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中药血竭的生物活性导向分离揭示龙血素B为PAI-1抑制剂。

Bioactivity-Guided Fractionation of the Traditional Chinese Medicine Resina Draconis Reveals Loureirin B as a PAI-1 Inhibitor.

作者信息

Jiang Yu, Zhang Guangping, Yan Dong, Yang Hong, Ye Zuguang, Ma Tonghui

机构信息

College of Life Science, Jilin Agricultural University, Changchun, China.

Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China.

出版信息

Evid Based Complement Alternat Med. 2017;2017:9425963. doi: 10.1155/2017/9425963. Epub 2017 Sep 18.

Abstract

Thrombotic diseases have become a global burden due to morbidity, mortality, and disability. Traditional Chinese medicine has been proven effective in removing blood stasis and promoting blood circulation, but the exact mechanisms remain unclear. Plasminogen activator inhibitor-1 (PAI-1) is a natural inhibitor of tissue-type and urokinase-type plasminogen activators. In this study, we screened four fractions of Resina Draconis (a traditional Chinese medicine) extract for PAI-1 inhibitory activity. Bioactivity-guided purification and chromogenic substrate-based assay led to the identification of loureirin B as the major PAI-1 inhibitor, with an IC value of 26.10 M. SDS-PAGE analysis showed that formation of the PAI-1/uPA complex was inhibited by loureirin B, and the inhibitory effect of loureirin B on PAI-1 was also confirmed by clot lysis assay. In vivo studies showed that loureirin B significantly prolonged the tail bleeding time and reduced the weight and size of arterial thrombus, reduced hydroxyproline level, and partly cured liver fibrosis in mice. Taken together, the results revealed loureirin B as a PAI-1 inhibitor, adding a new pharmacological target for loureirin B and uncovering a novel mechanism underlying the antithrombotic property of Resina Draconis, which might be useful in the treatment of cardiovascular diseases such as thrombosis and fibrosis.

摘要

由于发病率、死亡率和残疾率,血栓性疾病已成为全球负担。中药已被证明在活血化瘀方面有效,但其确切机制仍不清楚。纤溶酶原激活物抑制剂-1(PAI-1)是组织型和尿激酶型纤溶酶原激活物的天然抑制剂。在本研究中,我们筛选了血竭(一种中药)提取物的四个组分的PAI-1抑制活性。通过生物活性导向的纯化和基于显色底物的测定,鉴定出龙血素B是主要的PAI-1抑制剂,IC值为26.10μM。SDS-PAGE分析表明,龙血素B抑制了PAI-1/uPA复合物的形成,凝血块溶解试验也证实了龙血素B对PAI-1的抑制作用。体内研究表明,龙血素B显著延长了小鼠的尾部出血时间,减小了动脉血栓的重量和大小,降低了羟脯氨酸水平,并部分治愈了小鼠的肝纤维化。综上所述,结果表明龙血素B是一种PAI-1抑制剂,为龙血素B增加了一个新的药理学靶点,并揭示了血竭抗血栓特性的新机制,这可能对治疗血栓形成和纤维化等心血管疾病有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03de/5634571/eae2a5e58a6e/ECAM2017-9425963.001.jpg

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