Junlong Yang , Xianglong Lv , Yunting Chen , Changyu Shen , Huaqiao Chen , Lin Wang , Jing Yao , Yuanxin Huang
{"title":"脊髓非靶向代谢组学揭示银针热疗治疗肌筋膜疼痛综合征的镇痛机制","authors":"Junlong Yang , Xianglong Lv , Yunting Chen , Changyu Shen , Huaqiao Chen , Lin Wang , Jing Yao , Yuanxin Huang","doi":"10.1016/j.jrras.2025.101923","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>To elucidate the spinal analgesic mechanism of silver-needle thermotherapy in myofascial pain syndrome (MPS) using untargeted metabolomics.</div></div><div><h3>Methods</h3><div>An MPS rat model was established by blunt impact and treadmill exercise. Rats were divided into normal (N), model (M), and silver-needle thermotherapy (S) groups. Pain sensitivity was assessed via mechanical withdrawal threshold (MWT). Electromyography (EMG) recorded MTrP activity, hematoxylin-eosin (HE) staining evaluated muscle pathology, and immunofluorescence quantified spinal calcitonin gene-related peptide (CGRP) and substance P (SP) expression. Untargeted metabolomics of spinal cord tissue was performed using liquid chromatography tandem mass spectrometry (LC-MS/MS).</div></div><div><h3>Results</h3><div>Compared to group M, group S showed significantly increased MWT (<em>P</em> < 0.01), normalized EMG signals, and improved muscle histopathology. Silver-needle thermotherapy downregulated spinal CGRP and SP expression (<em>P</em> < 0.05). Metabolomics identified 52 differential metabolites in spinal cord tissue. Enrichment analysis revealed involvement of three key pathways: 2-oxocarboxylic acid metabolism (upregulated citric acid and 3-methyl-2-oxobutanoic acid; downregulated N-acetylornithine), cytochrome P450-mediated xenobiotic metabolism (upregulated nicotine), and starch/sucrose metabolism (downregulated D-fructose 6-phosphate).</div></div><div><h3>Conclusion</h3><div>Silver-needle thermotherapy alleviates MPS by modulating spinal metabolic pathways linked to neuronal excitability, neuroinflammation, and energy regulation. Untargeted metabolomics effectively uncovered these spinal mechanisms, advancing understanding of MPS pathophysiology and silver-needle analgesia.</div></div>","PeriodicalId":16920,"journal":{"name":"Journal of Radiation Research and Applied Sciences","volume":"18 4","pages":"Article 101923"},"PeriodicalIF":2.5000,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Untargeted metabolomics of spinal cord reveals analgesic mechanism of silver-needle thermotherapy for myofascial pain syndrome\",\"authors\":\"Junlong Yang , Xianglong Lv , Yunting Chen , Changyu Shen , Huaqiao Chen , Lin Wang , Jing Yao , Yuanxin Huang\",\"doi\":\"10.1016/j.jrras.2025.101923\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><div>To elucidate the spinal analgesic mechanism of silver-needle thermotherapy in myofascial pain syndrome (MPS) using untargeted metabolomics.</div></div><div><h3>Methods</h3><div>An MPS rat model was established by blunt impact and treadmill exercise. Rats were divided into normal (N), model (M), and silver-needle thermotherapy (S) groups. Pain sensitivity was assessed via mechanical withdrawal threshold (MWT). Electromyography (EMG) recorded MTrP activity, hematoxylin-eosin (HE) staining evaluated muscle pathology, and immunofluorescence quantified spinal calcitonin gene-related peptide (CGRP) and substance P (SP) expression. Untargeted metabolomics of spinal cord tissue was performed using liquid chromatography tandem mass spectrometry (LC-MS/MS).</div></div><div><h3>Results</h3><div>Compared to group M, group S showed significantly increased MWT (<em>P</em> < 0.01), normalized EMG signals, and improved muscle histopathology. Silver-needle thermotherapy downregulated spinal CGRP and SP expression (<em>P</em> < 0.05). Metabolomics identified 52 differential metabolites in spinal cord tissue. Enrichment analysis revealed involvement of three key pathways: 2-oxocarboxylic acid metabolism (upregulated citric acid and 3-methyl-2-oxobutanoic acid; downregulated N-acetylornithine), cytochrome P450-mediated xenobiotic metabolism (upregulated nicotine), and starch/sucrose metabolism (downregulated D-fructose 6-phosphate).</div></div><div><h3>Conclusion</h3><div>Silver-needle thermotherapy alleviates MPS by modulating spinal metabolic pathways linked to neuronal excitability, neuroinflammation, and energy regulation. Untargeted metabolomics effectively uncovered these spinal mechanisms, advancing understanding of MPS pathophysiology and silver-needle analgesia.</div></div>\",\"PeriodicalId\":16920,\"journal\":{\"name\":\"Journal of Radiation Research and Applied Sciences\",\"volume\":\"18 4\",\"pages\":\"Article 101923\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-09-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Radiation Research and Applied Sciences\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1687850725006351\",\"RegionNum\":4,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Radiation Research and Applied Sciences","FirstCategoryId":"103","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1687850725006351","RegionNum":4,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Untargeted metabolomics of spinal cord reveals analgesic mechanism of silver-needle thermotherapy for myofascial pain syndrome
Objective
To elucidate the spinal analgesic mechanism of silver-needle thermotherapy in myofascial pain syndrome (MPS) using untargeted metabolomics.
Methods
An MPS rat model was established by blunt impact and treadmill exercise. Rats were divided into normal (N), model (M), and silver-needle thermotherapy (S) groups. Pain sensitivity was assessed via mechanical withdrawal threshold (MWT). Electromyography (EMG) recorded MTrP activity, hematoxylin-eosin (HE) staining evaluated muscle pathology, and immunofluorescence quantified spinal calcitonin gene-related peptide (CGRP) and substance P (SP) expression. Untargeted metabolomics of spinal cord tissue was performed using liquid chromatography tandem mass spectrometry (LC-MS/MS).
Results
Compared to group M, group S showed significantly increased MWT (P < 0.01), normalized EMG signals, and improved muscle histopathology. Silver-needle thermotherapy downregulated spinal CGRP and SP expression (P < 0.05). Metabolomics identified 52 differential metabolites in spinal cord tissue. Enrichment analysis revealed involvement of three key pathways: 2-oxocarboxylic acid metabolism (upregulated citric acid and 3-methyl-2-oxobutanoic acid; downregulated N-acetylornithine), cytochrome P450-mediated xenobiotic metabolism (upregulated nicotine), and starch/sucrose metabolism (downregulated D-fructose 6-phosphate).
Conclusion
Silver-needle thermotherapy alleviates MPS by modulating spinal metabolic pathways linked to neuronal excitability, neuroinflammation, and energy regulation. Untargeted metabolomics effectively uncovered these spinal mechanisms, advancing understanding of MPS pathophysiology and silver-needle analgesia.
期刊介绍:
Journal of Radiation Research and Applied Sciences provides a high quality medium for the publication of substantial, original and scientific and technological papers on the development and applications of nuclear, radiation and isotopes in biology, medicine, drugs, biochemistry, microbiology, agriculture, entomology, food technology, chemistry, physics, solid states, engineering, environmental and applied sciences.