Suppr超能文献

血管舒张剂刺激磷蛋白丝氨酸239磷酸化作为一氧化氮/cGMP信号缺陷和内皮功能障碍的敏感监测指标。

Vasodilator-stimulated phosphoprotein serine 239 phosphorylation as a sensitive monitor of defective nitric oxide/cGMP signaling and endothelial dysfunction.

作者信息

Oelze M, Mollnau H, Hoffmann N, Warnholtz A, Bodenschatz M, Smolenski A, Walter U, Skatchkov M, Meinertz T, Münzel T

机构信息

Abteilung für Kardiologie, Universitäts-Krankenhaus Eppendorf, University of Hamburg, Hamburg, Germany.

出版信息

Circ Res. 2000 Nov 24;87(11):999-1005. doi: 10.1161/01.res.87.11.999.

Abstract

Studies with cGMP-dependent protein kinase I (cGK-I)-deficient human cells and mice demonstrated that cGK-I ablation completely disrupts the NO/cGMP pathway in vascular tissue, which indicates a key role of this protein kinase as a mediator of the NO/cGMP action. Analysis of the vasodilator-stimulated phosphoprotein phosphorylated at serine 239 (P-VASP) is a useful tool to monitor cGK-I activation in platelets and cultured endothelial and smooth muscle cells. Therefore, we investigated whether endothelial dysfunction and/or vascular NO bioavailability is reflected by decreased vessel wall P-VASP and whether improvement of endothelial dysfunction restores this P-VASP. Incubation of aortic tissue from New Zealand White Rabbits with the NOS inhibitor N:(G)-nitro-Ld-arginine and endothelial removal strikingly reduced P-VASP. Oxidative stress induced by inhibition of CuZn superoxide dismutase increased superoxide and decreased P-VASP. Endothelial dysfunction in hyperlipidemic Watanabe rabbits (WHHL) was associated with increased vascular superoxide and with decreased P-VASP. Treatment of WHHL with AT(1) receptor blockade improved endothelial dysfunction, reduced vascular superoxide, increased vascular NO bioavailability, and increased P-VASP. Therefore, the level of vessel P-VASP closely follows changes in endothelial function and vascular oxidative stress. P-VASP is suggested to represent a novel biochemical marker for monitoring the NO-stimulated sGC/cGK-I pathway and endothelial integrity in vascular tissue.

摘要

对依赖环磷酸鸟苷(cGMP)的蛋白激酶I(cGK-I)缺陷的人类细胞和小鼠进行的研究表明,cGK-I缺失会完全破坏血管组织中的一氧化氮(NO)/cGMP信号通路,这表明该蛋白激酶作为NO/cGMP作用的介质起着关键作用。分析在丝氨酸239处磷酸化的血管舒张剂刺激磷蛋白(P-VASP)是监测血小板以及培养的内皮细胞和平滑肌细胞中cGK-I激活的有用工具。因此,我们研究了血管壁P-VASP降低是否反映了内皮功能障碍和/或血管NO生物利用度,以及内皮功能障碍的改善是否能恢复这种P-VASP。用一氧化氮合酶(NOS)抑制剂N:(G)-硝基-L-精氨酸孵育新西兰白兔的主动脉组织并去除内皮,可显著降低P-VASP。抑制铜锌超氧化物歧化酶诱导的氧化应激会增加超氧化物并降低P-VASP。高脂血症渡边兔(WHHL)的内皮功能障碍与血管超氧化物增加和P-VASP降低有关。用血管紧张素II 1型(AT1)受体阻滞剂治疗WHHL可改善内皮功能障碍,降低血管超氧化物,增加血管NO生物利用度,并增加P-VASP。因此,血管P-VASP水平与内皮功能和血管氧化应激的变化密切相关。P-VASP被认为是监测血管组织中NO刺激的可溶性鸟苷酸环化酶(sGC)/cGK-I信号通路和内皮完整性的新型生化标志物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验