期刊文献+

短期抗心力衰竭治疗后心肌MMPs/TIMPs及白介素-15、18表达变化研究 被引量:4

Study of Analysis of Expression Change of MMPs/FIMPs and IL-15、18 of Myocardiac Tissue after Short Term Anti Heart Failure Treatment
原文传递
导出
摘要 目的观察在短期标准化治疗心功能不全的扩张型心肌病和缺血性心肌病患者,使其心功能得以改善后,MMPs/TIMPs系统和白介素家族成员-IL-15、IL-18表达的变化,并探讨其在监测病情变化以及临床疗效方面的价值。方法本研究入选51名受试者,年龄在4282岁之间,其中确诊为扩张型心肌病患者29名,缺血性心肌病患者9名以及13名健康者作为对照组。通过酶联免疫法(ELISA)检测患者在入院接受治疗,心功能不全控制前后血清中MMP-1、MMP-3、MMP-9、TIMP-1、IL-18以及IL-15水平的变化。结果研究发现,心功能不全患者,血MMP-1、MMP-3、IL-18以及IL-15水平较对照组明显降低。但在心功能不全的心肌疾病患者之间,上述检测指标的在血清中的水平与心功能分级无明显相关性。在经过短期治疗,心功能得到明显改善后,发现仅心功能不全患者TIMP-1血清水平显著升高,其余指标无明显变化。结论短期标准化治疗后心功能不全患者血中TIMP-1的表达变化,可能与患者心功能改变密切相关,可作为心功能不全患者短期抗心力衰竭治疗效果的监测指标。 Objective Change of matrix metalloproteinases(MMPS),tissue inhibitors of metalloproteinase(TIMP-1) and interleukin-18(IL-18) have been reported in heart failure patients secondary to cardiomyopathy(DCM or ICM).However,the short effect of treatment on the levels MMP-1,MMP-3,MMP-9,TIMP-1,IL-18,and IL-15 in patients with heart failure has not been elucidated.Methods We enrolled 51subjects with heart failure age range between 42-85 years old,29 DCM,9 ICM and 13 healthy subjects as control group;we measured the serum levels of these markers by using enzyme immunoassay(ELISA).Results The serum level of MMP-1,MMP-3,IL-18,IL-15 in heart failure patients were significant lower compared to that of control group before treatment.And the serum levels of TIMP-1 in heart failure patients were significant higher after one week treatment.But no significant difference between the patients with NYHA class II and NYHA class III-IV heart function before and after the treatment has been observed.Conclusion Therefore,the improvement of heart failure after one week of standard treatment could affect the expression of TIMP-1.And the change of the level of TIMP-1 in heart failure patients’ blood could reflect the effects of the treatment of heart failure.
出处 《医药论坛杂志》 2010年第23期1-6,共6页 Journal of Medical Forum
关键词 心力衰竭 金属基质蛋白酶 金属蛋白酶组织抑制物-1 白介素家族 Heart failure; metalloproteinases; Tissue inhibitor of metalloproteinases-1; Interleukins;
  • 相关文献

参考文献28

  • 1Jugdutt BI. Remodeling of the myocardium and potential targets in the collagen degradation and synthesis path- ways[ J]. Curr Drug Targets Cardiovasc Haematol Dis- ord,2003,3( 1 ) : 1-30.
  • 2Kelly D, Khan S, Cockerill G, et al. Circulating stromelysin - 1 (MMPs) : a novel predictor of LV dys- function, remodelling and all - cause mortality after a- cute myocardial infarction [ J ]. Eur J Heart Fail, 2008, i0 (2): 133-139.
  • 3Spinale FG, Coker ML, Thomas CV, et al. Time - De- pendent Changes in Matrix Metalloproteinase acti0itg and expression during the progression of congestive heart failure: relation to ventricular and myocyte function[ J ]. Circ Res, 1998,82 (4) :482-495.
  • 4Kukacka J, Prusa R, Kotaska K, et al. Matrix metallo- proteinases and their function in myocardium [ J 1- Bi- omed Pap Med Fac Univ Palacky Olomouc Czech Re- pub ,2005,149 ( 2 ) :225-236.
  • 5Tsuruda T, Costello - Boerrigter LC, Burnett JC Jr. Matrix metalloproteinases : pathways of induction by bio- active molecules[J]. Heart Fail Rev,2004,9 (1) : 53- 61.
  • 6Spinale FG. Matrix metalloproteinases: regulation and dysregulation in the failing heart [ J ]. Circ Res,2002, 90(5 ) :520-30.
  • 7Spinale FG, Coker ML, Heung LJ, et al. A Matrix Metalloproteinase Induction/Activation System Exists in the Human Left Ventricular Myocardium and Is Upregu- lated in Heart Failure [ J ]. Circulation, 2000, 102 (16) : 1944-1949.
  • 8ArendWP, PalmerG, Gabay C. IL-1, IL-18, and IL-33 families of cytokines[J]. Immunol Rev,2008, 223:20-38.
  • 9Wang M, Markel TA, Meldrum DR. lnterleukin 18 in the heart[J]. Shock,2008,30 ( 1 ) :3-10.
  • 10Apostolakis S, Vogiatzi K, Krambovitis E, et al. IL- 1 cytokines in cardiovascular disease: diagnostic, prog- nostic and therapeutic implications[ J]. Cardiovasc He- matol Agents Med Chem, 2008,6 ( 2 ) : 150-8.

同被引文献33

  • 1Cunningham MW. T cell mimicry in inflammatory heart disease [ J ]. Mol Immunol, 2004, 40 ( 14 - 15 ) : 1121 - 1127.
  • 2Wheeler DS. A formidable challenge: The diagnosis and treatment of- viral myocarditis in children[J]. Crit Care Clin, 2003, 19(3) : 365 -391.
  • 3Deguchi H, Kitaura Y, Hayashi T. Cell-mediated immune cardiocytei- njury in viral myocarditis of mice and patients[ J]. Jpn Circ J, 1989, 53(1) : 61 -77.
  • 4陈颖.血清白介素-6、白介素-8、超敏C反应蛋白测定在急性冠脉综合症中的临床意义[J].中国社区医师(医学专业),2007,9(20):116-116. 被引量:3
  • 5Parsanejad M, Zhang Y, Qu D. Regulation of the VHL/HIF-1 Pathway by DJ-I[-J3. J Neurosci. 2014,34(23),8043.
  • 6Li L,Huang K,You Y. Hypoxia-induced miR-210 in epithelial ovarian cancer enhances cancer cell viability via promoting pro- liferation and inhibiting apoptosis[J]. Int J Oncol. 2014, 44 (6) :2111.
  • 7Tekin D,Dursun A D,Xi L. Hypoxia inducible factor 1 (HIF- 1)and cardioprotection [J]. Acta Pharmaeol Sin. 2010,31(9): 1085.
  • 8Majmundar A J,Wong W J,Simon M C. Hypoxia-inducible fac- tors and the response to hypoxic stress[J]. Mol Cell,2010 ,40 (2) :294.
  • 9Voils SA,Cooper-DeHoff RM. Association between high sensi- tivity C-reactive protein and metabolic syndrome in subjects completing the National Health and Nutrition Examination Sur- vey (NHANES) 2009-10[J]. Diabetes Metab Syndr. 2014,8 (2) :88.
  • 10Li X,Chen C,Gan F. Plasma NT pro-BNP,hs-CRP and big-ET levels at admission as prognostic markers of survival in hospital- ized patients with dilated cardiomyopathy: a single-center cohort study[J]. BMC Cardiovasc Disord. 20 i4,11,14 (1) : 67.

引证文献4

二级引证文献23

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部