GENDER DIFFERENCES OF PERIPHERAL PLASMA AND LIVER METABOLIC PROFILING IN APP/PS1 TRANSGENIC AD MICE

被引:16
作者
Wu, Junfang [1 ]
Fu, Bin [2 ]
Lei, Hehua [1 ]
Tang, Huiru [1 ,3 ]
Wang, Yulan [1 ,4 ]
机构
[1] Chinese Acad Sci, State Key Lab Magnet Resonance & Atom & Mol Phys, CAS Key Lab Magnet Resonance Biol Syst, Wuhan Ctr Magnet Resonance,Wuhan Inst Phys & Math, Wuhan 430071, Peoples R China
[2] Hubei Prov Hosp Integrated Chinese & Western Med, Dept Neurol, Wuhan 430015, Peoples R China
[3] Fudan Univ, Collaborat Innovat Ctr Genet & Dev, State Key Lab Genet Engn,Metabon & Syst Biol Lab, Minist Educ,Key Lab Contemporary Anthropol,Sch Li, Shanghai 200438, Peoples R China
[4] Zhejiang Univ, Collaborat Innovat Ctr Diag & Treatment Infect Di, Hangzhou 310058, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; gender difference; metabonomics; peripheral; liver extracts; fatty acids; ESTIMATED DESATURASE ACTIVITIES; AMYLOID PRECURSOR PROTEIN; FATTY-ACID-COMPOSITION; ALZHEIMERS-DISEASE; SEX-DIFFERENCES; COGNITIVE IMPAIRMENT; PREFRONTAL CORTEX; NMR-SPECTROSCOPY; OXIDATIVE DAMAGE; MOUSE MODEL;
D O I
10.1016/j.neuroscience.2016.06.049
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD) is a neurodegenerative disorder characterized by progressive cognitive impairment. Currently, there is less knowledge of the involvement of the peripheral biofluid/organ in AD, compared with the central nervous system. In addition, with reported high morbidity in women in particular, it has become very important to explore whether gender difference in the peripheral metabolome is associated with AD. Here, we investigated metabolic responses of both plasma and liver tissues using an APP/PS1 double mutant transgenic mouse model with NMR spectroscopy, as well as analysis from serum biochemistry and histological staining. Fatty acid composition from plasma and liver extracts was analyzed using GC-FID/MS. We found clear gender differences in AD transgenic mice when compared with their wild-type counterparts. Female AD mice displayed more intensive responses, which were highlighted by higher levels of lipids, 3-hydroxybutyrate and nucleotide related metabolites, together with lower levels of glucose. These observations indicate that AD induces oxidative stress and impairs cellular energy metabolism in peripheral organs. Disturbances in AD male mice were milder with depletion of monounsaturated fatty acids. We also observed a higher activity of delta-6-desaturate and suppressed activity of delta-5-desaturate in female mice, whereas inhibited stearoyl-CoA-desaturase in male mice suggested that AD induced by the double mutant genes results in different fatty acids catabolism depending on gender. Our results provide metabolic clues into the peripheral biofluid/organs involved in AD, and we propose that a gender-specific scheme for AD treatment in men and women may be required. (C) 2016 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:160 / 169
页数:10
相关论文
共 67 条
  • [1] High-Fat Diet Induces Dynamic Metabolic Alterations in Multiple Biological Matrices of Rats
    An, Yanpeng
    Xu, Wenxin
    Li, Huihui
    Lei, Hehua
    Zhang, Limin
    Hao, Fuhua
    Duan, Yixuan
    Yan, Xing
    Zhao, Ying
    Wu, Junfang
    Wang, Yulan
    Tang, Huiru
    [J]. JOURNAL OF PROTEOME RESEARCH, 2013, 12 (08) : 3755 - 3768
  • [2] Cholesterol as a risk factor for dementia and cognitive decline: A systematic review of prospective studies with meta-analysis
    Anstey, Kaarin J.
    Lipnicki, Darren M.
    Low, Lee-Fay
    [J]. AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY, 2008, 16 (05) : 343 - 354
  • [3] Deficient Liver Biosynthesis of Docosahexaenoic Acid Correlates with Cognitive Impairment in Alzheimer's Disease
    Astarita, Giuseppe
    Jung, Kwang-Mook
    Berchtold, Nicole C.
    Nguyen, Vinh Q.
    Gillen, Daniel L.
    Head, Elizabeth
    Cotman, Carl W.
    Piomelli, Daniele
    [J]. PLOS ONE, 2010, 5 (09): : 1 - 8
  • [4] Avdulov NA, 1997, J NEUROCHEM, V69, P1746
  • [5] Alzheimer's disease beyond the genomic era: nuclear magnetic resonance (NMR) spectroscopy-based metabolomics
    Barba, Ignasi
    Fernandez-Montesinos, Rafael
    Garcia-Dorado, David
    Pozo, David
    [J]. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2008, 12 (5A) : 1477 - 1485
  • [6] Brain metabolism and brain disease: Is metabolic deficiency the proximate cause of Alzheimer dementia?
    Blass, JP
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 2001, 66 (05) : 851 - 856
  • [7] Demonstration of Amyloid Deposits and Neurofibrillary Changes in Whole Brain Sections
    Braak, Heiko
    Braak, Eva
    [J]. BRAIN PATHOLOGY, 1991, 1 (03) : 213 - 216
  • [8] Evidence of oxidative damage in Alzheimer's disease brain:: central role for amyloid β-peptide
    Butterfield, DA
    Drake, J
    Pocernich, C
    Castegna, A
    [J]. TRENDS IN MOLECULAR MEDICINE, 2001, 7 (12) : 548 - 554
  • [9] Pharmaco-metabonomic phenotyping and personalized drug treatment
    Clayton, TA
    Lindon, JC
    Cloarec, O
    Antti, H
    Charuel, C
    Hanton, G
    Provost, JP
    Le Net, JL
    Baker, D
    Walley, RJ
    Everett, JR
    Nicholson, JK
    [J]. NATURE, 2006, 440 (7087) : 1073 - 1077
  • [10] Involvement of oxidative stress-induced abnormalities in ceramide and cholesterol metabolism in brain aging and Alzheimer's disease
    Cutler, RG
    Kelly, J
    Storie, K
    Pedersen, WA
    Tammara, A
    Hatanpaa, K
    Troncoso, JC
    Mattson, MP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (07) : 2070 - 2075