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首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Attenuation of increased secretory leukocyte protease inhibitor, matricellular proteins and angiotensin II and left ventricular remodeling by candesartan and omapatrilat during healing after reperfused myocardial infarction
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Attenuation of increased secretory leukocyte protease inhibitor, matricellular proteins and angiotensin II and left ventricular remodeling by candesartan and omapatrilat during healing after reperfused myocardial infarction

机译:再灌注心肌梗死愈合过程中坎地沙坦和奥马修拉利对增加的分泌性白细胞蛋白酶抑制剂,基质细胞蛋白和血管紧张素II的衰减以及左心室重构

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While secretory-leukocyte-protease-inhibitor (SLPI) may promote skin wound healing, its role in infarct healing after reperfused myocardial infarction (RMI) remains unclear. Short-term intravenous angiotensin II (AngII) receptor blocker therapy with candesartan (CN) attenuates increased SLPI and markers of early matrix/left ventricular (LV) in acute RMI. To determine whether reducing effects of AngII with CN or the vasopeptidase inhibitor omapatrilat (OMA) during the healing phase after RMI attenuates SLPI and other mediators of healing and matrix/LV remodeling, we measured these in Sprague-Dawley rats randomized to oral placebo, CN (30 mg/kg/day) or OMA (10 mg/kg/day) therapy during healing between days 2 and 23 after RMI and sham. On day-25, RMI-placebo showed significant LV remodeling, systolic/diastolic dysfunction and impaired passive compliance, and ischemic zone increases in SLPI, secreted-protein-acidic-and- rich-in-cysteine (SPARC) and osteopontin (OPN) mRNA and protein. In addition, metalloproteinase (MMP)-9 and -2, a-disintegrin-and-metalloproteinase (ADAM)-10 and -17, inducible-nitric-oxide-synthase (iNOS), pro-inflammatory cytokines interleukin (IL)-6, and tumor necrosis factor-??, transforming growth factor (TGF)-??1 and its signaling molecule p-Smad-2, myeloperoxidase (MPO), AngII, MPO-positive granulocytes, MAC387-positive macrophages and monocytes, scar collagens, cardiomyocyte and fibroblast apoptosis, and microvascular no-reflow also increased whereas anti-inflammatory cytokine IL-10 decreased. Both CN and OMA attenuated all the changes except IL-10, which normalized. Thus, CN or OMA treatment during healing after RMI results in attenuation of SLPI as well as tissue AngII and mediators of inflammation and matrix/LV remodeling including SPARC, OPN, and ADAMs. Whether increasing SLPI on top of background AngII inhibition or therapy such as CN or OMA might produce added remodeling benefit needs study. ? 2013 Springer Science+Business Media New York.
机译:尽管分泌型白细胞蛋白酶抑制剂(SLPI)可以促进皮肤伤口愈合,但在再灌注心肌梗塞(RMI)后其在梗塞愈合中的作用仍不清楚。坎地沙坦(CN)短期静脉内血管紧张素II(AngII)受体阻滞剂治疗可减轻急性RMI中SLPI的升高和早期基质/左心室(LV)的标记。为了确定RMI减轻SLPI和其他介导的愈合以及基质/ LV重塑的介导因子在RMI减轻愈合阶段后,在CN或血管肽酶抑制剂omapatrilat(OMA)方面对AngII的降低作用,我们在随机分配给口服安慰剂CN的Sprague-Dawley大鼠中测量了这些(30 mg / kg /天)或OMA(10 mg / kg /天)治疗在RMI和假手术后第2至23天的愈合期间。第25天,RMI-安慰剂显示出严重的LV重塑,收缩/舒张功能障碍和被动顺应性受损,SLPI,分泌的蛋白质酸性和富含半胱氨酸(SPARC)和骨桥蛋白(OPN)的缺血区增加mRNA和蛋白质。此外,金属蛋白酶(MMP)-9和-2,α-解整合素和金属蛋白酶(ADAM)-10和-17,诱导型一氧化氮合酶(iNOS),促炎细胞因子白介素(IL)-6 ,肿瘤坏死因子-α,转化生长因子(TGF)-α-1及其信号分子p-Smad-2,髓过氧化物酶(MPO),AngII,MPO阳性粒细胞,MAC387阳性巨噬细胞和单核细胞,瘢痕胶原,心肌细胞和成纤维细胞凋亡以及微血管无回流也增加,而抗炎细胞因子IL-10减少。 CN和OMA都减弱了除归一化的IL-10以外的所有变化。因此,RMI愈合后的CN或OMA治疗会导致SLPI以及组织AngII和炎症介质和基质/ LV重塑的衰减,包括SPARC,OPN和ADAM。除背景AngII抑制之外增加SLPI还是采用CN或OMA等疗法可能还会产生额外的重塑益处,这需要进行研究。 ? 2013年Springer Science + Business Media纽约。

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