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E5510通过抑制核因子κB激活来拮抗凝血酶受体信号。

E5510 antagonizes thrombin receptor signals by inhibiting NF-kappa B activation.

作者信息

Nakajima T, Kitajima I, Shin H, Matsumoto W, Soejima Y, Maruyama I

机构信息

Department of Laboratory Medicine, Faculty of Medicine, University of Kagoshima, Japan.

出版信息

Biochem Biophys Res Commun. 1994 Sep 15;203(2):1181-7. doi: 10.1006/bbrc.1994.2307.

Abstract

We have recently demonstrated that NF-kappa B is involved in a thrombin-signaling and that the antisense oligodeoxynucleotides (ODNs) of NF-kappa B has a marked inhibitory effect on thrombin-induced cellular responses. In this study, we demonstrate that E5510 (4-cyano-5,5-bis(methoxyphenyl)-4-pentenoic acid), a compound with anti-platelet activity preferentially inhibits the thrombin-inducible NF-kappa B activation and then antagonizes the following thrombin-induced cellular responses, proliferation and cytokines production in vascular smooth muscle cell, and the adherency of differentiated HL-60 cells. These data suggest that E5510 is an anti-atherosclerotic or anti-restenotic drug induced by thrombin.

摘要

我们最近证明,核因子-κB参与凝血酶信号传导,并且核因子-κB的反义寡脱氧核苷酸(ODNs)对凝血酶诱导的细胞反应具有显著抑制作用。在本研究中,我们证明E5510(4-氰基-5,5-双(甲氧基苯基)-4-戊烯酸),一种具有抗血小板活性的化合物,优先抑制凝血酶诱导的核因子-κB活化,然后拮抗随后凝血酶诱导的细胞反应、血管平滑肌细胞的增殖和细胞因子产生,以及分化的HL-60细胞的黏附。这些数据表明,E5510是一种由凝血酶诱导的抗动脉粥样硬化或抗再狭窄药物。

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