Chronic β3 adrenergic agonist treatment improves neurovascular coupling responses, attenuates blood-brain barrier leakage and neuroinflammation, and enhances cognition in aged mice.

IF 3.9 3区 医学 Q2 CELL BIOLOGY
Aging-Us Pub Date : 2025-02-19 DOI:10.18632/aging.206203
Duraipandy Natarajan, Shoba Ekambaram, Stefano Tarantini, Raghavendra Y Nagaraja, Andriy Yabluchanskiy, Andria F Hedrick, Vibhudutta Awasthi, Madhan Subramanian, Anna Csiszar, Priya Balasubramanian
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引用次数: 0

Abstract

Microvascular endothelial dysfunction, characterized by impaired neurovascular coupling, reduced glucose uptake, blood-brain barrier disruption, and microvascular rarefaction, plays a critical role in the pathogenesis of age-related vascular cognitive impairment (VCI). Emerging evidence points to non-cell autonomous mechanisms mediated by adverse circulating milieu (an increased ratio of pro-geronic to anti-geronic circulating factors) in the pathogenesis of endothelial dysfunction leading to impaired cerebral blood flow and cognitive decline in the aging population. In particular, age-related adipose dysfunction contributes, at least in part, to an unfavorable systemic milieu characterized by chronic hyperglycemia, hyperinsulinemia, dyslipidemia, and altered adipokine profile, which together contribute to microvascular endothelial dysfunction. Hence, in the present study, we aimed to test whether thermogenic stimulation, an intervention known to improve adipose and systemic metabolism by increasing cellular energy expenditure, could mitigate brain endothelial dysfunction and improve cognition in the aging population. Eighteen-month-old C57BL/6J mice were treated with saline or β3-adrenergic agonist (CL 316, 243, CL) for 6 weeks followed by functional analysis to assess endothelial function and cognition. CL treatment improved neurovascular coupling responses and rescued brain glucose uptake in aged animals. In addition, CL treatment also attenuated blood-brain barrier leakage and associated neuroinflammation in the cortex and increased microvascular density in the hippocampus of aged mice. More importantly, these beneficial changes in microvascular function translated to improved cognitive performance in aged mice. Our results suggest that β3-adrenergic agonist treatment improves multiple aspects of cerebromicrovascular function and can be potentially repurposed for treating age-associated cognitive decline.

慢性β3肾上腺素能激动剂治疗可改善老年小鼠的神经血管偶联反应,减轻血脑屏障渗漏和神经炎症,增强认知能力。
微血管内皮功能障碍,以神经血管耦合受损、葡萄糖摄取减少、血脑屏障破坏和微血管稀疏为特征,在年龄相关性血管性认知障碍(VCI)的发病机制中起关键作用。新出现的证据表明,在导致老年人脑血流受损和认知能力下降的内皮功能障碍的发病机制中,不良循环环境(促衰老与抗衰老循环因子的比例增加)介导的非细胞自主机制。特别是,年龄相关的脂肪功能障碍至少部分地导致以慢性高血糖、高胰岛素血症、血脂异常和脂肪因子谱改变为特征的不利全身环境,这些共同导致微血管内皮功能障碍。因此,在本研究中,我们旨在测试产热刺激是否可以减轻脑内皮功能障碍并改善老年人的认知能力。产热刺激是一种已知的通过增加细胞能量消耗来改善脂肪和全身代谢的干预措施。18月龄C57BL/6J小鼠分别给予生理盐水或β3-肾上腺素能激动剂(cl316, 243, CL)治疗6周,随后进行功能分析,评估内皮功能和认知功能。CL治疗改善了老年动物的神经血管偶联反应和恢复脑葡萄糖摄取。此外,CL治疗还能减轻老年小鼠血脑屏障渗漏和皮层相关神经炎症,增加海马微血管密度。更重要的是,微血管功能的这些有益变化转化为老年小鼠认知能力的改善。我们的研究结果表明,β3-肾上腺素能激动剂治疗可改善脑血管功能的多个方面,并可潜在地用于治疗与年龄相关的认知衰退。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Aging-Us
Aging-Us CELL BIOLOGY-
CiteScore
10.00
自引率
0.00%
发文量
595
审稿时长
6-12 weeks
期刊介绍: Information not localized
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