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益气化痰活血法对AS粘附分子的影响及其与血脂异常证候的相关性
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摘要
目的:
     1通过观察调脂通脉颗粒对载脂蛋白E基因敲除(ApoE-/-)小鼠血脂水平及血清粘附分子sICAM-1、sVCAM-1的影响,对小鼠主动脉弓AS斑块的影响,及对小鼠主动脉弓NF-k B、ICAM-1和LFA-1表达的影响,探讨调脂通脉颗粒调节血脂及干预AS的可能作用机制,为益气化痰活血法指导血脂异常及AS的治疗提供实验依据。
     2通过观察血脂异常患者中医证候类型与血脂水平、血清粘附分子的关系,研究血脂异常患者证候分布规律,并初步探讨将TC、TG、HDL-C、s ICAM-1. sVCAM-1等血清检测指标作为血脂异常中医辨证依据的可行性,为血脂异常的中医辨证论治提供新思路。
     方法:
     1动物实验部分将40只6周龄ApoE-/-雄性小鼠随机分为模型组、血脂康组、调脂通脉颗粒低、中、高剂量组,每组8只,予高脂饮食结合药物饲养;另取8只相同遗传背景的C57BL/6雄性小鼠作为对照组,予普通饮食饲养。各组小鼠饲养12周后处死,血清学检测血脂、sICAM-1、sVCAM-1变化;主动脉弓根部石蜡切片苏木素伊红(HE)染色及马松(Masson)染色观察组织形态学变化;另取主动脉弓根部石蜡切片,行免疫组织化学染色法观察NF-k B、ICAM-1及LFA-1表达。收集数据后采用统计学方法分析,观察调脂通脉颗粒对以上指标的影响。
     2临床研究部分筛选120例于北京中医药大学东直门医院及北京市房山区大安山乡社区卫生服务中心门诊就诊的患者,根据相应纳入、排除标准收集血脂异常患者,签署知情同意书,采集患者一般资料并填写用于证候研究的临床调查量表,留取患者静脉血,血清学检测血脂、sICAM-1及sVCAM-1水平,另收集20例正常人作为对照组,研究内容同血脂异常患者。收集数据后进行统计分析观察血脂异常患者与正常人各项指标的差异;观察血脂异常不同证候类型间各项指标的差异;探讨将以上检测指标作为中医辨证依据的可行性。
     结果:
     1血脂检测表明,模型组、血脂康组、调脂通脉颗粒各组小鼠血清TC、LDL-C. HDL-C水平高于正常对照组;模型组、调脂通脉颗粒低剂量组TG水平高于正常对照组;调脂通脉颗粒中、高剂量组、血脂康组TG水平低于模型组。
     2ELISA法检测表明,调脂通脉颗粒各组、血脂康组、模型组小鼠血清sICAM-1、 sVCAM-1水平高于正常对照组;调脂通脉颗粒高剂量组血清sICAM-1、sVCAM-1水平低于模型组。
     3HE染色、Masson染色可见,对照组主动脉内膜光滑未见粥样斑块形成;模型组主动脉内膜增厚伴易损斑块形成;血脂康组及调脂通脉颗粒高剂量组内膜增厚伴稳定斑块形成。
     4免疫组化染色表明,模型组、血脂康组、调脂通脉颗粒各组主动脉弓NF-k B、ICAM-1及LFA-1表达高于正常对照组。调脂通脉颗粒高剂量组主动脉弓NF-k B、ICAM-1及LFA-1表达低于模型组。
     5临床研究发现,血脂异常患者证候分布比例由高到低依次为:肝肾阴虚组(40.83%)>阴虚阳亢组(25.83%)>痰浊阻滞组(20.83%)>脾肾阳虚组(8.33%)>气滞血瘀组(4.17%)。
     6各证候类型的血清TC水平由高到低依次为:气滞血瘀组>肝肾阴虚组>痰浊阻滞组>阴虚阳亢组>脾肾阳虚组>正常对照组。肝肾阴虚组、痰浊阻滞组、阴虚阳亢组及气滞血瘀组血清TC水平高于正常对照组。气滞血瘀组TC水平明显高于肝肾阴虚组及阴虚阳亢组。
     7各证候类型的血清TG水平由高到低依次为:痰浊阻滞组>阴虚阳亢组>肝肾阴虚组>脾肾阳虚组>气滞血瘀组>正常对照组。痰浊阻滞组及阴虚阳亢组TG水平高于正常对照组。痰浊阻滞组血清TG水平明显高于阴虚阳亢组。
     8各证候类型的血清HDL-C水平由低到高依次为肝肾阴虚组<正常对照组<阴虚阳亢组<脾肾阳虚组<痰浊阻滞组<气滞血瘀组,组间比较无差异。
     9血脂异常患者血清sICAM-1水平高于正常人,各证候类型血清sICAM-1水平由高到低依次为:阴虚阳亢组>肝肾阴虚组>脾肾阳虚组>痰浊阻滞组>气滞血瘀组>正常对照组。各证候组的血清sICAM-1水平均较正常对照组升高,但各证候组间无差异。
     10血脂异常患者血清sVCAM-1水平高于正常人,各证候类型血清sVCAM-1水平由高到低依次为:肝肾阴虚组>痰浊阻滞组>阴虚阳亢组>脾肾阳虚组>气滞血瘀组>正常对照组。各证候组的血清sVCAM-1水平均较正常对照组升高,但各证候组间无差异。
     结论:
     1以益气化痰活血法为指导的调脂通脉颗粒可在一定程度上缓解AS病理学改变,这可能与其降低血清TG、sICAM-1及sVCAM-1水平,抑制NF-kB. ICAM-1及LFA-1在斑块处的表达有关,抑制粘附分子及相关炎性因子表达可能是调脂通脉颗粒防治AS的作用机制之一。
     2肝肾阴虚证、阴虚阳亢证及痰浊阻滞证是血脂异常患者的重要证候类型,脾肾阳虚证出现较少,气滞血瘀证比例最少。
     3血脂异常患者的血清TC水平升高与气滞血瘀证密切相关;血清TG水平升高与痰浊阻滞证联系紧密;可考虑将其作为相应证候类型的辨证依据。
     4血脂异常患者的血清sICAM-1及sVCAM-1水平明显高于正常人,提示血脂异常早期阶段就已发生与AS相关的血管炎性反应。但本研究中未观察到其差异与不同证候类型存在相关性,暂不考虑将其作为辨证依据。
Objective:To study the effect of "Tiaozhitongmai" granules on serum lipid,atherosclerosis plaque and NF-κ B,ICAM-1and LFA-1's expressions in the aortic arch of ApoE-/-Mice. Provided experimental foundation for the method of reinforcing Qi as well as removing phlegm and stagnant blood to treat blood lipid abnormality and AS. To study the distribution rule of TCM syndromes of dysl ipidemia, and the relationship between that and serum level of TC, TG, HDL-C, sICAM-1and sVCAM-1.
     Methods:In the part of animal research, Six week-old male C57BL/6mice and ApoE-/-mice were divided into control group, model group, Xuezhikang group and "Tiaozhitongmai" granule group (low-,medium-, high-dosage) There were8mice in each group. They were fed by chow diet combined with medicine for12weeks. Changes in serum lipid, sICAM-1and sVCAM-1, as well as that of atherosclerosis and expressions of NF-k B, ICAM-1, and LFA-1in aortic arch were monitored by automatic biochemical serum analysis machine, ELISA, HE staining, and Immunohistochemical staining respectively. In the part of clinical research, we selected120patients with dyslipidemia according inclusion and exclusion criteria. Collecting their general information and finishing clinical research form after signed informed consent form. Then use automatic biochemical serum analysis machine and ELISA to monitor patients'serum level of lipid, sICAM-1and sVCAM-1respectively. Use statistic approach to analyze the relationship between patients'medical indexes of a test and TCM syndromes.
     Results:
     1By comparison to the control group, the serum levels of TC, LDL-C, and HDL-C have significantly increased in ApoE-/-mice (P<0.05), so was the serum levels of TG in the modeling group and in "Tiaozhitongmai" granule low-dosage group (P<0.05).
     2Compared with control group, serum level of sICAM-1and sVCAM-1significantly increased in ApoE-/-mice(P<0.05), and compared with model group, serum level of sICAM-1and sVCAM-1significantly decreased (P <0.05)
     3The HE staining showed that there were no atherosclerosis plaques formed in control group, yet vulnerable atherosclerosis plaques was formed in model group, and that stable atherosclerosis plaques were also formed in "Xuezhikang" group and "Tiaozhitongmai" granule high-dosage group.
     4In comparison to the control group, NF-κ B、ICAM-1and LFA-1expression significantly increased in ApoE-/-mice (P<0.05), while, expressions of NF-κ B、ICAM-1and LFA-1decreased (P<0.05) in "Tiaozhitongmai" granule high-dosage group comparing to the modeling group.
     5In clinical research, we found the distribution rule of TCM syndrome was:Ganshenyinxu (40.83%)> Yinxuyangkang (25.83%)> Tanzhuozuzhi (20.83%)>Pishenyangxu (8.33%)> Qizhixueyu (4.17%)
     6The syndrome type of TC level from high to low in the order was: Qizixueyu> Ganshenyinxu> Tanzhuozuzhi> Yinxuyangkang> Pishenyangxu>normal group. Syndrom of Ganshenyinxu, Tanzhuozuzhi, Yinxuyangkang and Qizhixueyu had higher TC level than normal group. Syndorm of Qizhixueyu had higher TC level than that of Ganshenyinxu and Yinxuyangkang.
     7The syndrome type of TG level from high to low in the order was: Tanzhuozuzhi> Yinxuyangkang> Ganshenyinxu> Pishenyangxu> Qizhixueyu>normal group. Syndrom of Tanzhuozuzhi and Yinxuyangkang had higher TG level than normal group. Syndorm of Tanzhuozuzhi had higher TG level than that of Yinxuyangkang.
     8The syndrome type of HDL-C level from low to high in the order was: Ganshenyinx     9The patients with dyslipidemia had higher serum sICAM-1level than normal group. The syndrome type of sICAM-1level from high to low in the order was:Yinxuyangkang> Ganshenyinxu> Pishenyangxu> Tanzhuozuzhi> Qizhixueyu> normal group. There was no significant difference between six groups.
     10The patients with dyslipidemia had higher serum sVCAM-1level than normal group. The syndrome type of sVCAM-1level from high to low in the order was:Ganshenyinxu> Tanzhuozuzhi> Yinxuyangkang> Pishenyangxu> Qizhixueyu> normal group. There was no significant difference between six groups.
     Conclusion:
     1"Tiaozhitongmai" granule appeared to be effective in decreasing the serum level of TG, sICAM-1and sVCAM-1, as well as the expressions of NF-κ B, ICAM-1, and LFA-1in the aortic arch of ApoE-/-mice.
     2The syndrome of Ganshenyinxu, Yinxuyangkang and Tanzhuozuzhi is one of the important syndrome types in patients with dyslipidemia, Pishenyangxu appear less, the lowest proportion is Qizhixueyu.
     3Dyslipidemia in patients with higher TC is closely related to the syndrome of Qizhixueyu, elevated TG and the syndrome of Tanzhuozuzhi connected, may identify those two syndrome based on serum TC and TG level.
     4The serum sICAM-1and sVCAM-1level of patients with dyslipidemia were significantly higher than normal people, that means the inflammatory reaction connected with AS had already happened in the early stage of dyslipidemia. But there was no correlation between serum adhesion molecular level and different syndrome types.
引文
[1]Libby P, Ridker PM, MaseriA. Inflammation in atherosclerosis [J]. Circulation,2002,105(9):1135-1143.
    [2]邓天真.心脑血管疾病的中医辨证治疗[J].当代医学,2013,19(11):148-149.
    [3]Moghadasian M H. Experimental atherosclerosis:a historical overview[J]. Life Sci,2002,70:855-865.
    [4]杨永宗.动脉粥样硬化性心血管病基础与临床[M].2版.北京:科学出版社,2009:53-102.
    [5]Jia G,Cheng G, Agrawal DK. Differential effects of insulin-like growth factor-1 and atherom a-associated cytokines on cell proliferation and apoptosis in plaque smooth muscle cells of symptomatic and asymptomatic patients with carotid stenosis [J]. Immunol Cell Biol, 2006,84(5):422-429.
    [6]阮秋蓉.干细胞/组细胞与动脉粥样硬化研究进展[J].中国动脉硬化杂志,2011,19(5):375-379.
    [7]杨琼,武春艳,江璐,等.剪切应力-内皮细胞-Caveolin-1信号通路在动脉粥样硬化中的作用[J].中国动脉硬化杂志,2009,17(3):237-240.
    [8]Frangogiannis NG. The immune system and cardiac repair [J]. Pharmacol Res,2008,58 (2):88-111.
    [9]Ross R. Atheroselerosis-an inflammatory disease[J]. N Engl J Med, 1999,340(2):125-126.
    [10]STOCKER R, KEANEY JF JR. Role of oxidative modifications in atherosclerosis[J]. Physiol Rev,2004,84:1381-1478.
    [11]Eikelenboom P, van Exel E, Hoozemans J, et al. Neuroinflammation-an early event in both the history and pathogenesis of Alzheimer's disease [J], Neurodegener Dis,2010,7 (1-3):38-41.
    [12]Aggarwal BB. Nuclear factor-kappa B:the enemy within [J]. Cancer Cell,2004,6:203-208.
    [13]Shishodia S, Aggarwal BB. Nuclear factor-kappa B activation mediates cellular transformation, proliferation, invasion angiogenesis and metastasis of cancer [J].CancerTreat Res,2004,119:139-173.
    [14]Neumann M, Naumann M. Beyond IJBs:alternative regulation of NF-κB activity [J]. FASEB J Rev,2007,21:2642-2654. &
    [15]Gordon JW, Shaw JA, Kirshenbaum LA. Multiple facets of NF-κ B in the heart:to be or not to NF-κ B [J]. Circ Res,2011,108 (9):1122-1132.
    [16]Kawamura N, Kubota T, Kawano S, et a.1 Blockade of NF-κ B improves cardiac function and survival without affecting inflammation in TNF-A-induced cardiomyopathy [J]. Cardiovasc Res,2005,66:520-529.
    [17]Brown M, Me Guinness M, Wright T, etal. Cardiac-specific blockade of NF-kB in cardiac pathophysiology:differences between acute and chronic stimuli in vivo[J]. Am J PhysiolHeartCirc Physio,12005, 289:H466-H476.
    [18]Wong ET, Tergaonkar V. Roles of NF-kappa B in health and disease: mechanisms and therapeutic potential[J]. Clin Sci (Lond),2009,116(6): 451-465.
    [19]Hayden MS, Ghosh S. Signaling toNF-kB [J]. Genes Dev,2004,18: 2195-2224.
    [20]Gilmore TD. Introduction to NF-JB:players, pathways, perspectives [J]. Onco-gene,2006,25:6680-6684.
    [21]Janssens S, Tschopp J. Signals from within:the DNA-damage-induced NF-k B response[J]. Cell Death Differ,2006,13:773-784 (review),21: 2642-2654
    [22]Neumann M, Naumann M. Beyond NF-kB s:alternative regulation of NF-kB activity [J].FASEB J Rev,2007,21:2642-2654.
    [23]Lorenzo 0, Picatoste B, Ares-Carrasco S, et al. Potential role of nuclear factor k B in diabetic cardiomyopathy[J].Mediators Inflamm,2011,2011:652097.
    [24]Perkins ND. Post-translational modifications regulating the activity and function of the nuclear factor kappa B pathway[J]. Oncogene, 2006,25 (51):6717-6730.
    [25]Rodriguez-Porcel M, Leman LO, Holmes DR Jr, et al. Chronic antioxidant supplementation attenuates nuclear factor-kappaB activation and preserve endothelial function in hypercholesterolemic pigs[J]. Cardiovasc Res,2002,53:1010-1018.
    [26]刘小玉,冯义朝.胃癌及癌前病变中COX-2和NF-k B65蛋白表达及其相关性研究[J].西部医学,2013,25(2):201-203.
    [27]Liu Shu-Fang, Asrar B. Malik. NF-k B activation as a Pathologioal Mechanism of septic shock and inflammation[J].physiol Lung Cell Mol Physiol,2006,290:L622-L645.
    [28]Jiang B, Xu S, Hou X, et al. Temporal control of NF-k B activation by ERK differentially regulates interleukin 13 induced gene expression[J]. BiolChem,2004,279(2):1323-1329.
    [29]Zhuang R, Lin MX, Song QY, et al. Effects of curcumin on the expression of nuclear factor kappaB and intercellular adhes ionmolecular 1 in rats with cerebral ischemia reperfusion injury[J].Nan Fang Yi Ke Da Xue Xue Bao,2009,29(6):1153-1155.
    [30]Gareus R, Kotsaki E, Xanthoulea S, et al. Endothelial cell-specific NF-k B inhibition protects mice from atherosclerosis [J]. Cell Metab, 2008,8(5):372-383.
    [31]LiaoPH, Du XK, Huang B, et al. Effect of act ivat ion of nuclear factor kappaB on modulation of secretion of intercellular adhesion molecule 1 by A549 cell[J]. Zhongguo Wei Zhong Bing Ji Jiu Yi Xue,2009,21(3): 151-154.
    [32]Liu M, Kluger MS, D'A lession A, et al. Regulation of arterial venous differences in tumor necrosis factor responsiveness of endothelial cells by anatomic context[J].Am J Pathol,2008,172(4): 1088-1099.
    [33]Rabquer BJ, Pakozdi A, Michel JE, et al. Junctional adhesion molecule C mediates leukocyte adhesion to rheumatoid arthritis synovium [J]. ArthritesRheum,2008,58(10):3020-3029.
    [34]Jianli NIU, Pappachan B. KOLATTUKUDY. Role of MCP-1 in cardiovascular disease:molecular mechanisms and clinical implications. Clinical Science.2009,117:95-109.
    [35]Francescato HD, Costa RS, Scavone C, et al. Parthenolide reduces cisplatin-induced renal damage [J]. Toxicology,2007,23, (1):64.
    [36]Menno PJ. De Winther, Edwin Kanters, Georg Kraal,et al. Nuelear Factor-KB Signaling in Atherogenesis[J],Arterioscler Thromb Vase Biol,2005,25:904-914.
    [37]Lu L, Liu H, Peng J, et al. Regulations of the key mediators in inflammation and atherosclerosis by aspirin in human macrophages [J]. Lipids Health Dis,2010,9:16.
    [38]岳兵,陈志坚,王彦富等.NF-k B在AngⅡ介导THP-1巨噬细胞源性泡沫细胞胆固醇流出及ABCA1表达调控过程中的作用研究[J].中国免疫学杂志,2008,24:398-402.
    [39]Newby AC. Metal loproteinase expression in monocytes and macrophages and its relationship to atherosclerotic plaque instability[J]. Arterioscler Thromb Vase Biol,2008,28(12):2108-2114.
    [40]Ye ZB,Li ZL, Song SD, et al. Effect of rosiglitazone on tumor necrosis factor alpha induced nuclear factor kappaB and coupl ing factor 6 expressions in human umbilical vein endothelial cells [J]. Nan Fang Yi Ke Da Xue Xue Bao,2008,28(9):1642-1645.
    [41]FunakoshiTago M, Tanabe S, TagoK, et al. Licochalcone a potently inhibits tumor necrosis factor alpha induced nuclear factor kappaB activation through the direct inhibition of I k B kinase complex activation[J]. MolPharmaco,1 2009,76(4):745-753.
    [42]Gacho 0, Legrand V, Biessaux X, et al. Long-term prognostic significance of high sensitivity C-reactive protein before and after coronary angioplasty in patients with stable angina pectoris[J]. Am J Cardio,12007,99(1):31-35.
    [43]范丹丹,翟桂兰,祝焕林.牛磺酸对动脉粥样硬化兔NF-KB信号转导途径的影响[J].中国现代医学杂志,2013,23(17):30-34.
    [44]Kumpf 0,Hamann L, Schlag PM, et al. Pre-and postoperative cytokine release after in vitro whole blood lipopolysaccharide stimulation and frequent Toll-like receptor 4 polymorphisms [J]. Shock.2006; 25(2): 123-128.
    [45]Gioannini TL, Weiss JP. Regulation of interactions of Gramnegative bacterial endo toxins with mammal ian cells [J]. Immunol Res. 2007; 39(13):249-260.
    [46]张代娟,刘同美,刘江月,等.青心酮防治动脉粥样硬化与TLR4信号转导途径的关系[J].中药新药与临床药理.2009,20(5):404-407.
    [47]陈嘉勤,柳维林,张川湘,等.TLR4信号通路参与有氧运动对ApoE-/-小鼠血管炎性损伤的修复[J].体育科学,2011,31(8):53-58.
    [48]杨娟,王洪新,张英杰,等.TLR4/NF-k B信号通路在黄芪甲苷抑制异丙肾上腺素诱导大鼠心肌肥厚中的作用[J].中国动脉硬化杂志,2013,21(7):577-582.
    [49]Rothlein R, Dustin ML, Marlin SD, et al. A human intercellular adhesion molecule-1 (ICAM-1) distinct from LFA-1[J]. J Immunol.1986, 137 (4):1270-1274.
    [50]Ghaisas NK, Shahi CN, Foley B, et al. Elevated levels of circulating soluble adhesion molecules in peripheral blood of patients with unstable angina [J]. Am J Cardiol,1997,80 (5):617-619.
    [51]Osborn L,Hession C,Tizard R,et al.Direct expression cloning of vascular cell adhesion molecule-1, a cytokine-induced endothelial protein that binds to lymphocytes. Cell.1989,59(6):1203-1211.
    [52]Gu HF, Ma J, Gu KT, et al. Association of intercellular adhesion molecule 1 (ICAM1) with diabetes and diabetic nephropathy [J]. Front Endocrinol (Lausanne),201,3:179.
    [53]Alcaide P, AuerbachS, Luscinskas F W. Neutrophil recruitment under shear flow:it's all about endothelial cell rings and gaps [J]. Microcirculation,2008,16(1):43.
    [54]刘应柯,张玉峰,刘尚岭,等.脂脉宁对动脉粥样硬化家兔氧化应激反应及LDL-R, VCAM-1基因表达的影响[J].中国实验方剂学杂志,2011,17(20):214.
    [55]白卫娜,陈英珠,闫静辉,等.柿叶总黄酮对apoE-/-小鼠动脉粥样硬化病变中粘附分子表达的影响[J].南京中医药大学学报,2013,29,(1):35-38.
    [56]王健美,王宇,闫承慧,等.西格列汀延缓或阻止动脉粥样硬化作用的实验研究[J].中国临床药理学杂志,2013,29(12):945-947.
    [57]张立涛,于织波,赵鹤龄.辛伐他汀预处理对脓毒症大鼠心肌细胞ICAM-1表达的影响及意义[J].河北医药,2013,35(19):2896-2898.
    [58]张彦红,朱磊,陈杰,等.益脑康对动脉粥样硬化性缺血中风大鼠脑组织和血液ICAM-1表达的影响[J].中医药临床杂志,2013,25(7):568-570.
    [59]陈文强,黄小波,王宁群,等.陈皮半夏对颈动脉硬化家兔血管细胞黏附分 子-1及基质金属蛋白酶-9表达的影响[J].中国中医药信息杂志,2013,20(11):34-36.
    [60]祝光礼,魏丽萍,刘昭.冠心合剂活性成分对TNF一α损伤人脐静脉内皮细胞分泌VCAM一1. ICAM-1及E-selectin的影响研究[J].中华中医药学刊,2013,31(8):1576-1578.
    [61]李骥.茯苓配合有氧运动对大鼠血脂和主动脉弓ICAM-1.LFA-1及TF表达的影响[D].武汉.武汉体育学院:2009.
    [62]吴文竹,张晓艳,周志上,等.老年颈动脉粥样硬化超声狭窄程度分型与中医证型的关系[J].武汉大学学报(医学版),2012,33(6):921-923.
    [63]韩轶,翟雪芹,王晓峰.冠心病中医证型与颈动脉粥样硬化斑块的相关性研究[J].陕西中医,2013,34(3):290-292.
    [64]徐辉,顾耘.颈动脉粥样硬化的中医症候特征及分类[J].中国老年学杂志,2012,11(32):4913-4915.
    [65]王玉燕,杜武勋,魏营,等.冠心病不同证型与颈动脉内-中膜厚度关系的研究[J].山西中医,2009,25(2):34-36.
    [66]杨东辉,孙博,郭艳艳.冠心病患者中医证型与颈动脉内膜中层厚度及踝臂指数的相关性研究[J].云南中医中药杂志,2009,30(9):5-6.
    [67]苏建春,于云华,塔衣尔江,等.下肢动脉粥样硬化与相关影响因素和疾病的中医证型特点分析[J].中华中医药杂志,2012,27(5):1461-1463.
    [68]陈颖,崔英子,邓悦.冠状动脉粥样硬化性心脏病中医证候特征的文献回顾分析[J]环球中医药,2012,5(12):889-892.
    [69]王椿野,赵振武,李新龙,等.基于现代文献的动脉粥样硬化中医病机研究[J].环球中医药,2013,6(2):92-95.
    [70]张燕,韩旭.冠状动脉粥样硬化性心脏病中医证候要素与现代化指标相关性的探讨[J].环球中医药,2012,5(12):893-896.
    [71]申定珠,陈川,陈久林,等.首参颗粒对颈动脉粥样硬化患者血脂及炎症因子的影响[J].中华中医药学刊,2014,32(1):22-24.
    [72]刘蓓,陈立新,郭鹏,等.四妙勇安汤活性部位对ApoE基因敲除小鼠动脉粥样硬化的药效学研究[J].中西医结合心脑血管病杂志,2013,11(4):450-451.
    [73]张海燕,唐农,葛金文,等.五脏温阳化瘀汤对动脉粥样硬化血管性痴呆大鼠海马组织Nrf2蛋白通路的影响[J].云南中医学院学报,2013,36(3):8-11.
    [74]谢心,吴坚,竺春玲,等.益气养阴方对动脉粥样硬化大鼠免疫炎症因子hs-CRP、sVCAM-1、sICAM-1影响的实验研究[J].江苏中医药,2013,45(3):73-74.
    [75]和殿峰.滋阴活血法治疗糖尿病合并冠状动脉粥样硬化性心脏病临床分析[J].中外医疗,2013,12:92-93.
    [76]陈刚.中药降脂汤治疗高脂血症54例临床观察[J].湖北科技学院学报(医学版),2013,27(4):323-325.
    [77]蔡云,张斌霞,王紫逸,等.血脉通颗粒治疗亚临床颈动脉粥样硬化(肾阴亏虚瘀互结证)的临床研究[J].2014,37(1):164-167.
    [78]贾燕珺.小檗碱的抗动脉粥样硬化作用及其机制[J].中国动脉硬化杂志。2013,21(4):364-368.
    [79]尹承华,毕大鹏,杜敏.通心络胶囊对阿司匹林抵抗患者血小板聚集的影响[J].中国中西医结合杂志,2010,30(4):380-382.
    [80]陈章强,洪浪,王洪,等.通心络胶囊对原发性高血压伴糖尿病患者血小板活化因子和炎症因子及内皮功能的影响[J].中国中西医结合杂志,2010,30(4):376-379.
    [1]Ross R. Atherosclerosis-an inflammatory disease. N Engl J Med, 1999,340(2):115-126
    [2]Libby P, Ridker PM, MaseriA. Inflammation in atherosclerosis [J].Circulation,2002,105(9):1135-1143.
    [3]邓天真.心脑血管疾病的中医辨证治疗[J].当代医学,2013,19(11):148-149.
    [4]Poston RN, Haskard DO, Coucher JR, et al. Expression of intercellular adhesion molecule-1 in atherosclerotic plaques [J].Am J Pathol,1992, 140:665-673.
    [5]Pr inteseva OY, Peclo MM, Gown AM. Various cell types in human atherosclerotic lesions express ICAM-1:Further immunocytechemical and immuno chemical studies employing monoclonal antibody 10 F3[J].Am J Pathol,1992,140:889-896.
    [6]Morishita R, Sugimoto T; Aoki M, et al. In vivo transfection of cis element "decoy" against Nuclearfactor-k B binding site prevents myocardial infarction [J].Nat Med,1997,3:894-899.
    [7]杨惠民,盛彤,韩丽蓓,等.调脂通脉颗粒治疗老年高脂血症痰瘀证的临床研究.中华中医药杂志[J]2005,20(4):247-248.
    [8]徐叔云,卞如濂,陈修.药理实验方法学[M].北京:人民卫生出版社,2002.
    [9]刘剑刚,董国菊,史大卓,等.载脂蛋白E基因敲除小鼠不同周龄动脉粥样硬化的病理变化.中国动脉硬化杂志,2005,13(6):689-692.
    [10]Sunny H. Zhang, Reddick RL,Piedrahita JA, Maeda N et al. Spontaneous hypercholesterolemia and arterial lesions in mice lacking aopolipoprotein E. Science,1992,258 (10):468-471.
    [11]Gleissner Ca, Leitinger N,Ley K.Effects of native and modified low-density lipoproteins on monocyte recruitment in atherosclerosis[J]. Hypertension,2007,50(2):276-283.
    [12]Benjamin JA, Mohamad N,Karol EW, et al.Antiinf lamma t or yp roper t ies of HDL[J].Circ Res,2004,95 (8):764-772.
    [13]中国成人血脂异常防治指南制订联合委员会,中国成人血脂异常防治指南,中华心血管病杂志,2007,35(5):390-419.
    [14]Stampter MJ, Krauss RM, Ma J, m,etal. A prospective study of tryiglyceride level, low-dens i ty lipoprotein par ticle diameter and risk of myocardial infarction[J]. JAMA,1996,276:882.
    [15]孙学刚,曾平,范钦等.动脉粥样硬化中医病机的探讨.江苏中医药.2010,42(2):7-8.
    [1]张庆军,刘德培,梁值权.动脉粥样硬化的基础研究[J].中华医学杂志,2005,85(6):428-431.
    [2]Alcaide P, Auerbach S, Luscinskas F W. Neutrophil recruitment under shear flow:it's all about endothelial cell rings and gaps [J].Microcirculation,2008,16(1):43.
    [3]刘应柯,张玉峰,刘尚岭,等.脂脉宁对动脉粥样硬化家兔氧化应激反应及LDL-R, VCAM-1基因表达的影响[J].中国实验方剂学杂志,2011,17(20):214.
    [4]王新陆.脑血辨证[M].北京:中国医药科技出版社,2002:82-99.
    [5]王中琳.“血浊”病因病机浅谈[J].中国中医药现代远程教育,2009,7(8):81-82.
    [6]高颖等.试沦浊毒在血管性痴呆发病的作用[J].中国中医急症,2000,9(6):266-267.
    [7]王椿野,赵振武,李新龙,李麒豫,董洪坦,郭蓉娟.基于现代文献的动脉粥样硬化中医病机研究[J].环球中医药,2013,6(2):92-95.
    [8]闻莉,刘松林,梅国强.高脂血症的中医临床证型分布及辨证规律研究[J].中国中医基础医学杂志,2008,14(3):220.
    [9]中国成人血脂异常防治指南制订联合委员会,中国成人血脂异常防治指南,中华心血管病杂志,2007,35(5):390-419.

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