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法舒地尔治疗慢性心力衰竭的临床疗效

Effect of Fasudil in Patients with Chronic Heart Failure
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摘要 目的:观察法舒地尔对慢性心力衰竭(CHF)的临床疗效及血浆脑钠肽(BNP)的影响。方法:将100例心功能(NYHA)Ⅲ~Ⅳ级冠心病慢性心力衰竭患者随机分为治疗组和对照组,各50例。两组均给予常规治疗:利尿剂、口服血管紧张素转换酶抑制剂、地高辛等,治疗组在此治疗基础上静脉滴注法舒地尔60mg/d,治疗前后观察两组患者血浆脑钠肽浓度变化及采用超声心动图、6min步行实验等方法进行疗效观察。结果:两组治疗后BNP、心功能、6min步行实验距离均明显改善(P〈0.01),治疗组较对照组更明显,BNP降低显著(398.2±105.3)/(456.5±106.4)ng/L(P〈0.05),左室射血分数(LVEF)分别为(53.4±9.9)/(46.5±8.3)%,左室射血分数增加明显(P〈0.05),6min步行距离明显增加(419.2±71.6)/(382.5±53.7)m(P〈0.05)。结论:法舒地尔能有效降低慢性心衰患者血浆BNP,改善心功能。 Objective: To explore the difference of brain natriuretic peptide(BNP) concentration and clinical effects in patients with chronic heart failure who received Fasudil : One hundred chronic heart failure patients with cardiac function(NYHA) III-IV were randomly divided into the treatment group(n=50) and the control group(n=50).The two groups were given conventional treatment, including diuretics, oral angiotensin-converting enzyme inhibitors, digoxin.Patients in treatment group on the basis of this treatment were treated with Fasudil 60 mg/d.The plasma levels of BNP was detected, LVEF and CO were observed by echocardiography, and the exercise endurance were eval;aated by 6-minutes walking test before and after the treatment.Results: The plasma levels of BNP, left ventrieular function(LVFF) and the distance of 6-minntes walking test were significantly improved after therapy in two groups(P〈0.01), especially in the treatment group(P〈0.05).The concentrations of BNP in treatment group were significantly decreased(398.2 ± 105.3)/(456.5± 106.4)ng/L(P〈0.05).LVEF of the patients in treatment group were increased significantly(53.4± 9.9)/(46.5± 8.3)%(P〈0.05).The distance of'6-minutes walking test of the patients in the treatment group were also significantly increased(419.2 ± 71.6)/(382.5 ± 53.7)m(P〈0.05).Conclusion: Fasudil can significantly improve cardiac function and decrease plasma BNP level of chronic heart failure patients.
机构地区 上海市浦东医院
出处 《中外医学研究》 2013年第22期6-8,共3页 CHINESE AND FOREIGN MEDICAL RESEARCH
关键词 法舒地尔 慢性心力衰竭 脑钠肽 6min步行实验 Fasudil Chronic heart failure Brain natriuretic peptide 6-minutes walking test
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参考文献13

  • 1无.慢性心力衰竭诊断治疗指南[J].中华心血管病杂志,2007,35(12):1076-1095. 被引量:3677
  • 2Shimokawa H.Rho-kinase as a novel therapeutic target in treatment of cardiovascular diseases[J].J Cardiovasc Pharmacol, 2002, 39(6): 319- 327. 被引量:1
  • 3Hu E, Lee D.Rho kinase inhibitors as potential therapeutic agents for cardiovasculardiseases[J].CurrOpinInvestigDrugs, 2003, 25(4):1065- 1075. 被引量:1
  • 4Kandabashi T, Shimokawa H, Miyata K, et al.Inhibition of myosin phosphatase by uprcgulated rho-kinase plays a key role for coronary artery spasm in a porcine model with interleukin-lbeta[J].Circulation, 2000, 101(2): 1319-1323. 被引量:1
  • 5Shimokawa H, Seto M, Katsumata N, et al.Rho-kinase-mediated pathway induces enhanced myosin light chain phosphorylations in a swine model of coronary artery spasm[J].Cardiovasc Res, 1999, 43(5): 1029- 1039. 被引量:1
  • 6Kandabashi T, Shimokawa H, Mukai Y, et al.Involvement of rho-kinase in agonists-induced contractions of arteriosclerotic human arteries[J]. ArteriosclerThrombVascBiol, 2002, 22(4): 243-248. 被引量:1
  • 7Shimokawa H, Mofishige K, Miyata K, et al.Long-term inhibition of Rho-kinase induces a regression of arteriosclerotic coronary lesions in a poreine model in vivo[J].Cardiovas Res, 2001, 45(3): 169-177. 被引量:1
  • 8Wang Y X, Da Cunha V, Martin-Mc Nulty B, et al.Inhibition of Rho- kinase by fasudil attenuated angiotensin Ⅱ-induced cardiac hypertrophy in apolipoprotein E deficient mice[J].Eur J Pharmacol, 2005, 512(2): 215- 222. 被引量:1
  • 9Ma Z, Zhang J, Du R, et al.Rho kinase inhibition by fasudil has anti- inflammatory effects in hypercholesterolemic rats[J].Biol Pharm Bull, 2011, 34(6): 1684-1689. 被引量:1
  • 10张曼,王文刚,曾定尹.法舒地尔对心力衰竭大鼠血流动力学和心肌细胞内钙离子浓度的影响[J].中国新药与临床杂志,2006,25(1):33-36. 被引量:17

二级参考文献55

  • 1张曼,曾定尹.法舒地尔对压力负荷心力衰竭大鼠的作用[J].中国医科大学学报,2004,33(6):484-486. 被引量:4
  • 2王方正,张澍,黄德嘉,华伟,孙宝贵,沈法荣,吴书林,王建安,方全,吴立群,王景峰,王冬梅,郭涛,陈新,中华医学会心电生理和起搏分会心脏再同步治疗专家工作组.心脏再同步治疗慢性心力衰竭的建议[J].中华心律失常学杂志,2006,10(2):90-102. 被引量:90
  • 3HISAOKA T, YANO M, OHKUSA T, et al. Enhancement of Rho/Rho kinase system in regulation of vascular smooth muscle contraction in tachycardia-induced heart failure[J]. Cardiovasc Res, 2001,49(2): 319-329.. 被引量:1
  • 4SUEMATSU N, SATOH S, KINUGAWA S, et al. Alph α1-adrenoceptor-Gq-RhoA signaling is up regulated to increase myofibrillar Ca2+ sensitivity in failing hearts[J]. Am J Physiol Heart Circ Physiol,2001, 281(2): H637-646.. 被引量:1
  • 5AOKI H, IZUMO S, SADOSHIMA J. Angiotensin Ⅱ activates RhoA in cardiac myocytes. A critical role of RhoA in angiotensin Ⅱ -induced premyofibrill formation[J] . Circ Res, 1998, 82: 666-676.. 被引量:1
  • 6SAH VP, HOSHLJIMA M, CHIEN KR, BROWN JH. Rho is required for Gq and α1 -adrenergic receptor signaling in cardiomyocytes.Dissociation of Ras and Rho pathways [J]. J Biol Chem, 1996, 271:31185-31190.. 被引量:1
  • 7SAH VP, MINAMISAWA S, TAM SP, et al. Cardiac-specific overexpression of RhoA results in sinus and atrioventricular nodal dysfunction and contractile failure[J]. J Clin Invest, 1999, 103: 1627-1634.. 被引量:1
  • 8KIMURA K, ITO M, AMANO M, et al. Regulation of myosin phosphatase by Rho and Rho-associated kinase (Rho-kinase) [J]. Science, 1996, 273: 245-248.. 被引量:1
  • 9SOMLYO AP ,SOMLYO AV. Signal transduction by G-protein rhokinase and protein phosphatase to smooth muscle and non-muscle myosin Ⅱ [J]. J Physiol, 2000,522 Pt 2: 177-185. 被引量:1
  • 10VATNER DE,KUNZE DL. Prologue: low-molecular-weight GTPases in the heart and circulation [J]. Am J Physiol Heart Cire Physiol, 2000,278(6) :H1733-H1735. 被引量:1

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