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氟伐他汀对自发性高血压大鼠心血管的保护作用 被引量:1

Experimental study on the protective effect of fluvastatin on cardiovascular system in spontaneously hypertension rats
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摘要 目的:探讨氟伐他汀对自发性高血压大鼠心血管系统的作用。方法:12周龄自发性高血压大鼠30只,随机分成3组,每组10只:安慰剂组给予安慰剂喂养,氟伐他汀组喂养氟伐他汀20mg/(kg·d);基础组入选后即处死留取血标本检测。分别测量治疗3个月前(后)收缩期血压、体质量、全心质量、左心室质量及血浆血管紧张素Ⅱ、血脂、血糖和尿素氮、肌酐、尿酸水平以及肠系膜三级动脉血管壁/腔面积比。结果:①氟伐他汀组治疗后收缩压(mmHg)均明显下降(163±4),与安慰剂组(174±7)比较,差异有显著性意义(F=3.12,P<0.05)。②氟伐他汀组全心质量和体质量比及左心室质量和体质量比明显下降(全心重/体质量:0.0051±0.0003和0.0049±0.0002;左室质量/体质量:0.0040±0.0003和0.0039±0.0001),与安慰剂组比较,差异有显著性意义(F=2.96,P<0.05)。③氟伐他汀治疗后血管紧张素Ⅱ(ng/L)水平无明显下降(241.50±45.68,F=1.26,P>0.05)。④氟伐他汀治疗后胆固醇(mmol/L)下降(1.23±0.46);三酰甘油水平(mmol/L)也明显变化(1.31±0.23),高密度脂蛋白水平(mmol/L)升高(1.20±0.51),与安慰剂组比较,差异有显著性意义(F=3.39,P<0.05)。⑤氟伐他汀治疗后血糖、血浆尿素氮、肌酐、尿酸水平水平无明显降低作用(F=1.76,P>0.05)。 AIM:To investigate the effects of fluvastatin in protecting the cardiovascular system of spontaneously hypertension rats. METHODS: Thirty spontaneously hypertension rats of 12 weeks old were randomly divided into 3 groups of 10 rats each: placebo group, fluvastatin group[20 mg/(kg·d)] and base group.Rats in the base group were sacrificed before treatment, and blood samples were detected. The systolic blood pressure(SBP),body mass, heart mass(HM), left ventricle mass(LVM),plasma concentration of angiotensin Ⅱ(Ang Ⅱ),lipid,glucose,urea nitrogen, creatinine, uric acid, and mesenteric arteries(3rd grade branch) wall to lumen ratio were determined 3 months before and after treatment respectively 3 months before and after treatment.respectively. RESULTS:①The SBP(mmHg) in the fluvastatins group(163±4) was obviously decreased, significantly different from that in the placebo group(174±7) (F=3.12,P< 0.05). ②The HM/body mass and LVM/body mass ratios in the fluvastatin group (0.005 1±0.000 3 and 0.004 0±0.000 3) were decreased obviously, significantly different from those in the placebo group (0.004 9±0.000 2 and 0.003 9±0.000 1)(F=2.96,P< 0.05).③Ang II level (ng/L) in the fluvastatin group was not significantly changed (241.50±45.68,F=1.26,P >0.05).④In the fluvastatin group, plasma cholesterol was decreased[(1.23±0.46) mmol/L], triglyceride was changed obviously[(1.31±0.23)mmol/L], high density lipoprotein was increased[(1.20±0.51)mmol/L], significantly different from that in the placebo group(F=3.39,P< 0.05). ⑤Plasma glucose, urea nitrogen, creatinine and uric acid in the fluvastatin group had no obvious changes(F=1.76,P >0.05). ⑥Mesenteric arteries W/L ratio was significantly higher in the placebo group (0.69±0.06) than the fluvastatin group(0.42±0.06)(F=3.61,P< 0.05).Fluvastatin can reduce the adverse effects of hypertension on cardiovascular system, and has protective effects on it.
出处 《中国临床康复》 CSCD 2004年第12期2268-2270,共3页 Chinese Journal of Clinical Rehabilitation
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参考文献19

  • 1舒茂琴,何作云,何国祥,宋志远,王国超.三酰甘油与冠心病危险性的相关性[J].中国临床康复,2004,8(3):450-451. 被引量:18
  • 2楚新梅,孟竹,何秉贤,戴文英,Chu Xinmei,MENG Zhu,He Bingxian,Dai Wenying.新疆地区维、汉民族冠状动脉粥样硬化性心脏病患者血脂分析(英文)[J].中国临床康复,2003,7(9):1408-1409. 被引量:30
  • 3徐峰,毕向军,王劲,李华,唐旭华.老年原发性高血压与舒血管活性物质的关系[J].中国临床康复,2003,7(21):2902-2903. 被引量:12
  • 4Ginsberg HN. Update on the treatment of hypercholesterolemia, with focus on HMG-COA reductase inhibitors and combination regimes. Clin Cardiol 1995: 18:307.
  • 5Corsini A, Bernini F, Quarato P, et al. Non-lipid-related effects of 3-hydroxy-3-methyglutaryl coenzyme A reductase inhibitors. Cardiology 1996; 87(6): 458.
  • 6Park JK, Muller DN, Mervaala EM, et al. Cerivastatin prevents angiotensin I-I-induced renal injury independent of blood pressure-and cholesterol-lowering effects. Kidney Int 2000; 58(4): 1420 - 30.
  • 7Brilla CG, Zhou G, Matsubara L, et al. Collagen metabolism in cultured adult rat fibroblasts: response to angiotensin Ⅱ and aldostrone. J Mol Cell Cardiol 1994:26:809 - 20.
  • 8Weber KT, Brilla CG. Pathological hypertrophy and cardiac interstitium. Fibrosis and renin-angiotensin-aldosterone system. Circulation 1991 ; 83:1849 - 65.
  • 9Su S, Hsiao C, Chu C, et aL Effects of pravastatin on left ventricular mass in patients with hyperlipidemia and essential hypertension. Am J Cardiol 2000; 86(5):514-8.
  • 10Pearson TA. Divergent approaches to the treatment of dvslipidemia with low levels of high-density lipoprotein cholesterol. Am J Cardiol ,2000; 86(12 Suppl 1):57 -61.

二级参考文献24

  • 1Castelli WP, Anderson K, Wilson PW, Levy D, Lipids and risk of coronary heart disease: the Framingham Study. Ann Epidemiol 1992; 2 ( 1 - 2) : 23 - 8.
  • 2Wierzbicki AS, Milchailidis DP, Beyond LDL-C-the importance of raising HDL-C.Curr Med Res Opin 2002:18(1):36-44.
  • 3Hokanson JE. Hypertriglyceridemia and risk of coronary heart disease. Curr Cardiol Rep 2002; 4 (6) : 488 - 93.
  • 4Clearfield MB. The national cholesterol education program adult treatment panel ill guidelines. J Am Osteopath Assoc 2003; 103(1 Suppl 1): 1 -5.
  • 5Expert panel on detection, evaluation, and treatment of high blood cholesterol in adults. Executive summary of the third report of the national cholesterol education program(NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel Ⅲ) . JAMA 2001; 285(19):2486 - 97.
  • 6Packard C, Nunn A, Hobbs R. Futme Forum Editorial Board. High density Lipoprotcin: guardian of the vascular system? Int J Clin Pract 2002; 56(10):761 -71.
  • 7Barbagallo CM, Polizzi F, Severino M, et al. Distribution of risk factors, plasma lipicls, lipoproteins and dyslipidemias in a small Mediterranean inland: the Ustica Project. Nutr Metab Cardiovasc Dis, 2002; 12(5):267 -74.
  • 8Nawawi HM, Nor IM, Noor IM, et al. Current status of coronary risk factors amnng rural Malavs in Malaysia. J Cardiovasc Risk 2002;9(1); 17 -23.
  • 9Menotti A, Lanti M. Coronary risk factors predicting early and late coronary deaths. Heart 2003;89(1): 19 -24.
  • 10Zoratti R. A review on ethnic differences in plasma triglycerides and high-density-Lipoprotein cholesterol: is the lipid pattern the key factor for the low coronary heart disease rate in people of African origin? Eur J Epidemiol 1998; 14(1):9 -21.

共引文献55

同被引文献9

  • 1沈晓君,孙婉萍,王玲.通脉降脂口服液和洛伐他汀对动脉粥样硬化患者血脂生化指标影响的对比研究[J].中国临床康复,2004,8(27):5888-5889. 被引量:6
  • 2Neuringer IP, Mannon RB, Coffman TM, et al. Immune cells in a mouse airway model of obliterative bronchiolitis. Am J Respir Cell Mol Biol 1998;19(3):379-86.
  • 3Valentine VG, Robbins RC, Berry GJ, et aL Actuarial survival of heart-lung and bilateral sequential lung transplant recipients with obliterative bronchiolitis. J Heart Lung Transplant 1996;15(4):371-83.
  • 4Johnson MD, Woodard A, Okediji EJ, et al. Lovastatin is a potent inhibitor of meningioma cell proliferation: evidence for inhibition of a mitogen associated protein kinase. J Neurooncol 2002;56(2):133-42.
  • 5Jakobisiak M, Bruno S, Skierski JS, et al. Cell cycle-specific effects of lovastatin. Proc Natl Acad Sci USA 1991;88(9):3628-32.
  • 6Aris RM, Walsh S, Chalermskulrat W. Growth factor upregulation during obliterative bronchiolitis in the mouse model. Am J Respir Crit Care Med 2002;166(3):417-22.
  • 7Al-Dossari GA, Jessurun J, Bolman RM, et al. Pathogenesis of obliterative bronchiolitis. Possible roles of platelet-derived growth factor and basic fibroblast growth factor. Transplantation 1995;59(1):143-5.
  • 8Kelynack KJ, Hewitson TD, Martic M, et al. Lovastatin downregulates renal myofibroblast function in vitro. Nephron 2002;91(4):701-7.
  • 9AIho HS, Inkinen KA, Salminen US, et al. Collagens Ⅰ and Ⅲ in a porcine bronchial model of obliterative bronchiolitis. Am J Respir Crit Care Med 2001;164:1519-25.

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