隔药饼灸对动脉粥样硬化兔血管内皮修复与基质细胞衍生因子1的影响
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  • 英文篇名:Effects of herbal-cake-separated moxibustion on the repair of vascular endothelial and SDF-1 in rabbits with atherosclerosis
  • 作者:沈菁 ; 刘涛 ; 刘霞 ; 葛君芸 ; 汪厚莲 ; 呙安林 ; 刘迈兰 ; 常小荣
  • 英文作者:SHEN Jing;LIU Tao;LIU Xia;GE Jun-yun;WANG Hou-lian;GUO An-lin;LIU Mai-lan;CHANG Xiao-rong;College of Acupuncture-Moxibustion and Tuina, Hunan University of CM;Hunan Junior College of TCM;Changsha Civil Vocational Technical School;
  • 关键词:动脉粥样硬化 ; 隔药饼灸 ; 总胆固醇 ; 三酰甘油 ; 低密度脂蛋白胆固醇 ; 高密度脂蛋白胆固醇 ; 基质细胞衍生因子1
  • 英文关键词:atherosclerosis;;herbal-cake-separated moxibustion;;total cholesterol (TC);;triglyceride (TG);;low-density lipoprotein cholesterol(LDL-C);;high-density lipoprotein cholesterol(HDL-C);;stromal cells derived factor 1(SDF-1)
  • 中文刊名:ZGZE
  • 英文刊名:Chinese Acupuncture & Moxibustion
  • 机构:湖南中医药大学针灸推拿学院;湖南中医药高等专科学校;长沙民政职业技术学院;
  • 出版日期:2019-02-03 19:24
  • 出版单位:中国针灸
  • 年:2019
  • 期:v.39;No.365
  • 基金:国家自然科学基金项目:81403486,81373716,81704182;; 国家973计划课题:2015CB554502
  • 语种:中文;
  • 页:ZGZE201902025
  • 页数:8
  • CN:02
  • ISSN:11-2024/R
  • 分类号:64-70+75
摘要
目的:观察隔药饼灸对动脉粥样硬化兔受损血管内皮结构的修复以及基质细胞衍生因子1(stromal cells derived factor 1,SDF-1)含量的影响。方法:将75只兔随机分为正常组、模型组、直接灸组、阿托伐他汀钙组与隔药饼灸组,每组15只,正常组采用普通饲料喂养,其余各组采用高胆固醇饲养法喂养12周制备动脉粥样硬化兔模型。隔药饼灸组与直接灸组选取两组穴位:"巨阙""天枢""丰隆"穴;"心俞""肝俞""脾俞"穴。每组穴隔日交替施灸,每穴灸30 min,每日1次,连续4周。阿托伐他汀钙组每天将阿托伐他汀钙片(1.96 mg·kg-1·d-1)碾成粉末后拌入第1餐饲料中喂食,造模后正常组、模型组不予上述干预处理,此3组同灸法时固定。以酶法测定总胆固醇(TC)、三酰甘油(TG)的含量;比色法测定低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)的含量;光学显微镜下观察兔主动脉血管壁形态结构;酶联免疫吸附法测定血清SDF-1的含量。结果:干预后,与正常组比较,模型组TC、TG、LDL-C明显升高(均P<0.01),HDL-C明显降低(P<0.01);与模型组比较,直接灸组、阿托伐他汀钙组、隔药饼灸组TC、TG、LDL-C均明显降低(均P<0.01),HDL-C升高(P<0.01,P<0.05)。与正常组相比,模型组主动脉壁结构受损明显;与模型组相比,阿托伐他汀钙组、隔药饼灸组内皮结构有显著好转,直接灸组的主动脉内皮病理变化也有减轻。干预后,与模型组相比,直接灸组、阿托伐他汀钙组、隔药饼灸组血清中SDF-1水平有不同程度的升高(P<0.05,P<0.01),隔药饼灸组血清中SDF-1水平高于直接灸组(P<0.05)。结论:隔药饼灸能促进血清SDF-1的表达,修复受损血管内皮结构。
        Objective To observe the effects of herbal-cake-separated moxibustion on the repair of damaged vascular endothelium structure and the content of stromal cells derived factor 1(SDF-1) in rabbits with atherosclerosis.Methods A total of 75 rabbits were randomly divided into a normal group, a model group, a direct moxibustion group,an atorvastatin calcium group and a herbal-cake-separated moxibustion group, 15 rabbits in each one. The rabbits in the normal group were fed with normal diet, and the remaining rabbits were fed with high-cholesterol diet for 12 weeks to prepare atherosclerotic model. Two groups of acupoints, one was "Juque"(CV 14), "Tianshu"(ST 25) and "Fenglong"(ST 40), the other one was "Xinshu"(BL 15), "Ganshu"(BL 18) and "Pishu"(BL 20), were applied in the direct moxibustion group and herbal-cake-separated moxibustion group; the two groups of acupoints were selected alternatively every other day. The moxibustion was given for 30 min per treatment, once a day for 4 weeks. The rabbits in the atorvastatin calcium group were treated with atorvastatin calcium tablets(1.96 mg·kg-1·d-1) which were crushed into powder and mixed into breakfast. After modeling, the rabbits in the normal group and model group received no treatment,and immobilized at the time when moxibustion was applied in other three groups. The levels of total cholesterol(TC)and triglyceride(TG) were measured by enzymic method; the low-density lipoprotein cholesterol(LDL-C) and high-density lipoprotein cholesterol(HDL-C) were measured by colorimetric method; the morphological structure of aortic wall was observed under optical microscope; the serum level of SDF-1 was determined by enzyme-linked immunosorbent assay(ELISA). Results After treatment, compared with the normal group, the levels of TC, TG and LDL-C were significantly increased in the model group(all P<0.01), and the level of HDL-C was decreased(P<0.01). Compared with the model group, the levels of TC, TG and LDL-C were significantly decreased(all P<0.01), and the level of HDL-C was significantly increased in the direct moxibustion group, atorvastatin calcium group and herbal-cake-separated moxibustion group(P<0.01, P<0.05). Compared with the normal group, the morphological structure of aortic wall was significantly damaged in the model group. Compared with the model group, the vascular endothelial structure was improved in the atorvastatin calcium group and herbal-cake-separated moxibustion group, and the pathological change of aorta endothelial in the direct moxibustion group was relieved. After treatment, compared with the model group, the level of SDF-1 was increased in the direct moxibustion group, atorvastatin calcium group and herbal-cake-separated moxibustion group(P<0.05, P<0.01); the level of SDF-1 in the herbal-cakeseparated moxibustion group was higher than that in the direct moxibustion group(P<0.05). Conclusion The herbalcake-separated moxibustion can promote the expression of SDF-1 in serum and repair the damaged aortic endothelial structure.
引文
[1]Roth GA,Johnson C,Abajobir A,et al.Global,regional,and national burden of cardiovascular diseases for 10 causes,1990 to2015[J].J Am Coll Cardiol,2017,70(1):1-25.
    [2]Goland S,Weinstein JM,Zalik A,et al.Angiogenic imbalance and residual myocardial injury in recovered peripartum cardiomyopathy patients[J].Circ Heart Fail,2016,9(11):e003349.
    [3]Krieger JR,Ogle ME,Mcfalinefigueroa J,et al.Spatially localized recruitment of anti-inflammatory monocytes by SDF-1α-releasing hydrogels enhances microvascular network remodeling[J].Biomaterials,2016,77:280-290.
    [4]Yu N,Zhang Z,Chen P,et al.Tetramethylpyrazine(TMP),an active ingredient of chinese herb medicine chuanxiong,attenuates the degeneration of trabecular meshwork through SDF-1/CXCR4axis[J].Plos One,2015,10(8):e0133055.
    [5]Puchert M,Engele J.The peculiarities of the SDF-1/CXCL12system:in some cells,CXCR4 and CXCR7 sing solos,in others,they sing duets[J].Cell Tissue Res,2014,355(2):239-253.
    [6]Yu P,Zhang Z,Li S,et al.Progesterone modulates endothelial progenitor cell(EPC)viability through the CXCL12/CXCR4/PI3K/Akt signalling pathway[J].Cell Proliferat,2016,49(1):48-57.
    [7]Silva M,Matthews ML,Jarvis C,et al.Meta-analysis of drug-induced adverse events associated with intensive-dose statin therapy[J].Clin Ther,2007,29(2):253-260.
    [8]哈略.艾灸对动脉粥样硬化小鼠炎性因子及MMP-9作用的实验研究[D].北京:北京中医药大学,2016.
    [9]卢享君.隔药饼灸对动脉粥样硬化兔胆固醇逆转运ABCA1的调节作用[D].长沙:湖南中医药大学,2016.
    [10]蔡海红,王玲玲,姜劲峰,等.温和灸对动脉粥样硬化家兔CD40-CD40L轴的影响[J].中国针灸,2014,34(1):55-60.
    [11]刘耀萌,崔莹雪,哈略,等.艾灸及艾烟对动脉粥样硬化模型小鼠血清TNF-α、hs-CRP及vWF的影响[J].中华中医药杂志,2016,31(4):1377-1379.
    [12]常小荣,周国平,严洁,等.隔药饼灸对高脂血症患者血清HDL-C、LDL-C及其它脂质含量的影响[J].针刺研究,1998,23(4):272-274.
    [13]常小荣,严洁,林亚平,等.隔药饼灸对高脂血症患者血浆TXB2、6-酮-PGF1α的影响[J].中国中医药科技,2000,7(5):329-330.
    [14]常小荣,严洁,易受乡,等.隔药饼灸治疗血脂异常的临床研究[J].中华中医药学刊,2010,28(1):8-10.
    [15]黄洁,曾文洁,常小荣.常小荣运用灸法治疗高脂血症经验[J].湖南中医杂志,2015,31(3):21-22.
    [16]刘未艾,常小荣,刘密,等.不同灸量隔药饼灸对高脂血症患者血脂及血液流变学的影响[J].辽宁中医杂志,2013,40(9):1787-1790.
    [17]王园园,龙民慧,周磊磊,等.兔动脉粥样硬化动物模型的建立和评价[J].实验动物科学,2008,25(3):18-21.
    [18]李忠仁.实验针灸学[M].北京:中国中医药出版社,2003:314-319.
    [19]岳增辉,严洁,常小荣,等.隔药饼灸对高脂血症兔主动脉内皮细胞超微结构的影响[J].中国针灸,2005,25(1):64-67.
    [20]岳增辉,常小荣,严洁,等.隔药饼灸对兔高脂血症合并动脉粥样硬化主动脉血管细胞粘附分子-1mRNA表达的影响[J].针刺研究,2006,31(3):145-148.
    [21]艾坤,艾潇,刘密,等.隔药饼灸对动脉粥样硬化兔总胆固醇和甘油三酯含量的影响[J].中华中医药学刊,2013,31(9):1857-1859.
    [22]常小荣,严洁,岳增辉,等.隔药饼灸对高脂血症兔血浆前列环素和血栓素含量的影响[J].中国组织工程研究,2004,8(33):7446-7447.
    [23]刘未艾,常小荣,刘密,等.隔药饼灸对动脉粥样硬化兔主动脉超微结构的影响[J].中华中医药学刊,2013,31(7):1499-1502.
    [24]常小荣,张亮,郁保生,等.隔药饼灸对动脉粥样硬化兔主动脉内皮细胞过氧化酶体增殖物激活型受体γ的影响[J].中医杂志,2011,52(8):683-685.
    [25]Yue ZH,He XQ,Chang XR,et al.The effect of herb-partition moxibustion on toll-like receptor 4 in rabbit aorta during atherosclerosis[J].J Acupunct Meridian Stud,2012,5(2):72-79.
    [26]刘未艾,常小荣,刘密,等.隔药饼灸对动脉粥样硬化兔主动脉内皮细胞PPARγ蛋白及斑块中MMP-9 mRNA表达的影响[J].中华中医药杂志,2013,28(1):193-197.
    [27]章海凤,刘密,常小荣,等.隔药饼灸对动脉粥样硬化兔主动脉内皮细胞NF-κB及ICAM-1 mRNA表达的影响[J].中华中医药杂志,2013,28(4):914-917.
    [28]吴焕淦,严洁,余曙光,等.灸法研究的现状与发展趋势[J].上海针灸杂志,2009,28(1):1-6.
    [29]Husna B,On T,Zhu YZ.Effects of purified salvia miltiorrhiza extract on cardiac vascular smooth muscle hypoxic cells[J].JPharmacol Sci,2007,104(3):202.
    [30]舒筱灿,周利玲,吴和平,等.大黄素对动脉粥样硬化的干预[J].中国组织工程研究,2007,11(34):6856-6859.
    [31]张兴燊,梁欣娜,王乃平,等.山楂水提液及山楂颗粒对高脂模型小鼠血脂的影响[J].时珍国医国药,2011,22(12):2905-2906.
    [32]罗玉梅,王贺振.山楂的化学成分及药理研究进展[J].时珍国医国药,2004,15(1):53-54.
    [33]洪行球,黄燕芬,符敏敏,等.二脱甲氧基姜黄素的降血脂和抗脂质过氧化作用[J].中国天然药物,2006,4(2):121-124.
    [34]李淑子,金在久,张善玉.泽泻不同提取物对高脂血症小鼠血脂及脂质过氧化的影响[J].中国实用医药,2008,3(32):7-9.
    [35]张春举,王丹,席蓓莉,等.泽泻对ox-LDL致血管内皮细胞损伤的保护作用[J].时珍国医国药,2013,24(4):796-798.
    [36]龙盼.血管内皮功能障碍与动脉粥样硬化[J].国际心血管病杂志,2011,38(2):79-81.
    [37]冉黎婧,史明霞,洪敏.间充质干细胞归巢机制研究进展[J].医学研究生学报,2014,27(4):423-426.
    [38]Rao S,Sengupta R,Choe EJ,et al.CXCL12 mediates trophic interactions between endothelial and tumor cells in glioblastoma[J].PLoS One,2012,7(3):e33005.
    [39]Newey SE,Tsaknakis G,Khoo CP,et al.The hematopoietic chemokine CXCL12 promotes integration of human endothelial colony forming cell-derived cells into imm ature vessel networks.[J].Stem Cells Dev,2014,23(22):2730-2743.
    [40]Ascione R,Rowlinson J,Avolio E,et al.Migration towards SDF-1selects angiogenin-expressing bone marrow monocytes endowed with cardiac reparative activity in patients with previous myocardial infarction[J].Stem Cell Res Ther,2015,6(1):53.
    [41]Wang J,Knaut H.Chemokine signaling in development and disease[J].Development,2014,141(22):4199.
    [42]张罡瑜,杭秋琦.趋化因子SDF-1研究进展[J].中国民族民间医药,2016,25(20):51-56.
    [43]Dai X,Tan Y,Cai S,et al.The role of CXCR7 on the adhesion,proliferation and angiogenesis of endothelial progenitor cells[J].JCell Mol Med,2011,15(6):1299-1309.
    [44]Yan X,Cai S,Xiong X,et al.Chemokine receptor CXCR7mediates human endothelial progenitor cells survival,angiogenesis,but not proliferation[J].J Cell Biochem,2012,113(4):1437-1446.
    [45]Oh BJ,Kim DK,Kim BJ,et al.Differences in donor CXCR4expression levelsare correlated with functional capacity and therapeutic outcome of angiogenic treatment with endothelial colony forming cells[J].Biochem Bioph Res Coc,2010,398(4):627-633.
    [46]Hocking AM.The role of chemokines in mesenchymal stem cell homing to wounds[J].Adv Skin Wound Care,2015,4(11):623.
    [47]Filippo TR,Galindo LT,Barnabe GF,et al.CXCL12 N-terminal end is sufficient to induce chemotaxis and proliferation of neural stem/progenitor cells[J].Stem Cell Research,2013,11(2):913-925.
    [48]Wu Y,Zhao RC.The role of chemokines in mesenchymal stem cell homing to myocardium[J].Stem Cell Rev,2012,8(1):243-250.
    [49]黎金凤.基质细胞衍生因子-1对外周血内皮祖细胞功能影响的研究进展[J].江西医药,2013,48(4):369-371.
    [50]Zhang M,Rehman J,Malik AB.Endothelial progenitor cells and vascular repair[J].Curr Opin Hematol,2014,21(3):224.
    [51]冯柳.SDF-1和VEGF对BMSCs向血管内皮细胞分化影响的研究[D].重庆:第三军医大学,2013.
    [52]秦臻,黄水清.当归补血汤对动脉粥样硬化兔内皮祖细胞及血清VEGF、SDF-1的影响[J].中国病理生理杂志,2012,28(2):211-215.
    [53]黎柏源,王茜云,赵永博,等.VEGF和SDF-1的协同作用对内皮祖细胞增殖与迁移的影响[J].现代生物医学进展,2016,16(11):2049-2053.
    [54]Jialal I,Fadini GP,Pollock K,et al.Circulating levels of endothelial progenitor cell mobilizing factors in the metabolic syndrome[J].Am J Cardiol,2010,106(11):1606-1608.

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