Kolovou Genovefa, Anagnostopoulou Katherine, Mikhailidis Dimitri P, Cokkinos Dennis V
Onassis Cardiac Surgery Center, 356 Sygrou Ave 176 74 Athens, Greece.
Curr Pharm Des. 2008;14(4):338-51. doi: 10.2174/138161208783497769.
Atherosclerosis is a multifactorial and long-lasting process in humans. Therefore, animal models where more rapid changes occur can be useful for the study of this process. Among such models are the apolipoprotein (apo) E knock out mice. Apo E deficient mice show impaired clearing of plasma lipoproteins and they develop atherosclerosis in a short time. The current review considers lipid metabolism and inflammation as well as nutritional and pharmacological agents affecting atherosclerosis, using the apo E knock out mouse model.
动脉粥样硬化是人类的一个多因素且持久的过程。因此,能发生更快速变化的动物模型对于研究这一过程可能是有用的。载脂蛋白(apo)E基因敲除小鼠就是这类模型之一。apo E基因缺陷小鼠表现出血浆脂蛋白清除受损,并且在短时间内就会发生动脉粥样硬化。本综述利用apo E基因敲除小鼠模型探讨了脂质代谢、炎症以及影响动脉粥样硬化的营养和药物因素。