Jhana O. Hendrickx, E. Calus, Peter Paul De Deyn, D. Van Dam, G. D. De Meyer
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引用次数: 0
摘要
由于全球人口增长,心血管疾病和痴呆症等老年相关疾病预计会增加。最近的数据表明,心血管疾病和神经变性之间存在联系,尤其是动脉僵化(AS)和阿尔茨海默病(AD)。有鉴于此,我们开展了一项研究,探讨长期一氧化氮合酶(NOS)同工酶抑制(导致动脉僵化)对神经行为表现的影响。我们还比较了 AD 模型和对照组小鼠的这些影响。在C57BL/6和hAPP23+/-小鼠(已建立的AD模型)的饮用水中添加0.5 mg/mL的N(G)-硝基-L-精氨酸甲酯(L-NAME),持续16周。我们的研究结果表明,慢性非选择性 NOS 抑制增加了 C57BL/6 和 hAPP23+/- 小鼠的 AS,并降低了它们的时空学习和记忆能力。这些影响在两组小鼠中都是一致的,强调了神经元NOS(nNOS)在认知衰老中的作用,与AD的遗传易感性无关。
Chronic Inhibition of Nitric Oxide Synthases Impairs Spatiotemporal Learning and Memory to a Similar Extent in C57BL/6 and hAPP23+/− Mice
Due to global population growth, age-related disorders like cardiovascular disease and dementia are anticipated to increase. Recent data suggests a connection between cardiovascular disease and neurodegeneration, especially focusing on arterial stiffness (AS) and Alzheimer’s disease (AD). In light of this, we conducted a study to explore the impact of long-term nitric oxide synthase (NOS) isoform inhibition, which leads to AS, on neurobehavioral performance. We also compared these effects in an AD model and control mice. C57BL/6 and hAPP23+/− mice (an established AD model) were given 0.5 mg/mL N(G)-Nitro-L-Arginine Methyl Ester (L-NAME) in their drinking water for 16 weeks. Our findings indicate that chronic non-selective NOS inhibition increased AS and reduced spatiotemporal learning and memory in both C57BL/6 and hAPP23+/− mice. These effects were consistent across both groups, emphasizing the role of neuronal NOS (nNOS) in cognitive aging, regardless of genetic predisposition to AD.