Iron Overload and Abdominal Aortic Aneurysm

被引:1
作者
Li, Yunyi [1 ,2 ]
Zhou, Quan [1 ,2 ]
Zhang, Kai [1 ,2 ]
Meng, Xiao [1 ,2 ]
机构
[1] Shandong Univ, Cheeloo Coll Med, Qilu Hosp, Chinese Natl Hlth Commiss,Chinese Minist Educ,Key, Jinan 250012, Shandong, Peoples R China
[2] Shandong Univ, Chinese Acad Med Sci, Cheeloo Coll Med, Dept Cardiol,Qilu Hosp,State & Shandong Prov Joint, Jinan 250012, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
iron overload; abdominal aortic aneurysm; inflammation; oxidative stress; endothelial function; ANGIOTENSIN-II; DIETARY IRON; ATHEROSCLEROTIC PLAQUE; OXIDATIVE STRESS; MACROPHAGE IRON; UP-REGULATION; INFLAMMATION; DYSFUNCTION; METABOLISM; INHIBITION;
D O I
10.31083/j.rcm2510361
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Abdominal aortic aneurysm (AAA) is a chronic vascular degenerative disease characterized by progressive segmental dilation of the abdominal aorta. The rupture of an AAA represents a leading cause of death in cardiovascular diseases. Despite numerous experimental and clinical studies examining potential drug targets and therapies, currently there are no pharmaceutical treatment to prevent AAA growth and rupture. Iron is an essential element in almost all living organisms and has important biological functions. Epidemiological studies have indicated that both iron deficiency and overload are associated with adverse clinical outcomes, particularly an increased risk of cardiovascular events. Recent evidence indicates that iron overload is involved in the pathogenesis of abdominal aortic aneurysms. In this review, we provide an overview of the role of iron overload in AAA progression and explore its potential pathological mechanisms. Although the exact molecular mechanisms of iron overload in the development of AAA remain to be elucidated, the inhibition of iron deposition may offer a promising strategy for preventing these aneurysms.
引用
收藏
页数:10
相关论文
共 67 条
[61]   Atherogenesis and iron: from epidemiology to cellular level [J].
Vinchi, Francesca ;
Muckenthaler, Martina U. ;
Da Silva, Milene C. ;
Balla, Gyoergy ;
Balla, Jozsef ;
Jeney, Viktoria .
FRONTIERS IN PHARMACOLOGY, 2014, 5
[62]   Iron deficiency and cardiovascular disease [J].
von Haehling, Stephan ;
Jankowska, Ewa A. ;
van Veldhuisen, Dirk J. ;
Ponikowski, Piotr ;
Anker, Stefan D. .
NATURE REVIEWS CARDIOLOGY, 2015, 12 (11) :659-669
[63]   Inhibition of reactive oxygen species attenuates aneurysm formation in a murine model [J].
Xiong, Wanfen ;
Mactaggart, Jason ;
Knispel, Rebecca ;
Worth, Jennifer ;
Zhu, Zhen ;
Li, Yulong ;
Sun, Yimin ;
Baxter, B. Timothy ;
Johanning, Jason .
ATHEROSCLEROSIS, 2009, 202 (01) :128-134
[64]   Evaluation of a smart activatable MRI nanoprobe to target matrix metalloproteinases in the early-stages of abdominal aortic aneurysms [J].
Yao, Yuyu ;
Cheng, Kai ;
Cheng, Zhen .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2020, 26
[65]   Role of iron metabolism in heart failure: From iron deficiency to iron overload [J].
Zhang, Hao ;
Zhabyeyev, Pavel ;
Wang, Shaohua ;
Oudit, Gavin Y. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2019, 1865 (07) :1925-1937
[66]   Inhibition of Soluble Epoxide Hydrolase Attenuated Atherosclerosis, Abdominal Aortic Aneurysm Formation, and Dyslipidemia [J].
Zhang, Le-Ning ;
Vincelette, Jon ;
Cheng, Ying ;
Mehra, Upasana ;
Chen, Dawn ;
Anandan, Sampath-Kumar ;
Gless, Richard ;
Webb, Heather K. ;
Wang, Yi-Xin .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2009, 29 (09) :1265-1270
[67]   Intracellular metal ion chelators inhibit TNFα-induced Sp-1 activation and adhesion molecule expression in human aortic endothelial cells [J].
Zhang, WJ ;
Frei, B .
FREE RADICAL BIOLOGY AND MEDICINE, 2003, 34 (06) :674-682