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金属蛋白酶抑制可改善肾血管性高血压大鼠的高血压状况,并预防血管功能障碍和重塑。

Metalloproteinase inhibition ameliorates hypertension and prevents vascular dysfunction and remodeling in renovascular hypertensive rats.

作者信息

Castro Michele M, Rizzi Elen, Figueiredo-Lopes Lívia, Fernandes Karla, Bendhack Lusiane M, Pitol Dimitrius Leonardo, Gerlach Raquel F, Tanus-Santos Jose E

机构信息

Department of Pharmacology, Faculty of Medicine of Ribeirao Preto, University of Sao Paulo, Av. Bandeirantes 3900, 14049-900 Ribeirao Preto, SP, Brazil.

出版信息

Atherosclerosis. 2008 Jun;198(2):320-31. doi: 10.1016/j.atherosclerosis.2007.10.011. Epub 2007 Dec 3.

Abstract

Altered activity of matrix metalloproteinases (MMPs) is implicated in the vascular remodeling of hypertension. We examined whether increased MMP-2 expression/activity plays a role in the vascular remodeling and dysfunction found in the two-kidney, one-clip (2K-1C) hypertension. Sham operated or 2K-1C hypertension rats were treated with doxycycline 30mg/(kgday) (or vehicle). Systolic blood pressure was monitored weekly. After 8 weeks of treatment, aortic rings were isolated to assess endothelium-dependent and independent relaxations. Quantitative morphometry of structural changes, collagen, and elastin contents in the aortic wall were studied in hematoxylin/eosin, Sirius Red, and Orceine stained aortic sections, respectively. Aortic MMP-2 levels were determined by gelatin zymography and aortic MMP-2 proteolytic activity was measured using DQ gelatin as the substrate after MMP-2 was captured by a specific antibody and immobilized on a microplate. Aortic MMP-2/tissue inhibitor of metalloproteinases (TIMP)-2 mRNA levels were determined by real time RT-PCR. Doxycycline attenuated 2K-1C hypertension (215+/-8mmHg versus 167+/-13mmHg in 2K-1C rats and 2K-1C+doxy rats, respectively; P<0.01) and prevented the 35% reduction in endothelium-dependent vasorelaxation found in 2K-1C rats. Doxycycline prevented the increases in media thickness, and was associated with lower media/lumen and cross-sectional areas (all P<0.01). Doxycycline also prevented excessive collagen and elastin deposition in the vascular wall. Increased MMP-2 and Pro-MMP-2 levels and MMP-2 activity were found in the aortas of 2K-1C rats (all P<0.05). A 21-fold increase (P<0.001) in the ratio of MMP-2/TIMP-2 mRNA expression was found in the 2K-1C group, whereas this ratio remained unaltered in 2K-1C+doxy rats. Our results suggest that MMP-2 plays a role in 2K-1C hypertension and its structural and functional vascular changes, which were attenuated by doxycycline.

摘要

基质金属蛋白酶(MMPs)活性改变与高血压的血管重塑有关。我们研究了MMP - 2表达/活性增加是否在两肾一夹(2K - 1C)高血压所致的血管重塑和功能障碍中起作用。对假手术或2K - 1C高血压大鼠给予强力霉素30mg/(kg·天)(或赋形剂)治疗。每周监测收缩压。治疗8周后,分离主动脉环以评估内皮依赖性和非依赖性舒张功能。分别在苏木精/伊红、天狼星红和orceine染色的主动脉切片中研究主动脉壁结构变化、胶原蛋白和弹性蛋白含量的定量形态学。通过明胶酶谱法测定主动脉MMP - 2水平,并在MMP - 2被特异性抗体捕获并固定在微孔板上后,以DQ明胶为底物测量主动脉MMP - 2的蛋白水解活性。通过实时RT - PCR测定主动脉MMP - 2/金属蛋白酶组织抑制剂(TIMP)- 2 mRNA水平。强力霉素减轻了2K - 1C高血压(2K - 1C大鼠和2K - 1C + 强力霉素大鼠的收缩压分别为215±8mmHg和167±13mmHg;P<0.01),并防止了2K - 1C大鼠中出现的内皮依赖性血管舒张功能降低35%的情况。强力霉素阻止了中膜厚度增加,并使其与中膜/管腔和横截面积降低相关(均P<0.01)。强力霉素还阻止了血管壁中胶原蛋白和弹性蛋白的过度沉积。在2K - 1C大鼠的主动脉中发现MMP - 2和前MMP - 2水平及MMP - 2活性增加(均P<0.05)。在2K - 1C组中,MMP - 2/TIMP - 2 mRNA表达比值增加了21倍(P<0.001),而在2K - 1C + 强力霉素大鼠中该比值保持不变。我们的结果表明,MMP - 2在2K - 1C高血压及其血管结构和功能变化中起作用,而强力霉素可减轻这些变化。

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