Age- and sex-dependent development of adrenocortical hyperactivity in a transgenic mouse model of Alzheimer's disease

被引:68
作者
Touma, C
Ambrée, O
Görtz, N
Keyvani, K
Lewejohann, L
Palme, R
Paulus, W
Schwarze-Eicker, K
Sachser, N
机构
[1] Univ Munster, Dept Behav Biol, D-48149 Munster, Germany
[2] Univ Hosp Munster, Inst Neuropathol, D-48149 Munster, Germany
[3] Univ Vet Med Vienna, Inst Biochem, A-1210 Vienna, Austria
关键词
Alzheimer's disease; amyloid-beta; transgenic mouse model TgCRND8; health check; explorative and anxiety related behavior; HPA axis; SAM system; adrenal tyrosine hydroxylase activity; plasma corticosterone; fecal corticosterone metabolites; adrenocortical hyperactivity; age- and sex-specific effects;
D O I
10.1016/j.neurobiolaging.2003.09.004
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
In this study, we investigated mice of the TgCRND8 line, an APP transgenic mouse model of Alzheimer's disease (AD), with respect to behavioral, endocrinological, and neuropathological parameters. Our results show that transgenic and wild-type mice did not differ in their general health status, exploratory and anxiety related behavior as well as in the activity of their sympathetic-adrenomedullary system. Significant differences, however, were found regarding body weight, amyloid plaque formation, and the activity of the hypothalamic-pituitary- adrenocortical (HPA) axis. Continuous monitoring of glucocorticoid (GC) concentrations over a period of 120 days, utilizing a noninvasive technique to measure corticosterone metabolites in fecal samples, revealed that transgenic animals showed adrenocortical hyperactivity, starting very early in males (from day 30) and later in females (around day 90). It is hypothesized that these changes in the activity of the HPA axis are linked to amyloid-beta associated pathological alterations in the hippocampus, causing degenerations in the negative feedback regulation of the HPA axis leading to hypersecretion of GC. Thus, the development of adrenocortical hyperactivity might be a key-element in the understanding of AD. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:893 / 904
页数:12
相关论文
共 109 条
[1]   TESTS FOR EMOTIONALITY IN RATS AND MICE - REVIEW [J].
ARCHER, J .
ANIMAL BEHAVIOUR, 1973, 21 (MAY) :205-235
[2]   The Topographical and Neuroanatomical Distribution of Neurofibrillary Tangles and Neuritic Plaques in the Cerebral Cortex of Patients with Alzheimer's Disease [J].
Arnold, Steven E. ;
Hyman, Bradley T. ;
Flory, Jill ;
Damasio, Antonio R. ;
Van Hoesen, Gary W. .
CEREBRAL CORTEX, 1991, 1 (01) :103-116
[3]   Learning and memory in Transgenic mice Modeling Alzheimer's disease [J].
Ashe, KH .
LEARNING & MEMORY, 2001, 8 (06) :301-308
[4]   STRESS HORMONES - THEIR INTERACTION AND REGULATION [J].
AXELROD, J ;
REISINE, TD .
SCIENCE, 1984, 224 (4648) :452-459
[5]  
Beynen AC, 1992, ANIM WELFARE, V1, P153
[6]   Plasma binding proteins as mediators of corticosteroid action in vertebrates [J].
Breuner, CW ;
Orchinik, M .
JOURNAL OF ENDOCRINOLOGY, 2002, 175 (01) :99-112
[7]   Augmented senile plaque load in aged female β-amyloid precursor protein-transgenic mice [J].
Callahan, MJ ;
Lipinski, WJ ;
Bian, F ;
Durham, RA ;
Pack, A ;
Walker, LC .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (03) :1173-1177
[8]   Genes, models and Alzheimer's disease [J].
Chapman, PF ;
Falinska, AM ;
Knevett, SG ;
Ramsay, MF .
TRENDS IN GENETICS, 2001, 17 (05) :254-261
[9]   Early-onset amyloid deposition and cognitive deficits in transgenic mice expressing a double mutant form of amyloid precursor protein 695 [J].
Chishti, MA ;
Yang, DS ;
Janus, C ;
Phinney, AL ;
Horne, P ;
Pearson, J ;
Strome, R ;
Zuker, N ;
Loukides, J ;
French, J ;
Turner, S ;
Lozza, G ;
Grilli, M ;
Kunicki, S ;
Morissette, C ;
Paquette, J ;
Gervais, F ;
Bergeron, C ;
Fraser, PE ;
Carlson, GA ;
St George-Hyslop, P ;
Westaway, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (24) :21562-21570
[10]   beta-amyloid deposition and other measures of neuropathology predict cognitive status in Alzheimer's disease [J].
Cummings, BJ ;
Pike, CJ ;
Shankle, R ;
Cotman, CW .
NEUROBIOLOGY OF AGING, 1996, 17 (06) :921-933