Wågsäter Dick, Vorkapic Emina, van Stijn Caroline M W, Kim Jason, Lusis Aldons J, Eriksson Per, Tangirala Rajendra K
Division of Drug research, Department of Medical and Health Sciences, Faculty of Health Science, Linköping University, Linköping, Sweden.
Division of Endocrinology, Diabetes and Hypertension, David Geffen School of Medicine, University of California, Los Angeles, USA.
Sci Rep. 2016 Sep 23;6:31414. doi: 10.1038/srep31414.
Abdominal aortic aneurysm (AAA) is a degenerative disease characterized by aortic dilation and rupture leading to sudden death. Currently, no non-surgical treatments are available and novel therapeutic targets are needed to prevent AAA. We investigated whether increasing plasma levels of adiponectin (APN), a pleiotropic adipokine, provides therapeutic benefit to prevent AngII-induced advanced AAA in a well-established preclinical model. In the AngII-infused hyperlipidemic low-density lipoprotein receptor-deficient mouse (LDLR) model, we induced plasma APN levels using a recombinant adenovirus expressing mouse APN (AdAPN) and as control, adenovirus expressing green florescent protein (AdGFP). APN expression produced sustained and significant elevation of total and high-molecular weight APN levels and enhanced APN localization in the artery wall. AngII infusion for 8 weeks induced advanced AAA development in AdGFP mice. Remarkably, APN inhibited the AAA development in AdAPN mice by suppressing aortic inflammatory cell infiltration, medial degeneration and elastin fragmentation. APN inhibited the angiotensin type-1 receptor (AT1R), inflammatory cytokine and mast cell protease expression, and induced lysyl oxidase (LOX) in the aortic wall, improved systemic cytokine profile and attenuated adipose inflammation. These studies strongly support APN therapeutic actions through multiple mechanisms inhibiting AngII-induced AAA and increasing plasma APN levels as a strategy to prevent advanced AAA.
腹主动脉瘤(AAA)是一种退行性疾病,其特征为主动脉扩张和破裂,可导致猝死。目前尚无非手术治疗方法,因此需要新的治疗靶点来预防AAA。我们研究了提高多效性脂肪因子脂联素(APN)的血浆水平是否能在一个成熟的临床前模型中为预防血管紧张素II(AngII)诱导的晚期AAA提供治疗益处。在AngII灌注的高脂血症低密度脂蛋白受体缺陷小鼠(LDLR)模型中,我们使用表达小鼠APN的重组腺病毒(AdAPN)诱导血浆APN水平,并作为对照,使用表达绿色荧光蛋白的腺病毒(AdGFP)。APN表达使总APN水平和高分子量APN水平持续显著升高,并增强了APN在动脉壁中的定位。在AdGFP小鼠中,AngII灌注8周可诱导晚期AAA的发展。值得注意的是,APN通过抑制主动脉炎性细胞浸润、中膜退变和弹性蛋白断裂,抑制了AdAPN小鼠中AAA的发展。APN抑制主动脉壁中的血管紧张素1型受体(AT1R)、炎性细胞因子和肥大细胞蛋白酶的表达,并诱导赖氨酰氧化酶(LOX),改善全身细胞因子谱并减轻脂肪炎症。这些研究有力地支持了APN通过多种机制发挥治疗作用,抑制AngII诱导的AAA,并提高血浆APN水平作为预防晚期AAA的一种策略。