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阿托伐他汀对人内皮细胞外核苷酸降解的刺激作用。

Stimulatory effects of atorvastatin on extracellular nucleotide degradation in human endothelial cells.

作者信息

Osman L, Amrani M, Isley C, Yacoub M H, Smolenski R T

机构信息

Heart Science Centre, Imperial College at Harefield Hospital, Harefield, UK.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2006;25(9-11):1125-8. doi: 10.1080/15257770600894196.

Abstract

Endothelial degradation of extracellular nucleotides is known to be an important mechanism in regulation of thrombosis, inflammation and immune response. It is possible that this pathway is a target for pleiotropic drugs such as atorvastatin. We studied therefore the effect of atorvastatin on extracellular nucleotide degradation in human endothelial cells. Atorvastatin treatment of human umbilical vein endothelial cells (HUVEC) and human microvascular endothelial cells (HMEC-1) resulted in significant increase in ATP breakdown and adenosine formation both if analysed in intact cell studies and as enzyme activity in cell lysates. We conclude that one of the beneficial effects of atorvastatin may include acceleration of extracellular nucleotide breakdown. This will attenuate nucleotide mediated pro-inflammatory effect and stimulate protective mechanisms of adenosine.

摘要

已知细胞外核苷酸的内皮降解是调节血栓形成、炎症和免疫反应的重要机制。这条途径有可能是阿托伐他汀等多效性药物的作用靶点。因此,我们研究了阿托伐他汀对人内皮细胞中细胞外核苷酸降解的影响。用阿托伐他汀处理人脐静脉内皮细胞(HUVEC)和人微血管内皮细胞(HMEC-1),无论是在完整细胞研究中分析,还是作为细胞裂解物中的酶活性分析,均导致ATP分解和腺苷形成显著增加。我们得出结论,阿托伐他汀的有益作用之一可能包括加速细胞外核苷酸分解。这将减弱核苷酸介导的促炎作用,并刺激腺苷的保护机制。

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