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阿托伐他汀通过香叶基香叶基焦磷酸中和凝血酶诱导的内皮细胞组织因子表达。

Atorvastatin neutralises the thrombin-induced tissue factor expresion in endothelial cells via geranylgeranyl pyrophosphate.

机构信息

Centro de Investigación, Hospital Universitario La Fe Avda, Campanar 21, 46009, Valencia, Spain,

出版信息

Cytotechnology. 2011 Jan;63(1):1-5. doi: 10.1007/s10616-010-9319-4. Epub 2010 Nov 4.

Abstract

Statins may have beneficial effects in atherogenesis given their antithrombotic properties involving non-lipid mechanisms that modify endothelial function of tissue factor induction by thrombin. In this study, we investigate the effect of atorvastatin on tissue factor (TF) activity in thrombin-stimulated endothelial cells and its regulation through mevalonate or its derivatives. First subculture of human umbilical endothelial cells was used for this study. Cells were treated with thrombin and atorvastatin for different time intervals and dosage. Tissue factor activity was measured as Factor Xa generation induced by Tissue Factor-Factor VIIa complex on confluent cells. Our results show that atorvastatin prevents the thrombin-induced up-regulation of tissue factor activity in a concentration-dependent manner. Mevalonate and geranylgeranyl pyrophosphate reversed this inhibitory effect of atorvastatin on tissue factor activity, while the presence of farnesyl pyrophosphate did not prevent the atorvastatin effect on thrombin-induced tissue factor activity. Rho-kinase inhibitor did not affect the thrombin stimulation of tissue factor activity. High amount of hydrophobic isoprenoid groups decreases the thrombin-induced TF activity and may promote endothelial cell anti-thrombotic action. Rho kinase pathways do not have a major role in the thrombin-mediated TF activity. The inhibitory effect of atorvastatin on thrombin-induced TF activity was partially reversed by MVA and GGPP but not FPP.

摘要

他汀类药物可能通过非脂质机制具有抗血栓作用,从而影响组织因子的诱导,对动脉粥样硬化形成有有益作用。在这项研究中,我们研究了阿托伐他汀对凝血酶刺激的内皮细胞组织因子(TF)活性的影响,以及其通过甲羟戊酸或其衍生物的调节作用。首先使用人脐静脉内皮细胞的亚培养物进行了这项研究。用凝血酶和阿托伐他汀处理不同时间间隔和剂量的细胞。组织因子活性通过组织因子-Factor VIIa 复合物在汇合细胞上诱导的因子 Xa 生成来测量。我们的结果表明,阿托伐他汀以浓度依赖的方式防止凝血酶诱导的组织因子活性上调。甲羟戊酸和香叶基香叶基焦磷酸逆转了阿托伐他汀对组织因子活性的这种抑制作用,而法尼基焦磷酸的存在并没有阻止阿托伐他汀对凝血酶诱导的组织因子活性的作用。Rho 激酶抑制剂不影响凝血酶刺激的组织因子活性。大量疏水性异戊二烯基团降低了凝血酶诱导的 TF 活性,并可能促进内皮细胞抗血栓作用。Rho 激酶途径在凝血酶介导的 TF 活性中没有主要作用。阿托伐他汀对凝血酶诱导的 TF 活性的抑制作用部分被 MVA 和 GGPP 逆转,但不是 FPP。

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