{"title":"[全度中胶囊()对软骨终板的保护作用,改善针刺所致的椎间盘退变]。","authors":"Songlin Liang, Nianhu Li, Jiawen Zhan, Hongyan Guo, Changjun Tie, Yanjie Zhu, Zhichao Li, Liqing Ke, Peng Zhang, Wenxiang Cheng","doi":"10.12200/j.issn.1003-0034.20240031","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To investigate the protective effect and underlying mechanism of <i>Quan Duzhong</i> Capsule () on acupuncture-induced caudal intervertebral disc degeneration in rats.</p><p><strong>Methods: </strong>Sixty male Sprague-Dawley rats were weight-stratified and randomly divided into 6 groups (10 rats per group). A 26 G needle was used to puncture the rat coccygeal vertebrae to establish an intervertebral disc degeneration model, while the control group only received acupuncture on the skin lateral to the coccygeal vertebrae. The model groups received either <i>Quan Duzhong</i> Capsule () at a dose of 300 mg·kg-1 or normal saline via intragastric administration. Samples were collected at 4 and 8 weeks post-modeling, respectively. Longitudinal assessment included weekly 3.0 T MRI scans to dynamically evaluate changes in the nucleus pulposus, with measurements of the nucleus pulposus height, area, signal value, and the disc height index(DHI). Isolated coccygeal segments underwent micro-computed tomography (Micro-CT) to analyze the morphological changes in the vertebrae at both ends of the modeled intervertebral discs, and bone microstructure parameters were analyzed. Coccygeal vertebral tissues were decalcified and embedded in paraffin. Hematoxylin-eosin (HE) staining and Toluidine Blue staining were used to assess the tissue morphology and cartilage damage. Immunohistochemistry was performed to analyze the expression of aggrecan (Acan) and typeⅡcollagen(ColⅡ). Total mRNA was extracted from the nucleus pulposus, and quantitative reverse transcription polymerase chain reaction(qRT-PCR) was used to detect the gene expression of Acan and ColⅡ.</p><p><strong>Results: </strong>MRI scan results showed that compared with the control group, the nucleus pulposus signal at the injured site in the model group gradually disappeared with the increase of time after acupuncture modeling, indicating the successful establishment of the acupuncture-induced caudal intervertebral disc degeneration model. Dynamic MRI acquisition data revealed that the T2WI signal value, height, area, and DHI of the nucleus pulposus in rats of the <i>Quan Duzhong</i> Capsule() administration group were significantly higher than those in the model group(<i>P</i><0.05). Micro-CT analysis results demonstrated that after 8 weeks of <i>Quan Duzhong</i> Capsule() treatment, the bone volume of the vertebrae adjacent to the nucleus pulposus injury site and the trabecular bone thickness were significantly increased compared with the model group (<i>P</i><0.05), while the bone surface area to bone volume ratio, structural model index, trabecular separation, and pattern factor were significantly decreased (<i>P</i><0.05). Histological staining results indicated that compared with the model group, the intervertebral disc tissue morphology in <i>Quan Duzhong</i> Capsule () administration group was relatively intact;Toluidine blue staining showed that the chondrocyte layer in <i>Quan Duzhong</i> Capsule () administration group was thicker than that in the model group; immunohistochemistry results revealed that the expressions of Acan and ColⅡ in the acupuncture-induced intervertebral discs of rats in <i>Quan Duzhong</i> Capsule () administration group were significantly higher than those in model group(<i>P</i><0.05). qRT-PCR results showed that after 8 weeks of <i>Quan Duzhong</i> Capsule() treatment, the mRNA expressions of Acan and ColⅡ were upregulated by 1.5 and 1.6 times, respectively, compared with the model group(<i>P</i><0.05).</p><p><strong>Conclusion: </strong><i>Quan Duzhong</i> Capsule () can alleviate acupuncture-induced caudal intervertebral disc degeneration in rats and inhibit the reduction of extracellular matrix in the intervertebral disc during the degeneration process.</p>","PeriodicalId":23964,"journal":{"name":"Zhongguo gu shang = China journal of orthopaedics and traumatology","volume":"39 4","pages":"407-18"},"PeriodicalIF":0.0000,"publicationDate":"2026-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Protecting effect of Quan Duzhong Capsule() on the cartilaginous endplate so as to improve acupuncture-induced intervertebral disc degeneration].\",\"authors\":\"Songlin Liang, Nianhu Li, Jiawen Zhan, Hongyan Guo, Changjun Tie, Yanjie Zhu, Zhichao Li, Liqing Ke, Peng Zhang, Wenxiang Cheng\",\"doi\":\"10.12200/j.issn.1003-0034.20240031\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To investigate the protective effect and underlying mechanism of <i>Quan Duzhong</i> Capsule () on acupuncture-induced caudal intervertebral disc degeneration in rats.</p><p><strong>Methods: </strong>Sixty male Sprague-Dawley rats were weight-stratified and randomly divided into 6 groups (10 rats per group). A 26 G needle was used to puncture the rat coccygeal vertebrae to establish an intervertebral disc degeneration model, while the control group only received acupuncture on the skin lateral to the coccygeal vertebrae. The model groups received either <i>Quan Duzhong</i> Capsule () at a dose of 300 mg·kg-1 or normal saline via intragastric administration. Samples were collected at 4 and 8 weeks post-modeling, respectively. Longitudinal assessment included weekly 3.0 T MRI scans to dynamically evaluate changes in the nucleus pulposus, with measurements of the nucleus pulposus height, area, signal value, and the disc height index(DHI). Isolated coccygeal segments underwent micro-computed tomography (Micro-CT) to analyze the morphological changes in the vertebrae at both ends of the modeled intervertebral discs, and bone microstructure parameters were analyzed. Coccygeal vertebral tissues were decalcified and embedded in paraffin. Hematoxylin-eosin (HE) staining and Toluidine Blue staining were used to assess the tissue morphology and cartilage damage. Immunohistochemistry was performed to analyze the expression of aggrecan (Acan) and typeⅡcollagen(ColⅡ). Total mRNA was extracted from the nucleus pulposus, and quantitative reverse transcription polymerase chain reaction(qRT-PCR) was used to detect the gene expression of Acan and ColⅡ.</p><p><strong>Results: </strong>MRI scan results showed that compared with the control group, the nucleus pulposus signal at the injured site in the model group gradually disappeared with the increase of time after acupuncture modeling, indicating the successful establishment of the acupuncture-induced caudal intervertebral disc degeneration model. Dynamic MRI acquisition data revealed that the T2WI signal value, height, area, and DHI of the nucleus pulposus in rats of the <i>Quan Duzhong</i> Capsule() administration group were significantly higher than those in the model group(<i>P</i><0.05). Micro-CT analysis results demonstrated that after 8 weeks of <i>Quan Duzhong</i> Capsule() treatment, the bone volume of the vertebrae adjacent to the nucleus pulposus injury site and the trabecular bone thickness were significantly increased compared with the model group (<i>P</i><0.05), while the bone surface area to bone volume ratio, structural model index, trabecular separation, and pattern factor were significantly decreased (<i>P</i><0.05). Histological staining results indicated that compared with the model group, the intervertebral disc tissue morphology in <i>Quan Duzhong</i> Capsule () administration group was relatively intact;Toluidine blue staining showed that the chondrocyte layer in <i>Quan Duzhong</i> Capsule () administration group was thicker than that in the model group; immunohistochemistry results revealed that the expressions of Acan and ColⅡ in the acupuncture-induced intervertebral discs of rats in <i>Quan Duzhong</i> Capsule () administration group were significantly higher than those in model group(<i>P</i><0.05). qRT-PCR results showed that after 8 weeks of <i>Quan Duzhong</i> Capsule() treatment, the mRNA expressions of Acan and ColⅡ were upregulated by 1.5 and 1.6 times, respectively, compared with the model group(<i>P</i><0.05).</p><p><strong>Conclusion: </strong><i>Quan Duzhong</i> Capsule () can alleviate acupuncture-induced caudal intervertebral disc degeneration in rats and inhibit the reduction of extracellular matrix in the intervertebral disc during the degeneration process.</p>\",\"PeriodicalId\":23964,\"journal\":{\"name\":\"Zhongguo gu shang = China journal of orthopaedics and traumatology\",\"volume\":\"39 4\",\"pages\":\"407-18\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2026-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zhongguo gu shang = China journal of orthopaedics and traumatology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.12200/j.issn.1003-0034.20240031\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhongguo gu shang = China journal of orthopaedics and traumatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12200/j.issn.1003-0034.20240031","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
摘要
目的:探讨全度中胶囊对针刺诱导大鼠椎间盘退变的保护作用及其机制。方法:雄性sd大鼠60只,按体重分层,随机分为6组,每组10只。采用26g针穿刺大鼠尾椎建立椎间盘退变模型,对照组仅针刺尾椎外侧皮肤。模型组大鼠分别灌胃全笃中胶囊(300 mg·kg-1)或生理盐水。分别于造模后4周和8周采集标本。纵向评估包括每周3.0 T MRI扫描,动态评估髓核的变化,测量髓核高度、面积、信号值和椎间盘高度指数(DHI)。对离体尾骨节段进行微计算机断层扫描(Micro-CT),分析模型椎间盘两端椎骨的形态变化,并分析骨微结构参数。尾椎组织脱钙,石蜡包埋。采用苏木精-伊红(HE)染色和甲苯胺蓝染色评价组织形态和软骨损伤情况。免疫组化分析聚集蛋白(Acan)和Ⅱ型胶原蛋白(ColⅡ)的表达。提取髓核总mRNA,采用定量逆转录聚合酶链反应(qRT-PCR)检测Acan和Col基因表达Ⅱ。结果:MRI扫描结果显示,与对照组相比,针刺造模后,模型组损伤部位髓核信号随着时间的增加逐渐消失,表明针刺诱导的椎弓根椎间盘退变模型建立成功。动态MRI采集数据显示,全独中胶囊()给药组大鼠髓核T2WI信号值、高度、面积、DHI均显著高于模型组(全独中胶囊()给药组);与模型组比较,髓核损伤部位附近椎体骨体积和骨小梁厚度均显著增加(PPQuan Duzhong Capsule()给药组相对完整;甲苯胺蓝染色显示全笃中胶囊()给药组软骨细胞层较模型组增厚;免疫组化结果显示,全毒中胶囊()给药组针刺大鼠椎间盘组织中Acan和ColⅡ的表达量显著高于模型组(全毒中胶囊()治疗组),Acan和ColⅡmRNA表达量分别较模型组上调1.5倍和1.6倍(p)。全度中胶囊()可减轻针刺诱导的大鼠椎间盘退变,抑制退变过程中椎间盘细胞外基质的减少。
[Protecting effect of Quan Duzhong Capsule() on the cartilaginous endplate so as to improve acupuncture-induced intervertebral disc degeneration].
Objective: To investigate the protective effect and underlying mechanism of Quan Duzhong Capsule () on acupuncture-induced caudal intervertebral disc degeneration in rats.
Methods: Sixty male Sprague-Dawley rats were weight-stratified and randomly divided into 6 groups (10 rats per group). A 26 G needle was used to puncture the rat coccygeal vertebrae to establish an intervertebral disc degeneration model, while the control group only received acupuncture on the skin lateral to the coccygeal vertebrae. The model groups received either Quan Duzhong Capsule () at a dose of 300 mg·kg-1 or normal saline via intragastric administration. Samples were collected at 4 and 8 weeks post-modeling, respectively. Longitudinal assessment included weekly 3.0 T MRI scans to dynamically evaluate changes in the nucleus pulposus, with measurements of the nucleus pulposus height, area, signal value, and the disc height index(DHI). Isolated coccygeal segments underwent micro-computed tomography (Micro-CT) to analyze the morphological changes in the vertebrae at both ends of the modeled intervertebral discs, and bone microstructure parameters were analyzed. Coccygeal vertebral tissues were decalcified and embedded in paraffin. Hematoxylin-eosin (HE) staining and Toluidine Blue staining were used to assess the tissue morphology and cartilage damage. Immunohistochemistry was performed to analyze the expression of aggrecan (Acan) and typeⅡcollagen(ColⅡ). Total mRNA was extracted from the nucleus pulposus, and quantitative reverse transcription polymerase chain reaction(qRT-PCR) was used to detect the gene expression of Acan and ColⅡ.
Results: MRI scan results showed that compared with the control group, the nucleus pulposus signal at the injured site in the model group gradually disappeared with the increase of time after acupuncture modeling, indicating the successful establishment of the acupuncture-induced caudal intervertebral disc degeneration model. Dynamic MRI acquisition data revealed that the T2WI signal value, height, area, and DHI of the nucleus pulposus in rats of the Quan Duzhong Capsule() administration group were significantly higher than those in the model group(P<0.05). Micro-CT analysis results demonstrated that after 8 weeks of Quan Duzhong Capsule() treatment, the bone volume of the vertebrae adjacent to the nucleus pulposus injury site and the trabecular bone thickness were significantly increased compared with the model group (P<0.05), while the bone surface area to bone volume ratio, structural model index, trabecular separation, and pattern factor were significantly decreased (P<0.05). Histological staining results indicated that compared with the model group, the intervertebral disc tissue morphology in Quan Duzhong Capsule () administration group was relatively intact;Toluidine blue staining showed that the chondrocyte layer in Quan Duzhong Capsule () administration group was thicker than that in the model group; immunohistochemistry results revealed that the expressions of Acan and ColⅡ in the acupuncture-induced intervertebral discs of rats in Quan Duzhong Capsule () administration group were significantly higher than those in model group(P<0.05). qRT-PCR results showed that after 8 weeks of Quan Duzhong Capsule() treatment, the mRNA expressions of Acan and ColⅡ were upregulated by 1.5 and 1.6 times, respectively, compared with the model group(P<0.05).
Conclusion: Quan Duzhong Capsule () can alleviate acupuncture-induced caudal intervertebral disc degeneration in rats and inhibit the reduction of extracellular matrix in the intervertebral disc during the degeneration process.