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Title: Resveratrol inhibits growth of experimental abdominal aortic aneurysm associated with upregulation of angiotensin-converting enzyme 2
Austin Authors: Moran, Corey S;Biros, Erik;Krishna, Smriti M;Wang, Yutang;Tikellis, Chris;Moxon, Joseph V;Cooper, Mark E;Norman, Paul E;Burrell, Louise M ;Thomas, Merlin C;Golledge, Jonathan
Affiliation: Department of Medicine, The University of Melbourne, Austin Health, Heidelberg, Victoria, Australia
Vascular Biology Unit, Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, Australia
School of Applied and Biomedical Sciences, Faculty of Science and Technology, Federation University Australia, Mount Helen, Victoria
Department of Diabetes, Central Clinical School, Monash University, Melbourne, Victoria, Australia
School of Surgery, Fremantle Hospital, University of Western Australia
Department of Vascular and Endovascular Surgery, Townsville Hospital, Queensland, Australia
Issue Date: Nov-2017 2017-09-21
Publication information: Arteriosclerosis, Thrombosis, and Vascular Biology 2017; 37(11): 2195-2203
Abstract: OBJECTIVE: Recent evidence suggests an important role for angiotensin-converting enzyme 2 (ACE2) in limiting abdominal aortic aneurysm (AAA). This study examined the effect of ACE2 deficiency on AAA development and the efficacy of resveratrol to upregulate ACE2 in experimental AAA. APPROACH AND RESULTS: Ace2 deletion in apolipoprotein-deficient mice (ApoE-/-Ace2-/y ) resulted in increased aortic diameter and spontaneous aneurysm of the suprarenal aorta associated with increased expression of inflammation and proteolytic enzyme markers. In humans, serum ACE2 activity was negatively associated with AAA diagnosis. ACE2 expression was lower in infrarenal biopsies of patients with AAA than organ donors. AAA was more severe in ApoE-/-Ace2-/y mice compared with controls in 2 experimental models. Resveratrol (0.05/100-g chow) inhibited growth of pre-established AAAs in ApoE-/- mice fed high-fat chow and infused with angiotensin II continuously for 56 days. Reduced suprarenal aorta dilatation in mice receiving resveratrol was associated with elevated serum ACE2 and increased suprarenal aorta tissue levels of ACE2 and sirtuin 1 activity. In addition, the relative phosphorylation of Akt and ERK (extracellular signal-regulated kinase) 1/2 within suprarenal aorta tissue and gene expression for nuclear factor of kappa light polypeptide gene enhancer in B cells 1, angiotensin type-1 receptor, and metallopeptidase 2 and 9 were significantly reduced. Upregulation of ACE2 in human aortic smooth muscle cells by resveratrol in vitro was sirtuin 1-dependent. CONCLUSIONS: This study provides experimental evidence of an important role for ACE2 in limiting AAA development and growth. Resveratrol upregulated ACE2 and inhibited AAA growth in a mouse model.
DOI: 10.1161/ATVBAHA.117.310129
ORCID: 0000-0003-1863-7539
PubMed URL:
Type: Journal Article
Subjects: Aneurysm
Angiotensin II
Appears in Collections:Journal articles

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