Department of Pharmacology and Toxicology, University of Navarra, Pamplona, Spain.
IdiSNA, Navarra Institute for Health Research, Pamplona, Spain.
Mol Neurobiol. 2018 Jun;55(6):5177-5183. doi: 10.1007/s12035-017-0700-6. Epub 2017 Sep 2.
Alzheimer's disease (AD) is characterized by the loss of synaptic contacts caused in part by cytoskeleton disruption. Adrenomedullin (AM) is involved in physiological functions such as vasodilation, hormone secretion, antimicrobial activity, cellular growth, and angiogenesis. In neurons, AM and related peptides are associated with some structural and functional cytoskeletal proteins, causing microtubule destabilization. Here, we describe the relationships between AM and other signs of AD in clinical specimens. Frontal cortex from AD patients and controls were studied for AM, acetylated tubulin, NCAM, Ox-42, and neurotransmitters. AM was increased in AD compared with controls, while levels of acetylated tubulin, NCAM, and neurotransmitters were decreased. Interestingly, increases in AM statistically correlated with the decrease in these markers. Furthermore, Ox42 overexpression in AD correlated with levels of AM. It is proposed that AD patients may have neural cytoskeleton failure associated with increase of AM levels, resulting in axon transport collapse and synaptic loss. These observations suggest that reducing AM expression may constitute a new avenue to prevent/treat AD.
阿尔茨海默病(AD)的特征是突触接触的丧失,部分原因是细胞骨架的破坏。肾上腺髓质素(AM)参与血管舒张、激素分泌、抗菌活性、细胞生长和血管生成等生理功能。在神经元中,AM 及相关肽与一些结构和功能细胞骨架蛋白有关,导致微管不稳定。在这里,我们描述了 AM 与临床标本中 AD 的其他迹象之间的关系。研究了 AD 患者和对照组的额皮质中的 AM、乙酰化微管蛋白、NCAM、Ox-42 和神经递质。与对照组相比,AD 中 AM 增加,而乙酰化微管蛋白、NCAM 和神经递质的水平降低。有趣的是,AM 的增加与这些标志物的减少呈统计学相关。此外,AD 中 Ox42 的过表达与 AM 水平相关。据提议,AD 患者可能存在与 AM 水平升高相关的神经细胞骨架功能障碍,导致轴突运输崩溃和突触丧失。这些观察结果表明,降低 AM 的表达可能是预防/治疗 AD 的新途径。