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Mechanisms of Dangua Fang in multi-target and multi-method regulation of glycolipid metabolism based on phosphoproteomics. 基于磷酸蛋白组学的丹桂方在多靶点、多方法调控糖脂代谢中的作用机制
Pub Date : 2024-04-01 DOI: 10.19852/j.cnki.jtcm.20230908.001
Heng Xianpei, Wang Zhita, L I Liang, Yang Liuqing, Huang Suping, Jin Lang, H E Weidong

Objective: To explore the mechanism of Dangua Fang (, DGR) in multi-target and multi-method regulation of glycolipid metabolism based on phosphoproteomics.

Methods: Sprague-Dawley rats with normal glucose levels were randomly divided into three groups, including a conventional diet control group (Group A), high-fat-high-sugar diet model group (Group B), and DGR group (Group C, high-fat-high-sugar diet containing 20.5 g DGR). After 10 weeks of intervention, the fasting blood glucose (FBG), 2 h blood glucose [PBG; using the oral glucose tolerance test (OGTT)], hemoglobin A1c (HbA1c), plasma total cholesterol (TC), and triglycerides (TG) were tested, and the livers of rats were removed to calculate the liver index. Then, hepatic portal TG were tested using the Gross permanent optimization-participatiory action planning enzymatic method and phosphoproteomics was performed using liquid chromatography with tandem mass spectrometry (LC-MS/MS) analysis followed by database search and bioinformatics analysis. Finally, cell experiments were used to verify the results of phosphoproteomics. Phosphorylated mitogen-activated protein kinase kinase kinase kinase 4 (MAP4k4) and phosphorylated adducin 1 (ADD1) were detected using western blotting.

Results: DGR effectively reduced PBG, TG, and the liver index (P < 0.05), and significantly decreased HbA1c, TC, and hepatic portal TG (P < 0.01), showed significant hematoxylin and eosin (HE) staining, red oil O staining, and Masson staining of liver tissue. The total spectrum was 805 334, matched spectrum was 260 471, accounting for accounting 32.3%, peptides were 19 995, modified peptides were 14 671, identified proteins were 4601, quantifiable proteins were 4417, identified sites were 15 749, and quantified sites were 14659. Based on the threshold of expression fold change ( > 1.2), DGR up-regulated the modification of 228 phosphorylation sites involving 204 corresponding function proteins, and down-regulated the modification of 358 phosphorylation sites involving 358 corresponding function proteins, which included correcting 75 phosphorylation sites involving 64 corresponding function proteins relating to glycolipid metabolism. Therefore, DGR improved biological tissue processes, including information storage and processing, cellular processes and signaling, and metabolism. The metabolic functions regulated by DGR mainly include energy production and conversion, carbohydrate transport and metabolism, lipid transport and metabolism, inorganic ion transport and metabolism, secondary metabolite biosynthesis, transport, and catabolism. In vitro phosphorylation validation based on cell experiments showed that the change trends in the phosphorylation level of MAP4k4 and ADD1 were consistent with that of previous phosphoproteomics studies.

Conclusion: DGR extensively corrects the modification of phosphorylation sites to improve corresp

目的方法:将血糖正常的Sprague-Dawley大鼠随机分为三组,包括常规饮食对照组(A组)、高脂高糖饮食模型组(B组)和高脂高糖饮食模型组(C组):将血糖正常的Sprague-Dawley大鼠随机分为三组,包括常规饮食对照组(A组)、高脂高糖饮食模型组(B组)和DGR组(C组,含20.5 g DGR的高脂高糖饮食)。干预10周后,检测空腹血糖(FBG)、2 h血糖[PBG;采用口服葡萄糖耐量试验(OGTT)]、血红蛋白A1c(HbA1c)、血浆总胆固醇(TC)和甘油三酯(TG),并切除大鼠肝脏计算肝脏指数。然后,使用毛永久优化-参与行动规划酶法检测肝门部甘油三酯,并使用液相色谱-串联质谱(LC-MS/MS)分析法进行磷蛋白组学研究,然后进行数据库搜索和生物信息学分析。最后,利用细胞实验验证了磷酸化蛋白质组学的结果。结果表明,DGR能有效降低PBG、TGF和PBD的浓度:DGR可有效降低PBG、TG和肝指数(P<0.05),显著降低HbA1c、TC和肝门部TG(P<0.01)。总图谱为 805 334,匹配图谱为 260 471,占 32.3%,肽段为 19 995,修饰肽段为 14 671,鉴定蛋白质为 4601,可定量蛋白质为 4417,鉴定位点为 15 749,定量位点为 14659。根据表达折变阈值(> 1.2),DGR 上调了 228 个磷酸化位点的修饰,涉及 204 个相应的功能蛋白;下调了 358 个磷酸化位点的修饰,涉及 358 个相应的功能蛋白,其中包括纠正了 75 个磷酸化位点的修饰,涉及 64 个相应的糖脂代谢功能蛋白。因此,DGR 改善了生物组织过程,包括信息存储和处理、细胞过程和信号传导以及新陈代谢。DGR 所调控的代谢功能主要包括能量产生和转化、碳水化合物转运和代谢、脂质转运和代谢、无机离子转运和代谢、次级代谢物的生物合成、转运和分解。基于细胞实验的体外磷酸化验证表明,MAP4k4 和 ADD1 磷酸化水平的变化趋势与之前的磷酸化蛋白质组学研究一致:结论:DGR广泛地纠正了磷酸化位点的修饰,改善了糖脂代谢紊乱大鼠相应的糖脂代谢相关蛋白的表达,从而通过多靶点、多方法调节糖脂代谢。
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引用次数: 0
Effectivenss of electroacupuncture for skeletal muscle pain in Parkinson's disease: a Clinical randomized controlled trial. 电针治疗帕金森病骨骼肌疼痛的疗效:临床随机对照试验。
Pub Date : 2024-04-01 DOI: 10.19852/j.cnki.jtcm.20240203.004
Wang Shaosong, Sun Jingqing, Feng Qingyin, L I Bin, Wang Xin, Yuan Fan, Cui Yingxue

Objective: To explore the effect of electroacupuncture on skeletal muscle pain in Parkinson's disease (PD).

Methods: A single-center randomized controlled trial was conducted with sixty patients with Parkinson's disease with skeletal muscle pain were randomly divided into electroacupuncture group and sham acupuncture control group with 30 patients each. The electric acupuncture group was treated with electric acupuncture, while the control group was treated with Park needle pseudoacupuncture. Both groups were treated 5 times a week for a total of 4 weeks, and both groups completed 20 treatments. King's Parkinson's Pain Scale (KPPS) and visual analog scale (VAS) were used before and after treatment to evaluate the pain degree of patients. Real-time shear wave elastography (SWE) and modified Ashworth score (MAS) were used to evaluate the changes of muscle tone. Parkinson's comprehensive Score Scale (MDS-UPDRS, including UPDRSⅡ and UPDRS Ⅲ) was used to evaluate exercise ability. Hamilton Depression Scale (HAMD) score was used to evaluate the emotional changes of patients. Spearman correlation analysis was used to explore the correlation between pain degree and muscle tone, exercise ability and emotion.

Results: During the study, one case fell off in the control group, and 30 cases were eventually included in the analysis and treatment group and 29 cases in the control group. After treatment, Young's modulus of biceps and quadriceps and shear wave velocity of biceps were decreased in electroacupuncture group compared with before treatment, while KPPS score, VAS score, UPDRSⅡ, UPDRS Ⅲ and modified Ashworth score were decreased, with statistical significance (P < 0.05). There was no statistical significance in control group (P > 0.05). After treatment, KPPS score, VAS score, UPDRSⅡ and UPDRS Ⅲ, MAS, HAMD score, Young's modulus of biceps and shear wave velocity in electroacupuncture group were significantly lower than those in control group (P < 0.05). Spearman correlation analysis showed that KPPS score was positively correlated with UPDRS Ⅲ (r = 0.414, P < 0.05). KPPS score was positively correlated with HAMD score (r = 0.576, P < 0.01).

Conclusion: Electroacupuncture therapy can effectively improve skeletal muscle pain in patients with Parkinson's disease, reduce the muscle hardness of patients, improve patients' daily life ability, and improve patients' emotional disorders. The degree of skeletal muscle pain in PD patients is correlated with motor ability and emotional disorders, but there is no significant correlation between the degree of skeletal muscle pain and the muscle tone of PD patients.

目的:探讨电针对帕金森病(PD)患者骨骼肌疼痛的影响:探讨电针对帕金森病(PD)骨骼肌疼痛的影响:采用单中心随机对照试验的方法,将60例伴有骨骼肌疼痛的帕金森病患者随机分为电针组和假针刺对照组,每组30例。电针组采用电针治疗,对照组采用朴针假针灸治疗。两组均每周治疗 5 次,共 4 周,两组均完成 20 次治疗。治疗前后采用帕金森氏疼痛金氏量表(KPPS)和视觉模拟量表(VAS)评估患者的疼痛程度。实时剪切波弹性成像(SWE)和改良阿什沃斯评分(MAS)用于评估肌张力的变化。帕金森综合评分量表(MDS-UPDRS,包括UPDRSⅡ和UPDRSⅢ)用于评估运动能力。汉密尔顿抑郁量表(HAMD)用于评估患者的情绪变化。采用斯皮尔曼相关分析探讨疼痛程度与肌张力、运动能力和情绪之间的相关性:研究期间,对照组有一例脱落,最终分析治疗组有 30 例,对照组有 29 例。治疗后,电针组肱二头肌、股四头肌的杨氏模量和肱二头肌剪切波速度较治疗前均有所下降,KPPS评分、VAS评分、UPDRSⅡ、UPDRSⅢ和改良Ashworth评分均有所下降,差异有统计学意义(P0.05)。对照组无统计学意义(P>0.05)。治疗后,电针组的 KPPS 评分、VAS 评分、UPDRSⅡ和 UPDRSⅢ、MAS、HAMD 评分、肱二头肌杨氏模量和剪切波速度均显著低于对照组(P 0.05)。斯皮尔曼相关分析显示,KPPS 评分与 UPDRS Ⅲ 呈正相关(r = 0.414,P 0.05)。KPPS评分与HAMD评分呈正相关(r = 0.576,P 0.01):结论:电针治疗能有效改善帕金森病患者的骨骼肌疼痛,减轻患者的肌肉硬度,提高患者的日常生活能力,改善患者的情绪障碍。帕金森病患者骨骼肌疼痛程度与运动能力和情绪障碍相关,但骨骼肌疼痛程度与帕金森病患者肌张力无明显相关性。
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引用次数: 0
Gehua Jiejiu Dizhi decoction ameliorates alcoholic fatty liver in mice by regulating lipid and bile acid metabolism and with exertion of antioxidant stress based on 4DLabel-free quantitative proteomic study. 基于四维无标记定量蛋白质组学研究,葛花解酒地黄汤通过调节脂质和胆汁酸代谢以及发挥抗氧化作用改善小鼠酒精性脂肪肝。
Pub Date : 2024-04-01 DOI: 10.19852/j.cnki.jtcm.20231018.001
Han Min, Y I Xu, You Shaowei, W U Xueli, Wang Shuoshi, H E Diancheng

Objective: To analyze the effect and molecular mechanism of Gehua Jiejiu Dizhi decoction (, GJDD) on alcoholic fatty live disease (AFLD) by using proteomic methods.

Methods: The male C57BL/6J mouse were randomly divided into four groups: control group, model group, GJDD group and resveratrol group. After the AFLD model was successfully prepared by intragastric administration of alcohol once on the basis of the Lieber-DeCarli classical method, the GJDD group and resveratrol group were intragastrically administered with GJDD (4900 mg/kg) and resveratrol (400 mg/kg) respectively, once a day for 9 d. The fat deposition of liver tissue was observed and evaluated by oil red O (ORO) staining. 4DLabel-free quantitative proteome method was used to determine and quantify the protein expression in liver tissue of each experimental group. The differentially expressed proteins were screened according to protein expression differential multiples, and then analyzed by Gene ontology classification and Kyoto Encyclopedia of Genes and Genomes pathway enrichment. Finally, expression validation of the differentially co-expressed proteins from control group, model group and GJDD group were verified by targeted proteomics quantification techniques.

Results: In semiquantitative analyses of ORO, all kinds of steatosis (ToS, MaS, and MiS) were evaluated higher in AFLD mice compared to those in GJDD or resveratrol-treated mice. 4DLabel-free proteomics analysis results showed that a total of 4513 proteins were identified, of which 3763 proteins were quantified and 946 differentially expressed proteins were screened. Compared with the control group, 145 proteins were up-regulated and 148 proteins were down-regulated in the liver tissue of model group. In addition, compared with the model group, 92 proteins were up-regulated and 135 proteins were down-regulated in the liver tissue of the GJDD group. 15 differentially co-expressed proteins were found between every two groups (model group vs control group, GJDD group vs model group and GJDD group vs control group), which were involved in many biological processes. Among them, 11 differentially co-expressed key proteins (Aox3, H1-5, Fabp5, Ces3a, Nudt7, Serpinb1a, Fkbp11, Rpl22l1, Keg1, Acss2 and Slco1a1) were further identified by targeted proteomic quantitative technology and their expression patterns were consistent with the results of 4D label-free proteomic analysis.

Conclusions: Our study provided proteomics-based evidence that GJDD alleviated AFLD by modulating liver protein expression, likely through the modulation of lipid metabolism, bile acid metabolism and with exertion of antioxidant stress.

目的采用蛋白质组学方法分析葛花解酒滴丸(GJDD)对酒精性脂肪活症(AFLD)的作用及分子机制:方法:将雄性C57BL/6J小鼠随机分为4组:对照组、模型组、GJDD组和白藜芦醇组。在Lieber-DeCarli经典方法基础上通过胃内注射酒精一次成功制备AFLD模型后,分别给GJDD组和白藜芦醇组胃内注射GJDD(4900 mg/kg)和白藜芦醇(400 mg/kg),每天一次,连续9 d。采用4D无标记定量蛋白质组方法测定和量化各实验组肝组织中的蛋白质表达。根据蛋白表达差异倍数筛选差异表达蛋白,然后进行基因本体分类和京都基因组百科全书通路富集分析。最后,通过靶向蛋白质组学定量技术验证了对照组、模型组和 GJDD 组差异共表达蛋白的表达情况:结果:在ORO的半定量分析中,AFLD小鼠的各种脂肪变性(ToS、MaS和MiS)均高于GJDD或白藜芦醇处理的小鼠。4D无标记蛋白质组学分析结果显示,共鉴定出4513个蛋白质,其中3763个蛋白质被定量,946个差异表达蛋白质被筛选。与对照组相比,模型组肝脏组织中有145个蛋白质上调,148个蛋白质下调。此外,与模型组相比,GJDD 组肝脏组织中有 92 个蛋白质上调,135 个蛋白质下调。在每两组(模型组与对照组、GJDD 组与模型组、GJDD 组与对照组)之间发现了 15 个差异共表达蛋白,它们参与了许多生物学过程。其中,11个差异共表达的关键蛋白(Aox3、H1-5、Fabp5、Ces3a、Nudt7、Serpinb1a、Fkbp11、Rpl22l1、Keg1、Acss2和Slco1a1)经靶向蛋白质组学定量技术进一步鉴定,其表达模式与4D无标记蛋白质组学分析结果一致:我们的研究提供了基于蛋白质组学的证据,证明 GJDD 可通过调节肝脏蛋白表达缓解 AFLD,这可能是通过调节脂质代谢、胆汁酸代谢和发挥抗氧化应激作用实现的。
{"title":"Gehua Jiejiu Dizhi decoction ameliorates alcoholic fatty liver in mice by regulating lipid and bile acid metabolism and with exertion of antioxidant stress based on 4DLabel-free quantitative proteomic study.","authors":"Han Min, Y I Xu, You Shaowei, W U Xueli, Wang Shuoshi, H E Diancheng","doi":"10.19852/j.cnki.jtcm.20231018.001","DOIUrl":"10.19852/j.cnki.jtcm.20231018.001","url":null,"abstract":"<p><strong>Objective: </strong>To analyze the effect and molecular mechanism of Gehua Jiejiu Dizhi decoction (, GJDD) on alcoholic fatty live disease (AFLD) by using proteomic methods.</p><p><strong>Methods: </strong>The male C57BL/6J mouse were randomly divided into four groups: control group, model group, GJDD group and resveratrol group. After the AFLD model was successfully prepared by intragastric administration of alcohol once on the basis of the Lieber-DeCarli classical method, the GJDD group and resveratrol group were intragastrically administered with GJDD (4900 mg/kg) and resveratrol (400 mg/kg) respectively, once a day for 9 d. The fat deposition of liver tissue was observed and evaluated by oil red O (ORO) staining. 4DLabel-free quantitative proteome method was used to determine and quantify the protein expression in liver tissue of each experimental group. The differentially expressed proteins were screened according to protein expression differential multiples, and then analyzed by Gene ontology classification and Kyoto Encyclopedia of Genes and Genomes pathway enrichment. Finally, expression validation of the differentially co-expressed proteins from control group, model group and GJDD group were verified by targeted proteomics quantification techniques.</p><p><strong>Results: </strong>In semiquantitative analyses of ORO, all kinds of steatosis (ToS, MaS, and MiS) were evaluated higher in AFLD mice compared to those in GJDD or resveratrol-treated mice. 4DLabel-free proteomics analysis results showed that a total of 4513 proteins were identified, of which 3763 proteins were quantified and 946 differentially expressed proteins were screened. Compared with the control group, 145 proteins were up-regulated and 148 proteins were down-regulated in the liver tissue of model group. In addition, compared with the model group, 92 proteins were up-regulated and 135 proteins were down-regulated in the liver tissue of the GJDD group. 15 differentially co-expressed proteins were found between every two groups (model group <i>vs</i> control group, GJDD group vs model group and GJDD group <i>vs</i> control group), which were involved in many biological processes. Among them, 11 differentially co-expressed key proteins (Aox3, H1-5, Fabp5, Ces3a, Nudt7, Serpinb1a, Fkbp11, Rpl22l1, Keg1, Acss2 and Slco1a1) were further identified by targeted proteomic quantitative technology and their expression patterns were consistent with the results of 4D label-free proteomic analysis.</p><p><strong>Conclusions: </strong>Our study provided proteomics-based evidence that GJDD alleviated AFLD by modulating liver protein expression, likely through the modulation of lipid metabolism, bile acid metabolism and with exertion of antioxidant stress.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 2","pages":"277-288"},"PeriodicalIF":0.0,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10927405/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140178404","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
Moxibustion of Zusanli (ST36) and Shenshu (BL23) alleviates the inflammation of rheumatoid arthritis in rats through regulating macrophage migration inhibitory factor/glucocorticoids signaling. 艾灸足三里(ST36)和神曲(BL23)可通过调节巨噬细胞迁移抑制因子/糖皮质激素信号传导,缓解大鼠类风湿性关节炎的炎症反应。
Pub Date : 2024-04-01 DOI: 10.19852/j.cnki.jtcm.20220602.001
Zhang Linlin, Zhong Yumei, L U Wenting, Shang Yanan, Guo Yanding, Luo Xiaochao, Chen Yang, Luo Kun, H U Danhui, Y U Huiling, Zhou Haiyan

Objective: To test the hypothesis that moxibustion may inhibit rheumatoid arthritis (RA) synovial inflammation by regulating the expression of macrophage migration inhibitory factor (MIF)/glucocorticoids (GCs).

Methods: Fifty male Sprague-Dawley rats were randomly divided into five groups (n = 10 each): blank Control (CON) group, RA Model (RA) group, Moxibustion (MOX) group, MIF inhibitor (S,R)-3-(4-hydroxyphenyl)-4,5-dihydro-5-isoxazole acetic acid methyl ester (ISO-1) group, and Moxibustion + MIF inhibitor ISO-1 (MOX + ISO-1) group. Rats in the ISO-1 group and ISO-1 + MOX group were intraperitoneally injected with the inhibitor ISO-1. The rats in the RA group, ISO-1 group, MOX group, and ISO-1 + MOX group were injected with Freund's complete adjuvant (FCA) in the right hind footpad to establish an experimental RA rat model. In the MOX group and MOX + ISO-1 group, rats were treated with Moxa. The thickness of the footpads of the rats in each group was measured at three-time points before, after modeling and after moxibustion treatment. The contents of serum MIF, corticosterone (CORT), tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) were detected by enzyme-linked immunosorbent assay; and the contents of synovial MIF were detected by Western blot. Hematoxylin-eosin (HE) staining method was used to observe the pathological changes of synovial tissue under a section light microscope, and pathological scoring was performed according to the grading standard of the degree of synovial tissue disease.

Results: Moxibustion was found to reduce the level of MIF and alleviate inflammation in RA rats in this study. In addition, after inhibiting the expression of MIF, the level of CORT increased, and the level of TNF-α decreased. Treating RA rats with inhibited MIF by moxibustion, the level of CORT was almost unchanged, but the level of TNF-α further decreased. The correlation analysis data suggested that MIF was positively related to the expression of TNF-α and negatively correlated with the expression of CORT.

Conclusion: Reducing MIF to increase CORT and decrease TNF-α by moxibustion treatment in RA. MIF may be a factor for moxibustion to regulate the expression of CORT, but the expression of TNF-α is due to the incomplete regulation of the MIF. This study added to the body of evidence pointing to moxibustion's anti-inflammatory mechanism in the treatment of RA.

目的方法:将 50 只雄性 Sprague-Dawley 大鼠随机分为 5 组(每组 10 只):空白对照组(CON)、RA 模型组(RA)、艾灸组(MOX):将50只雄性Sprague-Dawley大鼠随机分为5组(每组10只):空白对照组(CON)、RA模型组(RA)、艾灸组(MOX)、MIF抑制剂(S,R)-3-(4-羟基苯基)-4,5-二氢-5-异恶唑乙酸甲酯组(ISO-1)和艾灸+MIF抑制剂ISO-1组(MOX + ISO-1)。ISO-1 组和 ISO-1 + MOX 组大鼠腹腔注射抑制剂 ISO-1。RA组、ISO-1组、MOX组和ISO-1 + MOX组大鼠的右后足垫注射弗氏完全佐剂(FCA),以建立实验性RA大鼠模型。MOX组和MOX + ISO-1组大鼠接受艾灸治疗。在建模前、建模后和艾灸治疗后三个时间点测量各组大鼠足垫的厚度。用酶联免疫吸附法检测血清 MIF、皮质酮(CORT)、肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)的含量,用 Western 印迹法检测滑膜 MIF 的含量。采用苏木精-伊红(HE)染色法在切片光镜下观察滑膜组织的病理变化,并根据滑膜组织病变程度的分级标准进行病理评分:结果:本研究发现艾灸可降低MIF水平,缓解RA大鼠的炎症反应。此外,抑制 MIF 表达后,CORT 水平升高,TNF-α 水平降低。用艾灸抑制 MIF 的方法治疗 RA 大鼠,CORT 水平几乎没有变化,但 TNF-α 水平进一步下降。相关分析数据表明,MIF与TNF-α的表达呈正相关,而与CORT的表达呈负相关:结论:艾灸治疗RA可降低MIF,增加CORT,降低TNF-α。MIF可能是艾灸调节CORT表达的一个因素,但TNF-α的表达是由于MIF的不完全调节所致。这项研究为艾灸治疗RA的抗炎机制提供了更多证据。
{"title":"Moxibustion of Zusanli (ST36) and Shenshu (BL23) alleviates the inflammation of rheumatoid arthritis in rats through regulating macrophage migration inhibitory factor/glucocorticoids signaling.","authors":"Zhang Linlin, Zhong Yumei, L U Wenting, Shang Yanan, Guo Yanding, Luo Xiaochao, Chen Yang, Luo Kun, H U Danhui, Y U Huiling, Zhou Haiyan","doi":"10.19852/j.cnki.jtcm.20220602.001","DOIUrl":"10.19852/j.cnki.jtcm.20220602.001","url":null,"abstract":"<p><strong>Objective: </strong>To test the hypothesis that moxibustion may inhibit rheumatoid arthritis (RA) synovial inflammation by regulating the expression of macrophage migration inhibitory factor (MIF)/glucocorticoids (GCs).</p><p><strong>Methods: </strong>Fifty male Sprague-Dawley rats were randomly divided into five groups (<i>n =</i> 10 each): blank Control (CON) group, RA Model (RA) group, Moxibustion (MOX) group, MIF inhibitor (S,R)-3-(4-hydroxyphenyl)-4,5-dihydro-5-isoxazole acetic acid methyl ester (ISO-1) group, and Moxibustion + MIF inhibitor ISO-1 (MOX + ISO-1) group. Rats in the ISO-1 group and ISO-1 + MOX group were intraperitoneally injected with the inhibitor ISO-1. The rats in the RA group, ISO-1 group, MOX group, and ISO-1 + MOX group were injected with Freund's complete adjuvant (FCA) in the right hind footpad to establish an experimental RA rat model. In the MOX group and MOX + ISO-1 group, rats were treated with Moxa. The thickness of the footpads of the rats in each group was measured at three-time points before, after modeling and after moxibustion treatment. The contents of serum MIF, corticosterone (CORT), tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) were detected by enzyme-linked immunosorbent assay; and the contents of synovial MIF were detected by Western blot. Hematoxylin-eosin (HE) staining method was used to observe the pathological changes of synovial tissue under a section light microscope, and pathological scoring was performed according to the grading standard of the degree of synovial tissue disease.</p><p><strong>Results: </strong>Moxibustion was found to reduce the level of MIF and alleviate inflammation in RA rats in this study. In addition, after inhibiting the expression of MIF, the level of CORT increased, and the level of TNF-α decreased. Treating RA rats with inhibited MIF by moxibustion, the level of CORT was almost unchanged, but the level of TNF-α further decreased. The correlation analysis data suggested that MIF was positively related to the expression of TNF-α and negatively correlated with the expression of CORT.</p><p><strong>Conclusion: </strong>Reducing MIF to increase CORT and decrease TNF-α by moxibustion treatment in RA. MIF may be a factor for moxibustion to regulate the expression of CORT, but the expression of TNF-α is due to the incomplete regulation of the MIF. This study added to the body of evidence pointing to moxibustion's anti-inflammatory mechanism in the treatment of RA.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 2","pages":"353-361"},"PeriodicalIF":0.0,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10927400/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140178408","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
Polyphyllin I enhances tumor necrosis factor-related apoptosis-inducing ligand-induced inhibition of human osteosarcoma cell growth downregulating the Wnt/β-catenin pathway. Polyphyllin I 通过下调 Wnt/β-catenin 通路,增强肿瘤坏死因子相关凋亡诱导配体对人骨肉瘤细胞生长的抑制作用。
Pub Date : 2024-04-01 DOI: 10.19852/j.cnki.jtcm.2024.02.002
Chang Junli, Zhao Fulai, Sun Xingyuan, M A Xiaoping, Zhao Peng, Zhou Chujie, Shi Binhao, G U Wenchao, Wang Yongjun, Yang Yanping

Objective: To investigate the synergistic effects of polyphyllin I (PPI) combined with tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) on the growth of osteosarcoma cells through downregulating the Wnt/β-catenin signaling pathway.

Methods: Cell viability, apoptosis and cell cycle distribution were examined using cell counting kit-8 and flow cytometry assays. The morphology of cancer cells was observed with inverted phase contrast microscope. The migration and invasion abilities were examined by xCELLigence real time cell analysis DP system and transwell assays. The expressions of poly (adenosine diphosphate-ribose) polymerase, C-Myc, Cyclin B1, cyclin-dependent kinases 1, N-cadherin, Vimentin, Active-β-catenin, β-catenin, p-glycogen synthase kinase 3β (GSK-3β) and GSK-3β were determined by Western blotting assay.

Results: PPI sensitized TRAIL-induced decrease of viability, migration and invasion, as well as increase of apoptosis and cell cycle arrest of MG-63 and U-2 OS osteosarcoma cells. The synergistic effect of PPI with TRAIL in inhibiting the growth of osteosarcoma cells was at least partially realized through the inactivation of Wnt/β-catenin signaling pathway.

Conclusion: The combination of PPI and TRAIL is potentially a novel treatment strategy of osteosarcoma.

目的研究多粘菌素 I(PPI)与肿瘤坏死因子相关凋亡诱导配体(TRAIL)通过下调 Wnt/β-catenin 信号通路对骨肉瘤细胞生长的协同作用:方法:使用细胞计数试剂盒-8 和流式细胞术检测细胞活力、凋亡和细胞周期分布。倒置相差显微镜观察癌细胞的形态。迁移和侵袭能力由 xCELLigence 实时细胞分析 DP 系统和透孔试验检测。用 Western 印迹法测定了多(腺苷二磷酸核糖)聚合酶、C-Myc、细胞周期蛋白 B1、细胞周期蛋白依赖性激酶 1、N-钙粘蛋白、波形蛋白、活性-β-catenin、β-catenin、p-糖原合成酶激酶 3β (GSK-3β)和 GSK-3β 的表达:结果:PPI对TRAIL诱导的MG-63和U-2 OS骨肉瘤细胞活力、迁移和侵袭的降低以及细胞凋亡和细胞周期停滞的增加具有敏化作用。PPI与TRAIL在抑制骨肉瘤细胞生长方面的协同作用至少部分是通过Wnt/β-catenin信号通路的失活实现的:结论:PPI与TRAIL的联合应用可能是治疗骨肉瘤的一种新策略。
{"title":"Polyphyllin I enhances tumor necrosis factor-related apoptosis-inducing ligand-induced inhibition of human osteosarcoma cell growth downregulating the Wnt/β-catenin pathway.","authors":"Chang Junli, Zhao Fulai, Sun Xingyuan, M A Xiaoping, Zhao Peng, Zhou Chujie, Shi Binhao, G U Wenchao, Wang Yongjun, Yang Yanping","doi":"10.19852/j.cnki.jtcm.2024.02.002","DOIUrl":"10.19852/j.cnki.jtcm.2024.02.002","url":null,"abstract":"<p><strong>Objective: </strong>To investigate the synergistic effects of polyphyllin I (PPI) combined with tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) on the growth of osteosarcoma cells through downregulating the Wnt/β-catenin signaling pathway.</p><p><strong>Methods: </strong>Cell viability, apoptosis and cell cycle distribution were examined using cell counting kit-8 and flow cytometry assays. The morphology of cancer cells was observed with inverted phase contrast microscope. The migration and invasion abilities were examined by xCELLigence real time cell analysis DP system and transwell assays. The expressions of poly (adenosine diphosphate-ribose) polymerase, C-Myc, Cyclin B1, cyclin-dependent kinases 1, N-cadherin, Vimentin, Active-β-catenin, β-catenin, p-glycogen synthase kinase 3β (GSK-3β) and GSK-3β were determined by Western blotting assay.</p><p><strong>Results: </strong>PPI sensitized TRAIL-induced decrease of viability, migration and invasion, as well as increase of apoptosis and cell cycle arrest of MG-63 and U-2 OS osteosarcoma cells. The synergistic effect of PPI with TRAIL in inhibiting the growth of osteosarcoma cells was at least partially realized through the inactivation of Wnt/β-catenin signaling pathway.</p><p><strong>Conclusion: </strong>The combination of PPI and TRAIL is potentially a novel treatment strategy of osteosarcoma.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 2","pages":"251-259"},"PeriodicalIF":0.0,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10927409/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140178411","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
Efficacy and safety of extracorporeal shock wave therapy combined with sodium hyaluronate in treatment of knee osteoarthritis: a systematic review and Meta-analysis. 体外冲击波疗法联合透明质酸钠治疗膝骨关节炎的疗效和安全性:系统综述和 Meta 分析。
Pub Date : 2024-04-01 DOI: 10.19852/j.cnki.jtcm.20231226.002
Zhou Mingwang, Dong Zhuanli, Wei Changhao, Feng Lufang, Wang Xiaoping, Liu Haiping, J I Xing, Yang Kehu, L I Shenghua

Objective: To assess the efficacy and safety of extracorporeal shockwave therapy (ESWT) combined with sodium hyaluronate (HA) for the treatment of knee osteoarthritis (KOA).

Methods: PubMed, Embase, the Cochrane Library, Web of Science, China National Knowledge Infrastructure, Wanfang database, China Science and Technology Journal Database, and SinoMed were searched from inception to July 2020. The quality of the randomized controlled trials was evaluated independently by two reviewers according to the criteria in the Cochrane Collaboration for Systematic Reviews. The identified articles were then screened individually using EndnoteX9 for eligibility in this Meta-analysis. The heterogeneity among the articles was evaluated using I2.

Results: A total of 17 studies, comprising 2000 individuals, were included in this Meta-analysis. The results showed that a significant improvement was observed in knee pain and function based on the clinical efficacy of ESWT combined with HA. Statistical analysis of clinical efficacy showed that [relative risk (RR) = 1.21, 95% confidence interval (CI) (1.12, 1.30), P < 0.01]. Statistical analysis of visual analog scale showed that [standardized mean difference (SMD) = -2.84, 95%CI (-4.01, -1.66), P < 0.01]. Western Ontario and McMaster University osteoarthritis index statistical analysis showed that [SMD = -1.57, 95% CI (-2.52, -0.61), P < 0.01]. Lysholm score statistical analysis showed that [SMD = 1.71, 95% CI (0.98, 2.44), P < 0.01]. In addition, only minor side effects, such as redness and swelling of the skin, were observed.

Conclusions: Medium to low quality evidence showed that ESWT combined with HA offers an inexpensive, well-tolerated, safe, and effective method to improve pain and functionality in patients with KOA. However, tightly controlled, randomized, large multicenter trials are warranted to validate the current findings.

目的评估体外冲击波疗法(ESWT)联合透明质酸钠(HA)治疗膝骨关节炎(KOA)的有效性和安全性:方法:检索了PubMed、Embase、Cochrane图书馆、Web of Science、中国国家知识基础设施、万方数据库、中国科技期刊数据库和SinoMed从开始到2020年7月的数据。随机对照试验的质量由两名审稿人根据 Cochrane 协作系统综述的标准进行独立评估。然后使用 EndnoteX9 对确定的文章进行逐一筛选,以确定是否符合本 Meta 分析的条件。使用 I2 对文章之间的异质性进行评估:本次 Meta 分析共纳入了 17 项研究,涉及 2000 人。结果表明,根据 ESWT 联合 HA 的临床疗效,膝关节疼痛和功能均有明显改善。临床疗效统计分析显示[相对风险 (RR) = 1.21,95% 置信区间 (CI) (1.12, 1.30),P 0.01]。视觉模拟量表的统计分析显示[标准化平均差(SMD)=-2.84,95% 置信区间(-4.01,-1.66),P 0.01]。西安大略和麦克马斯特大学骨关节炎指数统计分析显示[SMD = -1.57, 95%CI (-2.52, -0.61),P 0.01]。Lysholm 评分统计分析显示[SMD = 1.71,95% CI (0.98,2.44),P 0.01]。此外,只观察到皮肤红肿等轻微副作用:中低质量的证据显示,ESWT 联合 HA 是改善 KOA 患者疼痛和功能的一种廉价、耐受性好、安全且有效的方法。然而,要验证目前的研究结果,还需要进行严格对照、随机、大型多中心试验。
{"title":"Efficacy and safety of extracorporeal shock wave therapy combined with sodium hyaluronate in treatment of knee osteoarthritis: a systematic review and Meta-analysis.","authors":"Zhou Mingwang, Dong Zhuanli, Wei Changhao, Feng Lufang, Wang Xiaoping, Liu Haiping, J I Xing, Yang Kehu, L I Shenghua","doi":"10.19852/j.cnki.jtcm.20231226.002","DOIUrl":"10.19852/j.cnki.jtcm.20231226.002","url":null,"abstract":"<p><strong>Objective: </strong>To assess the efficacy and safety of extracorporeal shockwave therapy (ESWT) combined with sodium hyaluronate (HA) for the treatment of knee osteoarthritis (KOA).</p><p><strong>Methods: </strong>PubMed, Embase, the Cochrane Library, Web of Science, China National Knowledge Infrastructure, Wanfang database, China Science and Technology Journal Database, and SinoMed were searched from inception to July 2020. The quality of the randomized controlled trials was evaluated independently by two reviewers according to the criteria in the Cochrane Collaboration for Systematic Reviews. The identified articles were then screened individually using EndnoteX9 for eligibility in this Meta-analysis. The heterogeneity among the articles was evaluated using I2.</p><p><strong>Results: </strong>A total of 17 studies, comprising 2000 individuals, were included in this Meta-analysis. The results showed that a significant improvement was observed in knee pain and function based on the clinical efficacy of ESWT combined with HA. Statistical analysis of clinical efficacy showed that [relative risk (<i>RR</i>) = 1.21, 95% confidence interval (<i>CI</i>) (1.12, 1.30), <i>P <</i> 0.01]. Statistical analysis of visual analog scale showed that [standardized mean difference (<i>SMD</i>) = -2.84, 95%<i>CI</i> (-4.01, -1.66), <i>P <</i> 0.01]. Western Ontario and McMaster University osteoarthritis index statistical analysis showed that [<i>SMD</i> = -1.57, 95% <i>CI</i> (-2.52, -0.61), <i>P <</i> 0.01]. Lysholm score statistical analysis showed that [<i>SMD</i> = 1.71, 95% <i>CI</i> (0.98, 2.44), <i>P <</i> 0.01]. In addition, only minor side effects, such as redness and swelling of the skin, were observed.</p><p><strong>Conclusions: </strong>Medium to low quality evidence showed that ESWT combined with HA offers an inexpensive, well-tolerated, safe, and effective method to improve pain and functionality in patients with KOA. However, tightly controlled, randomized, large multicenter trials are warranted to validate the current findings.</p>","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 2","pages":"243-250"},"PeriodicalIF":0.0,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10927402/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140178452","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
Network pharmacology and experimental validation to reveal the pharmacological mechanisms of Sini decoction against renal fibrosis. 通过网络药理学和实验验证,揭示西尼煎剂抗肾脏纤维化的药理机制。
Pub Date : 2024-04-01 DOI: 10.19852/j.cnki.jtcm.20230630.003
Wang Yan, Deng Fanying, Liu Shiqi, Wang Yingli

Objective: To investigate the mechanism by which Sini decoction (, SND) improves renal fibrosis (Rf) in rats based on transforming growth factor β1/Smad (TGF-β1/Smad) signaling pathway.

Methods: Network pharmacology was applied to obtain potentially involved signaling pathways in SND's improving effects on Rf. The targets of SND drug components and the targets of Rf were obtained by searching databases, such as the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCSMP) and GeenCard. The intersection targets of two searches were obtained and underwent signaling pathway analysis using a Venn diagram. Then experimental pharmacology was utilized to prove and investigate the effects of SND on target proteins in the TGF-β1/Smad signaling pathway. The Rf rat model was established by unilateral ureteral occlusion (UUO). The expression levels of transforming growth factor, matrix metalloproteinase-9 (MMP-9), matrix metal protease-2 (MMP-2), connective tissue growth factor (CTGF), and tissue inhibitor of metalloproteinase-1 (TIMP-1) were determined by Masson staining of rat renal tissue, and immunohistochemical methods. The expression levels of Smad3, Smad2, and Smad7 in renal tissue were determined by Western blotting (WB). The mechanism of the improving effects of SND on Rf was investigated based on TGF-β1/Smad signaling pathway.

Results: A total of 12 drug components of Fuzi (Radix Aconiti Lateralis Preparata), 5 drug components of Ganjiang (Rhizoma Zingiber), and 9 drug components of Gancao (Radix Glycy et Rhizoma) were obtained from the database search, and 207 shared targets were found. A total of 1063 Rf targets were found in the database search. According to the Venn diagram, in total, 96 intersection targets were found in two database searches. The metabolic pathways involved included TGF-β signaling pathway, phosphatidylinositol-3-kinase/serine-threonine protein kinase signaling (PI3K/Akt) pathway, and hypoxia-inducible factor-1 (HIF-1) signaling pathway. Masson staining analysis showed that compared with the model group, the renal interstitial collagen deposition levels in the SSN and SND groups were significantly lower (P < 0.05). Immunohistochemical analysis, compared with the control group, the positive cell area expression levels of MMP-9/TIMP-1 and MMP-2/TIMP-1 in the kidney tissue of the model group were significantly decreased (P < 0.05, P < 0.01), and the positive cell area expression levels of CTGF and TGF-β1 were significantly increased (P < 0.01). Compared with the model group, the positive cell area expression levels of MMP-9/TIMP-1 and MMP-2/TIMP-1 in the kidney tissue of the SSN and SND groups were significantly increased (P < 0.05, P < 0.01), and the positive cell area expression levels of CTGF and TGF-β1 in the kidney tissue were significantly decreased (P < 0.05

目的研究基于转化生长因子β1/Smad(TGF-β1/Smad)信号通路的西尼煎剂(SND)改善大鼠肾脏纤维化(Rf)的机制:方法:应用网络药理学获得SND改善Rf效应的潜在信号通路。通过检索中药系统药理学数据库与分析平台(TCSMP)和 GeenCard 等数据库,获得 SND 药物成分的靶点和 Rf 的靶点。两次搜索得到的交叉靶点通过维恩图进行信号通路分析。然后利用实验药理学证明并研究了SND对TGF-β1/Smad信号通路中靶蛋白的影响。通过单侧输尿管闭塞(UUO)建立了 Rf 大鼠模型。大鼠肾组织马森染色法和免疫组化法测定了转化生长因子、基质金属蛋白酶-9(MMP-9)、基质金属蛋白酶-2(MMP-2)、结缔组织生长因子(CTGF)和组织金属蛋白酶抑制剂-1(TIMP-1)的表达水平。大鼠肾组织中 Smad3、Smad2 和 Smad7 的表达水平通过 Western 印迹(WB)法测定。根据 TGF-β1/Smad 信号通路研究了 SND 对 Rf 改善作用的机制:结果:通过数据库检索获得了12种附子药物成分、5种赣江药物成分和9种甘草药物成分,发现了207个共有靶点。数据库检索共发现 1063 个 Rf 靶点。根据维恩图,两次数据库搜索共发现 96 个交叉靶标。涉及的代谢通路包括 TGF-β 信号通路、磷脂酰肌醇-3-激酶/丝氨酸-苏氨酸蛋白激酶信号通路(PI3K/Akt)和缺氧诱导因子-1(HIF-1)信号通路。马森染色分析显示,与模型组相比,SSN 组和 SND 组的肾间质胶原沉积水平明显降低(P 0.05)。免疫组化分析显示,与对照组相比,模型组肾脏组织中 MMP-9/TIMP-1 和 MMP-2/TIMP-1 的阳性细胞面积表达水平明显降低(P 0.05,P 0.01),CTGF 和 TGF-β1 的阳性细胞面积表达水平明显升高(P 0.01)。与模型组相比,SSN 组和 SND 组肾脏组织中 MMP-9/TIMP-1 和 MMP-2/TIMP-1 的阳性细胞面积表达水平明显升高(P 0.05,P 0.01),肾脏组织中 CTGF 和 TGF-β1 的阳性细胞面积表达水平明显降低(P 0.05,P 0.01)。WB结果显示,SSN组和SND组能减少Smad2和Smad3的表达(P 0.05),增加Smad7的表达(P 0.05)。
{"title":"Network pharmacology and experimental validation to reveal the pharmacological mechanisms of Sini decoction against renal fibrosis.","authors":"Wang Yan, Deng Fanying, Liu Shiqi, Wang Yingli","doi":"10.19852/j.cnki.jtcm.20230630.003","DOIUrl":"10.19852/j.cnki.jtcm.20230630.003","url":null,"abstract":"<p><strong>Objective: </strong>To investigate the mechanism by which Sini decoction (, SND) improves renal fibrosis (Rf) in rats based on transforming growth factor β1/Smad (TGF-β1/Smad) signaling pathway.</p><p><strong>Methods: </strong>Network pharmacology was applied to obtain potentially involved signaling pathways in SND's improving effects on Rf. The targets of SND drug components and the targets of Rf were obtained by searching databases, such as the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCSMP) and GeenCard. The intersection targets of two searches were obtained and underwent signaling pathway analysis using a Venn diagram. Then experimental pharmacology was utilized to prove and investigate the effects of SND on target proteins in the TGF-β1/Smad signaling pathway. The Rf rat model was established by unilateral ureteral occlusion (UUO). The expression levels of transforming growth factor, matrix metalloproteinase-9 (MMP-9), matrix metal protease-2 (MMP-2), connective tissue growth factor (CTGF), and tissue inhibitor of metalloproteinase-1 (TIMP-1) were determined by Masson staining of rat renal tissue, and immunohistochemical methods. The expression levels of Smad3, Smad2, and Smad7 in renal tissue were determined by Western blotting (WB). The mechanism of the improving effects of SND on Rf was investigated based on TGF-β1/Smad signaling pathway.</p><p><strong>Results: </strong>A total of 12 drug components of Fuzi (<i>Radix Aconiti Lateralis Preparata</i>), 5 drug components of Ganjiang (<i>Rhizoma Zingiber</i>), and 9 drug components of Gancao (<i>Radix Glycy et Rhizoma</i>) were obtained from the database search, and 207 shared targets were found. A total of 1063 Rf targets were found in the database search. According to the Venn diagram, in total, 96 intersection targets were found in two database searches. The metabolic pathways involved included TGF-β signaling pathway, phosphatidylinositol-3-kinase/serine-threonine protein kinase signaling (PI3K/Akt) pathway, and hypoxia-inducible factor-1 (HIF-1) signaling pathway. Masson staining analysis showed that compared with the model group, the renal interstitial collagen deposition levels in the SSN and SND groups were significantly lower (<i>P <</i> 0.05). Immunohistochemical analysis, compared with the control group, the positive cell area expression levels of MMP-9/TIMP-1 and MMP-2/TIMP-1 in the kidney tissue of the model group were significantly decreased (<i>P <</i> 0.05, <i>P <</i> 0.01), and the positive cell area expression levels of CTGF and TGF-β1 were significantly increased (<i>P <</i> 0.01). Compared with the model group, the positive cell area expression levels of MMP-9/TIMP-1 and MMP-2/TIMP-1 in the kidney tissue of the SSN and SND groups were significantly increased (<i>P <</i> 0.05, <i>P <</i> 0.01), and the positive cell area expression levels of CTGF and TGF-β1 in the kidney tissue were significantly decreased (<i>P <</i> 0.05","PeriodicalId":94119,"journal":{"name":"Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan","volume":"44 2","pages":"362-372"},"PeriodicalIF":0.0,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10927398/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140178409","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
Protective effect of thyroid and restores of ovarian function of Buzhong Yiqi granule on experimental autoimmune thyroiditis in female rats. 补中益气颗粒对雌性大鼠实验性自身免疫性甲状腺炎的甲状腺和卵巢功能恢复的保护作用
Pub Date : 2024-04-01 DOI: 10.19852/j.cnki.jtcm.20240203.008
Wang Yuezhu, Zhang Yuyang, Qiao Jiajun, L U Yuyuan, Xia Zhongyuan

Objective: To observe the effects of Buzhong Yiqi granule on thyroid function and ovarian function in rats with experimental autoimmune thyroiditis (EAT).

Methods: EAT model was replicate by using the method of mixing and injecting porcine thyroglobulin with Freund's adjuvant and high iodine. Rats were randomly divided into normal control (NC) group, EAT model (EAT) group, selenium yeast (PC) group, low dose Buzhong Yiqi (BZYQ-L) group, medium dose Buzhong Yiqi (BZYQ-M) group and high dose Buzhong Yiqi (BZYQ-H) group. After two months of drug intervention according to dosage, enzyme-linked immunosorbent assay (ELISA) was used to measure the levels of free triiodothyronine (FT3), free thyroxine (FT4), thyroid-stimulating hormone (TSH), anti-thyroid peroxidase antibody (TPOAb), thyroglobulin antibody (TGAb) in peripheral blood of rats. The pathological changes of rat thyroid tissues were observed under light microscope with HE staining; ELISA was used to determine estradiol (E2), follicle-stimulating hormone (FSH), luteinizing hormone (LH), testosterone (T), anti-müllerian hormone (AMH), and the pathological changes of rat ovarian tissues were observed under light microscope with hematoxylin and eosin staining.

Results: Compared with the NC group, BZYQ granule improved the thyroid and ovarian tissue morphology, and the levels of TPOAb, TGAb and TSH in the model group rats significantly increased (P < 0.05), the thyroid tissue was severely destroyed, the levels of E2, FSH, LH, T, AMH significantly increased (P < 0.05), and the ovary exhibited polycystic changes; Compared with the model group, TSH level in the BZYQ-L group rats decreased (P < 0.05), FSH, T, AMH levels decreased (P < 0.05), in the BZYQ-M group TPOAb, TSH levels decreased (P < 0.05), FSH, LH, T, AMH levels significantly decreased (P < 0.05), BZYQ-H group TPOAb, TGAb, TSH levels significantly decreased (P < 0.05), FSH, LH, T, AMH levels significantly decreased (P < 0.05), with the greatest improvement and significantly better than selenium yeast group (P < 0.05).

Conclusions: BZYQ granule could regulate the thyroid function of EAT rats, reduce thyroid antibody titers, then act on the ovarian function, regulate hormone disorders, and alleviate the pathological damage of rat's ovarian tissues. The effect of high dose Buzhong Yiqi granule is the best.

目的观察补中益气颗粒对实验性自身免疫性甲状腺炎(EAT)大鼠甲状腺功能和卵巢功能的影响:方法:采用猪甲状腺球蛋白与弗氏佐剂和高碘混合注射的方法复制实验性自身免疫性甲状腺炎模型。将大鼠随机分为正常对照(NC)组、EAT模型(EAT)组、硒酵母(PC)组、低剂量补中益气(BZYQ-L)组、中剂量补中益气(BZYQ-M)组和高剂量补中益气(BZYQ-H)组。按剂量干预两个月后,用酶联免疫吸附试验(ELISA)检测大鼠外周血中游离三碘甲状腺原氨酸(FT3)、游离甲状腺素(FT4)、促甲状腺激素(TSH)、抗甲状腺过氧化物酶抗体(TPOAb)、甲状腺球蛋白抗体(TGAb)的水平。光镜下HE染色观察大鼠甲状腺组织的病理变化;ELISA检测雌二醇(E2)、卵泡刺激素(FSH)、黄体生成素(LH)、睾酮(T)、抗苗勒氏激素(AMH);光镜下苏木精和伊红染色观察大鼠卵巢组织的病理变化:与NC组相比,BZYQ颗粒改善了甲状腺和卵巢组织形态,模型组大鼠TPOAb、TGAb和TSH水平显著升高(P 0.05),甲状腺组织破坏严重,E2、FSH、LH、T、AMH水平显著升高(P 0.05),卵巢呈多囊性改变;与模型组相比,BZYQ-L组大鼠TSH水平降低(P 0.05),FSH、T、AMH水平下降(P 0.05),BZYQ-M组TPOAb、TSH水平下降(P 0.05),FSH、LH、T、AMH水平明显下降(P 0.05),BZYQ-H组TPOAb、TGAb、TSH水平明显下降(P 0.05),FSH、LH、T、AMH水平明显下降(P 0.05),改善幅度最大,明显优于硒酵母组(P 0.05):结论:布中酵母颗粒能调节EAT大鼠的甲状腺功能,降低甲状腺抗体滴度,进而作用于卵巢功能,调节激素紊乱,减轻大鼠卵巢组织的病理损伤。大剂量补中益气颗粒的效果最好。
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引用次数: 0
Complementary and alternative medicine on cognitive defects and neuroinflammation after sepsis. 补充和替代医学对败血症后认知缺陷和神经炎症的影响。
Pub Date : 2024-04-01 DOI: 10.19852/j.cnki.jtcm.20240203.002
L I Zhenxuan, Wang Xuerui, Luis Ulloa, Ayman Youssef, Bai Yunjing, X U Xiaolong, Liu Qingquan

Sepsis-associated encephalopathy (SAE) is a common manifestation of sepsis, ranging from mild confusion and delirium to severe cognitive impairment and deep coma. SAE is associated with higher mortality and long-term outcomes, particularly substantial declines in cognitive function. The mechanisms of SAE probably include neuroinflammation that is mediated by systemic inflammation and ischemic lesions in the brain, a disrupted blood-brain barrier, oxidative stress, neurotransmitter dysfunction, and severe microglial activation. Increasing evidence suggests that complementary and alternative medicine, especially Traditional Chinese Medicine (TCM), is favorable in alleviating cognitive decline after sepsis. Here, we summarized the studies of traditional herbal remedies, TCM formulas and acupuncture therapy in animal models of neurological dysfunctions after sepsis in recent decades and reviewed their potential mechanisms.

脓毒症相关脑病(SAE)是脓毒症的一种常见表现,其范围从轻微的意识模糊和谵妄到严重的认知障碍和深度昏迷。SAE 与较高的死亡率和长期预后相关,尤其是认知功能的显著下降。SAE 的发病机制可能包括由全身炎症和大脑缺血性病变、血脑屏障破坏、氧化应激、神经递质功能障碍和严重的小胶质细胞活化介导的神经炎症。越来越多的证据表明,补充和替代医学,尤其是中医(TCM),有利于缓解脓毒症后的认知能力下降。在此,我们总结了近几十年来传统中草药、中药配方和针灸疗法在败血症后神经功能障碍动物模型中的研究,并回顾了其潜在机制。
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引用次数: 0
Pharmacological potential of (L.) P. Royen (Sapodilla): a narrative review. (L.) P. Royen(无患子)的药理潜力:叙述性综述。
Pub Date : 2024-04-01 DOI: 10.19852/j.cnki.jtcm.2024.02.001
Priyanka Sharma, Aakash Deep, Harish Kumar, Nitin Bansal, Sanjiv Kumar, Arun, Davinder Kumar

Herbal medicine is safe and effective in treating various diseases. Traditional herbal medicine plays a tremendous role in treatment of various diseases and accompanying complications, hence herbal medicine requires remarkable attention in further research for the development of numerous active formulations for treatment of health troubles. The plant needs special consideration for development and research of unidentified compound and characterization of novel active molecules that overcome multiple pathological abnormalities. The genus Manilkara contains 135 plants around the world. This overview discusses all the virtues of most important and commonly used plant Manilkara zapota (L.) P. Royen (M. zapota), also known as Sapodilla. M. zapota has various traditional beneficial effects in treatment of various diseases and disorders dating back to prehistoric times and used in ancient traditional system of herbal medicine.

草药在治疗各种疾病方面安全有效。传统草药在治疗各种疾病和伴随的并发症方面发挥着巨大作用,因此,草药需要在进一步研究中得到高度重视,以开发出多种治疗健康问题的活性配方。在开发和研究未知化合物以及表征能克服多种病理异常的新型活性分子时,需要特别考虑到这种植物。Manilkara 属在全世界有 135 种植物。本综述讨论了最重要、最常用的植物 Manilkara zapota (L.) P. Royen(M. zapota)(又名 Sapodilla)的所有优点。Manilkara zapota 在治疗各种疾病和失调方面具有多种传统功效,其历史可追溯到史前时代,并被用于古老的传统草药系统中。
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引用次数: 0
期刊
Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan
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