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Insights into the activity, differential expression, mutual regulation, and functions of matrix metalloproteinases and a disintegrin and metalloproteinases in hypertension and cardiac disease.基质金属蛋白酶和去整合素金属蛋白酶在高血压和心脏疾病中的活性、差异表达、相互调节及功能研究
J Vasc Res. 2013;50(1):52-68. doi: 10.1159/000345240. Epub 2012 Nov 17.
2
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.
3
Matrix metalloproteinase activity causes VEGFR-2 cleavage and microvascular rarefaction in rat mesentery.基质金属蛋白酶活性导致大鼠肠系膜中 VEGFR-2 的裂解和微血管稀疏。
Microcirculation. 2011 Apr;18(3):228-37. doi: 10.1111/j.1549-8719.2011.00082.x.
4
Nuclear factor kappa B and matrix metalloproteinase induced receptor cleavage in the spontaneously hypertensive rat.核因子-κB 和基质金属蛋白酶诱导的受体裂解在自发性高血压大鼠中。
Hypertension. 2011 Feb;57(2):261-8. doi: 10.1161/HYPERTENSIONAHA.110.158709. Epub 2011 Jan 10.
5
Crosstalk of reactive oxygen species and NF-κB signaling.活性氧与 NF-κB 信号通路的相互作用。
Cell Res. 2011 Jan;21(1):103-15. doi: 10.1038/cr.2010.178. Epub 2010 Dec 28.
6
Matrix metalloproteinases cleave the beta2-adrenergic receptor in spontaneously hypertensive rats.基质金属蛋白酶在自发性高血压大鼠中裂解β2-肾上腺素能受体。
Am J Physiol Heart Circ Physiol. 2010 Jul;299(1):H25-35. doi: 10.1152/ajpheart.00620.2009. Epub 2010 Apr 9.
7
Enhanced matrix metalloproteinase activity in the spontaneously hypertensive rat: VEGFR-2 cleavage, endothelial apoptosis, and capillary rarefaction.自发性高血压大鼠中基质金属蛋白酶活性增强:血管内皮生长因子受体-2裂解、内皮细胞凋亡和毛细血管稀疏
J Vasc Res. 2010;47(5):423-31. doi: 10.1159/000281582. Epub 2010 Feb 6.
8
Imbalance between matrix metalloproteinases and tissue inhibitor of metalloproteinases in hypertensive vascular remodeling.高血压血管重构中基质金属蛋白酶与金属蛋白酶组织抑制剂失衡。
Matrix Biol. 2010 Apr;29(3):194-201. doi: 10.1016/j.matbio.2009.11.005. Epub 2009 Dec 5.
9
Molecular mechanisms of hypertension: role of Nox family NADPH oxidases.高血压的分子机制:Nox家族NADPH氧化酶的作用
Curr Opin Nephrol Hypertens. 2009 Mar;18(2):122-7. doi: 10.1097/MNH.0b013e32832923c3.
10
Antioxidant treatment reduces matrix metalloproteinase-2-induced vascular changes in renovascular hypertension.抗氧化剂治疗可减轻基质金属蛋白酶-2诱导的肾血管性高血压中的血管变化。
Free Radic Biol Med. 2009 May 1;46(9):1298-307. doi: 10.1016/j.freeradbiomed.2009.02.011. Epub 2009 Feb 25.

氧自由基调控自发性高血压大鼠 MMP-9 和转录因子的表达。

The oxygen free radicals control MMP-9 and transcription factors expression in the spontaneously hypertensive rat.

机构信息

Department of Bioengineering, Institute of Engineering in Medicine, University of California, San Diego, La Jolla, CA 92093-0412, USA; Division of Physiology, Department of Preclinical Science, Faculty of Medicine, Thammasat University, Pathum Thani 12121, Thailand.

出版信息

Microvasc Res. 2013 Nov;90:154-61. doi: 10.1016/j.mvr.2013.09.003. Epub 2013 Sep 21.

DOI:10.1016/j.mvr.2013.09.003
PMID:24060804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4642998/
Abstract

Oxygen free radical and matrix metalloproteinases-9 (MMP-9) play an important pathophysiological role in the development of chronic hypertension. MMP-9 activities are regulated at different levels. We hypothesize that as mediators of the expression of MMP-9 the transcription factors like nuclear factor kappa B (NF-κB), c-fos and retinoic acid receptors-α (RAR-α) with binding sites to the MMP-9 promoter are overexpressed in the spontaneously hypertensive rat (SHR) in a process that is regulated by oxygen free radicals. Transcription factor NF-κB, c-fos and RAR-α expression levels were determined by immunohistochemistry in renal, cardiac and mesentery microcirculation of the SHR and its normotensive control, the Wistar Kyoto (WKY) rat. The animals were treated with a superoxide scavenger (Tempol) for eight weeks. The elevated plasma levels of thiobarbituric acid reactive substances and MMP-9 levels in the SHR were significantly decreased by Tempol treatment (P<0.05). The NF-κB, c-fos and RAR-α expression levels in renal glomerular, heart and mesentery microvessels were enhanced in the SHR and could also be reduced by Tempol compared to untreated animals (P<0.05). The enhanced MMP-9 levels in SHR microvessels co-express with transcription factors. These results suggest that elevated NF-κB, c-fos and RAR-α expressions and MMP-9 activity in the SHR are superoxide-dependent.

摘要

氧自由基和基质金属蛋白酶-9(MMP-9)在慢性高血压的发展中起着重要的病理生理作用。MMP-9 的活性在不同水平上受到调节。我们假设,作为 MMP-9 表达的介质,转录因子如核因子 kappa B(NF-κB)、c-fos 和维甲酸受体-α(RAR-α)与 MMP-9 启动子的结合位点在自发性高血压大鼠(SHR)中过度表达,这个过程受氧自由基调节。通过免疫组织化学方法测定 SHR 及其正常血压对照 Wistar Kyoto(WKY)大鼠的肾、心和肠系膜微循环中转录因子 NF-κB、c-fos 和 RAR-α 的表达水平。动物用超氧化物清除剂(Tempol)处理 8 周。Tempol 治疗可显著降低 SHR 血浆中硫代巴比妥酸反应性物质和 MMP-9 水平(P<0.05)。SHR 肾小球、心脏和肠系膜微血管中 NF-κB、c-fos 和 RAR-α 的表达水平升高,与未处理动物相比,Tempol 也可降低其表达水平(P<0.05)。SHR 微血管中 MMP-9 水平升高与转录因子共表达。这些结果表明,SHR 中升高的 NF-κB、c-fos 和 RAR-α 表达和 MMP-9 活性依赖于超氧化物。