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黄芩苷元在心血管系统中的生物学特性。

Biological properties of baicalein in cardiovascular system.

作者信息

Huang Yu, Tsang Suk-Ying, Yao Xiaoqiang, Chen Zhen-Yu

机构信息

Department of Physiology, Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.

出版信息

Curr Drug Targets Cardiovasc Haematol Disord. 2005 Apr;5(2):177-84. doi: 10.2174/1568006043586206.

Abstract

The dried roots of Scutellaria baicalensis (S. baicalensis) Georgi (common name: Huangqin in China) have been widely employed for many centuries in traditional Chinese herbal medicine as popular antibacterial and antiviral agents. They are effective against staphylococci, cholera, dysentery, pneumococci and influenza virus. Baicalein, one of the major flavonoids contained in the dried roots, possesses a multitude of pharmacological activities. The glycoside of baicalein, baicalin is a potent anti-inflammatory and anti-tumor agent. This review describes the biological properties of baicalein (Table 1), which are associated with the prevention and treatment of cardiovascular diseases. Baicalein is a potent free radical scavenger and xanthine oxidase inhibitor, thus improving endothelial function and conferring cardiovascular protective actions against oxidative stress-induced cell injury. Baicalein lowers blood pressure in renin-dependent hypertension and the in vivo hypotensive effect may be partly attributed to its inhibition of lipoxygenase, resulting in reduced biosynthesis and release of arachidonic acid-derived vasoconstrictor products. On the other hand, baicalein enhances vasoconstricting sensitivity to receptor-dependent agonists such as noradrenaline, phenylephrine, serotonin, U46619 and vasopressin in isolated rat arteries. The in vitro effect is likely caused by inhibition of an endothelial nitric oxide-dependent mechanism. The anti-thrombotic, anti-proliferative and anti-mitogenic effects of the roots of S. baicalensis and baicalein are also reported. Baicalein inhibits thrombin-induced production of plasminogen activator inhibitor-1, and interleukin-1beta- and tumor necrosis factor-alpha-induced adhesion molecule expression in cultured human umbilical vein endothelial cells. The pharmacological findings have highlighted the therapeutic potentials of using plant-derived baicalein and its analogs for the treatment of arteriosclerosis and hypertension.

摘要

黄芩(在中国俗名:黄芩)的干燥根在传统中药中已被广泛使用了几个世纪,是常用的抗菌和抗病毒药物。它们对葡萄球菌、霍乱、痢疾、肺炎球菌和流感病毒有效。黄芩苷是干燥根中所含的主要黄酮类化合物之一,具有多种药理活性。黄芩苷的糖苷黄芩苷是一种有效的抗炎和抗肿瘤剂。本综述描述了黄芩苷(表1)的生物学特性,这些特性与心血管疾病的预防和治疗有关。黄芩苷是一种有效的自由基清除剂和黄嘌呤氧化酶抑制剂,因此可改善内皮功能,并赋予心血管对氧化应激诱导的细胞损伤的保护作用。黄芩苷可降低肾素依赖性高血压患者的血压,其体内降压作用可能部分归因于其对脂氧合酶的抑制,从而减少花生四烯酸衍生的血管收缩产物的生物合成和释放。另一方面,黄芩苷可增强离体大鼠动脉对去甲肾上腺素、苯肾上腺素、5-羟色胺、U46619和血管加压素等受体依赖性激动剂的血管收缩敏感性。体外作用可能是由内皮一氧化氮依赖性机制的抑制引起的。还报道了黄芩根和黄芩苷的抗血栓、抗增殖和抗有丝分裂作用。黄芩苷抑制凝血酶诱导的人脐静脉内皮细胞中纤溶酶原激活物抑制剂-1的产生,以及白细胞介素-1β和肿瘤坏死因子-α诱导的黏附分子表达。药理学研究结果突出了使用植物来源的黄芩苷及其类似物治疗动脉硬化和高血压的治疗潜力。

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