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Catechins Green Tea GMB4 Clone Increases mRNA of ABCA1 through LXR Signaling in Cultured Macrophage Exposed OX-LDL

机译:儿茶素绿茶GMB4克隆通过培养的巨噬细胞暴露的OX-LDL中的LXR信号增加ABCA1的mRNA

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Inhibition of atherogenesis through inhibition of lipid metabolism has not been explored while other inhibition s through inflammation, endothelial dysfunction and free radicals have done. Inhibition of atherogenesis via inhibition of lipid metabolism can be done through the mechanism of Reverse Cholesterol Transport (RCT). Signaling pathways that play a role in this mechanism is LXR signaling. LXR activation by an LXR agonist led increasing cholesterol efflux. Catechins based on bioinformatics study showed as a potent candidate LXR agonists that can be used as an inhibitor of atherogenesis. This study aims to prove that the administration Catechins green tea Clone GMB4 can prevent atherosclerosis through increasing mechanism cholesterol efflux from macrophage by taking effect of ABCA1, ABCG1, SRB1 gene expression in cultured macrophages were exposed ox-LDL. Long-term goals of the outcome of the research are the use of Catechins Green Tea Clones GMB4 as an inhibitor of atherogenesis so that it can be used as a complementary therapy for the treatment of atherosclerosis and cardiovascular diseases. Th e research is divided into 5 groups, namely the culture of macrophages without exposed o x-LDL, culture exposed ox-LDL and groups of Catechins dose I, II, III. In vitro study showed that administration of Catechins increases mRNA of ABCA1, whereas mRNA ABCG1 and SRB1 decreased at all three doses given. The result of protein profilling was identified a protein with a molecular weight of 70 kDa by SDS-PGE with silver staining.
机译:尚未探索通过抑制脂质代谢来抑制动脉粥样硬化,而其他通过炎症,内皮功能障碍和自由基引起的抑制作用也已被探索。通过抑制脂质代谢来抑制动脉粥样硬化可以通过胆固醇逆向转运(RCT)机制来完成。在该机制中起作用的信号传导途径是LXR信号传导。 LXR激动剂激活LXR导致胆固醇外排增加。基于生物信息学研究的儿茶素显示作为有效的候选LXR激动剂,可以用作动脉粥样硬化的抑制剂。这项研究旨在证明,通过在暴露于ox-LDL的培养的巨噬细胞中利用ABCA1,ABCG1,SRB1基因表达的作用,施用Catechins绿茶克隆GMB4可以通过增加巨噬细胞的胆固醇外流机制来预防动脉粥样硬化。研究结果的长期目标是使用儿茶素绿茶克隆GMB4作为动脉粥样硬化的抑制剂,以便可以用作动脉粥样硬化和心血管疾病的辅助疗法。研究分为5组,即无暴露于x-LDL的巨噬细胞培养物,暴露于ox-LDL的培养物和儿茶素剂量组I,II,III。 体外研究表明,给予儿茶素会增加ABCA1的mRNA表达,而在所有三种剂量下mRNA ABCG1和SRB1都会降低。蛋白质填充的结果通过银染的SDS-PGE鉴定为分子量为70 kDa的蛋白质。

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