Differential effects of duration and age on the consequences of neuroinflammation in the hippocampus

被引:25
作者
Bardou, Isabelle [1 ]
Brothers, Holly M. [1 ]
Kaercher, Roxanne M. [1 ]
Hopp, Sarah C. [2 ]
Wenk, Gary L. [1 ]
机构
[1] Ohio State Univ, Dept Psychol, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Neurosci, Columbus, OH 43210 USA
关键词
Lipopolysaccharide; Rats; Water pool task; Aging; PCR; Cytokines; Migroglia; ALZHEIMERS-DISEASE; PARKINSONS-DISEASE; MICROGLIAL ACTIVATION; TAU PATHOLOGY; MOUSE MODEL; TNF-ALPHA; BRAIN; RISK; INFLAMMATION; DEMENTIA;
D O I
10.1016/j.neurobiolaging.2013.03.034
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The current study investigated the hypothesis that the duration of the proinflammatory environment plays a critical role in the brain's response that results in negative consequences on cognition, biochemistry, and pathology. Lipopolysaccharide or artificial cerebrospinal fluid was slowly (250 eta g/h) infused into the fourth ventricle of young (3-month-old), adult (9-month-old), or aged (23-month-old) male F-344 rats for 21 or 56 days. The rats were then tested in the water pool task and endogenous hippocampal levels of pro-and anti-inflammatory proteins and genes and indicators of glutamatergic function were determined. The duration of the lipopolysaccharide infusion, compared with the age of the rat, had the greatest effect on (1) spatial working memory; (2) the density and distribution of activated microglia within the hippocampus; and (3) the cytokine protein and gene expression profiles within the hippocampus. The duration-and age-dependent consequences of neuroinflammation might explain why human adults respond positively to anti-inflammatory therapies and aged humans do not. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:2293 / 2301
页数:9
相关论文
共 69 条
  • [1] Risk of dementia in Parkinson's disease - A community-based, prospective study
    Aarsland, D
    Andersen, K
    Larsen, JP
    Lolk, A
    Nielsen, H
    Kragh-Sorensen, P
    [J]. NEUROLOGY, 2001, 56 (06) : 730 - 736
  • [2] Lipopolysaccharide interaction with cell surface toll-like receptor 4-MD-2: Higher affinity than that with MD-2 or CD14
    Akashi, S
    Saitoh, S
    Wakabayashi, Y
    Kikuchi, T
    Takamura, N
    Nagai, Y
    Kusumoto, Y
    Fukase, K
    Kusumoto, S
    Adachi, Y
    Kosugi, A
    Miyake, K
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (07) : 1035 - 1042
  • [3] Inflammation and Alzheimer's disease
    Akiyama, H
    Barger, S
    Barnum, S
    Bradt, B
    Bauer, J
    Cole, GM
    Cooper, NR
    Eikelenboom, P
    Emmerling, M
    Fiebich, BL
    Finch, CE
    Frautschy, S
    Griffin, WST
    Hampel, H
    Hull, M
    Landreth, G
    Lue, LF
    Mrak, R
    Mackenzie, IR
    McGeer, PL
    O'Banion, MK
    Pachter, J
    Pasinetti, G
    Plata-Salaman, C
    Rogers, J
    Rydel, R
    Shen, Y
    Streit, W
    Strohmeyer, R
    Tooyoma, I
    Van Muiswinkel, FL
    Veerhuis, R
    Walker, D
    Webster, S
    Wegrzyniak, B
    Wenk, G
    Wyss-Coray, T
    [J]. NEUROBIOLOGY OF AGING, 2000, 21 (03) : 383 - 421
  • [4] Depression and the risk of Alzheimer disease
    Andersen, K
    Lolk, A
    Kragh-Sorensen, P
    Petersen, NE
    Green, A
    [J]. EPIDEMIOLOGY, 2005, 16 (02) : 233 - 238
  • [5] Early Stage Drug Treatment That Normalizes Proinflammatory Cytokine Production Attenuates Synaptic Dysfunction in a Mouse Model That Exhibits Age-Dependent Progression of Alzheimer's Disease-Related Pathology
    Bachstetter, Adam D.
    Norris, Christopher M.
    Sompol, Pradoldej
    Wilcock, Donna M.
    Goulding, Danielle
    Neltner, Janna H.
    Clair, Daret St.
    Watterson, D. Martin
    Van Eldik, Linda J.
    [J]. JOURNAL OF NEUROSCIENCE, 2012, 32 (30) : 10201 - 10210
  • [6] Balakrishnan K, 2005, J ALZHEIMERS DIS, V8, P269
  • [7] Bardou I., 2012, Health, V4, P679
  • [8] Barrientos RM, 2010, AGING DIS, V1, P212
  • [9] Increased risk of Alzheimer's disease in Type II diabetes: insulin resistance of the brain or insulin-induced amyloid pathology?
    Biessels, GJ
    Kappelle, LJ
    [J]. BIOCHEMICAL SOCIETY TRANSACTIONS, 2005, 33 : 1041 - 1044
  • [10] Early-life infection is a vulnerability factor for aging-related glial alterations and cognitive decline
    Bilbo, Staci D.
    [J]. NEUROBIOLOGY OF LEARNING AND MEMORY, 2010, 94 (01) : 57 - 64