Literature DB >> 26306842

Emerging Pharmacological Treatments to Prevent Abdominal Aortic Aneurysm Growth and Rupture.

Rodrigo A Fraga-Silva, Bram Trachet, Nikolaos Stergiopulos1.   

Abstract

Abdominal aortic aneurysm (AAA) is a local expansion of the abdominal aorta wall caused by a complex multifactorial maladaptive vascular remodeling. Despite recent advances in the management of cardiovascular diseases, there currently is no established drug therapy for AAA. Since the probability of death from a ruptured AAA still remains high, preventive elective repair of AAAs larger than 5.5 cm in luminal diameter is considered the best treatment option. However, perioperative complications are problematic as elective AAA repair comes with numerous intrinsic risks. Impelled by the need of improving AAA therapy, significant efforts have been made to identify pharmacological tools that would slow down AAA enlargement and lower the risk of rupture, thereby reducing the necessity of surgical intervention. In this review, we discuss recent findings addressing molecular targets that could potentially treat AAA, particularly addressing: statins, classical renin angiotensin system (RAS) blockers, the protective arm of RAS, renin inhibitors, tetracyclines, interleukin-1β inhibition, anti-angiogenic agents and urocortins.

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Year:  2015        PMID: 26306842

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  3 in total

1.  Alterations in phenotype and gene expression of adult human aneurysmal smooth muscle cells by exogenous nitric oxide.

Authors:  Kurt Farrell; Phillip Simmers; Gautam Mahajan; Ludovic Boytard; Andrew Camardo; Jyotsna Joshi; Anand Ramamurthi; Florence Pinet; Chandrasekhar R Kothapalli
Journal:  Exp Cell Res       Date:  2019-08-29       Impact factor: 3.905

2.  Inhibitory effects of cycloastragenol on abdominal aortic aneurysm and its related mechanisms.

Authors:  Yunxia Wang; Cong Chen; Qinyu Wang; Yini Cao; Lu Xu; Rong Qi
Journal:  Br J Pharmacol       Date:  2018-12-04       Impact factor: 8.739

3.  K-134, a phosphodiesterase 3 inhibitor, reduces vascular inflammation and hypoxia, and prevents rupture of experimental abdominal aortic aneurysms.

Authors:  Naoki Unno; Hiroki Tanaka; Tatsuro Yata; Takafumi Kayama; Yuta Yamanaka; Hajime Tsuyuki; Masaki Sano; Kazunori Inuzuka; Ena Naruse; Hiroya Takeuchi
Journal:  JVS Vasc Sci       Date:  2020-10-22
  3 in total

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