Sjögren Magnus, Mielke Michelle, Gustafson Deborah, Zandi Peter, Skoog Ingmar
Department of Experimental Geriatrics, Neurotec, Karolinska Institute, Huddinge, Sweden.
Mech Ageing Dev. 2006 Feb;127(2):138-47. doi: 10.1016/j.mad.2005.09.020. Epub 2005 Dec 5.
The predominating theory on the pathophysiology of Alzheimer's disease (AD) concerns the mis-metabolism of amyloid precursor protein (APP). As a result of this mis-metabolism, there is an increased production of the 42 amino acid form of beta-amyloid (Abeta42) that rapidly will form oligomers that initiates a cascade of events leading to the accumulation of amyloid plaques. Commonly recognised as vascular factors, hypertension, hypercholesterolemia and diabetes and the inheritance of the epsilon4 allele of the APOE gene, are also risk factors for AD. These risks have been found to promote the production of Abeta42. An association between cholesterol and the development of AD was suggested in the early 1990s and ever since, an increasing amount of research has confirmed that there is a link between cholesterol and the development of AD. A high cholesterol levels in mid-life is a risk for AD and statins, i.e., cholesterol-lowering drugs, reduce this risk. Statins may not only inhibit enzymes involved in the endogenous synthesis of cholesterol but also affect enzymes involved in Abeta metabolism, i.e., alpha-secretase and beta-secretase. This normalises the breakdown of APP thereby promoting the non-amyloidogenic pathway. In this review, investigations focusing on cholesterol and Alzheimer's disease are presented.
关于阿尔茨海默病(AD)病理生理学的主流理论涉及淀粉样前体蛋白(APP)的代谢异常。由于这种代谢异常,β-淀粉样蛋白42氨基酸形式(Aβ42)的产生增加,其会迅速形成寡聚体,引发一系列事件,导致淀粉样斑块的积累。通常被认为是血管因素的高血压、高胆固醇血症和糖尿病以及APOE基因ε4等位基因的遗传,也是AD的危险因素。已发现这些风险会促进Aβ42的产生。20世纪90年代初有人提出胆固醇与AD发病之间存在关联,从那时起,越来越多的研究证实胆固醇与AD发病之间存在联系。中年时高胆固醇水平是AD的一个风险因素,而他汀类药物,即降胆固醇药物,可降低这种风险。他汀类药物不仅可能抑制参与胆固醇内源性合成的酶,还可能影响参与Aβ代谢的酶,即α-分泌酶和β-分泌酶。这使APP的分解正常化,从而促进非淀粉样生成途径。在本综述中,将介绍聚焦于胆固醇与阿尔茨海默病的研究。