Department of Cardiology, Rui Jin Hospital, Shanghai Jiaotong University School of Medicine, 197 Rui Jin Road II, Shanghai 200025, People's Republic of China.
Eur Heart J. 2012 Sep;33(18):2297-306. doi: 10.1093/eurheartj/ehs122. Epub 2012 May 29.
We here investigated the endothelial effects of the chromogranin A-derived peptide vasostatin-2 and its relation to coronary artery disease (CAD).
We assessed the impact of recombinant vasostatin-1 and vasostatin-2 on tumour necrosis factor-alpha (TNFα)-, angiotensin II-, and oxidized low-density lipoprotein (oxLDL)-induced expression of adhesion molecules in human arterial endothelial cells. Vasostatin-1 and vasostatin-2 levels were examined in coronary endarterectomy specimens (n= 23), atherosclerotic aortas (n= 16), non-significant-atherosclerotic internal mammary arteries (n= 30), and non-atherosclerotic aortas (n= 10), as well as in peripheral blood mononuclear cells (PBMCs) from severe CAD patients (n= 50) and healthy volunteers (n= 21). Serum levels of vasostatin-2 were analysed in 968 consecutive patients undergoing coronary angiography. Vasostatin-1 and vasostatin-2 concentration-dependently inhibited TNFα-, angiotensin II-, and oxLDL-induced expression of adhesion molecules; and attenuated TNFα-induced adhesion of U937 monocytes to endothelial cells. Vasostatin-2 levels were significantly decreased in endarterectomy samples and atherosclerotic aortas compared with non-atherosclerotic internal mammary arteries and aortas, as well as in PBMCs of severe CAD patients compared with healthy controls (all P< 0.05). Serum vasostatin-2 levels were significantly lower in CAD patients (diameter stenosis ≥ 50%, n= 554) than in controls (normal arteries or diameter stenosis <30%, n= 281) (P< 0.001). Its concentrations correlated with the number of diseased coronary arteries and Syntax score in CAD patients (all P< 0.05). At multivariable regression analysis, decreased vasostatin-2 levels remained associated with CAD when other variables were taken into account.
Vasostatin-2 has anti-inflammatory properties and is decreased in atherosclerotic plaque specimens and in PBMC of CAD patients. Decreased serum vasostatin-2 levels are associated with the presence and severity of CAD.
本研究旨在探讨嗜铬粒蛋白 A 衍生肽血管抑肽-2 的内皮细胞效应及其与冠状动脉疾病(CAD)的关系。
我们评估了重组血管抑肽-1 和血管抑肽-2 对肿瘤坏死因子-α(TNFα)、血管紧张素 II 和氧化型低密度脂蛋白(oxLDL)诱导的人动脉内皮细胞黏附分子表达的影响。在冠状动脉内膜切除术标本(n=23)、粥样硬化主动脉(n=16)、非粥样硬化性内乳动脉(n=30)和非粥样硬化性主动脉(n=10)中检测了血管抑肽-1 和血管抑肽-2 的水平,以及严重 CAD 患者(n=50)和健康志愿者(n=21)的外周血单核细胞(PBMC)中。对 968 例连续接受冠状动脉造影的患者进行了血清血管抑肽-2 水平分析。血管抑肽-1 和血管抑肽-2 浓度依赖性地抑制了 TNFα、血管紧张素 II 和 oxLDL 诱导的黏附分子表达,并减弱了 TNFα 诱导的 U937 单核细胞与内皮细胞的黏附。与非粥样硬化性内乳动脉和主动脉以及严重 CAD 患者的 PBMC 相比,内膜切除术标本和粥样硬化主动脉中的血管抑肽-2 水平显著降低(所有 P<0.05)。与对照组(正常动脉或直径狭窄<30%,n=281)相比,CAD 患者(直径狭窄≥50%,n=554)的血清血管抑肽-2 水平显著降低(P<0.001)。在 CAD 患者中,其浓度与病变冠状动脉的数量和Syntax 评分相关(所有 P<0.05)。在多元回归分析中,当考虑其他变量时,降低的血管抑肽-2 水平与 CAD 仍然相关。
血管抑肽-2 具有抗炎作用,在粥样斑块标本和 CAD 患者的 PBMC 中减少。血清血管抑肽-2 水平降低与 CAD 的存在和严重程度相关。