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Amelioration of Metabolic Syndrome-Associated Cognitive Impairments in Mice via a Reduction in Dietary Fat Content or Infusion of Non-Diabetic Plasma

  • Lance A. Johnson
  • , Kristen L. Zuloaga
  • , Tara L. Kugelman
  • , Kevin S. Mader
  • , Jeff T. Morré
  • , Damian G. Zuloaga
  • , Sydney Weber
  • , Tessa Marzulla
  • , Amelia Mulford
  • , Dana Button
  • , Jonathan R. Lindner
  • , Nabil J. Alkayed
  • , Jan F. Stevens
  • , Jacob Raber

Research output: Contribution to journalArticlepeer-review

66 Scopus citations

Abstract

Obesity, metabolic syndrome (MetS) and type 2 diabetes (T2D) are associated with decreased cognitive function. While weight loss and T2D remission result in improvements in metabolism and vascular function, it is less clear if these benefits extend to cognitive performance. Here, we highlight the malleable nature of MetS-associated cognitive dysfunction using a mouse model of high fat diet (HFD)-induced MetS. While learning and memory was generally unaffected in mice with type 1 diabetes (T1D), multiple cognitive impairments were associated with MetS, including deficits in novel object recognition, cued fear memory, and spatial learning and memory. However, a brief reduction in dietary fat content in chronic HFD-fed mice led to a complete rescue of cognitive function. Cerebral blood volume (CBV), a measure of vascular perfusion, was decreased during MetS, was associated with long term memory, and recovered following the intervention. Finally, repeated infusion of plasma collected from age-matched, low fat diet-fed mice improved memory in HFD mice, and was associated with a distinct metabolic profile. Thus, the cognitive dysfunction accompanying MetS appears to be amenable to treatment, related to cerebrovascular function, and mitigated by systemic factors.

Original languageEnglish
Pages (from-to)26-42
Number of pages17
JournalEBioMedicine
Volume3
DOIs
StatePublished - Jan 1 2016

Bibliographical note

Publisher Copyright:
© 2015 The Authors.

Funding

L.A.J. was supported by NIEHS grant T32-ES07060 , NIH grant T32-HL094294 , NSF grant SMA-1408653 , the Collins Medical Trust , an OHSU Tartar Award, the Oregon Tax Check-off Program for Alzheimer's Research administered by the Layton Aging & Alzheimer's Disease Center at OHSU, and the OHSU development account of J.R. K.L.Z. was supported by NIH F32NS082017 . N.J.A. was supported by NIH R21AG043857 . D.G.Z. was supported by NIDA T32DA007262 . J.F.S. was supported by NIH grant S10RR027878 and the OSU Mass Spectrometry Core Facility of the Environmental Health Sciences Center grant P30ES000210 . The funding sources had no role in the writing of the manuscript or the decision to submit it for publication. The contents of the manuscript are solely the responsibility of the authors and do not necessarily represent the official views of the funding agencies.

FundersFunder number
Collins Medical Trust
Oregon Health and Science University
National Institutes of Health (NIH)
National Science Foundation Arctic Social Science Program1408653, SMA-1408653
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke CouncilF32NS082017
Author National Institute on Drug Abuse DA031791 Mark J Ferris National Institute on Drug Abuse DA006634 Mark J Ferris National Institute on Alcohol Abuse and Alcoholism AA026117 Mark J Ferris National Institute on Alcohol Abuse and Alcoholism AA028162 Elizabeth G Pitts National Institute of General Medical Sciences GM102773 Elizabeth G Pitts Peter McManus Charitable Trust Mark J Ferris National Institute on Drug AbuseT32DA007262
National Center for Research ResourcesS10RR027878
National Heart, Lung, and Blood Institute (NHLBI)T32HL094294
National Institutes of Health/National Institute of Environmental Health SciencesT32ES007060, P30ES000210
Oregon Tax Check-off Program for Alzheimer's ResearchR21AG043857, F32NS082017
U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging)R21AG043857
OSU Mass Spectrometry Core Facility of the Environmental Health Sciences CenterP30ES000210

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Brain
    • Cerebrovascular
    • Cognitive
    • Diabetes
    • Metabolic syndrome
    • Obesity
    • Plasma

    ASJC Scopus subject areas

    • General Medicine
    • General Biochemistry, Genetics and Molecular Biology

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