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高胆固醇血症血小板中鞘氨醇-1-磷酸的释放增强:在高胆固醇血症动脉粥样硬化发展中的作用。

Enhanced release of sphingosine-1-phosphate from hypercholesterolemic platelets: role in development of hypercholesterolemic atherosclerosis.

作者信息

Son Dong Ju, Lee Hyoung Woo, Shin Hyun Woo, Lee Jung Jin, Yoo Hwan Soo, Kim Tack Joong, Yun Yeo Pyo, Hong Jin Tae

机构信息

College of Pharmacy and CBITRC, Chungbuk National University, Cheongju, Chungbuk 361-763, Republic of Korea.

出版信息

Prostaglandins Leukot Essent Fatty Acids. 2008 Jun;78(6):383-90. doi: 10.1016/j.plefa.2008.04.010. Epub 2008 Jun 20.

Abstract

Although it is well known that sphingosine-1-phosphate (S1P), which induces many biological responses, is present in plasma and is mainly released from activated platelets, little is known whether the release of S1P is increased when platelets are activated in the hypercholesterolemic condition, and what are the roles of increased S1P generation in the development or progression of the atherosclerosis. Results show that 0.5% cholesterol diet for 16 weeks induces platelet hyperaggregability to low doses of agonists as well as development of hypercholesterolemic atherosclerosis in the rabbits. The generation and released level of S1P were significantly increased in the hypersensitized platelets and blood plasma in hypercholesterolemic rabbits. We also demonstrated that S1P increased VSMC proliferation via endothelial differentiation gene (EDG)-1 receptor dependent pathway. Our results indicate that release of S1P from activated platelets was increased by enhanced platelet sensitivity in hypercholesterolemia, which potentiated the ox-LDL-induced VSMC proliferation via EDG-1 receptor pathway.

摘要

虽然众所周知,诱导多种生物学反应的1-磷酸鞘氨醇(S1P)存在于血浆中,且主要由活化的血小板释放,但对于在高胆固醇血症条件下血小板活化时S1P的释放是否增加,以及S1P生成增加在动脉粥样硬化发生或发展中的作用知之甚少。结果表明,给兔子喂食16周0.5%胆固醇饮食会诱导血小板对低剂量激动剂产生高聚集性,并引发高胆固醇血症性动脉粥样硬化。高胆固醇血症兔子的超敏血小板和血浆中S1P的生成和释放水平显著增加。我们还证明,S1P通过内皮分化基因(EDG)-1受体依赖性途径增加血管平滑肌细胞(VSMC)增殖。我们的结果表明,高胆固醇血症中血小板敏感性增强会增加活化血小板释放S1P,这通过EDG-1受体途径增强了氧化型低密度脂蛋白(ox-LDL)诱导的VSMC增殖。

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