Key result
Adiponectin gene transfer cuts Angiotensin II-accelerated atherosclerotic lesions ~48% independent of blood pressure.
Why the study?
It is unknown whether adiponectin provides atheroprotection under conditions of renin angiotensin system activation leading to vascular damage in metabolic syndrome.
Does sustained adiponectin expression via adenoviral gene transfer prevent atherosclerosis and vascular inflammation in a hypertensive and accelerated atherosclerosis model?
Does sustained adiponectin expression via adenoviral gene transfer prevent atherosclerosis and vascular inflammation in a hypertensive and accelerated atherosclerosis model?
Effect estimate: 48% reduction
p-value: p=<0.01
Increasing adiponectin levels via gene transfer provides atheroprotection and reduces vascular inflammation in a model of RAS activation, suggesting a potential therapeutic strategy for metabolic syndrome-associated cardiovascular disease.
Adiponectin modulation warrants further preclinical study in Ang II models; clinical translation remains untested.
Adiponectin (APN), an adipocytokine produced by adipose tissue, exerts pleiotropic actions regulating inflammation, metabolism and vascular homeostasis. APN levels are inversely correlated with obesity, type-2 diabetes, hypertension and cardiovascular disease. Although renin angiotensin system (RAS) activation in these interrelated metabolic syndrome components increases angiotensin II (AngII) levels leading to vascular damage, it is unknown whether APN under these conditions provides atheroprotection. We investigated whether increasing plasma APN provides atheroprotection in a hypertensive and accelerated atherosclerosis model. Using adenoviral gene transfer, sustained APN expression increased plasma levels of total and high-molecular weight APN, leading to a significant elevation of plasma HDL-cholesterol (HDL-C). Elevated APN levels were strongly atheroprotective, yet had no impact on blood pressure. Notably, gene expression analyses revealed that APN significantly inhibited the expression of pro-inflammatory and atherogenic genes while it increased the expression of the anti-inflammatory cytokine, IL-10 and the cholesterol efflux transporters, ABCA1 and ABCG1 in the artery wall. These findings suggest that increasing APN levels may be an effective therapeutic strategy to inhibit vascular inflammation and accelerated atherosclerosis associated with RAS activation in the metabolic syndrome.
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Stijn et al. (2014) studied Angiotensin II-induced accelerated atherosclerosis and hypertension (n=44). Adenoviral gene transfer of adiponectin (AdAPN) vs. Control adenovirus expressing GFP (AdGFP) or PBS was evaluated on Atherosclerotic lesion area in entire aortas (en face analysis) (48% reduction, p=<0.01). Adenoviral expression of adiponectin significantly reduced Angiotensin II-accelerated atherosclerotic lesion development by 48% (p<0.01) without lowering blood pressure.
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