医学
氯沙坦
厄贝沙坦
主动脉夹层
动脉瘤
主动脉瘤
二甲双胍
疾病
药品
重症监护医学
血管紧张素II
药理学
内科学
外科
糖尿病
主动脉
受体
内分泌学
血压
作者
Bitao Xiang,Shichao Zhu,Jun Li,Hao Lai,Chunsheng Wang,Kai Zhu
出处
期刊:Journal of Cardiovascular Pharmacology
[Ovid Technologies (Wolters Kluwer)]
日期:2021-08-01
卷期号:78 (2): 211-220
被引量:1
标识
DOI:10.1097/fjc.0000000000001054
摘要
Aortic aneurysm (AA) remains one of the primary causes of death worldwide. Of the major treatments, prophylactic operative repair is used for AA to avoid potential aortic dissection or rupture. To halt the development of AA and alleviate its progression into aortic dissection, pharmacological treatment has been investigated for years. Currently, β-adrenergic blocking agents, losartan, irbesartan, angiotensin-converting-enzyme inhibitors, statins, antiplatelet agents, doxycycline, and metformin have been investigated as potential candidates for preventing AA progression. However, the paradox between preclinical successes and clinical failures still exists, with no medical therapy currently available for ideally negating the disease progression. This review describes the current drugs used for pharmacological management of AA and their individual potential mechanisms. Preclinical models for drug screening and evaluation are also discussed to gain a better understanding of the underlying pathophysiology and ultimately find new therapeutic targets for AA.
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