Aging drives cerebrovascular network remodeling and functional changes in the mouse brain

Abstract

AbstractAging is the largest risk factor for neurodegenerative disorders, and commonly associated with compromised cerebrovasculature and pericytes. However, we do not know how normal aging differentially impacts the vascular structure and function in different brain areas. Here we utilize mesoscale microscopy methods (serial two-photon tomography and light sheet microscopy) andin vivoimaging (wide field optical spectroscopy and two-photon imaging) to determine detailed changes in aged cerebrovascular networks. Whole-brain vascular tracing showed an overall ~10% decrease in vascular length and branching density, and light sheet imaging with 3D immunolabeling revealed increased arteriole tortuosity in aged brains. Vasculature and pericyte densities showed significant reductions in the deep cortical layers, hippocampal network, and basal forebrain areas. Moreover,in vivoimaging in awake mice identified delays in neurovascular coupling and disrupted blood oxygenation. Collectively, we uncover regional vulnerabilities of cerebrovascular network and physiological changes that can mediate cognitive decline in normal aging.Highlight-Brain-wide mapping of vasculature and pericyte changes with normal aging-Simplified vascular network with tortuous vessels in aged brains-Vascular rarefication in the deep cortical layers, hippocampus, and the basal forebrain-Slowed hemodynamic response in aged animals