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小鼠体内循环血小板衍生生长因子-BB升高时的血管和代谢反应:一项多参数磁共振成像研究。

Vascular and metabolic responses to elevated circulating PDGF-BB in mice: A multiparametric MRI study.

作者信息

Yang Xiuli, Wang Jiekang, Li Yuguo, Wan Mei, Wei Zhiliang

机构信息

Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Department of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Health Metab. 2025;2(2). doi: 10.53941/hm.2025.100009. Epub 2025 Feb 11.

Abstract

Elevated circulating platelet-derived growth factor-BB (PDGF-BB) has been implicated in various aged-related pathologies and, therefore, is recognized as a potential pro-aging factor. Despite extensive studies on the pathological characterizations centering PDGF-BB/PDGFRβ signaling alterations, there is limited research on the neurofunctional responses to elevated circulating PDGF-BB, primarily because measurements are generally required for studying neurofunction. To address this knowledge gap, we characterized the vascular and metabolic responses to elevated circulating PDGF-BB using multiparametric non-invasive non-contrast MRI techniques in a conditional transgenic mouse model (Pdgfb) at 6 months of age. We found that Pdgfb mice exhibited decreased cerebral blood flow (P = 0.025), elevated oxygen extraction (P = 0.002), and increased metabolic rate of oxygen (P = 0.035), which replicated the changes observed in human aging. Compared to naturally aged mice, the rate of change in vascular and metabolic measurements was prominently higher (≥ 200.3%). Our study provides neurofunctional evidence that elevated circulating PDGF-BB accelerates neurovascular aging.

摘要

循环血小板衍生生长因子-BB(PDGF-BB)水平升高与多种衰老相关病理状况有关,因此被认为是一种潜在的促衰老因子。尽管围绕PDGF-BB/PDGFRβ信号改变的病理特征进行了广泛研究,但对于循环PDGF-BB水平升高时神经功能反应的研究却很有限,主要原因是研究神经功能通常需要进行测量。为了填补这一知识空白,我们在6月龄的条件转基因小鼠模型(Pdgfb)中,使用多参数无创非对比MRI技术,对循环PDGF-BB水平升高时的血管和代谢反应进行了表征。我们发现,Pdgfb小鼠表现出脑血流量减少(P = 0.025)、氧摄取增加(P = 0.002)和氧代谢率升高(P = 0.035),这些变化与人类衰老过程中观察到的变化一致。与自然衰老小鼠相比,血管和代谢测量的变化率显著更高(≥200.3%)。我们的研究提供了神经功能方面的证据,表明循环PDGF-BB水平升高会加速神经血管衰老。

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