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Lycium barbarum glycopeptide ameliorates motor and visual deficits in autoimmune inflammatory diseases

视神经脊髓炎 医学 神经保护 视神经炎 多发性硬化 脊髓 促炎细胞因子 神经科学 神经免疫学 脊髓炎 视神经 实验性自身免疫性脑脊髓炎 病理 中枢神经系统 免疫学 炎症 药理学 生物 内科学 解剖 精神科
作者
Li Xu,Lu Yang,Huiming Xu,Yuhan Li,Fuhua Peng,Wei Qiu,Changyong Tang
出处
期刊:Phytomedicine [Elsevier BV]
卷期号:129: 155610-155610 被引量:15
标识
DOI:10.1016/j.phymed.2024.155610
摘要

Lycium barbarum glycopeptide (LbGp), extracted from the Traditional Chinese medicine (TCM) of Lycium barbarum (LB), provides a neuroprotective effect against neurodegenerative and neuroimmune disorders contributing to its immunomodulatory and anti-inflammatory roles. Neuromyelitis optica spectrum disorders (NMOSD) is an autoimmune-mediated central nervous system (CNS) demyelinating disease, clinically manifested as transverse myelitis (TM) and optic neuritis. However, no drug has been demonstrated to be effective in relieving limb weakness and visual impairment of NMOSD patients. This study investigates the potential role of LbGp in ameliorating pathologic lesions and improving neurological dysfunction during NMOSD progression, and to elucidate the underlying mechanisms for the first time. We administrate LbGp in experimental NMOSD models in ex vivo and in vivo to explore its effect on NMOSD. To evaluate motor function, both rotarod and gait tasks were performed in systemic NMOSD mice models. Furthermore, we assessed the severity of NMO-like lesions of astrocytes, organotypic cerebellar slices, as well as brain, spinal cord and optic nerve sections from NMOSD mouse models with LbGp treatment by immunofluorescent staining. In addition, demyelination levels in optic nerve were measured by G-ratio through Electro-microscopy (EM). And inflammation response was explored through detecting the protein levels of proinflammatory cytokines and NF-κB signaling in astrocytic culture medium and spinal cord homogenates respectively by Elisa and by Western blotting. LbGp could significantly reduce astrocytes injury, demyelination, and microglial activation in NMOSD models. In addition, LbGp also improved locomotor and visual dysfunction through preventing neuron and retinal ganglion cells (RGCs) from inflammatory attack in a systemic mouse model. Mechanically, LbGp inhibits proinflammatory factors release via inhibition of NF-κB signaling in NMOSD models. This study provides evidence to develop LbGp as a functional TCM for the clinical treatment of NMOSD.
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