Ketogenic diet enhances neurovascular function with altered gut microbiome in young healthy mice

David Ma, Amy C. Wang, Ishita Parikh, Stefan J. Green, Jared D. Hoffman, George Chlipala, M. Paul Murphy, Brent S. Sokola, Björn Bauer, Anika M.S. Hartz, Ai Ling Lin

Producción científica: Articlerevisión exhaustiva

279 Citas (Scopus)

Resumen

Neurovascular integrity, including cerebral blood flow (CBF) and blood-brain barrier (BBB) function, plays a major role in determining cognitive capability. Recent studies suggest that neurovascular integrity could be regulated by the gut microbiome. The purpose of the study was to identify if ketogenic diet (KD) intervention would alter gut microbiome and enhance neurovascular functions, and thus reduce risk for neurodegeneration in young healthy mice (12-14 weeks old). Here we show that with 16 weeks of KD, mice had significant increases in CBF and P-glycoprotein transports on BBB to facilitate clearance of amyloid-beta, a hallmark of Alzheimer's disease (AD). These neurovascular enhancements were associated with reduced mechanistic target of rapamycin (mTOR) and increased endothelial nitric oxide synthase (eNOS) protein expressions. KD also increased the relative abundance of putatively beneficial gut microbiota (Akkermansia muciniphila and Lactobacillus), and reduced that of putatively pro-inflammatory taxa (Desulfovibrio and Turicibacter). We also observed that KD reduced blood glucose levels and body weight, and increased blood ketone levels, which might be associated with gut microbiome alteration. Our findings suggest that KD intervention started in the early stage may enhance brain vascular function, increase beneficial gut microbiota, improve metabolic profile, and reduce risk for AD.

Idioma originalEnglish
Número de artículo6670
PublicaciónScientific Reports
Volumen8
N.º1
DOI
EstadoPublished - dic 1 2018

Nota bibliográfica

Publisher Copyright:
© 2018 The Author(s).

Financiación

This research was supported by NIH/NIA grants R01AG054459 and K01AG040164, NIH/CTSA grant UL1TR000117, and American Federation for Aging Research Grant #A12474 to A-LL, NIH/NIA grant R01AG039621 to AMSH, NIH/NINDS grant R01NS079507 to BB, and NIH/NIDDK Training Grant T32DK007778 to JDH. This research was supported by NIH/NIA grants R01AG054459 and K01AG040164, NIH/CTSA grant UL1TR000117, and American Federation for Aging Research Grant #A12474 to A-LL, NIH/NIA grant R01AG039621 to AMSH, NIH/NINDS grant R01NS079507 to BB, and NIH/NIDDK Training Grant T32DK007778 to JDH. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute on Aging or the National Institutes of Health. The MRI imaging and data were processed using MANGO software developed by the Research Imaging Institute of the University of Texas Health Science Center at San Antonio. The 7 T ClinScan small animal MRI scanner of UK was funded by the S10 NIH Shared Instrumentation Program Grant (1S10RR029541-01). We thank Vikas Bakshi, Janet Guo, Max Baker, Stephanie Edelmann, and Ralf Rempe of the University of Kentucky for assisting the experiments.

FinanciadoresNúmero del financiador
Hartford Foundation/American Federation12474
National Institutes of Health (NIH)
National Institute on AgingR01AG039621, R01AG054459, K01AG040164
National Institute on Aging
National Institute of Diabetes and Digestive and Kidney Diseases1S10RR029541-01, T32DK007778
National Institute of Diabetes and Digestive and Kidney Diseases
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke CouncilR01NS079507
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke Council
American Federation for Aging Research#A12474
American Federation for Aging Research
Georgia Clinical and Translational Science AllianceUL1TR000117
Georgia Clinical and Translational Science Alliance

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