Potential benefits of phytochemicals for abdominal aortic aneurysm

被引:14
|
作者
Hosseini, Azar [1 ]
Penson, Peter E. [2 ]
Cicero, Arrigo F. G. [3 ]
Golledge, Jonathan [4 ,5 ]
Al-Rasadi, Khalid [6 ]
Jamialahmadi, Tannaz [7 ,8 ]
Sahebkar, Amirhossein [9 ,10 ,11 ]
机构
[1] Mashhad Univ Med Sci, Pharmacol Res Ctr Med Plants, Mashhad, Razavi Khorasan, Iran
[2] Liverpool John Moores Univ, Sch Pharm & Biomol Sci, Liverpool, Merseyside, England
[3] Univ Bologna, St Orsola Malpighi Hosp, Med & Surg Sci Dept, Atherosclerosis Res Unit, Bologna, Italy
[4] James Cook Univ, Coll Med & Dent, Queensland Res Ctr Peripheral Vasc Dis, Townsville, Qld, Australia
[5] Univ Hosp, Dept Vasc & Endovasc Surg, Townsville, Qld, Australia
[6] Sultan Qaboos Univ Hosp, Dept Clin Biochem, Muscat, Oman
[7] Islamic Azad Univ, Dept Food Sci & Technol, Quchan Branch, Quchan, Iran
[8] Mashhad Univ OfMed Sci, Fac Med, Dept Nutr, Mashhad, Razavi Khorasan, Iran
[9] Mashhad Univ Med Sci, Biotechnol Res Ctr, Pharmaceut Technol Inst, Mashhad, Razavi Khorasan, Iran
[10] Mashhad Univ Med Sci, Appl Biomed Res Ctr, Mashhad, Razavi Khorasan, Iran
[11] Mashhad Univ Med Sci, Sch Pharm, Mashhad, Razavi Khorasan, Iran
基金
英国医学研究理事会;
关键词
Abdominal aortic aneurysm; oxidative stress; phytotherapy; inflammation; plant medicine; phytochemicals; RENIN-ANGIOTENSIN SYSTEM; REDUCES OXIDATIVE STRESS; N-TERMINAL KINASE; ASTRAGALOSIDE-IV; GINKGO-BILOBA; KAPPA-B; ANTIINFLAMMATORY ACTIVITY; HEPATOCELLULAR-CARCINOMA; CHEMOPREVENTIVE AGENT; MOUSE MODEL;
D O I
10.2174/0929867328666210614113116
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Abdominal aortic aneurysms (AAAs) are a leading cause of death in older adults due to aortic rupture. There are currently no effective medical therapies for AAA, with surgery being the only acceptable treatment. There is frequently an extended period between AAA diagnosis and treatment by corrective surgery, during which an effective drug therapy could prevent or delay the need for AAA repair. Objective: This review aimed to critically summarize prior research investigating the potential benefits of phytochemicals in preventing or treating AAA. Methods: In vitro, in vivo, and human studies examining the effect of phytochemicals in AAA models and patients were critically summarised. Results: Some preliminary data support the further investigation of curcumin, radix astragali, grape seed polyphenols, resveratrol, Ginkgo biloba extract (EGb 761), Ginsenoide Rb1, Dan Hong, Epigallocatechin-3-gallate, Baicalein, Fucoidan, Quercetin, and Salvianolic acid as potential treatments for AAA. Conclusion: Experimental in vivo and in vitro studies suggest the potential benefits of a number of medicinal herbs and phytochemicals in preventing or reducing the progression of AAA. In order to assess whether these findings can be translated into proven treatments, adequately designed double-blind randomized clinical trials will be required.
引用
收藏
页码:8595 / 8607
页数:13
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