Mendiola Perenkita J, O'Herron Philip, Xie Kun, Brands Michael W, Bush Weston, Patterson Rachel E, Di Stefano Valeria, Filosa Jessica A
Department of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
bioRxiv. 2024 Oct 24:2024.10.21.619509. doi: 10.1101/2024.10.21.619509.
Blood pressure variability (BPV) has emerged as a novel risk factor for cognitive decline and dementia, independent of alterations in average blood pressure (BP). However, the underlying consequences of large BP fluctuations on the neurovascular complex are unknown. We developed a novel mouse model of BPV in middle-aged mice based on intermittent Angiotensin II infusions. Using radio telemetry, we demonstrated that the 24-hr BP averages of these mice were similar to controls, indicating BPV without hypertension. Chronic (20-25 days) BPV led to a blunted bradycardic response and cognitive deficits. Two-photon imaging of parenchymal arterioles showed enhanced pressure-evoked constrictions (myogenic response) in BPV mice. Sensory stimulus-evoked dilations (neurovascular coupling) were greater at higher BP levels in control mice, but this pressure-dependence was lost in BPV mice. Our findings support the notion that large BP variations impair vascular function at the neurovascular complex and contribute to cognitive decline.
血压变异性(BPV)已成为认知功能下降和痴呆的一种新的风险因素,独立于平均血压(BP)的改变。然而,大幅血压波动对神经血管复合体的潜在影响尚不清楚。我们基于间歇性输注血管紧张素II,开发了一种中年小鼠的新型BPV小鼠模型。使用无线电遥测技术,我们证明这些小鼠的24小时平均血压与对照组相似,表明存在无高血压的BPV。慢性(20 - 25天)BPV导致心动过缓反应减弱和认知缺陷。实质小动脉的双光子成像显示,BPV小鼠中压力诱发的收缩(肌源性反应)增强。在对照小鼠中,感觉刺激诱发的扩张(神经血管耦合)在较高血压水平时更大,但这种压力依赖性在BPV小鼠中丧失。我们的研究结果支持这样的观点,即大幅血压变化会损害神经血管复合体的血管功能,并导致认知功能下降。