School of Biomedical Sciences, Ulster University, Coleraine, Northern Ireland, UK.
CNS Drugs. 2012 Oct 1;26(10):871-82. doi: 10.2165/11635890-000000000-00000.
The current understanding of neurodegenerative processes in sporadic diseases such as Alzheimer's disease (AD), Parkinson's disease (PD) or multiple sclerosis is very limited. Several risk factors have been identified that may shed light on the underlying mechanisms that initiate the neurodegeneration. Type 2 diabetes mellitus has been identified as a risk factor for AD and PD. In AD patients, desensitization of insulin receptors in the brain has been shown, even in non-diabetic patients. Insulin acts as a growth factor in the brain and supports neuronal repair, dendritic sprouting and synaptogenesis, and protection from oxidative stress. Importantly, several drugs have been developed to treat type 2 diabetes that re-sensitize insulin receptors and may be of use to prevent neurodegenerative processes. Glucagon-like peptide-1 (GLP-1) is a hormone that facilitates insulin release under high blood sugar conditions. Interestingly, GLP-1 also has very similar growth factor-like properties to insulin, and has been shown to reduce a range of degenerative processes. In pre-clinical studies, GLP-1 and longer-lasting protease-resistant analogues cross the blood-brain barrier, protect memory formation (AD) or motor activity (PD), protect synapses and synaptic functions, enhance neurogenesis, reduce apoptosis, protect neurons from oxidative stress, and reduce plaque formation and the chronic inflammation response in the brains of mouse models of AD, PD, amyotrophic lateral sclerosis, stroke and other degenerative diseases. GLP-1 signalling does not affect blood sugar levels in non-diabetic people and therapies that affect GLP-1 signalling have a good safety profile as shown by the chronic application of drugs currently on the market (liraglutide, Victoza(®); NovoNordisk, Copenhagen, Denmark, and exendin-4, Byetta(®); Amylin, San Diego, CA, USA). Based on the extensive evidence, several clinical trials are currently underway, testing liraglutide and exendin-4 in AD and PD patients. Therefore, GLP-1 analogues show great promise as a novel treatment for AD or other neurodegenerative conditions.
目前,人们对散发性疾病(如阿尔茨海默病(AD)、帕金森病(PD)或多发性硬化症)中的神经退行性过程的认识非常有限。已经确定了一些危险因素,这些危险因素可能揭示引发神经退行性变的潜在机制。2 型糖尿病已被确定为 AD 和 PD 的危险因素。在 AD 患者中,即使在非糖尿病患者中,也已经显示出大脑中的胰岛素受体脱敏。胰岛素在大脑中充当生长因子,支持神经元修复、树突棘发芽和突触形成,并防止氧化应激。重要的是,已经开发出几种治疗 2 型糖尿病的药物来重新敏感胰岛素受体,可能有助于预防神经退行性过程。胰高血糖素样肽-1(GLP-1)是一种在高血糖条件下促进胰岛素释放的激素。有趣的是,GLP-1 也具有与胰岛素非常相似的生长因子样特性,并已被证明可减少一系列退行性过程。在临床前研究中,GLP-1 和更持久的蛋白酶抗性类似物可穿过血脑屏障,保护记忆形成(AD)或运动活动(PD),保护突触和突触功能,增强神经发生,减少细胞凋亡,保护神经元免受氧化应激,并减少 AD、PD、肌萎缩侧索硬化症、中风和其他退行性疾病的小鼠模型中的斑块形成和慢性炎症反应。GLP-1 信号不会影响非糖尿病患者的血糖水平,并且目前市场上的药物的慢性应用表明,影响 GLP-1 信号的疗法具有良好的安全性概况(利拉鲁肽、Victoza®;诺和诺德,丹麦哥本哈根,和 exendin-4、Byetta®;Amylin,圣地亚哥,CA,美国)。基于广泛的证据,目前正在进行几项临床试验,测试利拉鲁肽和 exendin-4 在 AD 和 PD 患者中的应用。因此,GLP-1 类似物作为 AD 或其他神经退行性疾病的新型治疗方法具有广阔的前景。