Age-related changes in neural volume and microstructure associated with interleukin-6 are ameliorated by a calorie-restricted diet in old rhesus monkeys

被引:50
|
作者
Willette, A. A. [2 ]
Bendlin, B. B. [1 ,4 ]
McLaren, D. G. [1 ,3 ,4 ]
Canu, E. [1 ]
Kastman, E. K. [1 ,4 ]
Kosmatka, K. J. [4 ]
Xu, G. [1 ]
Field, A. S. [6 ]
Alexander, A. L. [5 ]
Colman, R. J. [7 ]
Weindruch, R. H. [1 ,4 ,6 ]
Coe, C. L.
Johnson, S. C. [1 ,4 ,7 ]
机构
[1] William S Middleton Mem Vet Adm Med Ctr, Geriatr Res Educ & Clin Ctr, Madison, WI 53705 USA
[2] Dept Psychol, Harlow Primate Lab, Madison, WI 53715 USA
[3] Univ Wisconsin, Neurosci Training Program, Madison, WI 53706 USA
[4] Univ Wisconsin, Dept Med, Madison, WI 53705 USA
[5] Univ Wisconsin, Waisman Imaging Ctr, Madison, WI 53705 USA
[6] Univ Wisconsin, Dept Radiol, Madison, WI 53792 USA
[7] Wisconsin Natl Primate Res Ctr, Madison, WI 53715 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Monkey; Voxel-based morphometry; Calorie restriction; Aging; Interleukin-6; Atrophy; VOXEL-BASED MORPHOMETRY; ALZHEIMERS-DISEASE; IN-VIVO; SICKNESS BEHAVIOR; ADIPOSE-TISSUE; CHRONIC NEURODEGENERATION; INFLAMMATORY BIOMARKERS; FRACTIONAL ANISOTROPY; GENE-EXPRESSION; MATTER VOLUME;
D O I
10.1016/j.neuroimage.2010.03.015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Systemic levels of proinflammatory cytokines such as interleukin-6 (IL-6) increase in old age and may contribute to neural atrophy in humans. We investigated IL-6 associations with age in T1-weighted segments and microstructural diffusion indices using MRI in aged rhesus monkeys (Macaca mulatto). Further, we determined if long-term 30% calorie restriction (CR) reduced IL-6 and attenuated its association with lower tissue volume and density. Voxel-based morphometry (VBM) and diffusion-weighted voxelwise analyses were conducted. IL-6 was associated with less global gray and white matter (GM and WM), as well as smaller parietal and temporal GM volumes. Lower fractional anisotropy (FA) was associated with higher IL-6 levels along the corpus callosum and various cortical and subcortical tracts. Higher IL-6 concentrations across subjects were also associated with increased mean diffusivity (MD) throughout many brain regions. particularly in corpus callosum, cingulum, and parietal, frontal, and prefrontal areas. CR monkeys had significantly lower IL-6 and less associated atrophy. An IL-6 x CR interaction across modalities also indicated that CR mitigated IL-6 related changes in several brain regions compared to controls. Peripheral IL-6 levels were correlated with atrophy in regions sensitive to aging, and this relationship was decreased by CR. Published by Elsevier Inc.
引用
收藏
页码:987 / 994
页数:8
相关论文
共 4 条
  • [1] A Calorie-Restricted Diet Decreases Brain Iron Accumulation and Preserves Motor Performance in Old Rhesus Monkeys
    Kastman, Erik K.
    Willette, Auriel A.
    Coe, Christopher L.
    Bendlin, Barbara B.
    Kosmatka, Kris J.
    McLaren, Donald G.
    Xu, Guofan
    Canu, Elisa
    Field, Aaron S.
    Alexander, Andrew L.
    Voytko, Mary Lou
    Beasley, T. Mark
    Colman, Ricki J.
    Weindruch, Richard H.
    Johnson, Sterling C.
    JOURNAL OF NEUROSCIENCE, 2010, 30 (23) : 7940 - 7947
  • [2] Age-Related Changes in Sirtuin 7 Expression in Calorie-Restricted and Refed Rats
    Gerstorf, Denis
    Bertram, Lars
    Lindenberger, Ulman
    Pawelec, Graham
    Demuth, Ilja
    Steinhagen-Thiessen, Elisabeth
    Wagner, Gert G.
    GERONTOLOGY, 2016, 62 (03) : 311 - 315
  • [3] Age-related decline in striatal volume in rhesus monkeys: assessment of long-term calorie restriction
    Matochik, JA
    Chefer, SI
    Lane, MA
    Roth, GS
    Mattison, JA
    London, ED
    Ingram, DK
    NEUROBIOLOGY OF AGING, 2004, 25 (02) : 193 - 200
  • [4] Plasticity of lifelong calorie-restricted C57BL/6J mice in adapting to a medium-fat diet intervention at old age
    Rusli, Fenni
    Boekschoten, Mark V.
    Borelli, Vincenzo
    Sun, Chen
    Lute, Carolien
    Menke, Aswin L.
    van den Heuvel, Joost
    Salvioli, Stefano
    Franceschi, Claudio
    Muller, Michael
    Steegenga, Wilma T.
    AGING CELL, 2018, 17 (02)