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对称二甲基精氨酸通过单核细胞中储存式钙内流增加活性氧在血管损伤中的作用。

Role of symmetric dimethylarginine in vascular damage by increasing ROS via store-operated calcium influx in monocytes.

作者信息

Schepers Eva, Glorieux Griet, Dhondt Annemieke, Leybaert Luc, Vanholder Raymond

机构信息

Renal Division, Department of Internal Medicine, University Hospital Gent, Gent, Belgium.

出版信息

Nephrol Dial Transplant. 2009 May;24(5):1429-35. doi: 10.1093/ndt/gfn670. Epub 2008 Dec 4.

Abstract

BACKGROUND

The guanidines asymmetric dimethylarginine (ADMA), a marker of endothelial dysfunction, and its counterpart symmetric dimethylarginine (SDMA), considered inert, are accumulated in chronic kidney disease (CKD). The present study evaluates their effect on monocyte function, since previous data demonstrated leukocyte activation by other guanidino compounds.

METHODS

The effect of ADMA and SDMA on reactive oxygen species (ROS) production in human whole blood at baseline and after N-formyl-methionine-leucine-phenylalanine (fMLP) stimulation was evaluated. By using the fluorescent probe Fluo3-AM, the role of changes in monocytic cytoplasmic calcium ([Ca2+]i) was studied. Thapsigargin, and removal followed by addition of extracellular Ca2+ (Ca2+(ex)), was used to investigate the contribution of store-operated Ca2+-channels (SOCs). SKF96365 was used as a selective inhibitor of the SOCs. A pharmacologic intervention with captopril, known to affect Ca2+ influx, was tested.

RESULTS

SDMA enhanced ROS production in fMLP-stimulated monocytes using heparinized blood, and this effect was abolished in EDTA-anticoagulated blood. In the presence of SDMA, an increased Ca2+ entry from the extracellular milieu resulted in an elevated amplitude of the peak [Ca2+]i change triggered by fMLP. None of these effects were seen with ADMA. Depletion of the intracellular stores with thapsigargin in the absence of Ca2+(ex), followed by re-addition of Ca2+(ex) triggered a significantly larger Ca2+ entry after SDMA treatment versus saline. This effect was prevented with SKF96365, as was the SDMA-enhanced oxidative burst after fMLP. Pre-incubation with captopril also reduced the increased ROS production seen with SDMA.

CONCLUSIONS

SDMA, a uraemic retention solute considered inert, stimulates ROS production of monocytes by acting on Ca2+ entry via SOCs. This pro-inflammatory effect may trigger vascular pathology and may be involved in altering the prevalence of cardiovascular disease in CKD.

摘要

背景

内皮功能障碍标志物胍类物质不对称二甲基精氨酸(ADMA)及其相对应的被认为无活性的对称二甲基精氨酸(SDMA)在慢性肾脏病(CKD)中会蓄积。本研究评估它们对单核细胞功能的影响,因为先前的数据表明其他胍基化合物可激活白细胞。

方法

评估了ADMA和SDMA对人全血在基线时以及在N-甲酰甲硫氨酸-亮氨酸-苯丙氨酸(fMLP)刺激后活性氧(ROS)产生的影响。通过使用荧光探针Fluo3-AM,研究了单核细胞胞质钙([Ca2+]i)变化的作用。使用毒胡萝卜素,并在去除后添加细胞外Ca2+(Ca2+(ex)),以研究储存操纵性Ca2+通道(SOCs)的作用。SKF96365用作SOCs的选择性抑制剂。测试了已知会影响Ca2+内流的卡托普利的药物干预作用。

结果

使用肝素化血液时,SDMA增强了fMLP刺激的单核细胞中ROS的产生,而在EDTA抗凝血液中这种作用消失。在存在SDMA的情况下,细胞外环境中Ca2+的进入增加导致fMLP触发的[Ca2+]i变化峰值幅度升高。ADMA未观察到这些作用。在不存在Ca2+(ex)的情况下用毒胡萝卜素耗尽细胞内储存,然后重新添加Ca2+(ex),与生理盐水相比,SDMA处理后触发了明显更大的Ca2+内流。SKF96365可阻止这种作用,fMLP后SDMA增强的氧化爆发也可被阻止。用卡托普利预孵育也减少了SDMA所见的ROS产生增加。

结论

SDMA是一种被认为无活性的尿毒症潴留溶质,通过作用于经由SOCs的Ca2+进入来刺激单核细胞的ROS产生。这种促炎作用可能触发血管病变,并可能参与改变CKD中心血管疾病的患病率。

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