首页 > 最新文献

Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan最新文献

英文 中文
International standard of Traditional Chinese Medicine Techniques: Traditional Chinese Medicine guidelines for acute primary headache (2022). 国际中医药技术标准:中医治疗急性原发性头痛指南(2022 年)。
Pub Date : 2024-08-01 DOI: 10.19852/j.cnki.jtcm.2024.04.005
Yao Yuning, Cao Kegang, Zhang Genming, Liu Jianping, Chen Wei, Cao Junling, Yang Wenming, Yan Yongmei, Geng Chang, J U Yi, Zhao Dexi, Q U Mia, L I Xiaoli, Sun Li, Han Zhenyun, H E Liyun, Cui Fangyuan, F U Caihong, Zhou Bo, Liao Shuqin

Objective: To summarize the evidence from Traditional Chinese Medicine (TCM) practice in the treatment of acute primary headache and provide clinical practice guidance.

Methods: The guidelines were developed in accordance with the World Health Organization guideline development manual. After the establishment of steering committee, panel and the registration and protocol formulation, the evidence on TCM for acute primary headache from published guidelines, clinical evidence, and expert experience and consensus were collected. The grading of recommendations assessment, development and evaluation method was used to grade the evidence and make the recommendations.

Results: Based on the available evidence, the guidelines recommended three TCM herbal decoctions, six Chinese patent medicines, and two kinds of external application of Chinese herbal medicines. Diagnostic recommendations based on the expert experience and consensus were also included in the guidelines.

Conclusion: TCM diagnosis and treatment of decoction, Chinese patent medicine and external application for treating acute primary headache were recommended. We hope these guidelines will be helpful in standardize the TCM acute treatment of primary headache.

目的:总结中医治疗急性原发性头痛的证据,并为临床实践提供指导:总结中医治疗急性原发性头痛的实践证据,并提供临床实践指导:方法:根据世界卫生组织指南制定手册制定指南。方法:本指南按照世界卫生组织指南制定手册制定,在成立指导委员会、专家组、注册和制定方案后,从已发表的指南、临床证据、专家经验和共识中收集中医药治疗急性原发性头痛的证据。采用建议分级评估、制定和评价方法对证据进行分级并提出建议:根据现有证据,指南推荐了三种中药煎剂、六种中成药和两种中药外敷药。基于专家经验和共识的诊断建议也被纳入指南:结论:推荐了治疗急性原发性头痛的煎剂、中成药和外敷药的中医诊疗方法。我们希望这些指南将有助于规范原发性头痛的中医急性期治疗。
{"title":"International standard of Traditional Chinese Medicine Techniques: Traditional Chinese Medicine guidelines for acute primary headache (2022).","authors":"Yao Yuning, Cao Kegang, Zhang Genming, Liu Jianping, Chen Wei, Cao Junling, Yang Wenming, Yan Yongmei, Geng Chang, J U Yi, Zhao Dexi, Q U Mia, L I Xiaoli, Sun Li, Han Zhenyun, H E Liyun, Cui Fangyuan, F U Caihong, Zhou Bo, Liao Shuqin","doi":"10.19852/j.cnki.jtcm.2024.04.005","DOIUrl":"10.19852/j.cnki.jtcm.2024.04.005","url":null,"abstract":"<p><strong>Objective: </strong>To summarize the evidence from Traditional Chinese Medicine (TCM) practice in the treatment of acute primary headache and provide clinical practice guidance.</p><p><strong>Methods: </strong>The guidelines were developed in accordance with the World Health Organization guideline development manual. After the establishment of steering committee, panel and the registration and protocol formulation, the evidence on TCM for acute primary headache from published guidelines, clinical evidence, and expert experience and consensus were collected. The grading of recommendations assessment, development and evaluation method was used to grade the evidence and make the recommendations.</p><p><strong>Results: </strong>Based on the available evidence, the guidelines recommended three TCM herbal decoctions, six Chinese patent medicines, and two kinds of external application of Chinese herbal medicines. Diagnostic recommendations based on the expert experience and consensus were also included in the guidelines.</p><p><strong>Conclusion: </strong>TCM diagnosis and treatment of decoction, Chinese patent medicine and external application for treating acute primary headache were recommended. We hope these guidelines will be helpful in standardize the TCM acute treatment of primary headache.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 4","pages":"839-850"},"PeriodicalIF":0.0,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11337266/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768332","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tuina alleviates neuropathic pain through regulate the activation of microglia and the secretion of inflammatory cytokine in spinal cord. 推拿通过调节脊髓小胶质细胞的活化和炎症细胞因子的分泌来缓解神经性疼痛。
Pub Date : 2024-08-01 DOI: 10.19852/j.cnki.jtcm.20240515.002
W U Zhiwei, Zhu Qingguang, Kong Lingjun, Song Pengfei, Zhou Xin, Guo Guangxin, Zhang Shuaipan, H E Tianxiang, Cheng Yanbin, Fang Min

Objective: To observe the analgesic effects of Tuina on neuropathic pain (NPP) and the underlying mechanisms.

Methods: Forty-eight Sprague-Dawley (SD) rats were assigned by random into three treatment groups: sham, chronic constriction injury (CCI), and Tuina. Each group contained sixteen rats. CCI model was generated by ligating the right sciatic nerve. Behavioral changes of CCI were assessed by the paw withdrawal threshold (PWT) and paw withdrawal latency (PWL). In addition, biochemical techniques such as immunofluorescence staining, enzyme-linked immunosorbent assay (ELISA) and Western blotting were used to profile levels of microglia activation and inflammatory factors in the spinal dorsal horn (SDH) of rats. Tuina (clockwise pressing and rubbing) was performed at Chengshan (BL57) to observe the analgesic effects on CCI rats and the underlying mechanisms.

Results: Rats with CCI experienced significant reduction in the PWT and PWL of the right hind paw relative to CCI group at day 3. Tuina treatment rescued this situation significantly on days 10 and 14. Besides, Iba-1, microglia M1 receptor CD68, tumor necrosis factor-α (TNF-α), and interleukin-1β (IL-1β) were higher in the right SDH for CCI group compared to the sham group on day 14. As expected, Tuina partially downregulated the CCI-induced overexpressed Iba-1, CD68, TNF-α, and IL-1β in the SDH of CCI model.

Conclusion: Tuina induces a time-dependent cumulative analgesic effect in CCI rats by inhibiting the activation of microglia and the secretion of IL-1β and TNF-α in SDH.

目的:观察推拿对神经病理性疼痛(NPP)的镇痛作用及其机制:观察推拿对神经病理性疼痛(NPP)的镇痛作用及其机制:将 48 只 Sprague-Dawley (SD) 大鼠随机分为三个治疗组:假组、慢性收缩性损伤 (CCI) 组和推拿组。每组十六只大鼠。CCI模型通过结扎右坐骨神经产生。通过爪退缩阈值(PWT)和爪退缩潜伏期(PWL)评估CCI的行为变化。此外,还使用免疫荧光染色、酶联免疫吸附试验(ELISA)和Western印迹等生化技术来分析大鼠脊髓背角(SDH)的小胶质细胞活化和炎症因子水平。在成山(BL57)上进行推拿(顺时针按揉),观察对CCI大鼠的镇痛效果及其内在机制:结果:与CCI组相比,CCI大鼠在第3天右后爪的脉搏波速度和脉搏波速度明显降低。推拿治疗在第 10 天和第 14 天明显缓解了这一状况。此外,在第14天,CCI组与假组相比,右侧SDH中的Iba-1、小胶质细胞M1受体CD68、肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)含量更高。正如预期的那样,推拿可部分下调CCI诱导的CCI模型SDH中过表达的Iba-1、CD68、TNF-α和IL-1β:结论:通过抑制小胶质细胞的活化以及SDH中IL-1β和TNF-α的分泌,推拿对CCI大鼠具有时间依赖性的累积镇痛效果。
{"title":"Tuina alleviates neuropathic pain through regulate the activation of microglia and the secretion of inflammatory cytokine in spinal cord.","authors":"W U Zhiwei, Zhu Qingguang, Kong Lingjun, Song Pengfei, Zhou Xin, Guo Guangxin, Zhang Shuaipan, H E Tianxiang, Cheng Yanbin, Fang Min","doi":"10.19852/j.cnki.jtcm.20240515.002","DOIUrl":"10.19852/j.cnki.jtcm.20240515.002","url":null,"abstract":"<p><strong>Objective: </strong>To observe the analgesic effects of Tuina on neuropathic pain (NPP) and the underlying mechanisms.</p><p><strong>Methods: </strong>Forty-eight Sprague-Dawley (SD) rats were assigned by random into three treatment groups: sham, chronic constriction injury (CCI), and Tuina. Each group contained sixteen rats. CCI model was generated by ligating the right sciatic nerve. Behavioral changes of CCI were assessed by the paw withdrawal threshold (PWT) and paw withdrawal latency (PWL). In addition, biochemical techniques such as immunofluorescence staining, enzyme-linked immunosorbent assay (ELISA) and Western blotting were used to profile levels of microglia activation and inflammatory factors in the spinal dorsal horn (SDH) of rats. Tuina (clockwise pressing and rubbing) was performed at Chengshan (BL57) to observe the analgesic effects on CCI rats and the underlying mechanisms.</p><p><strong>Results: </strong>Rats with CCI experienced significant reduction in the PWT and PWL of the right hind paw relative to CCI group at day 3. Tuina treatment rescued this situation significantly on days 10 and 14. Besides, Iba-1, microglia M1 receptor CD68, tumor necrosis factor-α (TNF-α), and interleukin-1β (IL-1β) were higher in the right SDH for CCI group compared to the sham group on day 14. As expected, Tuina partially downregulated the CCI-induced overexpressed Iba-1, CD68, TNF-α, and IL-1β in the SDH of CCI model.</p><p><strong>Conclusion: </strong>Tuina induces a time-dependent cumulative analgesic effect in CCI rats by inhibiting the activation of microglia and the secretion of IL-1β and TNF-α in SDH.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 4","pages":"762-769"},"PeriodicalIF":0.0,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11337246/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768391","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Integration of serum pharmacochemistry with network pharmacology to reveal the potential mechanism of Yangqing Chenfei formula for the treatment of silicosis. 将血清药理化学与网络药理学相结合,揭示阳清陈妃方治疗矽肺病的潜在机制
Pub Date : 2024-08-01 DOI: 10.19852/j.cnki.jtcm.20240610.005
H U Yuanyuan, Liu Xinguang, Zhao Peng, W U Jinyan, Yan Xinhua, Hou Runsu, Wang Xiangcheng, Yang Fan, Tian Xinrong, L I Jiansheng

Objective: To explore the mechanisms of Yangqing Chenfei formula (, YCF) in the treatment of silicosis through a comprehensive strategy consisting of serum pharmacochemistry, network pharmacology analysis, and in vitro validation.

Methods: An ultrahigh-performance liquid chroma-tography-tandem mass spectrometry method was used to confirm the active components in YCF-medicated serum. Then, we obtained targets for active components and genes for silicosis from multiple databases. Furthermore, a protein-protein interaction network was constructed, and Kyoto Encyclopedia of Genes and Genomes pathway and biological process analyses were conducted to elucidate the mechanisms of YCF for the treatment of silicosis. Finally, we validated the important components and mechanisms in vitro.

Results: Altogether, 19 active components were identified from rat serum after YCF administration. We identified 724 targets for 19 components, which were mainly related to inflammation [phosphatidy linositol 3 kinase/protein kinase B, forkhead box O, hypoxia inducible factor, and T-cell receptor signaling pathway, nitric oxide biosynthetic process], fibrotic processes [vascular endothelial growth factor signaling pathway, extracellular signal regulated kinase (ERK) 1 and ERK2 cascade, smooth muscle cell proliferation], and apoptosis (negative regulation of apoptotic process). In addition, 218 genes for silicosis were identified and were mainly associated with the inflammatory response and immune process [cytokine?cytokine receptor interaction, tumor necrosis factor alpha (TNF-α), toll-like receptor, and nucleotide binding oligomerization domain-like receptor signaling pathway]. Taking an intersection of active component targets and silicosis genes, we obtained 61 common genes that were mainly related to the inflammatory response and apoptosis, such as the phosphatidylinositol-3-kinase/protein kinase B signaling pathway, mitogen activated protein kinases signaling pathway, TNF signaling pathway, toll-like receptor signaling pathway, biosynthesis of nitric oxide, and apoptotic process. In the herb-component-gene-pathway network, paeoniflorin, rutin and nobiletin targeted the most genes. In vitro, paeoniflorin, rutin and nobiletin decreased the mRNA levels of inflammatory factors [interleukin (IL)-6, TNF-α, and IL-1β], suppressed p-AKT and cleaved caspase-3, and increased B cell lymphoma (Bcl)-2 protein expression in silica-induced macrophages in a concentration-dependent manner.

Conclusion: YCF could significantly relieve the inflammatory response of silicosis via suppression of the AKT/Bcl-2/Caspase-3 pathway.

目的通过血清药理、网络药理学分析和体外验证等综合策略,探讨阳清陈妃方治疗矽肺的机理:方法:采用超高效液相色谱-串联质谱法确认了YCF药物血清中的活性成分。然后,我们从多个数据库中获得了活性成分的靶标和矽肺病基因。此外,我们还构建了蛋白质-蛋白质相互作用网络,并进行了京都基因和基因组百科全书的通路和生物过程分析,以阐明 YCF 治疗矽肺的机制。最后,我们在体外对重要成分和机制进行了验证:结果:服用 YCF 后,从大鼠血清中总共鉴定出 19 种活性成分。我们为 19 种成分确定了 724 个靶点,这些靶点主要与炎症有关[磷脂酰亚肌醇 3 激酶/蛋白激酶 B、叉头框 O、低氧诱导因子、T 细胞受体信号通路、一氧化氮生物合成过程]、纤维化过程[血管内皮生长因子信号通路、细胞外信号调节激酶(ERK)1 和 ERK2 级联、平滑肌细胞增殖]和细胞凋亡(凋亡过程的负调控)。此外,还发现了 218 个矽肺病基因,这些基因主要与炎症反应和免疫过程有关[细胞因子与细胞因子受体相互作用、肿瘤坏死因子α(TNF-α)、类收费受体和核苷酸结合寡聚域样受体信号通路]。将活性成分靶标与矽肺病基因进行交叉分析,我们得到了61个常见基因,这些基因主要与炎症反应和细胞凋亡有关,如磷脂酰肌醇-3-激酶/蛋白激酶B信号通路、丝裂原活化蛋白激酶信号通路、TNF信号通路、类收费受体信号通路、一氧化氮的生物合成和细胞凋亡过程。在草药-成分-基因-通路网络中,芍药苷、芦丁和金没药苷靶向的基因最多。在体外,芍药苷、芦丁和金没药苷以浓度依赖的方式降低了白细胞介素(IL)-6、TNF-α和IL-1β等炎症因子的mRNA水平,抑制了p-AKT和裂解的caspase-3,并增加了硅诱导的巨噬细胞中B细胞淋巴瘤(Bcl)-2蛋白的表达:结论:YCF可通过抑制AKT/Bcl-2/Caspase-3通路明显缓解矽肺的炎症反应。
{"title":"Integration of serum pharmacochemistry with network pharmacology to reveal the potential mechanism of Yangqing Chenfei formula for the treatment of silicosis.","authors":"H U Yuanyuan, Liu Xinguang, Zhao Peng, W U Jinyan, Yan Xinhua, Hou Runsu, Wang Xiangcheng, Yang Fan, Tian Xinrong, L I Jiansheng","doi":"10.19852/j.cnki.jtcm.20240610.005","DOIUrl":"10.19852/j.cnki.jtcm.20240610.005","url":null,"abstract":"<p><strong>Objective: </strong>To explore the mechanisms of Yangqing Chenfei formula (, YCF) in the treatment of silicosis through a comprehensive strategy consisting of serum pharmacochemistry, network pharmacology analysis, and <i>in vitro</i> validation.</p><p><strong>Methods: </strong>An ultrahigh-performance liquid chroma-tography-tandem mass spectrometry method was used to confirm the active components in YCF-medicated serum. Then, we obtained targets for active components and genes for silicosis from multiple databases. Furthermore, a protein-protein interaction network was constructed, and Kyoto Encyclopedia of Genes and Genomes pathway and biological process analyses were conducted to elucidate the mechanisms of YCF for the treatment of silicosis. Finally, we validated the important components and mechanisms <i>in vitro</i>.</p><p><strong>Results: </strong>Altogether, 19 active components were identified from rat serum after YCF administration. We identified 724 targets for 19 components, which were mainly related to inflammation [phosphatidy linositol 3 kinase/protein kinase B, forkhead box O, hypoxia inducible factor, and T-cell receptor signaling pathway, nitric oxide biosynthetic process], fibrotic processes [vascular endothelial growth factor signaling pathway, extracellular signal regulated kinase (ERK) 1 and ERK2 cascade, smooth muscle cell proliferation], and apoptosis (negative regulation of apoptotic process). In addition, 218 genes for silicosis were identified and were mainly associated with the inflammatory response and immune process [cytokine?cytokine receptor interaction, tumor necrosis factor alpha (TNF-α), toll-like receptor, and nucleotide binding oligomerization domain-like receptor signaling pathway]. Taking an intersection of active component targets and silicosis genes, we obtained 61 common genes that were mainly related to the inflammatory response and apoptosis, such as the phosphatidylinositol-3-kinase/protein kinase B signaling pathway, mitogen activated protein kinases signaling pathway, TNF signaling pathway, toll-like receptor signaling pathway, biosynthesis of nitric oxide, and apoptotic process. In the herb-component-gene-pathway network, paeoniflorin, rutin and nobiletin targeted the most genes. <i>In vitro</i>, paeoniflorin, rutin and nobiletin decreased the mRNA levels of inflammatory factors [interleukin (IL)-6, TNF-α, and IL-1β], suppressed p-AKT and cleaved caspase-3, and increased B cell lymphoma (Bcl)-2 protein expression in silica-induced macrophages in a concentration-dependent manner.</p><p><strong>Conclusion: </strong>YCF could significantly relieve the inflammatory response of silicosis <i>via</i> suppression of the AKT/Bcl-2/Caspase-3 pathway.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 4","pages":"784-793"},"PeriodicalIF":0.0,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11337247/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768330","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Electroacupuncture ameliorates blood-brain barrier disruption after ischemic stroke through histone acetylation regulation at the matrix metalloproteinase 9 and tissue inhibitor of metalloproteinase 2 genes. 电针通过调节基质金属蛋白酶9和组织金属蛋白酶2抑制剂基因的组蛋白乙酰化,改善缺血性脑卒中后血脑屏障的破坏。
Pub Date : 2024-08-01 DOI: 10.19852/j.cnki.jtcm.20240610.004
Chen Yonglin, Ouyang Ling, Meng Lingling, W U Bufan, Peng Rou, Liu Sitong, Hou Dan, Wang Yaling, Jing Xinyue, L U Shengfeng, F U Shuping

Objective: To explore whether the regulation of matrix metalloproteinase 9 (MMP-9)/ tissue inhibitors of MMPs (TIMPs) gene expression through histone acetylation is a possible mechanism by which electroacupuncture (EA) protects blood-brain barrier (BBB) integrity in a middle cerebral artery occlusion (MCAO) rat model.

Methods: Male Sprague-Dawley rats were divided into four groups: the sham group, the MCAO group, the MCAO + EA (MEA) group, and the MCAO + EA + HAT inhibitor (HATi) group. The MCAO model was generated by blocking the middle cerebral artery. EA was applied to Baihui (GV20). Samples were collected 1 or 3 d after reperfusion. Neurological function scores and Evans blue extravasation were employed to evaluate the poststroke injury. The effect of EA on MMP-9/TIMPs gene expression was assessed by real-time fluorescence quantitative polymerase chain reaction (RT-qPCR) and chromatin immunoprecipitation (ChIP).

Results: Our results showed that EA treatment prominently improved neurological function and ameliorated BBB disruption. The RT-qPCR assay showed that EA reduced the expression of MMP-9 and promoted TIMP-2 mRNA expression, but HATi reversed these effects of EA. In addition, ChIP results revealed that EA decreased the enrichment of H3K9ace/H3K27ace at MMP-9 promoters and notably stimulated the recruitment of H3K9ace/H3K27ace at TIMP-2 promoter.

Conclusion: EA treatment at Baihui (GV20) regulates the transcription of MMP-9 and TIMP-2 through histone acetylation modification in the acute stage of stroke, which preserves the structural integrity of the BBB in MCAO rats. These findings suggested that the histone acetylation-mediated transcriptional activity of target genes may be a crucial mechanism of EA treatment in stroke.

目的探讨通过组蛋白乙酰化调控基质金属蛋白酶9(MMP-9)/MMPs组织抑制剂(TIMPs)基因表达是否是电针(EA)在大脑中动脉闭塞(MCAO)大鼠模型中保护血脑屏障(BBB)完整性的可能机制:雄性 Sprague-Dawley 大鼠分为四组:假组、MCAO 组、MCAO + EA(MEA)组和 MCAO + EA + HAT 抑制剂(HATi)组。MCAO 模型通过阻断大脑中动脉产生。EA应用于百汇(GV20)。再灌注后 1 或 3 d 采集样本。采用神经功能评分和埃文斯蓝外渗来评估脑卒中后的损伤。通过实时荧光定量聚合酶链反应(RT-qPCR)和染色质免疫沉淀(ChIP)评估了EA对MMP-9/TIMPs基因表达的影响:结果:我们的研究结果表明,EA治疗显著改善了神经功能,并改善了BBB的破坏。RT-qPCR测定显示,EA降低了MMP-9的表达,促进了TIMP-2 mRNA的表达,但HATi逆转了EA的这些影响。此外,ChIP结果显示,EA降低了MMP-9启动子上H3K9ace/H3K27ace的富集,并显著刺激了TIMP-2启动子上H3K9ace/H3K27ace的招募:结论:百会(GV20)EA通过组蛋白乙酰化修饰调节脑卒中急性期MMP-9和TIMP-2的转录,从而保护MCAO大鼠BBB结构的完整性。这些研究结果表明,组蛋白乙酰化介导的靶基因转录活性可能是EA治疗中风的重要机制。
{"title":"Electroacupuncture ameliorates blood-brain barrier disruption after ischemic stroke through histone acetylation regulation at the matrix metalloproteinase 9 and tissue inhibitor of metalloproteinase 2 genes.","authors":"Chen Yonglin, Ouyang Ling, Meng Lingling, W U Bufan, Peng Rou, Liu Sitong, Hou Dan, Wang Yaling, Jing Xinyue, L U Shengfeng, F U Shuping","doi":"10.19852/j.cnki.jtcm.20240610.004","DOIUrl":"10.19852/j.cnki.jtcm.20240610.004","url":null,"abstract":"<p><strong>Objective: </strong>To explore whether the regulation of matrix metalloproteinase 9 (MMP-9)/ tissue inhibitors of MMPs (TIMPs) gene expression through histone acetylation is a possible mechanism by which electroacupuncture (EA) protects blood-brain barrier (BBB) integrity in a middle cerebral artery occlusion (MCAO) rat model.</p><p><strong>Methods: </strong>Male Sprague-Dawley rats were divided into four groups: the sham group, the MCAO group, the MCAO + EA (MEA) group, and the MCAO + EA + HAT inhibitor (HATi) group. The MCAO model was generated by blocking the middle cerebral artery. EA was applied to Baihui (GV20). Samples were collected 1 or 3 d after reperfusion. Neurological function scores and Evans blue extravasation were employed to evaluate the poststroke injury. The effect of EA on MMP-9/TIMPs gene expression was assessed by real-time fluorescence quantitative polymerase chain reaction (RT-qPCR) and chromatin immunoprecipitation (ChIP).</p><p><strong>Results: </strong>Our results showed that EA treatment prominently improved neurological function and ameliorated BBB disruption. The RT-qPCR assay showed that EA reduced the expression of MMP-9 and promoted TIMP-2 mRNA expression, but HATi reversed these effects of EA. In addition, ChIP results revealed that EA decreased the enrichment of H3K9ace/H3K27ace at MMP-9 promoters and notably stimulated the recruitment of H3K9ace/H3K27ace at TIMP-2 promoter.</p><p><strong>Conclusion: </strong>EA treatment at Baihui (GV20) regulates the transcription of MMP-9 and TIMP-2 through histone acetylation modification in the acute stage of stroke, which preserves the structural integrity of the BBB in MCAO rats. These findings suggested that the histone acetylation-mediated transcriptional activity of target genes may be a crucial mechanism of EA treatment in stroke.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 4","pages":"734-744"},"PeriodicalIF":0.0,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11337257/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768328","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acupuncture improves the live birth of patients with repeated implantation failure: a retrospective cohort study. 针灸可提高反复植入失败患者的活产率:一项回顾性队列研究。
Pub Date : 2024-08-01 DOI: 10.19852/j.cnki.jtcm.20240515.006
Sun Junjian, Xie Henghui, L I Huanhuan, Tian Xiangming, Fang Yigong, Zhou Wenhui

Objective: To explore the therapeutic efficacy of acupuncture treatment on repeated implantation failure (RIF) patients with cryo-thawed embryo transfer (CET).

Methods: In a retrospective cohort study, all eligible women undergoing RIF were recruited in our center from January 1, 2018 to December 31, 2021. The patients were grouped by whether an acceptance of acupuncture treatment before CET, including the acupuncture group (Acu-group, 55 cycles) and control group (Con-group, 244 cycles). Data were analyzed by using binary logistic regression to explore the relationship of acupuncture treatment with pregnancy outcomes.

Results: The Acu-group had higher live-birth rate (LBR) [54.5% vs41.0%, respectively; odds ratio (OR) = 1.105, 95% confidence interval (CI) (1.029, 1.187), P =0.006] and ongoing pregnancy rate (OPR) [56.4% vs43.0%, respectively; OR= 1.100, 95% CI(1.025, 1.181), P =0.008] than the Con-group. There were no significant between-group differences in the rates of implantation [OR= 1.070, 95% CI(0.996, 1.149), P =0.064], clinical pregnancy [OR= 1.065, 95% CI(0.997, 1.138), P =0.061], biochemical pregnancy [OR= 1.002, 95% CI(0.903, 1.112), P =0.967], or miscarriage [OR= 0.778, 95% CI(0.551, 1.099), P =0.155]. Perinatal outcomes did not differ significantly between the two groups.

Conclusions: Acupuncture treatment could improve the LBR and OPR in RIF patients with CET cycles, suggesting a potential adjuvant therapy of acupuncture to improve the pregnancy outcomes in RIF patients.

目的探讨针灸治疗对冷冻解冻胚胎移植(CET)反复着床失败(RIF)患者的疗效:在一项回顾性队列研究中,我中心从 2018 年 1 月 1 日至 2021 年 12 月 31 日招募了所有符合条件的 RIF 患者。患者按CET前是否接受针灸治疗分组,包括针灸组(Acu-group,55个周期)和对照组(Con-group,244个周期)。采用二元逻辑回归分析数据,探讨针灸治疗与妊娠结局的关系:结果:针刺组的活产率(LBR)[分别为54.5% vs41.0%;比值比(OR)= 1.105,95%置信区间(CI)(1.029, 1.187),P =0.006]和持续妊娠率(OPR)[分别为56.4% vs43.0%;比值比(OR)= 1.100,95%置信区间(CI)(1.025, 1.181),P =0.008]均高于对照组。植入率[OR= 1.070,95% CI(0.996,1.149),P =0.064]、临床妊娠率[OR= 1.065,95% CI(0.997,1.138),P =0.061]、生化妊娠[OR= 1.002,95% CI(0.903,1.112),P =0.967]或流产[OR= 0.778,95% CI(0.551,1.099),P =0.155]。两组围产期结果无明显差异:结论:针灸治疗可改善CET周期RIF患者的LBR和OPR,表明针灸可能成为改善RIF患者妊娠结局的辅助疗法。
{"title":"Acupuncture improves the live birth of patients with repeated implantation failure: a retrospective cohort study.","authors":"Sun Junjian, Xie Henghui, L I Huanhuan, Tian Xiangming, Fang Yigong, Zhou Wenhui","doi":"10.19852/j.cnki.jtcm.20240515.006","DOIUrl":"10.19852/j.cnki.jtcm.20240515.006","url":null,"abstract":"<p><strong>Objective: </strong>To explore the therapeutic efficacy of acupuncture treatment on repeated implantation failure (RIF) patients with cryo-thawed embryo transfer (CET).</p><p><strong>Methods: </strong>In a retrospective cohort study, all eligible women undergoing RIF were recruited in our center from January 1, 2018 to December 31, 2021. The patients were grouped by whether an acceptance of acupuncture treatment before CET, including the acupuncture group (Acu-group, 55 cycles) and control group (Con-group, 244 cycles). Data were analyzed by using binary logistic regression to explore the relationship of acupuncture treatment with pregnancy outcomes.</p><p><strong>Results: </strong>The Acu-group had higher live-birth rate (LBR) [54.5% <i>vs</i>41.0%, respectively; odds ratio (<i>OR</i>) = 1.105, 95% confidence interval (<i>CI</i>) (1.029, 1.187), <i>P =</i>0.006] and ongoing pregnancy rate (OPR) [56.4% <i>vs</i>43.0%, respectively; <i>OR</i>= 1.100, 95% <i>CI</i>(1.025, 1.181), <i>P =</i>0.008] than the Con-group. There were no significant between-group differences in the rates of implantation [<i>OR</i>= 1.070, 95% <i>CI</i>(0.996, 1.149), <i>P =</i>0.064], clinical pregnancy [<i>OR</i>= 1.065, 95% <i>CI</i>(0.997, 1.138), <i>P =</i>0.061], biochemical pregnancy [<i>OR</i>= 1.002, 95% <i>CI</i>(0.903, 1.112), <i>P =</i>0.967], or miscarriage [<i>OR</i>= 0.778, 95% <i>CI</i>(0.551, 1.099), <i>P =</i>0.155]. Perinatal outcomes did not differ significantly between the two groups.</p><p><strong>Conclusions: </strong>Acupuncture treatment could improve the LBR and OPR in RIF patients with CET cycles, suggesting a potential adjuvant therapy of acupuncture to improve the pregnancy outcomes in RIF patients.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 4","pages":"830-838"},"PeriodicalIF":0.0,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11337250/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768380","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Saponin Ⅰ from Shuitianqi () inhibits metastasis by negatively regulating the transforming growth factor-β1/Smad7 network and epithelial-mesenchymal transition in the intrahepatic metastasis Bagg's Albino/c mouse model. 水天芪皂苷Ⅰ通过负向调节转化生长因子-β1/Smad7网络和上皮-间质转化抑制肝内转移Bagg's Albino/c小鼠模型的转移。
Pub Date : 2024-08-01 DOI: 10.19852/j.cnki.jtcm.2024.04.006
Lyu Meixian, Zhou Huan, Zhi Limin, Zhou Jinling, Gan Rizhi, Qin Yanping, H E Nengting, Zuo Qiqi, L I Hao, Dong Min, Liang Gang

Objective: To examine the influence of Saponin I from Shuitianqi (Rhizoma Schizocapasae Plantagineae) (SSPH I) on hepatocellular carcinoma (HCC) metastasis, and to elucidate the underlying mechanism.

Methods: The intrahepatic metastasis Bagg's Albino/c (BALB/c) mouse model was established with human hepatocellular carcinomas (HepG2) cells, then treated with normal saline (once per day), cisplatin (2 mg/kg, once every 2 d), and SSPH Ⅰ (25, 50, and 75 mg/kg, once per day). Then, we assessed alterations in the hepatic pathology and target protein expressions in the intrahepatic metastasis BALB/c mouse model using a series of molecular biology techniques.

Results: Based on our analysis, SSPH Ⅰ significantly alleviated hepatocyte necrosis and tumor cells infiltration. Moreover, SSPH Ⅰ suppressed extracellular matrix (ECM) degradation and angiogenesis viaa decrease in matrix etalloproteinase-2 (MMP-2), MMP-9, CD31, CD34, and vascular endothelial growth factor (VEGF) levels. Furthermore, SSPH Ⅰ repressed invasion and meta-stasis by suppressing the transforming growth factor-β1 (TGF-β1)/Smad7 axis and epithelial-mesenchymal transition (EMT), as evidenced by the scarce TGF-β1, N-cadherin, and Vimentin expressions, and elevated Smad7 and E-cadherin expressions.

Conclusion: The SSPH Ⅰ-mediated negative regulation of the TGF-β1/Smad7 axis and EMT are critical for the inhibition of HCC invasion and metastasis.

研究目的研究水天齐皂苷 I(SSPH I)对肝细胞癌(HCC)转移的影响,并阐明其作用机制:用人肝癌(HepG2)细胞建立肝内转移Bagg's Albino/c(BALB/c)小鼠模型,然后用生理盐水(每天一次)、顺铂(2 mg/kg,每2 d一次)和SSPH Ⅰ(25、50和75 mg/kg,每天一次)治疗。然后,我们利用一系列分子生物学技术评估了肝内转移 BALB/c 小鼠模型的肝脏病理变化和靶蛋白表达:结果:根据我们的分析,SSPH Ⅰ能明显减轻肝细胞坏死和肿瘤细胞浸润。此外,SSPH Ⅰ通过降低基质等蛋白酶-2(MMP-2)、MMP-9、CD31、CD34和血管内皮生长因子(VEGF)的水平,抑制了细胞外基质(ECM)降解和血管生成。此外,SSPHⅠ还通过抑制转化生长因子-β1(TGF-β1)/Smad7轴和上皮-间质转化(EMT)来抑制侵袭和元停滞,这体现在TGF-β1、N-cadherin和Vimentin的表达量减少,而Smad7和E-cadherin的表达量升高:结论:SSPH Ⅰ介导的对TGF-β1/Smad7轴和EMT的负调控是抑制HCC侵袭和转移的关键。
{"title":"Saponin Ⅰ from Shuitianqi () inhibits metastasis by negatively regulating the transforming growth factor-β1/Smad7 network and epithelial-mesenchymal transition in the intrahepatic metastasis Bagg's Albino/c mouse model.","authors":"Lyu Meixian, Zhou Huan, Zhi Limin, Zhou Jinling, Gan Rizhi, Qin Yanping, H E Nengting, Zuo Qiqi, L I Hao, Dong Min, Liang Gang","doi":"10.19852/j.cnki.jtcm.2024.04.006","DOIUrl":"10.19852/j.cnki.jtcm.2024.04.006","url":null,"abstract":"<p><strong>Objective: </strong>To examine the influence of Saponin I from Shuitianqi (<i>Rhizoma Schizocapasae Plantagineae</i>) (SSPH I) on hepatocellular carcinoma (HCC) metastasis, and to elucidate the underlying mechanism.</p><p><strong>Methods: </strong>The intrahepatic metastasis Bagg's Albino/c (BALB/c) mouse model was established with human hepatocellular carcinomas (HepG2) cells, then treated with normal saline (once per day), cisplatin (2 mg/kg, once every 2 d), and SSPH Ⅰ (25, 50, and 75 mg/kg, once per day). Then, we assessed alterations in the hepatic pathology and target protein expressions in the intrahepatic metastasis BALB/c mouse model using a series of molecular biology techniques.</p><p><strong>Results: </strong>Based on our analysis, SSPH Ⅰ significantly alleviated hepatocyte necrosis and tumor cells infiltration. Moreover, SSPH Ⅰ suppressed extracellular matrix (ECM) degradation and angiogenesis <i>via</i>a decrease in matrix etalloproteinase-2 (MMP-2), MMP-9, CD31, CD34, and vascular endothelial growth factor (VEGF) levels. Furthermore, SSPH Ⅰ repressed invasion and meta-stasis by suppressing the transforming growth factor-β1 (TGF-β1)/Smad7 axis and epithelial-mesenchymal transition (EMT), as evidenced by the scarce TGF-β1, N-cadherin, and Vimentin expressions, and elevated Smad7 and E-cadherin expressions.</p><p><strong>Conclusion: </strong>The SSPH Ⅰ-mediated negative regulation of the TGF-β1/Smad7 axis and EMT are critical for the inhibition of HCC invasion and metastasis.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 4","pages":"642-651"},"PeriodicalIF":0.0,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11337245/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768384","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Study on the effect and mechanism of Yanghe decoction Huacai on tissue repair ofsyndrome after anal fistula surgery. 阳和水煎华彩对肛瘘术后综合征组织修复的作用及机制研究
Pub Date : 2024-08-01 DOI: 10.19852/j.cnki.jtcm.20240515.004
W U Yijuan, Sun Xinghong, Guo Haixia, Zhang Xiangan

Objective: To observe the clinical efficacy and safety of Yanghe decoction Huacai for the repair of Yin syndrome wounds with slow-healing after anal fistula surgery.

Methods: A total of 120 patients with slow-healing negative wounds with after low-grade anal fistula surgery who met the inclusion criteria were divided into a treatment group and a control group based on a random number table method, with 60 patients in the treatment group and 60 patients in the control group. The treatment group was given Yanghe decoction Huacai in combination with routine treatment; the control group was only given routine treatment, in which the wound surface was disinfected with iodine, and then covered with sterile gauze. The course of treatment in both groups was 10 d. After treatment, the wound secretion score, wound granulation tissue score, the expression levels of basic fibroblast growth factor (bFGF), transforming growth factor β1 (TGF-β1), and epidermal growth factor (EGF) in the wound, wound healing time and clinical efficacy were compared.

Results: There was no significant difference in age or gender between the two groups (P > 0.05). On the 10th and 15th days after the surgery, the wound secretion scores were higher in the treatment group than in the control group (P < 0.01). Comparing the two groups at the 10th and 15th day after surgery, the granulation tissue growth scores in the treatment group were better than the in control group (P < 0.01). On the 10th and 15th day after operation, the expression levels of bFGF, TGF-β1 and EGF factors in the treatment group were stronger than those in the control group. The healing time of the wounds in the treatment group was significantly shorter than in the control group (P < 0.01). The clinical efficacy of the two groups after treatment was compared, and the overall efficacy of the treatment group was significantly higher than that of the control group (P < 0.01).

Conclusions: Yanghe decoction Huacai have significant efficacy in the treatment of slow-healing wounds with Yin syndrome after anal fistula surgery. It improves wound secretions, promotes the growth of wound granulation tissue, and shortens wound healing time. Its mechanism of action may be related to the control of wound inflammation. It is related to increasing the expression of bFGF, TGF-β1 and EGF in wound tissue, and promoting wound angiogenesis and fibroblast proliferation.

目的观察洋河煎剂华蟾素修复肛瘘术后阴证伤口的临床疗效和安全性:方法:将120例符合纳入标准的低位肛瘘术后阴性伤口缓慢愈合患者按照随机数字表法分为治疗组和对照组,治疗组60例,对照组60例。治疗组在常规治疗的基础上给予洋河煎剂华彩;对照组仅给予常规治疗,即用碘伏消毒创面,然后用无菌纱布覆盖。两组疗程均为 10 d,比较治疗后伤口分泌物评分、伤口肉芽组织评分、伤口中碱性成纤维细胞生长因子(bFGF)、转化生长因子β1(TGF-β1)和表皮生长因子(EGF)的表达水平、伤口愈合时间和临床疗效:两组患者的年龄和性别无明显差异(P>0.05)。术后第 10 天和第 15 天,治疗组的伤口分泌物评分高于对照组(P < 0.01)。两组在术后第 10 天和第 15 天的肉芽组织生长评分比较,治疗组优于对照组(P < 0.01)。术后第 10 天和第 15 天,治疗组 bFGF、TGF-β1 和 EGF 因子的表达水平均强于对照组。治疗组的伤口愈合时间明显短于对照组(P < 0.01)。比较两组治疗后的临床疗效,治疗组的总疗效明显高于对照组(P < 0.01):结论:洋河煎剂华蟾素治疗肛瘘术后阴证伤口愈合缓慢有显著疗效。结论:洋河煎剂华蟾素对肛瘘术后阴证伤口愈合缓慢有明显疗效,能改善伤口分泌物,促进伤口肉芽组织生长,缩短伤口愈合时间。其作用机制可能与控制伤口发炎有关。它与增加伤口组织中 bFGF、TGF-β1 和 EGF 的表达,促进伤口血管生成和成纤维细胞增殖有关。
{"title":"Study on the effect and mechanism of Yanghe decoction Huacai on tissue repair ofsyndrome after anal fistula surgery.","authors":"W U Yijuan, Sun Xinghong, Guo Haixia, Zhang Xiangan","doi":"10.19852/j.cnki.jtcm.20240515.004","DOIUrl":"10.19852/j.cnki.jtcm.20240515.004","url":null,"abstract":"<p><strong>Objective: </strong>To observe the clinical efficacy and safety of Yanghe decoction Huacai for the repair of <i>Yin</i> syndrome wounds with slow-healing after anal fistula surgery.</p><p><strong>Methods: </strong>A total of 120 patients with slow-healing negative wounds with after low-grade anal fistula surgery who met the inclusion criteria were divided into a treatment group and a control group based on a random number table method, with 60 patients in the treatment group and 60 patients in the control group. The treatment group was given Yanghe decoction Huacai in combination with routine treatment; the control group was only given routine treatment, in which the wound surface was disinfected with iodine, and then covered with sterile gauze. The course of treatment in both groups was 10 d. After treatment, the wound secretion score, wound granulation tissue score, the expression levels of basic fibroblast growth factor (bFGF), transforming growth factor β1 (TGF-β1), and epidermal growth factor (EGF) in the wound, wound healing time and clinical efficacy were compared.</p><p><strong>Results: </strong>There was no significant difference in age or gender between the two groups (<i>P</i> > 0.05). On the 10th and 15th days after the surgery, the wound secretion scores were higher in the treatment group than in the control group (<i>P</i> < 0.01). Comparing the two groups at the 10th and 15th day after surgery, the granulation tissue growth scores in the treatment group were better than the in control group (<i>P</i> < 0.01). On the 10th and 15th day after operation, the expression levels of bFGF, TGF-β1 and EGF factors in the treatment group were stronger than those in the control group. The healing time of the wounds in the treatment group was significantly shorter than in the control group (<i>P</i> < 0.01). The clinical efficacy of the two groups after treatment was compared, and the overall efficacy of the treatment group was significantly higher than that of the control group (<i>P</i> < 0.01).</p><p><strong>Conclusions: </strong>Yanghe decoction Huacai have significant efficacy in the treatment of slow-healing wounds with <i>Yin</i> syndrome after anal fistula surgery. It improves wound secretions, promotes the growth of wound granulation tissue, and shortens wound healing time. Its mechanism of action may be related to the control of wound inflammation. It is related to increasing the expression of bFGF, TGF-β1 and EGF in wound tissue, and promoting wound angiogenesis and fibroblast proliferation.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 4","pages":"813-721"},"PeriodicalIF":0.0,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11393818/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768388","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
High-throughput sequencing analysis of differential microRNA expression in the process of blocking the progression of chronic atrophic gastritis to gastric cancer by Xianglian Huazhuo formula. 高通量测序分析湘莲化癥方阻断慢性萎缩性胃炎向胃癌进展过程中microRNA的差异表达
Pub Date : 2024-08-01 DOI: 10.19852/j.cnki.jtcm.20240617.002
Guo Yuxi, L I Ze, Cheng Nan, Jia Xuemei, Wang Jie, M A Hongyu, Zhao Runyuan, L I Bolin, Xue Yucong, Cai Yanru, Yang Qian

Objective: To explore the mechanism of Xianglian Huazhuo formula (, XLHZ) blocking the development of chronic atrophic gastritis (CAG) to gastric cancer (GC) through bioinformatics analysis and in vitro.

Methods: Pathological morphology of gastric mucosa of rats were observed. High-throughput sequencing was used to analyze the miRNA expression profile of gastric mucosa. The miRanda, miRDB and miRWalk databases were used to predict the differential target genes. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis were performed for differential target genes. Real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to verify the differentially expressed miRNAs and target genes. Western blot, EdU, wound healing and flow cytometry were used to observe the effect of XLHZ on epithelial-mesenchymal transition (EMT) markers, proliferation, migration, apoptosis and cell cycle of CAG cells in vitro.

Results: A total of five differentially expressed miRNAs and four differential target genes were screened in this study. GO analysis showed that the target genes were enriched in regulation of neuron development, regulation of transcription factor activity and regulation of RNA polymerase. KEGG pathways database differences in gene enrichment of target genes in the Wnt signaling pathway, Phospholipase D signaling pathway and mitogen-activated protein kinase signaling pathway. qRT-PCR confirmed that miRNAs and its target genes were consistent with the screening results. In vitro, our study revealed that XLHZ could increase the expression of E-cadherin, decrease the expression of transforming growth factor β1, vimentin and β-catenin, inhibite the proliferation and migration of CAG cells, cause cell cycle arrest at G0/G1 and G2/M phase, induce the apoptosis of CAG cells, and prevent the progression of CAG to GC.

Conclusion: This study provided a new idea for the mechanism of blocking the progression of CAG to GC by XLHZ, which may be related to the expression of miR-20a-3p, miR-320-3p, miR-34b-5p, miR-483-3p and miR-883-3p and their target genes transferrin receptor, nuclear receptor subfamily 4 member 2, delta like canonical Notch ligand 1 and a kinase anchor protein 12 in CAG. In the future, we will continue to investigate the linkage between the active ingredients of XLHZ and the relevant miRNAs and their target genes, so as to provide more sufficient experimental basis for clinically effective prevention of CAG to GC.

目的通过生物信息学分析和体外实验,探讨湘莲化滞方(XLHZ)阻断慢性萎缩性胃炎(CAG)向胃癌(GC)发展的机制:方法:观察大鼠胃黏膜的病理形态。方法:观察大鼠胃黏膜的病理形态,采用高通量测序分析胃黏膜的 miRNA 表达谱。利用 miRanda、miRDB 和 miRWalk 数据库预测差异靶基因。对差异靶基因进行了基因本体(GO)和京都基因组百科全书(KEGG)富集分析。采用实时定量反转录聚合酶链反应(qRT-PCR)验证差异表达的 miRNA 和靶基因。采用Western blot、EdU、伤口愈合和流式细胞术观察XLHZ对体外CAG细胞上皮-间质转化(EMT)标志物、增殖、迁移、凋亡和细胞周期的影响:结果:本研究共筛选出5个差异表达的miRNA和4个差异表达的靶基因。GO分析表明,目标基因富集于神经元发育调控、转录因子活性调控和RNA聚合酶调控。KEGG通路数据库显示,在Wnt信号通路、磷脂酶D信号通路和丝裂原活化蛋白激酶信号通路中,靶基因的富集存在差异。qRT-PCR证实,miRNA及其靶基因与筛选结果一致。体外研究发现,XLHZ能增加E-cadherin的表达,降低转化生长因子β1、波形蛋白和β-catenin的表达,抑制CAG细胞的增殖和迁移,使细胞周期停滞在G0/G1和G2/M期,诱导CAG细胞凋亡,阻止CAG向GC进展:本研究为XLHZ阻断CAG向GC发展的机制提供了新思路,这可能与CAG中miR-20a-3p、miR-320-3p、miR-34b-5p、miR-483-3p和miR-883-3p及其靶基因转铁蛋白受体、核受体亚家族4成员2、delta like canonical Notch配体1和激酶锚蛋白12的表达有关。今后,我们将继续研究XLHZ的有效成分与相关miRNA及其靶基因之间的联系,为临床有效预防CAG转为GC提供更充分的实验依据。
{"title":"High-throughput sequencing analysis of differential microRNA expression in the process of blocking the progression of chronic atrophic gastritis to gastric cancer by Xianglian Huazhuo formula.","authors":"Guo Yuxi, L I Ze, Cheng Nan, Jia Xuemei, Wang Jie, M A Hongyu, Zhao Runyuan, L I Bolin, Xue Yucong, Cai Yanru, Yang Qian","doi":"10.19852/j.cnki.jtcm.20240617.002","DOIUrl":"10.19852/j.cnki.jtcm.20240617.002","url":null,"abstract":"<p><strong>Objective: </strong>To explore the mechanism of Xianglian Huazhuo formula (, XLHZ) blocking the development of chronic atrophic gastritis (CAG) to gastric cancer (GC) through bioinformatics analysis and <i>in vitro</i>.</p><p><strong>Methods: </strong>Pathological morphology of gastric mucosa of rats were observed. High-throughput sequencing was used to analyze the miRNA expression profile of gastric mucosa. The miRanda, miRDB and miRWalk databases were used to predict the differential target genes. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis were performed for differential target genes. Real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to verify the differentially expressed miRNAs and target genes. Western blot, EdU, wound healing and flow cytometry were used to observe the effect of XLHZ on epithelial-mesenchymal transition (EMT) markers, proliferation, migration, apoptosis and cell cycle of CAG cells <i>in vitro</i>.</p><p><strong>Results: </strong>A total of five differentially expressed miRNAs and four differential target genes were screened in this study. GO analysis showed that the target genes were enriched in regulation of neuron development, regulation of transcription factor activity and regulation of RNA polymerase. KEGG pathways database differences in gene enrichment of target genes in the Wnt signaling pathway, Phospholipase D signaling pathway and mitogen-activated protein kinase signaling pathway. qRT-PCR confirmed that miRNAs and its target genes were consistent with the screening results. <i>In vitro</i>, our study revealed that XLHZ could increase the expression of E-cadherin, decrease the expression of transforming growth factor β1, vimentin and β-catenin, inhibite the proliferation and migration of CAG cells, cause cell cycle arrest at G0/G1 and G2/M phase, induce the apoptosis of CAG cells, and prevent the progression of CAG to GC.</p><p><strong>Conclusion: </strong>This study provided a new idea for the mechanism of blocking the progression of CAG to GC by XLHZ, which may be related to the expression of miR-20a-3p, miR-320-3p, miR-34b-5p, miR-483-3p and miR-883-3p and their target genes transferrin receptor, nuclear receptor subfamily 4 member 2, delta like canonical Notch ligand 1 and a kinase anchor protein 12 in CAG. In the future, we will continue to investigate the linkage between the active ingredients of XLHZ and the relevant miRNAs and their target genes, so as to provide more sufficient experimental basis for clinically effective prevention of CAG to GC.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 4","pages":"703-712"},"PeriodicalIF":0.0,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11337255/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768329","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sanhua Tang protects against ischemic stroke by preventing blood-brain barrier injury: a network pharmacology and experiments. 三花汤通过防止血脑屏障损伤预防缺血性中风:网络药理学与实验
Pub Date : 2024-08-01 DOI: 10.19852/j.cnki.jtcm.20240515.001
Luo Shan, Yang Fan, Chen Yuanchun, Zhao Ruoxi, Liu Haiye, Gao Fei, M A Wencan, Gao Weijuan, Y U Wentao

Objective: To assess the effect and mechanism of Sanhua Tang (, SHT) in treating ischemic stroke (IS) through the "Kaitong Xuanfu" theory by using network pharmacology and animal experiments.

Methods: The active ingredients and targets of SHT and IS were screened by public databases such as Traditional Chinese Medicine systems pharmacology, GeneCards, and online mendelian inheritance in man. Visual network topographies were constructed using R, Cytoscape 3.6.0, AutoDockTools, a user-sponsored molecular visualization system on an open-source foundation, and other software to analyze the correlation between targets and active ingredients. The middle cerebral artery occlusion (MCAO) model was established by operation. Animals were divided into the Sham group, MCAO group (M group), aloe-emodin (AE) group (MCAO rats treated with aloe-emodin), SHT at low dosage (SL group) (MCAO rats treated with SL), SHT at medium dosage (SM group), and SHT at high dosage (SH group). 2,3,5-triphenyl tetrazolium chloride staining was used to detect the volume of cerebral infarction; Nissl staining was used to observe the morphology of neuronal cells; transmission electron microscopy was used to observe the integrity of the blood-brain barrier (BBB); enzyme-linked immunosorbent assay was used to detect the content of interleukin-6 (IL-6), IL-10, tumor necrosis factor α (TNF-α) in serum. Western blot was used to detect the expression of vascular endothelial growth factor A (VEGFA) protein in the cerebral ischemic penumbra.

Results: Using network pharmacology and molecular docking validation, four active ingredients (lignan, naringenin, aloe-rhodopsin, and β-sitosterol), seven target proteins (protein kinase b 1, IL-6, TNF, VEGFA, TP53, jun proto-oncogene, and cysteinyl aspartate specific proteinase 3), and inflammatory signaling pathways were identified. Animal experiments showed that the SH and AE groups had fewer neurological deficits, reduced brain infarct volumes, decreased serum inflammatory factor levels, increased expression of VEGFA protein, and less structural damage to neurons and BBB.

Conclusion: The present study found that the therapeutic mechanism of SHT against IS may be related to the inhibition of BBB inflammatory damage, which is also the mechanism of "Kaitong Xuanfu." The high-dose group of SHT was relatively effective in regulating inflammatory factors, improving BBB permeability, and protecting neuronal cells from damage.

目的利用网络药理学和动物实验,通过 "开窍醒脑 "理论评估三花汤治疗缺血性中风(IS)的作用和机制:方法:通过中药系统药理学、GeneCards等公共数据库和在线人类孟德尔遗传学,筛选三花汤和IS的有效成分和靶点。使用R、Cytoscape 3.6.0、AutoDockTools(一个由用户发起的开源分子可视化系统)等软件构建可视化网络拓扑图,分析靶点与活性成分之间的相关性。通过手术建立大脑中动脉闭塞(MCAO)模型。动物被分为 Sham 组、MCAO 组(M 组)、芦荟大黄素组(AE 组)(用芦荟大黄素治疗 MCAO 大鼠)、SHT 低剂量组(SL 组)(用 SL 治疗 MCAO 大鼠)、SHT 中剂量组(SM 组)和 SHT 高剂量组(SH 组)。2,3,5-三苯基氯化四氮唑染色检测脑梗死体积;Nissl染色观察神经细胞形态;透射电镜观察血脑屏障(BBB)的完整性;酶联免疫吸附试验检测血清中白细胞介素-6(IL-6)、IL-10、肿瘤坏死因子α(TNF-α)的含量。用 Western 印迹法检测脑缺血半影中血管内皮生长因子 A(VEGFA)蛋白的表达:结果:通过网络药理学和分子对接验证,确定了四种活性成分(木脂素、柚皮苷、芦荟黄酮素和β-谷甾醇)、七种靶蛋白(蛋白激酶b 1、IL-6、TNF、VEGFA、TP53、jun原癌基因和半胱氨酰天冬氨酸特异性蛋白酶3)和炎症信号通路。动物实验表明,SH组和AE组神经功能缺损较少,脑梗死体积缩小,血清炎症因子水平降低,VEGFA蛋白表达增加,神经元和BBB结构损伤较轻:本研究发现,SHT对IS的治疗机制可能与抑制BBB炎症损伤有关,这也是 "开窍散 "的作用机制。大剂量SHT组在调节炎症因子、改善BBB通透性、保护神经细胞免受损伤方面相对有效。
{"title":"Sanhua Tang protects against ischemic stroke by preventing blood-brain barrier injury: a network pharmacology and experiments.","authors":"Luo Shan, Yang Fan, Chen Yuanchun, Zhao Ruoxi, Liu Haiye, Gao Fei, M A Wencan, Gao Weijuan, Y U Wentao","doi":"10.19852/j.cnki.jtcm.20240515.001","DOIUrl":"10.19852/j.cnki.jtcm.20240515.001","url":null,"abstract":"<p><strong>Objective: </strong>To assess the effect and mechanism of Sanhua Tang (, SHT) in treating ischemic stroke (IS) through the \"Kaitong Xuanfu\" theory by using network pharmacology and animal experiments.</p><p><strong>Methods: </strong>The active ingredients and targets of SHT and IS were screened by public databases such as Traditional Chinese Medicine systems pharmacology, GeneCards, and online mendelian inheritance in man. Visual network topographies were constructed using R, Cytoscape 3.6.0, AutoDockTools, a user-sponsored molecular visualization system on an open-source foundation, and other software to analyze the correlation between targets and active ingredients. The middle cerebral artery occlusion (MCAO) model was established by operation. Animals were divided into the Sham group, MCAO group (M group), aloe-emodin (AE) group (MCAO rats treated with aloe-emodin), SHT at low dosage (SL group) (MCAO rats treated with SL), SHT at medium dosage (SM group), and SHT at high dosage (SH group). 2,3,5-triphenyl tetrazolium chloride staining was used to detect the volume of cerebral infarction; Nissl staining was used to observe the morphology of neuronal cells; transmission electron microscopy was used to observe the integrity of the blood-brain barrier (BBB); enzyme-linked immunosorbent assay was used to detect the content of interleukin-6 (IL-6), IL-10, tumor necrosis factor α (TNF-α) in serum. Western blot was used to detect the expression of vascular endothelial growth factor A (VEGFA) protein in the cerebral ischemic penumbra.</p><p><strong>Results: </strong>Using network pharmacology and molecular docking validation, four active ingredients (lignan, naringenin, aloe-rhodopsin, and β-sitosterol), seven target proteins (protein kinase b 1, IL-6, TNF, VEGFA, TP53, jun proto-oncogene, and cysteinyl aspartate specific proteinase 3), and inflammatory signaling pathways were identified. Animal experiments showed that the SH and AE groups had fewer neurological deficits, reduced brain infarct volumes, decreased serum inflammatory factor levels, increased expression of VEGFA protein, and less structural damage to neurons and BBB.</p><p><strong>Conclusion: </strong>The present study found that the therapeutic mechanism of SHT against IS may be related to the inhibition of BBB inflammatory damage, which is also the mechanism of \"Kaitong Xuanfu.\" The high-dose group of SHT was relatively effective in regulating inflammatory factors, improving BBB permeability, and protecting neuronal cells from damage.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 4","pages":"794-803"},"PeriodicalIF":0.0,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11337263/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768334","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
International standard of Traditional Chinese Medicine techniques: the operating specifications for Chinese medicated bath (2022). 中医药技术国际标准:中药浴操作规范(2022 年)》。
Pub Date : 2024-08-01 DOI: 10.19852/j.cnki.jtcm.20240610.001
Zhang Jing, Wang Chunhui, Jin Xinyan, Y U Miao, Fan Yingyi, Han Xiaoli, Pei Xiaohua

Chinese medicated bath is one of the external therapies in Traditional Chinese Medicine (TCM), which has been widely used clinically. The "International Standard of Traditional Chinese Medicine Techniques: The Operating Specifications for Chinese Medicated Bath" is drawn up by the Beijing University of Chinese Medicine Third Affiliated Hospital and Beijing University of Chinese Medicine Xiamen Hospital in collaboration with domestic TCM universities and hospitals. The specification includes definition, operating process, points for attention and contraindications. It is targeted to provide reference for TCM providers at home and abroad with TCM background in clinical decision-making.

中药药浴是中医外治法之一,在临床上应用广泛。中药药浴操作规范》由北京中医药大学第三附属医院制定:中药浴操作规范》由北京中医药大学第三附属医院和北京中医药大学厦门医院联合国内中医药大学和医院共同制定。该规范包括定义、操作流程、注意事项及禁忌等内容。旨在为国内外具有中医背景的中医医疗机构提供临床决策参考。
{"title":"International standard of Traditional Chinese Medicine techniques: the operating specifications for Chinese medicated bath (2022).","authors":"Zhang Jing, Wang Chunhui, Jin Xinyan, Y U Miao, Fan Yingyi, Han Xiaoli, Pei Xiaohua","doi":"10.19852/j.cnki.jtcm.20240610.001","DOIUrl":"10.19852/j.cnki.jtcm.20240610.001","url":null,"abstract":"<p><p>Chinese medicated bath is one of the external therapies in Traditional Chinese Medicine (TCM), which has been widely used clinically. The \"International Standard of Traditional Chinese Medicine Techniques: The Operating Specifications for Chinese Medicated Bath\" is drawn up by the Beijing University of Chinese Medicine Third Affiliated Hospital and Beijing University of Chinese Medicine Xiamen Hospital in collaboration with domestic TCM universities and hospitals. The specification includes definition, operating process, points for attention and contraindications. It is targeted to provide reference for TCM providers at home and abroad with TCM background in clinical decision-making.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 4","pages":"851-854"},"PeriodicalIF":0.0,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11337249/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141768331","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1