Multisensory gamma stimulation promotes glymphatic clearance of amyloid

Mitchell H. Murdock(Massachusetts Institute of Technology), Cheng-Yi Yang(Massachusetts Institute of Technology), Na Sun(Broad Institute), Ping‐Chieh Pao(Massachusetts Institute of Technology), Cristina Blanco‐Duque(Massachusetts Institute of Technology), Martin C. Kahn(Massachusetts Institute of Technology), TaeHyun Kim(Massachusetts Institute of Technology), Nicolas Lavoie(Massachusetts Institute of Technology), Matheus B. Victor(Massachusetts Institute of Technology), Md. Rezaul Islam(Massachusetts Institute of Technology), Fabiola Galiana-Melendez(Massachusetts Institute of Technology), Noelle Leary(Massachusetts Institute of Technology), Sidney Wang(Massachusetts Institute of Technology), Adele Bubnys(Massachusetts Institute of Technology), Emily Ma(Massachusetts Institute of Technology), Leyla Anne Akay(Massachusetts Institute of Technology), Madison A. Sneve(Howard Hughes Medical Institute), Yong Qian(Howard Hughes Medical Institute), Cuixin Lai(Westlake University), Michelle M. McCarthy(Boston University), Nancy Kopell(Boston University), Manolis Kellis(Broad Institute), Kiryl D. Piatkevich(Howard Hughes Medical Institute), Edward S. Boyden(Howard Hughes Medical Institute), Li‐Huei Tsai(Broad Institute)
Nature
February 28, 2024
Cited by 290Open Access
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Abstract

Abstract The glymphatic movement of fluid through the brain removes metabolic waste 1–4 . Noninvasive 40 Hz stimulation promotes 40 Hz neural activity in multiple brain regions and attenuates pathology in mouse models of Alzheimer’s disease 5–8 . Here we show that multisensory gamma stimulation promotes the influx of cerebrospinal fluid and the efflux of interstitial fluid in the cortex of the 5XFAD mouse model of Alzheimer’s disease. Influx of cerebrospinal fluid was associated with increased aquaporin-4 polarization along astrocytic endfeet and dilated meningeal lymphatic vessels. Inhibiting glymphatic clearance abolished the removal of amyloid by multisensory 40 Hz stimulation. Using chemogenetic manipulation and a genetically encoded sensor for neuropeptide signalling, we found that vasoactive intestinal peptide interneurons facilitate glymphatic clearance by regulating arterial pulsatility. Our findings establish novel mechanisms that recruit the glymphatic system to remove brain amyloid.


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