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利用脑脊液脂质组学阐明三叉神经痛中的分子脂质扰动。

Elucidating molecular lipid perturbations in trigeminal neuralgia using cerebrospinal fluid lipidomics.

作者信息

Xu Dongyuan, Dai Xuan, He Qianwen, Mei Zhimin, Zhou Yixuan, Zhao Jingwei, Xiong Nanxiang

机构信息

Department of Neurosurgery, Zhongnan Hospital of Wuhan University, No. 169, Donghu Road, Wuhan, 430071, China.

Department of Anesthesiology, Zhongnan Hospital of Wuhan University, Wuhan, 430071, P. R. China.

出版信息

Sci Rep. 2025 Apr 6;15(1):11777. doi: 10.1038/s41598-025-89755-x.

Abstract

Trigeminal neuralgia (TN) is a neuropathic facial pain disorder characterized by severe stabbing pain along the trigeminal nerve. While its pathogenesis remains unclear, nerve demyelination and inflammation are likely involved. Current research has primarily focused on various blood-based omics approaches, which do not fully capture the lipid alterations occurring during TN progression in brain. In contrast, our study is the first to investigate cerebrospinal fluid (CSF) lipidomic profiles in TN patients, aiming to elucidate potential disease mechanisms. CSF samples were collected from 22 TN patients and 18 healthy controls, followed by untargeted lipidomic analysis using high-performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry. A pipeline for lipid identification and relative quantification, combined with statistical analysis, revealed 188 lipid species across 21 classes. We found significant upregulation of Cer-NPs, LPCs, PCs, TGs, and OxTGs in TN patients, while stigmasterol hexoside was downregulated. Moderate correlations were observed between lipid species and clinical parameters. These findings highlight considerable CSF lipidome alterations in TN, suggesting roles for nerve demyelination, neuroinflammation, and pain sensitization in its pathogenesis. Our study provides novel insights into lipid targets that may offer therapeutic potential for managing TN.

摘要

三叉神经痛(TN)是一种神经性面部疼痛疾病,其特征为沿三叉神经出现严重的刺痛。虽然其发病机制尚不清楚,但神经脱髓鞘和炎症可能与之相关。目前的研究主要集中在各种基于血液的组学方法上,这些方法并不能完全捕捉到TN进展过程中大脑中发生的脂质变化。相比之下,我们的研究首次调查了TN患者的脑脊液(CSF)脂质组学特征,旨在阐明潜在的疾病机制。从22例TN患者和18例健康对照中收集CSF样本,然后使用高效液相色谱-四极杆飞行时间质谱联用进行非靶向脂质组学分析。结合统计分析的脂质鉴定和相对定量流程揭示了21类中的188种脂质。我们发现TN患者中神经酰胺纳米颗粒(Cer-NPs)、溶血磷脂酰胆碱(LPCs)、磷脂酰胆碱(PCs)、甘油三酯(TGs)和氧化甘油三酯(OxTGs)显著上调,而豆甾醇己糖苷下调。观察到脂质种类与临床参数之间存在中等程度的相关性。这些发现突出了TN患者脑脊液脂质组的显著变化,表明神经脱髓鞘、神经炎症和疼痛敏化在其发病机制中的作用。我们的研究为可能为TN治疗提供潜在治疗价值的脂质靶点提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e098/11973149/6c5aa98e3936/41598_2025_89755_Fig1_HTML.jpg

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