Li Wenjing, Li Jifu, Hao Panpan, Chen Wenqiang, Meng Xiao, Li Hongxuan, Zhang Yun, Zhang Cheng, Yang Jianmin
The Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education and Chinese Ministry of Public Health, Qilu Hospital, Shandong University, P.R. China Fine Arts School of Shandong University, P.R. China.
The Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education and Chinese Ministry of Public Health, Qilu Hospital, Shandong University, P.R. China.
J Renin Angiotensin Aldosterone Syst. 2016 Jul 18;17(3). doi: 10.1177/1470320316659618. Print 2016 Jul.
Our previous studies found that angiotensin-(1-7) (Ang-(1-7)) is an endogenous counter-factor of angiotensin II (Ang-II). However, the balance between Ang-II and Ang-(1-7) in the development of human coronary atherosclerosis is not determined.
The plasma levels of Ang-II and Ang-(1-7) were detected by enzyme-linked immunosorbent assay (ELISA) in 112 patients with known or suspected coronary artery disease (CAD) undergoing coronary angiography. Patients were divided into three groups based on the coronary angiography as follows: (1) normal (n = 13); (2) noncritical CAD (<50% stenosis, n = 17); and (3) critical CAD (⩾50% stenosis, n = 82). The plasma levels of Ang-II, Ang-(1-7) and the ratio of Ang-II and Ang-(1-7) (Ang-II/Ang-(1-7) were comparable between the normal and noncritical CAD groups. However, Ang-II, Ang-(1-7), and especially Ang-II/Ang-(1-7), were elevated in patients with critical CAD, compared with patients with normal or noncritical CAD. The level of Ang-II/Ang-(1-7) was positively associated with serious coronary stenosis, and correlated with tumor necrosis factor-alpha (TNF-α) level.
Both Ang-II and Ang-(1-7) expression are significantly increased in patients with critical CAD. However, increased Ang-II/Ang-(1-7) ratios may lead to Ang-II over-activation and aggravate atherosclerosis progression.
我们之前的研究发现血管紧张素 -(1 - 7)(Ang -(1 - 7))是血管紧张素II(Ang - II)的内源性拮抗因子。然而,在人类冠状动脉粥样硬化发展过程中Ang - II与Ang -(1 - 7)之间的平衡尚未明确。
采用酶联免疫吸附测定法(ELISA)检测了112例已知或疑似冠心病(CAD)且接受冠状动脉造影的患者血浆中Ang - II和Ang -(1 - 7)的水平。根据冠状动脉造影结果将患者分为三组:(1)正常组(n = 13);(2)非严重CAD组(狭窄<50%,n = 17);(3)严重CAD组(狭窄⩾50%,n = 82)。正常组和非严重CAD组之间血浆Ang - II、Ang -(1 - 7)水平以及Ang - II与Ang -(1 - 7)的比值(Ang - II/Ang -(1 - 7))相当。然而,与正常或非严重CAD患者相比,严重CAD患者的Ang - II、Ang -(1 - 7)水平,尤其是Ang - II/Ang -(1 - 7)升高。Ang - II/Ang -(1 - 7)水平与严重冠状动脉狭窄呈正相关,并与肿瘤坏死因子 -α(TNF -α)水平相关。
严重CAD患者中Ang - II和Ang -(1 - 7)的表达均显著增加。然而,Ang - II/Ang -(1 - 7)比值升高可能导致Ang - II过度激活并加重动脉粥样硬化进展。