Chronic phase advances reduces recognition memory and increases vascular cognitive dementia-like impairments in aged mice

• Published in: Scientific reports 2024-04, Vol.14 (1), p.7760-7760, Article 7760
• Main Authors: Liu, Jennifer A., Bumgarner, Jacob R., Walker, William H., Meléndez-Fernández, O. Hecmarie, Walton, James C., DeVries, A. Courtney, Nelson, Randy J.
• Format: Article
• Language: English
• Subjects: 631/378/1385; 631/378/1595/1636; 631/378/1595/3922; 631/378/1689/1283; 631/378/2612; 692/499; Animals; Associative learning; Auditory discrimination learning; Circadian rhythm; Circadian Rhythm - physiology; Circadian rhythms; Cognition; Cognitive ability; Dementia; Dementia disorders; Dementia, Vascular - etiology; Female; Health risks; Humanities and Social Sciences; Inflammation; Information processing; Ischemia; Male; Mice; multidisciplinary; Photoperiod; Recognition, Psychology; Risk factors; Science; Science (multidisciplinary); Spontaneous alternation; Synchronization; Vascular dementia; Vascular diseases
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-57511-2

Disrupted or atypical light–dark cycles disrupts synchronization of endogenous circadian clocks to the external environment; extensive circadian rhythm desynchrony promotes adverse health outcomes. Previous studies suggest that disrupted circadian rhythms promote neuroinflammation and neuronal damage post-ischemia in otherwise healthy mice, however, few studies to date have evaluated these health risks with aging. Because most strokes occur in aged individuals, we sought to identify whether, in addition to being a risk factor for poor ischemic outcome, circadian rhythm disruption can increase risk for vascular cognitive impairment and dementia (VCID). We hypothesized that repeated 6 h phase advances (chronic jet lag; CJL) for 8 weeks alters cerebrovascular architecture leading to increased cognitive impairments in aged mice. Female CJL mice displayed impaired spatial processing during a spontaneous alternation task and reduced acquisition during auditory-cued associative learning. Male CJL mice displayed impaired retention of the auditory-cued associative learning task 24 h following acquisition. CJL increased vascular tortuosity in the isocortex, associated with increased risk for vascular disease. These results demonstrate that CJL increased sex-specific cognitive impairments coinciding with structural changes to vasculature in the brain. We highlight that CJL may accelerate aged-related functional decline and could be a crucial target against disease progression.