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The Role of An Experimental Model of Atherosclerosis: apoE-knockout Mice in Developing New Drugs against Atherogenesis

机译:动脉粥样硬化实验模型的作用:apoE基因敲除小鼠在开发新的抗动脉粥样硬化药物方面的作用

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Although atherosclerosis was previously thought to be mainly a degenerative disease, it is now well ascertained that its pathogenesis is inflammatory. There was a pivotal role of apoE-knockout mice in understanding the inflammatory background of atherosclerosis. Currently, atherosclerosis is known as a chronic inflammatory disease, in most cases initiated by hypercholesterolemia. Recently, the mouse has become the best model for experimental atherosclerosis. It was in 1992 that the first line of gene targeted mice, namely apolipoprotein E-knockout mice was developed. The apoE-deficient model develops extensive atherosclerotic lesions on a chow diet. The LDL receptor - deficient model has elevated LDL levels, but no lesions, or only very small lesions, form on the chow diet. However, robust lesions do form on the western-type diet. The creation of apoE- knockout mice has changed the face of atherosclerosis research. Gene-targeted mouse models has changed the face of atherosclerotic research and helped in creation of the new theory of atherosclerosis: as an inflammatory disease. Recently, the mouse has become the best model for experimental atherosclerosis. It was in 1992 that the first line of gene targeted mice, namely apolipoprotein E-knockout mice was developed. The apoE-deficient model develops extensive atherosclerotic lesions on a chow diet. It is also the model in which the lesions have been characterized most thoroughly. The lesions develop into fibrous plaques; however, there is no evidence that plaque rupture occurs in this model. The LDL receptor - deficient model has elevated LDL levels, but no lesions, or only very small lesions, form on the chow diet. However, robust lesions do form on the western-type diet. The creation of apoE-knockout mice has changed the face of atherosclerosis research. Gene-targeted mouse models has changed the face of atherosclerotic research and helped in creation of the new theory of atherosclerosis: as an inflammatory disease. Nowadays, apoE- knockout mice model is therefore used in developing new drugs against atherosclerosis. This review describes how new groups of agents are searched.
机译:尽管以前认为动脉粥样硬化是主要的退行性疾病,但现在已经确定其发病机理是炎症性的。在了解动脉粥样硬化的炎症背景中,apoE基因敲除小鼠具有关键作用。当前,动脉粥样硬化被称为慢性炎性疾病,在大多数情况下是由高胆固醇血症引发的。最近,鼠标已成为实验性动脉粥样硬化的最佳模型。在1992年,开发了第一批基因靶向小鼠,即载脂蛋白E基因敲除小鼠。缺乏apoE的模型会在日常饮食中发展出广泛的动脉粥样硬化病变。 LDL受体缺陷型大鼠的LDL水平升高,但在日粮中没有形成病变,或只有很小的病变。但是,在西式饮食中确实会形成牢固的病变。载脂蛋白E敲除小鼠的创建改变了动脉粥样硬化研究的面貌。以基因为靶标的小鼠模型改变了动脉粥样硬化研究的面貌,并有助于创建新的动脉粥样硬化理论:作为一种炎症性疾病。最近,鼠标已成为实验性动脉粥样硬化的最佳模型。在1992年,开发了第一批基因靶向小鼠,即载脂蛋白E基因敲除小鼠。缺乏apoE的模型会在日常饮食中发展出广泛的动脉粥样硬化病变。这也是病变最充分表征的模型。病变发展成纤维斑块。但是,没有证据表明该模型发生斑块破裂。 LDL受体缺陷型大鼠的LDL水平升高,但在日粮中没有形成病变,或只有很小的病变。但是,在西式饮食中确实会形成牢固的病变。 apoE基因敲除小鼠的创建改变了动脉粥样硬化研究的面貌。以基因为靶标的小鼠模型改变了动脉粥样硬化研究的面貌,并有助于创建新的动脉粥样硬化理论:作为一种炎症性疾病。因此,如今,apoE基因敲除小鼠模型被用于开发抗动脉粥样硬化的新药。该评论描述了如何搜索新的座席组。

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