虾青素减轻大鼠与醋酸脱氧皮质酮盐诱导的高血压相关的心血管功能障碍。

IF 1.5 4区 医学 Q3 PERIPHERAL VASCULAR DISEASE
Suzan A Khodir, Eman Sweed, Marwa Gadallah, Anwaar Shabaan
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引用次数: 3

摘要

背景:高血压是一个主要的全球性健康问题。它是心血管疾病的主要危险因素。研究降压作用最常用的实验模型之一是醋酸脱氧皮质酮(DOCA)盐高血压大鼠。本研究旨在探讨虾青素(astaxanthin, ASX)在doca盐致高血压中的心血管保护作用及其可能的机制。方法:将48只成年雄性Wistar白化大鼠分为对照组、DOCA组和DOCA + ASX组。测量血压、血清心脏酶水平、一些氧化应激和炎症生物标志物水平以及血脂水平。计算左心室重量与胫骨长度之比。研究了主动脉组织和心脏组织的细胞凋亡检测和总基因组DNA提取。对心脏和主动脉的凋亡标志物BAX进行免疫组织化学检测。结果:与对照组相比,DOCA组血压、血清心酶水平、氧化应激和炎症生物标志物水平、血脂(除血清高密度脂蛋白)、左心室重量与胫骨长度、左心室和主动脉总释放DNA片段水平显著升高,还原性谷胱甘肽(GSH)和HDL显著降低。与DOCA组相比,DOCA + ASX组明显改善了DOCA引起的变化。结论:ASX通过DNA片段保护、细胞凋亡抑制、抗氧化、抗炎及对血脂水平的影响,对doca盐诱导的高血压具有有益的保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Astaxanthin attenuates cardiovascular dysfunction associated with deoxycorticosterone acetate-salt-induced hypertension in rats.

Background: Hypertension is a major global health problem. It is a major risk factor of cardiovascular disease. One of the most used experimental models in studying antihypertensive action is the deoxycorticosterone acetate (DOCA)-salt hypertensive rat. This study aimed to investigate the cardiovascular protective effect of astaxanthin (ASX) in DOCA-salt-induced hypertension and its possible underlying mechanisms.

Methods: A total of 48 adult male Wistar albino rats were divided into three groups: control, DOCA, and DOCA + ASX. Blood pressure, serum cardiac enzyme levels, some oxidative stress and inflammatory biomarker levels, and lipid profile levels were measured. The weight of the left ventricle to tibial length ratio was calculated. Apoptosis detection and total genomic DNA extraction in aortic and cardiac tissues were investigated. The apoptotic marker BAX was also immunohistochemically assessed in the heart and aorta.

Results: Compared to the control group, the DOCA group was associated with a significant increase in blood pressure, serum cardiac enzyme levels, oxidative stress and inflammatory biomarker levels, lipid profile except serum high-density lipoprotein (HDL), weight of the left ventricle to tibial length, and total released DNA fragmentation level of the left ventricle and aorta and a significant decrease in reduced glutathione (GSH) and HDL. Compared to the DOCA group, the DOCA + ASX group significantly improved the DOCA-induced changes.

Conclusion: ASX has beneficial protective effects on DOCA-salt-induced hypertension via DNA fragmentation protection, apoptosis inhibition, antioxidant, anti-inflammatory, and its effects on lipid levels.

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来源期刊
CiteScore
3.90
自引率
0.80%
发文量
66
审稿时长
6-12 weeks
期刊介绍: Clinical and Experimental Hypertension is a reputable journal that has converted to a full Open Access format starting from Volume 45 in 2023. While previous volumes are still accessible through a Pay to Read model, the journal now provides free and open access to its content. It serves as an international platform for the exchange of up-to-date scientific and clinical information concerning both human and animal hypertension. The journal publishes a wide range of articles, including full research papers, solicited and unsolicited reviews, and commentaries. Through these publications, the journal aims to enhance current understanding and support the timely detection, management, control, and prevention of hypertension-related conditions. One notable aspect of Clinical and Experimental Hypertension is its coverage of special issues that focus on the proceedings of symposia dedicated to hypertension research. This feature allows researchers and clinicians to delve deeper into the latest advancements in this field. The journal is abstracted and indexed in several renowned databases, including Pharmacoeconomics and Outcomes News (Online), Reactions Weekly (Online), CABI, EBSCOhost, Elsevier BV, International Atomic Energy Agency, and the National Library of Medicine, among others. These affiliations ensure that the journal's content receives broad visibility and facilitates its discoverability by professionals and researchers in related disciplines.
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