• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

原发性高血压患者基质金属蛋白酶-9和金属蛋白酶组织抑制因子-1水平。与左心室质量及降压治疗的关系。

Matrix metalloproteinase-9 and tissue inhibitor metalloproteinase-1 levels in essential hypertension. Relationship to left ventricular mass and anti-hypertensive therapy.

作者信息

Li-Saw-Hee F L, Edmunds E, Blann A D, Beevers D G, Lip G Y

机构信息

Haemostasis Thrombosis and Vascular Biology Unit, University Department of Medicine, City Hospital, B18 7QH, Birmingham, UK.

出版信息

Int J Cardiol. 2000 Aug;75(1):43-7. doi: 10.1016/s0167-5273(00)00274-6.

DOI:10.1016/s0167-5273(00)00274-6
PMID:11054505
Abstract

To test the hypothesis that the activity of enzymes degrading the extracellular matrix in hypertensive patients are abnormal, and that the treatment of hypertension will normalise these abnormalities, we measured the serum levels of metalloproteinase MMP-9, and its inhibitor, tissue metalloproteinase inhibitor (TIMP-1). Thirty-two patients with untreated hypertension (BP 168/96) had significantly lower levels of both MMP-9 and TIMP-1 when compared to 24 matched normotensive controls (BP 123/80) (P<0.001). There was no significant correlation between MMP-9 and TIMP-1 levels (P>0.2). In the patients, there were no significant correlations observed between left ventricular mass, Doppler V(E)/V(A) ratio (an index of diastolic function), blood pressure, left ventricular mass index and either MMP-9 or TIMP-1 levels (all P=NS). Levels of MMP-9 and TIMP-1 were not significantly altered after 2 months of antihypertensive treatment of 29 patients despite mean blood pressure falling from 170/96 to 143/85 mmHg (P<0.001). Correspondingly, there were also no significant alterations in indices of diastolic function and left ventricular mass. Our study suggests that the proteolytic activities of MMP-9 and TIMP-l are depressed in hypertensive patients and were not significantly affected by short-term antihypertensive treatment. The relationship between collagen metabolism in hypertensive subjects, especially in those with cardiac hypertrophy, and the effects of treatment needs to be further explored in larger trials over a longer period of time.

摘要

为验证高血压患者中降解细胞外基质的酶活性异常,且高血压治疗可使这些异常恢复正常这一假说,我们测定了金属蛋白酶MMP-9及其抑制剂组织金属蛋白酶抑制剂(TIMP-1)的血清水平。与24名匹配的血压正常对照者(血压123/80)相比,32名未经治疗的高血压患者(血压168/96)的MMP-9和TIMP-1水平均显著降低(P<0.001)。MMP-9与TIMP-1水平之间无显著相关性(P>0.2)。在患者中,左心室质量、多普勒V(E)/V(A)比值(舒张功能指标)、血压、左心室质量指数与MMP-9或TIMP-1水平之间均未观察到显著相关性(所有P=无显著性差异)。29名患者接受2个月的抗高血压治疗后,尽管平均血压从170/96降至143/85 mmHg(P<0.001),但MMP-9和TIMP-1水平并未显著改变。相应地,舒张功能指标和左心室质量也无显著变化。我们的研究表明,高血压患者中MMP-9和TIMP-1的蛋白水解活性降低,且不受短期抗高血压治疗的显著影响。高血压患者尤其是心脏肥大患者的胶原代谢与治疗效果之间的关系,需要在更大规模、更长时间的试验中进一步探索。

相似文献

1
Matrix metalloproteinase-9 and tissue inhibitor metalloproteinase-1 levels in essential hypertension. Relationship to left ventricular mass and anti-hypertensive therapy.原发性高血压患者基质金属蛋白酶-9和金属蛋白酶组织抑制因子-1水平。与左心室质量及降压治疗的关系。
Int J Cardiol. 2000 Aug;75(1):43-7. doi: 10.1016/s0167-5273(00)00274-6.
2
Tissue inhibitor of metalloproteinase-1 and matrix metalloproteinase-9 levels in patients with hypertension Relationship to tissue Doppler indices of diastolic relaxation.高血压患者中基质金属蛋白酶-1组织抑制剂和基质金属蛋白酶-9水平与舒张期松弛组织多普勒指标的关系
Am J Hypertens. 2004 Sep;17(9):770-4. doi: 10.1016/j.amjhyper.2004.06.023.
3
Abnormalities of the extracellular degradation of collagen type I in essential hypertension.原发性高血压中I型胶原细胞外降解异常。
Circulation. 1998 Aug 11;98(6):535-40. doi: 10.1161/01.cir.98.6.535.
4
Serum levels of MMP-9 and TIMP-1 in primary hypertension and effect of antihypertensive treatment.原发性高血压患者血清基质金属蛋白酶-9和金属蛋白酶组织抑制因子-1水平及降压治疗的影响
Eur J Intern Med. 2009 Jul;20(4):369-72. doi: 10.1016/j.ejim.2008.10.003. Epub 2008 Nov 28.
5
Matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 in hypertension and their relationship to cardiovascular risk and treatment: a substudy of the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT).基质金属蛋白酶-9和金属蛋白酶组织抑制因子-1在高血压中的作用及其与心血管风险和治疗的关系:盎格鲁-斯堪的纳维亚心脏结局试验(ASCOT)的一项子研究
Am J Hypertens. 2004 Sep;17(9):764-9. doi: 10.1016/j.amjhyper.2004.05.019.
6
Altered matrix metalloproteinase 9 and tissue inhibitor of metalloproteinases 1 levels in children with primary hypertension.原发性高血压患儿基质金属蛋白酶9和金属蛋白酶组织抑制剂1水平的改变
J Hypertens. 2016 Sep;34(9):1815-22. doi: 10.1097/HJH.0000000000001024.
7
[Effects of renin-angiotensin system blockers on left ventricular hypertrophy and biochemical markers of collagen balance in patients with hypertensive hypertrophy].[肾素-血管紧张素系统阻滞剂对高血压性肥厚患者左心室肥厚及胶原平衡生化标志物的影响]
Ter Arkh. 2009;81(5):64-71.
8
Matrix metalloproteinases/tissue inhibitors of metalloproteinases: relationship between changes in proteolytic determinants of matrix composition and structural, functional, and clinical manifestations of hypertensive heart disease.基质金属蛋白酶/金属蛋白酶组织抑制剂:基质成分蛋白水解决定因素的变化与高血压性心脏病的结构、功能及临床表现之间的关系
Circulation. 2006 May 2;113(17):2089-96. doi: 10.1161/CIRCULATIONAHA.105.573865. Epub 2006 Apr 24.
9
Long-term effects of benidipine hydrochloride on severe left ventricular hypertrophy and collagen metabolism in patients with essential hypertension.盐酸贝尼地平对原发性高血压患者严重左心室肥厚及胶原代谢的长期影响。
J Cardiol. 2002 Apr;39(4):195-204.
10
Impact of the metalloproteinase-9/tissue inhibitor of metalloproteinase-1 system on large arterial stiffness in patients with essential hypertension.金属蛋白酶-9/金属蛋白酶组织抑制剂-1系统对原发性高血压患者大动脉僵硬度的影响。
Hypertens Res. 2007 Oct;30(10):959-63. doi: 10.1291/hypres.30.959.

引用本文的文献

1
Matrix Metalloproteinases in Cardioembolic Stroke: From Background to Complications.心肌梗死后心脏破裂的危险因素分析
Int J Mol Sci. 2023 Feb 11;24(4):3628. doi: 10.3390/ijms24043628.
2
Angiotensin-converting enzyme inhibitors increase anti-fibrotic biomarkers in African Americans with left ventricular hypertrophy.血管紧张素转换酶抑制剂增加左心室肥厚的非裔美国人的抗纤维化生物标志物。
J Clin Hypertens (Greenwich). 2021 May;23(5):1008-1016. doi: 10.1111/jch.14206. Epub 2021 Mar 10.
3
Matrix Metalloproteinases and Hypertension-Mediated Organ Damage: Current Insights.
基质金属蛋白酶与高血压介导的器官损伤:当前见解
Integr Blood Press Control. 2020 Nov 2;13:157-169. doi: 10.2147/IBPC.S223341. eCollection 2020.
4
Matrix metalloproteinase-9 as a messenger in the cross talk between obstructive sleep apnea and comorbid systemic hypertension, cardiac remodeling, and ischemic stroke: a literature review.基质金属蛋白酶-9 在阻塞性睡眠呼吸暂停与共病系统性高血压、心脏重构和缺血性卒中的串扰中的信使作用:文献综述。
J Clin Sleep Med. 2021 Mar 1;17(3):567-591. doi: 10.5664/jcsm.8928.
5
Plasma levels of matrix metalloproteinase-9 are elevated in individuals with hypertensive crisis.高血压危象患者的基质金属蛋白酶-9 血浆水平升高。
BMC Cardiovasc Disord. 2020 Mar 12;20(1):132. doi: 10.1186/s12872-020-01412-5.
6
The effect of antihypertensive treatment on arterial stiffness and serum concentration of selected matrix metalloproteinases.抗高血压治疗对动脉僵硬度及所选基质金属蛋白酶血清浓度的影响。
Arch Med Sci. 2017 Jun;13(4):760-770. doi: 10.5114/aoms.2016.58825. Epub 2016 Mar 23.
7
Serum Concentrations of Endothelin-1 and Matrix Metalloproteinases-2, -9 in Pre-Hypertensive and Hypertensive Patients with Type 2 Diabetes.2型糖尿病前期高血压和高血压患者血清内皮素-1及基质金属蛋白酶-2、-9的浓度
Int J Mol Sci. 2016 Aug 1;17(8):1182. doi: 10.3390/ijms17081182.
8
Beneficial effects of renal sympathetic denervation on cardiovascular inflammation and remodeling in essential hypertension.肾交感神经去神经术对原发性高血压患者心血管炎症和重构的有益作用。
Clin Res Cardiol. 2015 Feb;104(2):175-84. doi: 10.1007/s00392-014-0773-4. Epub 2014 Oct 18.
9
Effect of a dipeptidyl peptidase-IV inhibitor, des-fluoro-sitagliptin, on neointimal formation after balloon injury in rats.二肽基肽酶-4 抑制剂地氟噻嗪对大鼠球囊损伤后新生内膜形成的影响。
PLoS One. 2012;7(4):e35007. doi: 10.1371/journal.pone.0035007. Epub 2012 Apr 6.
10
An emerging role of degrading proteinases in hypertension and the metabolic syndrome: autodigestion and receptor cleavage.降解蛋白酶在高血压和代谢综合征中的新作用:自身消化和受体裂解。
Curr Hypertens Rep. 2012 Feb;14(1):88-96. doi: 10.1007/s11906-011-0240-9.