Voluntary running enhances glymphatic influx in awake behaving, young mice

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Voluntary running enhances glymphatic influx in awake behaving, young mice. / von Holstein-Rathlou, Stephanie; Petersen, Nicolas Caesar; Nedergaard, Maiken.

In: Neuroscience Letters, Vol. 662, 2018, p. 253-258.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

von Holstein-Rathlou, S, Petersen, NC & Nedergaard, M 2018, 'Voluntary running enhances glymphatic influx in awake behaving, young mice', Neuroscience Letters, vol. 662, pp. 253-258. https://doi.org/10.1016/j.neulet.2017.10.035

APA

von Holstein-Rathlou, S., Petersen, N. C., & Nedergaard, M. (2018). Voluntary running enhances glymphatic influx in awake behaving, young mice. Neuroscience Letters, 662, 253-258. https://doi.org/10.1016/j.neulet.2017.10.035

Vancouver

von Holstein-Rathlou S, Petersen NC, Nedergaard M. Voluntary running enhances glymphatic influx in awake behaving, young mice. Neuroscience Letters. 2018;662:253-258. https://doi.org/10.1016/j.neulet.2017.10.035

Author

von Holstein-Rathlou, Stephanie ; Petersen, Nicolas Caesar ; Nedergaard, Maiken. / Voluntary running enhances glymphatic influx in awake behaving, young mice. In: Neuroscience Letters. 2018 ; Vol. 662. pp. 253-258.

Bibtex

@article{aab1ea956a3044fbb7556f6894296daf,
title = "Voluntary running enhances glymphatic influx in awake behaving, young mice",
abstract = "Vascular pathology and protein accumulation contribute to cognitive decline, whereas exercise can slow vascular degeneration and improve cognitive function. Recent investigations suggest that glymphatic clearance measured in aged mice while anesthetized is enhanced following exercise. We predicted that exercise would also stimulate glymphatic activity in awake, young mice with higher baseline glymphatic function. Therefore, we assessed glymphatic function in young female C57BL/6J mice following five weeks voluntary wheel running and in sedentary mice. The active mice ran a mean distance of 6km daily. We injected fluorescent tracers in cisterna magna of awake behaving mice and in ketamine/xylazine anesthetized mice, and later assessed tracer distribution in coronal brain sections. Voluntary exercise consistently increased CSF influx during wakefulness, primarily in the hypothalamus and ventral parts of the cortex, but also in the middle cerebral artery territory. While glymphatic activity was higher under ketamine/xylazine anesthesia, we saw a decrease in glymphatic function during running in awake mice after five weeks of wheel running. In summary, daily running increases CSF flux in widespread areas of the mouse brain, which may contribute to the pro-cognitive effects of exercise.",
keywords = "Journal Article",
author = "{von Holstein-Rathlou}, Stephanie and Petersen, {Nicolas Caesar} and Maiken Nedergaard",
note = "Copyright {\textcopyright} 2017 Elsevier B.V. All rights reserved.",
year = "2018",
doi = "10.1016/j.neulet.2017.10.035",
language = "English",
volume = "662",
pages = "253--258",
journal = "Neuroscience letters. Supplement",
issn = "0167-6253",
publisher = "Elsevier Ireland Ltd",

}

RIS

TY - JOUR

T1 - Voluntary running enhances glymphatic influx in awake behaving, young mice

AU - von Holstein-Rathlou, Stephanie

AU - Petersen, Nicolas Caesar

AU - Nedergaard, Maiken

N1 - Copyright © 2017 Elsevier B.V. All rights reserved.

PY - 2018

Y1 - 2018

N2 - Vascular pathology and protein accumulation contribute to cognitive decline, whereas exercise can slow vascular degeneration and improve cognitive function. Recent investigations suggest that glymphatic clearance measured in aged mice while anesthetized is enhanced following exercise. We predicted that exercise would also stimulate glymphatic activity in awake, young mice with higher baseline glymphatic function. Therefore, we assessed glymphatic function in young female C57BL/6J mice following five weeks voluntary wheel running and in sedentary mice. The active mice ran a mean distance of 6km daily. We injected fluorescent tracers in cisterna magna of awake behaving mice and in ketamine/xylazine anesthetized mice, and later assessed tracer distribution in coronal brain sections. Voluntary exercise consistently increased CSF influx during wakefulness, primarily in the hypothalamus and ventral parts of the cortex, but also in the middle cerebral artery territory. While glymphatic activity was higher under ketamine/xylazine anesthesia, we saw a decrease in glymphatic function during running in awake mice after five weeks of wheel running. In summary, daily running increases CSF flux in widespread areas of the mouse brain, which may contribute to the pro-cognitive effects of exercise.

AB - Vascular pathology and protein accumulation contribute to cognitive decline, whereas exercise can slow vascular degeneration and improve cognitive function. Recent investigations suggest that glymphatic clearance measured in aged mice while anesthetized is enhanced following exercise. We predicted that exercise would also stimulate glymphatic activity in awake, young mice with higher baseline glymphatic function. Therefore, we assessed glymphatic function in young female C57BL/6J mice following five weeks voluntary wheel running and in sedentary mice. The active mice ran a mean distance of 6km daily. We injected fluorescent tracers in cisterna magna of awake behaving mice and in ketamine/xylazine anesthetized mice, and later assessed tracer distribution in coronal brain sections. Voluntary exercise consistently increased CSF influx during wakefulness, primarily in the hypothalamus and ventral parts of the cortex, but also in the middle cerebral artery territory. While glymphatic activity was higher under ketamine/xylazine anesthesia, we saw a decrease in glymphatic function during running in awake mice after five weeks of wheel running. In summary, daily running increases CSF flux in widespread areas of the mouse brain, which may contribute to the pro-cognitive effects of exercise.

KW - Journal Article

U2 - 10.1016/j.neulet.2017.10.035

DO - 10.1016/j.neulet.2017.10.035

M3 - Journal article

C2 - 29079431

VL - 662

SP - 253

EP - 258

JO - Neuroscience letters. Supplement

JF - Neuroscience letters. Supplement

SN - 0167-6253

ER -

ID: 185945162