School of Biomedical Sciences, Ulster University, Cromore Road, Coleraine BT52 1SA, UK.
Biochem Soc Trans. 2011 Aug;39(4):891-7. doi: 10.1042/BST0390891.
Surprisingly little is known about the mechanisms that trigger the onset of AD (Alzheimer's disease) in sporadic forms. A number of risk factors have been identified that may shed light on the mechanisms that may trigger or facilitate the development of AD. Recently, T2DM (Type 2 diabetes mellitus) has been identified as a risk factor for AD. A common observation for both conditions is the desensitization of insulin receptors in the brain. Insulin acts as a growth factor in the brain and is neuroprotective, activates dendritic sprouting, regeneration and stem cell proliferation. The impairment of this important growth factor signal may facilitate the development of AD. Insulin as well as other growth factors have shown neuroprotective properties in preclinical and clinical trials. Several drugs have been developed to treat T2DM, which re-sensitize insulin receptors and may be of use to prevent neurodegenerative processes in the brain. In particular, the incretins GLP-1 (glucagon-like peptide-1) and GIP (glucose-dependent insolinotropic polypeptide) are hormones that re-sensitize insulin signalling. Incretins also have similar growth-factor-like properties as insulin and are neuroprotective. In mouse models of AD, GLP-1 receptor agonists reduce amyloid plaque formation, reduce the inflammation response in the brain, protect neurons from oxidative stress, induce neurite outgrowth, and protect synaptic plasticity and memory formation from the detrimental effects caused by β-amyloid production and inflammation. Other growth factors such as BDNF (brain-derived neurotrophic factor), NGF (nerve growth factor) or IGF-1 (insulin-like growth factor 1) also have shown a range of neuroprotective properties in preclinical studies. These results show that these growth factors activate similar cell signalling mechanisms that are protective and regenerative, and suggest that the initial process that may trigger the cascade of neurodegenerative events in AD could be the impairment of growth factor signalling such as early insulin receptor desensitization.
令人惊讶的是,人们对散发性 AD(阿尔茨海默病)发病机制知之甚少。已经确定了许多危险因素,这些危险因素可能揭示触发或促进 AD 发展的机制。最近,2 型糖尿病(T2DM)已被确定为 AD 的危险因素。这两种疾病的一个共同观察结果是大脑中胰岛素受体的脱敏。胰岛素在大脑中充当生长因子,具有神经保护作用,可激活树突棘发芽、再生和干细胞增殖。这种重要生长因子信号的损伤可能会促进 AD 的发展。胰岛素和其他生长因子在临床前和临床试验中显示出神经保护特性。已经开发出几种用于治疗 T2DM 的药物,这些药物可以重新敏化胰岛素受体,可能有助于预防大脑中的神经退行性过程。特别是,肠促胰岛素 GLP-1(胰高血糖素样肽-1)和 GIP(葡萄糖依赖性胰岛素促分泌多肽)是重新敏化胰岛素信号的激素。肠促胰岛素还具有与胰岛素相似的生长因子样特性,具有神经保护作用。在 AD 的小鼠模型中,GLP-1 受体激动剂可减少淀粉样斑块形成,减少大脑中的炎症反应,保护神经元免受氧化应激,诱导神经突生长,并保护突触可塑性和记忆形成免受由β-淀粉样蛋白产生和炎症引起的有害影响。其他生长因子,如 BDNF(脑源性神经营养因子)、NGF(神经生长因子)或 IGF-1(胰岛素样生长因子 1),在临床前研究中也表现出多种神经保护特性。这些结果表明,这些生长因子激活了相似的细胞信号转导机制,具有保护和再生作用,并表明可能触发 AD 中神经退行性事件级联反应的初始过程可能是生长因子信号的损伤,如早期胰岛素受体脱敏。