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丹参中提取的丹参酮的抗动脉粥样硬化作用及分子靶点

Atheroprotective Effects and Molecular Targets of Tanshinones Derived From Herbal Medicine Danshen.

机构信息

Department of Pharmacy, Huadu District People's Hospital,Southern Medical University, 48 Xinhua Road, Guangzhou, 510800, China.

Pharmacy Australia Centre of Excellence (PACE), School of Pharmacy, The University of Queensland, Woolloongabba, QLD, 4102, Australia.

出版信息

Med Res Rev. 2018 Jan;38(1):201-228. doi: 10.1002/med.21438. Epub 2017 Feb 16.

Abstract

Medicinal plant-derived bioactive compounds modulate multiple therapeutic targets in cardiovascular diseases (CVDs), rendering herb-derived phytochemicals effective against one of the major CVDs-atherosclerosis. Danshen (Salvia milthiorriza Bunge) is a Chinese medicine that has been used in cardio- and cerebro-vascular therapeutic remedies in Asian countries for many years. Emerging evidence from cellular, animal, and clinical studies suggests that major lipophilic tanshinones from Danshen can treat atherosclerotic CVDs. In this review, we highlight recent advances in understanding the molecular mechanisms of tanshinones in treating atherosclerosis, ranging from endothelial dysfunction to chronic inflammation. We also overview new molecular targets of tanshinones, including endothelial nitric oxide synthase, AMP-activated protein kinase, ABC transporter A1, heme oxygenase 1, soluble epoxide hydrolase, 11β-hydroxysteroid dehydrogenase, estrogen receptor, and proprotein convertase subtilisin/kexin type 9. Thus, this review provides a new perspective for advancing our understanding of the "ancient" herb Danshen from "modern" biomedical perspectives, supporting the possibility of exploiting tanshinones and derivatives as effective therapeutics against atherosclerosis-related cardiovascular and metabolic diseases.

摘要

植物源生物活性化合物调节心血管疾病 (CVDs) 的多个治疗靶点,使植物源植物化学物质成为对抗主要 CVDs-动脉粥样硬化的有效药物。丹参(Salvia milthiorriza Bunge)是一种中药,多年来一直被用于亚洲国家的心脏和脑血管治疗药物中。来自细胞、动物和临床研究的新证据表明,丹参中的主要脂溶性丹参酮可治疗动脉粥样硬化性 CVDs。在这篇综述中,我们强调了近年来对丹参酮治疗动脉粥样硬化分子机制的理解的最新进展,范围从内皮功能障碍到慢性炎症。我们还概述了丹参酮的新分子靶点,包括内皮型一氧化氮合酶、AMP 激活蛋白激酶、ABC 转运蛋白 A1、血红素加氧酶 1、可溶性环氧化物水解酶、11β-羟甾醇脱氢酶、雌激素受体和脯肽酶枯草溶菌素/激肽释放酶 9。因此,本综述从“现代”生物医学角度为深入了解“古老”草药丹参提供了新的视角,支持了利用丹参酮及其衍生物作为治疗与动脉粥样硬化相关的心血管和代谢疾病的有效治疗方法的可能性。

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