Impact of SMTP Targeting Plasminogen and Soluble Epoxide Hydrolase on Thrombolysis, Inflammation, and Ischemic Stroke.

Impact of SMTP Targeting Plasminogen and Soluble Epoxide Hydrolase on Thrombolysis, Inflammation, and Ischemic Stroke.
复制标题

DOI:
10.3390/ijms22020954
复制
发表时间:
2021-01-19
影响因子:
5.6
通讯作者:
Suzuki E
Suzuki E
中科院分区:
生物学2区
文献类型:
--
作者:
Hasumi K;Suzuki E

文献摘要

参考文献

被引文献

相似文献

Stachybotrys microspora triprenyl phenol (SMTP)是一种源自真菌S. microspora的小分子化合物。SMTP作为一种酶原调节剂(特别是纤溶酶原调节剂),改变纤溶酶原的构象,增强其与纤维蛋白的结合和随后的纤维蛋白溶解。某些SMTP同源物通过靶向可溶性环氧化物水解酶发挥抗炎作用。具有纤溶酶原调节活性和抗炎活性的SMTP同源体可以改善啮齿动物和灵长类动物缺血性卒中的各个方面。SMTP疗效的一个显著特征是抑制出血转化,而传统的溶栓治疗会加重出血转化。目前还没有开发出具有这种特性的药物,SMTP将是第一个促进溶栓但抑制疾病相关出血的药物。在这些发现的基础上,一种SMTP同系物正在临床研究和开发中。本文综述了SMTP的发现、作用机制、药理活性及研究进展。
Stachybotrys microspora triprenyl phenol (SMTP) is a large family of small molecules derived from the fungus S. microspora. SMTP acts as a zymogen modulator (specifically, plasminogen modulator) that alters plasminogen conformation to enhance its binding to fibrin and subsequent fibrinolysis. Certain SMTP congeners exert anti-inflammatory effects by targeting soluble epoxide hydrolase. SMTP congeners with both plasminogen modulation activity and anti-inflammatory activity ameliorate various aspects of ischemic stroke in rodents and primates. A remarkable feature of SMTP efficacy is the suppression of hemorrhagic transformation, which is exacerbated by conventional thrombolytic treatments. No drug with such properties has been developed yet, and SMTP would be the first to promote thrombolysis but suppress disease-associated bleeding. On the basis of these findings, one SMTP congener is under clinical study and development. This review summarizes the discovery, mechanism of action, pharmacological activities, and development of SMTP.
DOI: 10.1021/bi901433n
发表时间: 2009-11-03
期刊: BIOCHEMISTRY
影响因子: 2.9
作者:
Battistel, Marcos D.;Grishaev, Alexander;Llinas, Miguel
通讯作者: Llinas, Miguel
DOI: 10.2183/pjab.86.484
发表时间: 2010
期刊: Proceedings of the Japan Academy. Series B, Physical and biological sciences
影响因子: --
作者:
Endo A
通讯作者: Endo A
DOI: 10.1021/jo0508494
发表时间: 2005-09-16
影响因子: 3.6
作者:
Alajarín, M;Sánchez-Andrada, P;Alvarez, A
通讯作者: Alvarez, A
DOI: 10.1001/archneurol.2010.175
发表时间: 2010-08
影响因子: --
作者:
Goldstein, Joshua N.;Marrero, Marisela;Masrur, Shihab;Pervez, Muhammad;Barrocas, Alex M.;Abdullah, Abdul;Oleinik, Alexandra;Rosand, Jonathan;Smith, Eric E.;Dzik, Walter H.;Schwamm, Lee H.
通讯作者: Schwamm, Lee H.
DOI: 10.2174/157340310791658730
发表时间: 2010-08
影响因子: 1.9
作者:
Arboix A;Alió J
通讯作者: Alió J