Perinatal Choline Supplementation Improves Cognitive Functioning and Emotion Regulation in the Ts65Dn Mouse Model of Down Syndrome

被引:98
作者
Moon, Jisook [1 ]
Chen, May [1 ]
Gandhy, Shruti U. [1 ]
Strawderman, Myla [1 ]
Levitsky, David A. [1 ,2 ]
Maclean, Kenneth N. [3 ]
Strupp, Barbara J. [1 ,2 ]
机构
[1] Cornell Univ, Div Nutr Sci, Ithaca, NY 14853 USA
[2] Cornell Univ, Dept Psychol, Ithaca, NY 14853 USA
[3] Univ Colorado, Sch Med, Dept Pediat, Boulder, CO 80309 USA
关键词
Down syndrome; choline-early exposure delayed effects; Alzheimer's disease; attention; arousal; AVAILABILITY MODULATES HIPPOCAMPAL; ENHANCED VISUOSPATIAL MEMORY; ALZHEIMERS-DISEASE; BASAL FOREBRAIN; NUCLEUS BASALIS; DIETARY SUPPLEMENTATION; ALCOHOL EXPOSURE; GENE-EXPRESSION; SPATIAL MEMORY; ADULT RATS;
D O I
10.1037/a0019590
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
In addition to mental retardation, individuals with Down syndrome (DS) also develop the neuropathological changes typical of Alzheimer's disease (AD) and the majority of these individuals exhibit dementia. The Ts65Dn mouse model of DS exhibits key features of these disorders, including early degeneration of cholinergic basal forebrain (CBF) neurons and impairments in functions dependent on the two CBF projection systems; namely, attention and explicit memory. Herein, we demonstrate that supplementing the maternal diet with excess choline during pregnancy and lactation dramatically improved attentional function of the adult trisomic offspring. Specifically, the adult offspring of choline-supplemented Ts65Dn dams performed significantly better than unsupplemented Ts65Dn mice on a series of 5 visual attention tasks, and in fact, on some tasks did not differ from the normosomic (2N) controls. A second area of dysfunction in the trisomic animals, heightened reactivity to committing an error, was partially normalized by the early choline supplementation. The 2N littermates also benefited from increased maternal choline intake on 1 attention task. These findings collectively suggest that perinatal choline supplementation might significantly lessen cognitive dysfunction in DS and reduce cognitive decline in related neurodegenerative disorders such as AD.
引用
收藏
页码:346 / 361
页数:16
相关论文
共 91 条
[1]   Maternal dietary choline availability alters mitosis, apoptosis and the localization of TOAD-64 protein in the developing fetal rat septum [J].
Albright, CD ;
Friedrich, CB ;
Brown, EC ;
Mar, MH ;
Zeisel, SH .
DEVELOPMENTAL BRAIN RESEARCH, 1999, 115 (02) :123-129
[2]   Choline availability during embryonic development alters the localization of calretinin in develovina and aaina mouse hippocampus [J].
Albright, CD ;
Siwek, DF ;
Craciunescu, CN ;
Mar, MH ;
Kowall, NW ;
Williams, CL ;
Zeisel, SH .
NUTRITIONAL NEUROSCIENCE, 2003, 6 (02) :129-134
[3]   Choline availability alters embryonic development of the hippocampus and septum in the rat [J].
Albright, CD ;
Tsai, AY ;
Friedrich, CB ;
Mar, MH ;
Zeisel, SH .
DEVELOPMENTAL BRAIN RESEARCH, 1999, 113 (1-2) :13-20
[4]  
[Anonymous], 2001, Int. J. Comp. Psychol.
[5]   Differential gene expression studies to explore the molecular pathophysiology of Down syndrome [J].
Antonarakis, SE ;
Lyle, R ;
Chrast, R ;
Scott, HS .
BRAIN RESEARCH REVIEWS, 2001, 36 (2-3) :265-274
[6]   Imprinting of hippocampal metabolism of choline by its availability during gestation: Implications for cholinergic neurotransmission [J].
Blusztajn, JK ;
Cermak, JM ;
Holler, T ;
Jackson, DA .
JOURNAL OF PHYSIOLOGY-PARIS, 1998, 92 (3-4) :199-203
[7]   Developmental neuroscience - Choline, a vital amine [J].
Blusztajn, JK .
SCIENCE, 1998, 281 (5378) :794-795
[8]   LOCALIZATION OF A RETROVIRAL ELEMENT WITHIN THE RD GENE CODING FOR THE BETA-SUBUNIT OF CGMP PHOSPHODIESTERASE [J].
BOWES, C ;
LI, TS ;
FRANKEL, WN ;
DANCIGER, M ;
COFFIN, JM ;
APPLEBURY, ML ;
FARBER, DB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :2955-2959
[9]   Down syndrome: Advances in molecular biology and the neurosciences [J].
Capone, GT .
JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS, 2001, 22 (01) :40-59
[10]  
Cataldo AM, 2003, J NEUROSCI, V23, P6788