Biwer Lauren A, D'souza Karen M, Abidali Ali, Tu Danni, Siniard Ashley L, DeBoth Matthew, Huentelman Matthew, Hale Taben M
Department of Basic Medical Sciences, University of Arizona, College of Medicine-Phoenix, Phoenix AZ, USA.
Neurogenomics Division, The Translational Genomics Research Institute, Phoenix, AZ, USA.
Hypertens Res. 2016 Jan;39(1):8-18. doi: 10.1038/hr.2015.107. Epub 2015 Oct 22.
We have previously demonstrated that angiotensin-converting enzyme (ACE) inhibition with enalapril produces persistent effects that protect against future nitric oxide synthase (NOS) inhibitor (L-arginine methyl ester, L-NAME)-induced cardiac dysfunction and outer wall collagen deposition in spontaneously hypertensive rats (SHR). In the present study, we dissect the cytokine/chemokine release profile during NOS inhibition, its correlation to pathological cardiac remodeling and the impact of transient ACE inhibition on these effects. Adult male SHR were treated with enalapril (E+L) or tap water (C+L) for 2 weeks followed by a 2-week washout period. Rats were then subjected to 0, 3, 7 or 10 days of L-NAME treatment. The temporal response to NOS inhibition was evaluated by measuring arterial pressure, cardiac remodeling and cytokine/chemokine levels. L-NAME equivalently increased blood pressure and myocardial and vascular injury in C+L and E+L rats. However, pulse pressure (PP) was only transiently altered in C+L rats. The levels of several inflammatory mediators were increased during L-NAME treatment. However, interleukin-6 (IL-6) and IL-10 and monocyte chemoattractant protein-1 were uniquely increased in C+L hearts; whereas IL-4 and fractalkine were only elevated in E+L hearts. By days 7 and 10 of L-NAME treatment, there was a significant increase in the cardiac density of macrophages and proliferating cells, respectively only in C+L rats. Although myocardial injury was similar in both treatment groups, PP was not changed and there was a distinct cardiac chemokine/cytokine signature in rats previously treated with enalapril that may be related to the lack of proliferative response and macrophage infiltration in these hearts.
我们之前已经证明,依那普利抑制血管紧张素转换酶(ACE)会产生持久效应,可预防未来一氧化氮合酶(NOS)抑制剂(L-精氨酸甲酯,L-NAME)诱导的自发性高血压大鼠(SHR)心脏功能障碍和外壁胶原沉积。在本研究中,我们剖析了NOS抑制过程中的细胞因子/趋化因子释放谱、其与病理性心脏重塑的相关性以及短暂ACE抑制对这些效应的影响。成年雄性SHR用依那普利(E+L)或自来水(C+L)处理2周,随后有2周的洗脱期。然后大鼠接受0、3、7或10天的L-NAME处理。通过测量动脉血压、心脏重塑和细胞因子/趋化因子水平来评估对NOS抑制的时间反应。L-NAME同等程度地增加了C+L和E+L大鼠的血压以及心肌和血管损伤。然而,C+L大鼠的脉压(PP)仅出现短暂改变。在L-NAME处理期间,几种炎症介质的水平升高。然而,白细胞介素-6(IL-6)、IL-10和单核细胞趋化蛋白-1仅在C+L心脏中独特地增加;而IL-4和 fractalkine仅在E+L心脏中升高。到L-NAME处理的第7天和第10天,仅在C+L大鼠中,巨噬细胞和增殖细胞的心脏密度分别显著增加。尽管两个治疗组的心肌损伤相似,但PP没有变化,并且在先前用依那普利治疗的大鼠中存在独特的心脏趋化因子/细胞因子特征,这可能与这些心脏中缺乏增殖反应和巨噬细胞浸润有关。