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舒血宁注射液对冠心病患者血液流变学和炎性因子的影响 被引量:5

Effects of Shuxuening injection on hemorheology and inflammatory factors in patients with coronary heart disease
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摘要 目的:观察舒血宁注射液对冠心病患者血液流变学和炎性因子的影响。方法:238例冠心病患者随机分为治疗组(129例)和对照组(109例),对照组采用常规西药治疗;治疗组在常规治疗基础上给予舒血宁注射液20ml,用5%葡萄糖注射液稀释成250ml,静脉滴注,1次/d。两组患者均治疗14d为1疗程。结果:①治疗组总有效率(86.0%)显著好于和对照组(64.2%),P<0.05;②治疗后治疗组全血黏度高切变率[ηbH(3.8±1.1)mPa/s∶(5.9±1.2)mPa/s]、全血黏度低切变率[ηbL(12.8±2.1)mPa/s∶(15.2±2.0)mPa/s]、血浆比黏度[ηp(2.2±0.2)mPa/s∶(3.0±0.4)mPa/s]、全血还原黏度[ηH(10.8±2.2)mPa/s∶(13.9±3.5)mPa/s]、血细胞比容[HCT(0.7±0.1)∶(0.8±0.1)]和纤维蛋白原[Fib(4.0±0.9)g/L∶(4.4±1.1)]g/L均较治疗前明显下降(P均<0.05),而对照组治疗前后比较除HCT、Fib外其它指标差异无显著性(P>0.05);治疗后两组比较,治疗组除HCT、Fib外其它指标明显优于对照组(P<0.05);③治疗后两组白细胞介素-6[治疗组(23.5±14.5)ng/L∶(59.3±12.1)ng/L,对照组(40.3±16.2)ng/L∶(61.6±14.7)ng/L]、肿瘤坏死因子α[治疗组(40.3±16.2)ng/L∶(254.4±55.6)ng/L,对照组(127.5±31.8)ng/L∶(257.0±44.9)ng/L]和高敏C反应蛋白[治疗组(4.1±0.9)mg/ml∶(6.1±1.2)mg/ml,对照组(5.0±1.0)mg/ml∶(6.0±1.1)mg/ml]均较治疗前明显下降(P均<0.05),治疗后两组比较,治疗组各指标均明显优于对照组(P均<0.05);④治疗后治疗组的一氧化氮[NO(48.2±7.2)mmol/L∶(43.4±8.5)mmol/L]、内皮素[ET(82.7±7.3)ng/L∶(89.2±12.5)ng/L]及NO/ET[(0.58±0.14)∶(0.49±0.11)]均较治疗前有非常明显的改善(P均<0.05),而对照组治疗前后差异则无显著性(P均>0.05)。结论:舒血宁注射液能明显降低冠心病患者的血液黏度,炎性因子水平,进而调节血管内皮活性,增加供血量,显著提高疗效。 Objective: To investigate the effects of Shuxuening injection on hemorheology and inflammatory factors in patients with coronary heart disease (CHD), Methods: A total of 238 eases with CHD were randomly divided into treatment group (n= 129) and control group (n= 109) . The control group was given routine therapy. The treatment group were given Shuxuening injection 20 ml (1 time/d, iv drop) based on routine therapy. The two group were trea- ted for 14d all. Results: (1)The total effective rate (86.0%) of treatment group was more than that of control group (64. 2%), P〈O. 05; (2)After treatment, η/bH [(3. 8±1.1) mPa/s vs. (5.9±1.2) mPa/s], ηbL [(12. 8±2. 1) roPa/s vs. (15.2±2.0) mPa/s], r/p [ (2.2±0.2) mPa/s vs. (3.0±0.4) mPa/s], r/H [ (10.8±2.2) mPa/s vs. (13.9± 3.5) mPa/s], HCT [ (0.7±0.1) vs. (0.8±0.1)], and Fib [Fib (4.0±0.9) g/L vs. (4.4±1.1) g/L] in treat- ment group were significantly decreased compared with before therapy (P〈0.05 all) , while there were no significant difference except for HCT and Fib in control group (P〉0.05). There were significant difference in above indexes ex- cept for HCT and Fib between the two groups after treatment (P〈0.05) ; (3)After treatment, IL--6 [treatment group (23.5±14.5) ng/L vs. (59.3±12.1) ng/L, control group (40. 3±6.2) ng/L vs. (61.6±14.7) ng/L], TNF-α [treatment group (40. 33±16.2) ng/L vs. (254.4±55.6) ng/L, control group (127.5±31.8) ng/L vs. (257. 0± 44. 9) ng/L], and hs--CRP [treatment group (4. 1:]=0. 9) mg/ml vs, (6.1±1.2) mg/ml, control group (5.0±1. 0) mg/ml vs. (6.0±1.1) mg/ml] in the two groups were significantly decreased (P〈0.05 all), but the treatment group had a better result compared with control group (P〈20.05) ; (4)After treatment, NO [(48.2±7.2) mmol/L vs. (43.4 ±8.5) mmol/L], ET[(82.7±7.3) ng/Lvs. (89.2±12.5) ng/L], and NO/ET [(0. 58±0.14) vs. (0.49±0.11)] were significantly improved in treatment group (P〈0. 05 all), but the control group no produced significant difference (P〉0. 05 all). Conclusion: Shuxuening injection can significantly reduce blood viscosity, inflammatory factors, im- prove blood vassel endothelial function and increase blood stream and therapeutiz effect.
出处 《心血管康复医学杂志》 CAS 2010年第5期552-555,共4页 Chinese Journal of Cardiovascular Rehabilitation Medicine
关键词 冠状动脉疾病 C反应蛋白质 血液粘度 Coronary artery disease C reactive protein Blood viscosity
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参考文献7

  • 1丁芳.冠心病血清超敏C-反应蛋白和血清淀粉样蛋白A,脂联素的关系[J].心血管康复医学杂志,2009,18(5):442-444. 被引量:5
  • 2Danesh J, W heeler JG, Hirschfield GM, et al.C-reactive protein and other circulating markers of inflammation in the prediction of coronary heart disease[J].N Engl J Med, 2004, 350:1387-1397.
  • 3Yeh ET,Willerson JT.Coming of age of C-reactive protein: Using inflammation markers in cardiology[J].Circulation, 2003, 107:370-372.
  • 4Weissberg PL.Atherogenesis current understanding of the cause of atheroma[J].Heart, 2000, 83(1):247-252.
  • 5Luppi P, Licata A, Haluszczak C,et al.Analysis of TCR Vβ repertoire and cytokine gene expression in patients with idiopathy dilated cardiomyopathy[J].J Autoimmun, 2001,16(1):3-13.
  • 6Ahlemeyer B,Krieglstein J.Neuroprotective effects of Ginkgo biloba extract[J].Cell Mol Life Sci, 2003, 60(9):1779-1792.
  • 7Sun BL,Zhang J,Wang XC,et al.Effects of extract of Ginkgo biloba on spasms of the basilar artery and cerebral microcirculatory perfusion in rats with subarachnoid hemorrhage[J].Clin Hemorheol Microcire,2003,29(3-4):231-238.

二级参考文献14

  • 1Rose R. Atherosclerosis, an inflammatory disease [J]. N Engl J Med, 1999, 340:115-126.
  • 2Katayama T, Nakashima H, Yonekura T, et al. Significance of acute-phase inflammatory reactants as an indicator of prognosis after acuter myocardial infarction: which is the most useful predictor? [J]. J Cardiol, 2003, 42: 49-56.
  • 3Ouehi N, Kihara S, Ayita Y, et al. Adipocyte derived plasma protein adiponectin, suppresses lipid accumulation and class A scavenger receptor expression in human monocyte derived macrophages [J]. Circulation, 2001, 103: 1057-1063.
  • 4Carr S, Farb A, Pearce WH. Atherosclerotie qlaque rupture in symptomatic carotid artery stenosis [J]. J Vase Surg, 1996, 23 (5): 755-765.
  • 5Sellmayer A, Limmert T, Hoffmann U. High sensitivity C-reactive, protein in cardiovascular risk assessment, CRP mania or useful screening? [J]. Int Angiol Mar, 2003, 22: 15-23.
  • 6Meek RL, Urieli-Shoval S, Benditt EP. Expression of apolipoprotein serum amyloid A mRNA in human atherosclerotic lesions and cultured vascular cells,implications for serum amyloid A function [J]. Proc Natl Acad Sci USA, 1994,91 : 3186-3199.
  • 7Ouchi N, Kisara S, Arita Y, et al. Nover modulator for eudothelial adbesion mdecule: adippoeyte derived plasma protein adipronectin [J]. Circulation, 1999, 25 (2): 473-476.
  • 8Kumada M, Kihara S, Sumitsuji S, et al. Association of hypoadiponectinemia with coronary artery disease in men [J]. Arterioscler Thromb Vasc Biol, 2003, 23 (1): 85-89.
  • 9Nakamura Y, Shimada K, Fukuda D, et al. Implications of plasma concentration of adiponectin in patients with coronary artery disease [J]. Heart, 2004, 90:528-533.
  • 10Fruebis J, Tsao TS, Javorschi S, et al. Proteolytic cleavage product of 30 - kDA adipocyte complement- related protein increases fatty acid oxidation in muscle and causes weight loss in mice [J]. Proc Natl Acad Sei USA, 2001, 98 (4): 2005-2010.

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