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通过聚腺苷酸测序利用腰交感神经切除术鉴定改善神经损伤大鼠冷敏感性的基因

Identification of Genes for Improving Cold Sensitivity in Nerve-Damaged Rats Via Lumbar Sympathectomy Using Poly(A)-seq.

作者信息

Meng Xi, Fan Hanrui, Xu Ping, Yang Lei, Fei Yong, Zhang Wenping

机构信息

College of Life Sciences and Medicine, Zhejiang Sci-Tech University, 310053 Hangzhou, Zhejiang, China.

Department of Pain Medicine, Affiliated Hospital of Jiaxing University, 314000 Jiaxing, Zhejiang, China.

出版信息

J Integr Neurosci. 2025 Jun 20;24(6):36253. doi: 10.31083/JIN36253.

Abstract

BACKGROUND

Lumbar sympathectomy improves blood flow to the lower limbs and is widely used in clinical practice to treat lower limb pain and cold. However, the therapeutic mechanisms underlying lumbar sympathectomy for limb coldness resulting from nerve injury remain unclear. This study aimed to investigate the effect of lumbar sympathectomy on cold allodynia in rats with spared nerve injury (SNI) and identify potential target genes associated with its analgesic effects.

METHODS

A rat model of SNI was established. Mechanical and cold pain thresholds were assessed in rats with SNI to explore the analgesic effects of lumbar sympathetic neurectomy on cold allodynia. Poly(A)-seq was used to analyze the transcriptional profile of the spinal cord. Differentially expressed genes (DEGs) were screened and analyzed using bioinformatics and validated by quantitative PCR analysis.

RESULTS

Lumbar sympathectomy improved mechanical pain, cold allodynia, and cold sensitivity in the ipsilateral hind paw of SNI rats (all < 0.05). Poly(A)-seq identified 278 DEGs (177 upregulated and 101 downregulated) in the spinal cords of SNI model rats compared with control rats. We identified 174 DEGs in the gene expression profile of lumbar sympathectomized SNI rats, including 69 upregulated and 105 downregulated genes, compared with SNI model rats. Functional analysis of the DEGs revealed that the most significantly enriched pathways included immune-related pathways and cellular molecular components, which mediate neuroinflammation, central sensitization, and chronic pain. To explore the correlation among the DEGs, we used the STRING database to construct protein-protein interaction networks. Finally, quantitative PCR analysis revealed six potential target genes associated with cold analgesic effects epithelial mitogen gene (), histone cluster 2 H3 family member C2 (), small integral membrane protein 6 (), family with sequence similarity 187 member a (), , and .

CONCLUSIONS

Lumbar sympathectomy may alleviate cold allodynia in SNI model rats. We identified key genes associated with pain mitigation, offering potential therapeutic targets. These genes may serve as targets for treating nerve injury-induced cold allodynia. These findings provide valuable insights for the development of new treatments for nerve-related pain disorders.

摘要

背景

腰交感神经切除术可改善下肢血流,在临床实践中广泛用于治疗下肢疼痛和寒冷。然而,腰交感神经切除术治疗神经损伤所致肢体寒冷的治疗机制仍不清楚。本研究旨在探讨腰交感神经切除术对 spared 神经损伤(SNI)大鼠冷痛觉过敏的影响,并确定与其镇痛作用相关的潜在靶基因。

方法

建立 SNI 大鼠模型。评估 SNI 大鼠的机械性和冷痛阈值,以探讨腰交感神经切除术对冷痛觉过敏的镇痛作用。使用 Poly(A)-seq 分析脊髓的转录谱。使用生物信息学筛选和分析差异表达基因(DEGs),并通过定量 PCR 分析进行验证。

结果

腰交感神经切除术改善了 SNI 大鼠同侧后爪的机械性疼痛、冷痛觉过敏和冷敏感性(均 P<0.05)。与对照大鼠相比,Poly(A)-seq 在 SNI 模型大鼠脊髓中鉴定出 278 个 DEGs(177 个上调和 101 个下调)。与 SNI 模型大鼠相比,我们在腰交感神经切除的 SNI 大鼠基因表达谱中鉴定出 174 个 DEGs,包括 69 个上调和 105 个下调基因。DEGs 的功能分析表明,最显著富集的途径包括免疫相关途径和细胞分子成分,它们介导神经炎症、中枢敏化和慢性疼痛。为了探索 DEGs 之间的相关性,我们使用 STRING 数据库构建蛋白质-蛋白质相互作用网络。最后,定量 PCR 分析揭示了与冷镇痛作用相关的六个潜在靶基因,即上皮有丝分裂原基因()、组蛋白簇 2 H3 家族成员 C2()、小整合膜蛋白 6()、序列相似性家族 187 成员 a()、()和()。

结论

腰交感神经切除术可能减轻 SNI 模型大鼠的冷痛觉过敏。我们鉴定出与疼痛减轻相关的关键基因,提供了潜在的治疗靶点。这些基因可能作为治疗神经损伤诱导的冷痛觉过敏的靶点。这些发现为开发治疗神经相关疼痛疾病的新疗法提供了有价值的见解。

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