Petrella Carla, Di Certo Maria Grazia, Barbato Christian, Gabanella Francesca, Ralli Massimo, Greco Antonio, Possenti Roberta, Severini Cinzia
Department of Sense Organs, CNR, Institute of Cell Biology and Neurobiology, University Sapienza of Rome, Viale del Policlinico 155, 00161 Rome, Italy.
Department of Sense Organs, University Sapienza of Rome, Viale del Policlinico 155, 00161 Rome, Italy.
Curr Alzheimer Res. 2019;16(6):544-558. doi: 10.2174/1567205016666190503152555.
Neuropeptides are small proteins broadly expressed throughout the central nervous system, which act as neurotransmitters, neuromodulators and neuroregulators. Growing evidence has demonstrated the involvement of many neuropeptides in both neurophysiological functions and neuropathological conditions, among which is Alzheimer's disease (AD). The role exerted by neuropeptides in AD is endorsed by the evidence that they are mainly neuroprotective and widely distributed in brain areas responsible for learning and memory processes. Confirming this point, it has been demonstrated that numerous neuropeptide-containing neurons are pathologically altered in brain areas of both AD patients and AD animal models. Furthermore, the levels of various neuropeptides have been found altered in both Cerebrospinal Fluid (CSF) and blood of AD patients, getting insights into their potential role in the pathophysiology of AD and offering the possibility to identify novel additional biomarkers for this pathology. We summarized the available information about brain distribution, neuroprotective and cognitive functions of some neuropeptides involved in AD. The main focus of the current review was directed towards the description of clinical data reporting alterations in neuropeptides content in both AD patients and AD pre-clinical animal models. In particular, we explored the involvement in the AD of Thyrotropin-Releasing Hormone (TRH), Cocaine- and Amphetamine-Regulated Transcript (CART), Cholecystokinin (CCK), bradykinin and chromogranin/secretogranin family, discussing their potential role as a biomarker or therapeutic target, leaving the dissertation of other neuropeptides to previous reviews.
神经肽是一类在中枢神经系统广泛表达的小蛋白质,它们作为神经递质、神经调质和神经调节剂发挥作用。越来越多的证据表明,许多神经肽参与神经生理功能和神经病理状况,其中包括阿尔茨海默病(AD)。神经肽在AD中发挥的作用得到了以下证据的支持:它们主要具有神经保护作用,并且广泛分布于负责学习和记忆过程的脑区。证实这一点的是,已证明在AD患者和AD动物模型的脑区中,许多含神经肽的神经元发生了病理改变。此外,在AD患者的脑脊液(CSF)和血液中均发现各种神经肽水平发生了改变,这有助于深入了解它们在AD病理生理学中的潜在作用,并为该疾病识别新的生物标志物提供了可能性。我们总结了有关参与AD的一些神经肽的脑部分布、神经保护和认知功能的现有信息。本综述的主要重点是描述报告AD患者和AD临床前动物模型中神经肽含量变化的临床数据。特别是,我们探讨了促甲状腺激素释放激素(TRH)、可卡因和苯丙胺调节转录物(CART)、胆囊收缩素(CCK)、缓激肽和嗜铬粒蛋白/分泌粒蛋白家族在AD中的作用,讨论了它们作为生物标志物或治疗靶点的潜在作用,而将其他神经肽的论述留给以前的综述。