pain and related comorbidity requires further investigation. In the present study, the excitability of the vlPAG-LC pathway was found to be increased in spared nerve injury (SNI) mice. Activating of the vlPAG-LC pathway using chemogenetic approach produced antinociceptive and anxiolytic effects in SNI mice. Intrathecal administration of α2-adrenergic receptor antagonist reversed analgesic effect of the vlPAG-LC pathway in SNI mice. However, the anxiolytic effect of this neural pathway was unaffected. A previously unrecognized vlPAG-LC-anterior cingulate cortex (ACC) tertiary pathway was identified in the current work. The excitability of ACC increased in SNI mice, whereas decreased following activation of the vlPAG-LC pathway. Activation of the ACC pyramidal neurons blocked the vlPAG-LC pathway-mediated anxiolytic effect but not analgesic effect in SNI mice. Furthermore, the anxiolytic effect of the vlPAG-LC pathway in SNI mice was altered after activation of the LC-ACC pathway or microinjection of norepinephrine into ACC. The present results underscored spinal dorsal horn and ACC as the potential downstream targets for analgesic and anxiolytic effects of the vlPAG-LC neural pathway in SNI mice, respectively. • The excitability of the vlPAG-LC neural pathway is enhanced in SNI mice. • Activation of the vlPAG-LC neural pathway exhibits analgesic and anxiolytic effects in SNI mice. • The analgesic effect of the vlPAG-LC neural pathway relies on the α2-adrenergic receptor located in the SDH. • The anxiolytic effect of the vlPAG-LC neural pathway acts via the ACC.
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