Mechanistic Insights on Cardioprotective Properties of Ursolic Acid: Regulation of Mitochondrial and Non-mitochondrial Pathways.

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY Current pharmaceutical design Pub Date : 2025-01-01 DOI:10.2174/0113816128344497241120025757
Hesan Soleimani Roudi, Rozhan Safaei, Mohammad Mahdi Dabbaghi, Mohammad Saleh Fadaei, Mahsa Saberifar, Katayoun Sakhaee, Vafa Baradaran Rahimi, Vahid Reza Askari
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Abstract

Ursolic acid, a natural pentacyclic triterpenoid compound, has been shown to have significant cardioprotective effects in various preclinical studies. This article reviews the various mechanisms by which ursolic acid achieves its cardioprotective effects, highlighting its potent anti-oxidant, anti-inflammatory, and anti- apoptotic properties. Ursolic acid upregulates anti-oxidant enzymes such as superoxide dismutase (SOD) and glutathione peroxidase (GPx), effectively reducing oxidative stress, thereby decreasing reactive oxygen species (ROS) and improving lipid peroxidation levels. Furthermore, ursolic acid downregulates pro-inflammatory cytokines and inhibits key inflammatory pathways, such as nuclear factor kappa B (NF-κB), which results in its anti-inflammatory effects. These actions help in protecting cardiac tissues from acute and chronic inflammation. Ursolic acid also promotes mitochondrial function and energy metabolism by enhancing mitochondrial biogenesis and reducing dysfunction, which is critical during ischemia-reperfusion (I/R) injury. Additionally, ursolic acid influences multiple molecular pathways, including B-cell leukemia/lymphoma 2 protein (Bcl- 2)/Bcl-2 associated x-protein (Bax), miR-21/extracellular signal-regulated kinase (ERK), and phosphoinositide 3-kinase (PI3K)/protein kinase B (Akt), to reduce cardiomyocyte apoptosis. Collectively, these properties make ursolic acid a promising therapeutic agent for cardiovascular diseases (CVDs), warranting further research and clinical trials to harness its potential fully.

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熊果酸心脏保护特性的机制:线粒体和非线粒体途径的调节。
熊果酸是一种天然的五环三萜化合物,在各种临床前研究中已被证明具有显著的心脏保护作用。本文综述了熊果酸实现其心脏保护作用的各种机制,重点介绍了其有效的抗氧化、抗炎和抗凋亡特性。熊果酸上调超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx)等抗氧化酶,有效降低氧化应激,从而降低活性氧(ROS),改善脂质过氧化水平。熊果酸还能下调促炎细胞因子,抑制关键炎症通路,如核因子κB (NF-κB),从而发挥抗炎作用。这些作用有助于保护心脏组织免受急性和慢性炎症的影响。熊果酸还通过促进线粒体生物发生和减少功能障碍来促进线粒体功能和能量代谢,这在缺血再灌注(I/R)损伤中是至关重要的。此外,熊果酸影响多种分子通路,包括B细胞白血病/淋巴瘤2蛋白(Bcl- 2)/Bcl-2相关x蛋白(Bax)、miR-21/细胞外信号调节激酶(ERK)和磷酸肌苷3激酶(PI3K)/蛋白激酶B (Akt),以减少心肌细胞凋亡。总的来说,这些特性使熊果酸成为心血管疾病(cvd)的有希望的治疗剂,需要进一步的研究和临床试验来充分利用其潜力。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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