Katusic Zvonimir S, Austin Susan A
Department of Anesthesiology, Vascular Biology Laboratory, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
Eur Heart J. 2014 Apr;35(14):888-94. doi: 10.1093/eurheartj/eht544. Epub 2013 Dec 18.
Endothelial nitric oxide (NO) is generated by constitutively active endothelial nitric oxide synthase (eNOS), an essential enzyme responsible for cardiovascular homeostasis. Historically, endothelial NO was first recognized as a major vasodilator involved in control of vasomotor function and local blood flow. In this review, our attention is focused on the emerging role of endothelial NO in linking cerebrovascular function with cognition. We will discuss the recognized ability of endothelial NO to modulate processing of amyloid precursor protein (APP), influence functional status of microglia, and affect cognitive function. Existing evidence suggests that the loss of NO in cultured human cerebrovascular endothelium causes increased expression of APP and β-site APP-cleaving enzyme 1 (BACE1) thereby resulting in increased secretion of amyloid β peptides (Aβ1-40 and Aβ1-42). Furthermore, increased expression of APP and BACE1 as well as increased production of Aβ peptides was detected in the cerebral microvasculature and brain tissue of eNOS-deficient mice. Since Aβ peptides are considered major cytotoxic molecules responsible for the pathogenesis of Alzheimer's disease, these observations support the concept that a loss of endothelial NO might significantly contribute to the initiation and progression of cognitive decline. In addition, genetic inactivation of eNOS causes activation of microglia and promotes a pro-inflammatory phenotype in the brain. Behavioural analysis revealed that eNOS-deficient mice exhibit impaired cognitive performance thereby indicating that selective loss of endothelial NO has a detrimental effect on the function of neuronal cells. Together with findings from prior studies demonstrating the ability of endothelial NO to affect synaptic plasticity, mitochondrial biogenesis, and function of neuronal progenitor cells, it is becoming apparent that the role of endothelial NO in the control of central nervous system function is very complex. We propose that endothelial NO represents the key molecule linking cerebrovascular and neuronal function.
内皮型一氧化氮(NO)由组成型活性内皮型一氧化氮合酶(eNOS)生成,eNOS是维持心血管稳态的一种重要酶。从历史上看,内皮型NO最初被认为是一种主要的血管舒张剂,参与血管舒缩功能和局部血流的控制。在本综述中,我们将注意力集中在内皮型NO在连接脑血管功能与认知方面的新作用上。我们将讨论内皮型NO调节淀粉样前体蛋白(APP)加工、影响小胶质细胞功能状态以及影响认知功能的公认能力。现有证据表明,培养的人脑血管内皮细胞中NO的缺失会导致APP和β位点APP裂解酶1(BACE1)表达增加,从而导致淀粉样β肽(Aβ1-40和Aβ1-42)分泌增加。此外,在eNOS缺陷小鼠的脑微血管和脑组织中检测到APP和BACE1表达增加以及Aβ肽生成增加。由于Aβ肽被认为是导致阿尔茨海默病发病机制的主要细胞毒性分子,这些观察结果支持这样一种观点,即内皮型NO的缺失可能对认知衰退的起始和进展有显著影响。此外,eNOS的基因失活会导致小胶质细胞活化,并促进大脑中的促炎表型。行为分析表明,eNOS缺陷小鼠表现出认知能力受损,从而表明内皮型NO的选择性缺失对神经元细胞功能有不利影响。结合先前研究发现内皮型NO能够影响突触可塑性、线粒体生物发生和神经元祖细胞功能,内皮型NO在控制中枢神经系统功能中的作用显然非常复杂。我们认为内皮型NO是连接脑血管和神经元功能的关键分子。