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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Meso-dihydroguaiaretic acid inhibits rat aortic vascular smooth muscle cell proliferation by suppressing phosphorylation of platelet-derived growth factor receptor beta
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Meso-dihydroguaiaretic acid inhibits rat aortic vascular smooth muscle cell proliferation by suppressing phosphorylation of platelet-derived growth factor receptor beta

机译:中二氢愈创木酸通过抑制血小板衍生的生长因子受体β的磷酸化来抑制大鼠主动脉血管平滑肌细胞的增殖

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摘要

Abnormal proliferation of vascular smooth muscle cells (VSMCs) plays an essential functional role in the pathogenesis of vascular disorders, such as atherosclerosis, restenosis, and neointimal hyperplasia. In this study, we examined the effects of meso-dihydroguaiaretic acid (MDGA) On platelet-derived growth factor (PDGF)-BB-induced proliferation and the molecular basis of its underlying mechanism of action in rat aortic VSMCs. Incubation of resting VSMCs with MDGA for 24 h significantly diminished PDGF-BB-induced DNA synthesis in a dose-dependent manner. We also examined the effects of MDGA on PDGF-BB signal transduction. Pre-treatment of VSMCs with MDGA inhibited PDGF-BB-induced phosphorylation of extracellular signal-regulated kinases 1/2 (ERK1/2), p38, and C-Jun N-terminal kinase (JNK). MDGA also effectively inhibited phosphorylation of Akt, phospholipase C gamma 1 (PLC gamma 1), and PDGF receptor beta (PDGFR beta). These results indicate that MDGA may inhibit proliferation of VSMCs by suppressing autophosphorylation of PDGFR beta, and may be useful in the treatment of VSMC-associated vascular disease such as atherosclerosis, restenosis, and neointimal hyperplasia after angioplasty. (C) 2014 Elsevier B.V. All rights reserved.
机译:血管平滑肌细胞(VSMC)的异常增殖在诸如动脉粥样硬化,再狭窄和新内膜增生等血管疾病的发病机理中起着至关重要的作用。在这项研究中,我们研究了中二氢愈创木酸(MDGA)对大鼠主动脉VSMC中血小板衍生的生长因子(PDGF)-BB诱导的增殖及其潜在作用机理的分子基础。将静止的VSMC与MDGA一起孵育24小时,以剂量依赖的方式显着减少了PDGF-BB诱导的DNA合成。我们还检查了MDGA对PDGF-BB信号转导的影响。用MDGA预处理VSMC可抑制PDGF-BB诱导的细胞外信号调节激酶1/2(ERK1 / 2),p38和C-Jun N端激酶(JNK)的磷酸化。 MDGA还有效抑制Akt,磷脂酶Cγ1(PLCγ1)和PDGF受体beta(PDGFR beta)的磷酸化。这些结果表明,MDGA可以通过抑制PDGFRβ的自身磷酸化来抑制VSMC的增殖,并且可以用于治疗VSMC相关的血管疾病,例如血管成形术后的动脉粥样硬化,再狭窄和新内膜增生。 (C)2014 Elsevier B.V.保留所有权利。

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