Impact of different saturated fatty acid, polyunsaturated fatty acid and cholesterol containing diets on beta-amyloid accumulation in APP/PS1 transgenic mice

被引:244
作者
Oksman, M.
Livonen, H.
Hogyes, E.
Amtul, Z.
Penke, B.
Leenders, I.
Broersen, L.
Luetjohann, D.
Hartmann, T.
Tanila, H.
机构
[1] Univ Kuopio, AI Virtanen Inst, Dept Neurobiol, FIN-70211 Kuopio, Finland
[2] Univ Kuopio, Dept Neurosci & Neurol, FIN-70211 Kuopio, Finland
[3] Univ Heidelberg, Ctr Mol Biol, D-6900 Heidelberg, Germany
[4] Univ Szeged, Prot Chem Res Grp, Hungarian Acad Sci, H-6720 Szeged, Hungary
[5] Numico Res BV, Biomed Res Dept, Wageningen, Netherlands
[6] Univ Bonn, Dept Clin Pharmacol, D-5300 Bonn, Germany
[7] Kuopio Univ Hosp, Dept Neurol, SF-70210 Kuopio, Finland
关键词
lipid; DHA; PUFA; omega-3; n-3; Alzheimer's disease; amyloid plaque;
D O I
10.1016/j.nbd.2006.04.013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The present study assessed the influence of dietary lipids on accumulation of amyloid beta-peptide (A beta) in the brain. Seven experimental diets with varying n-6/n-3-ratio, saturated and polyunsaturated fatty acid and cholesterol contents were fed to transgenic APPswe/PS1dE9 mice for 3-4 months beginning at a young adult age (6 months). Hippocampal AD levels were determined with ELISA and 7 using immunocytochemistry. A typical Western diet plaque load by with 40% saturated fatty acids and 1% of cholesterol increased, while diets supplemented with docosahexaenoic acid (DHA) decreased AD levels compared to regular (soy oil based) diet. DHA diet also decreased the number of activated microglia in hippocampus and increased exploratory activity of transgenic mice, but did not improve their spatial learning in the water maze. The favorable effect of DHA on AD production was verified in two different cell lines. Regulation of dietary lipid intake may offer a new tool to reduce the risk of Alzheimer's disease at the population level. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:563 / 572
页数:10
相关论文
共 40 条
[1]   Fish, meat, and risk of dementia:: cohort study [J].
Barberger-Gateau, P ;
Letenneur, L ;
Deschamps, V ;
Pérès, K ;
Dartigues, JF ;
Renaud, S .
BRITISH MEDICAL JOURNAL, 2002, 325 (7370) :932-+
[2]  
Bourre JM, 2005, J NUTR HEALTH AGING, V9, P31
[3]   Docosahexaenoic acid protects from dendritic pathology in an Alzheimer's disease mouse model [J].
Calon, F ;
Lim, GP ;
Yang, FS ;
Morihara, T ;
Teter, B ;
Ubeda, O ;
Rostaing, P ;
Triller, A ;
Salem, N ;
Ashe, KH ;
Frautschy, SA ;
Cole, GM .
NEURON, 2004, 43 (05) :633-645
[4]   Mean age of onset in familial Alzheimer's disease is determined by amyloid beta 42 [J].
Duering, M ;
Grimm, MOW ;
Grimm, HS ;
Schröder, J ;
Hartmann, T .
NEUROBIOLOGY OF AGING, 2005, 26 (06) :785-788
[5]  
DYERBERG J, 1995, J AM COLL NUTR, V14, P213
[6]   Rectal diazepam gel for treatment of acute repetitive seizures in adults [J].
Cereghino, JJ ;
Cloyd, JC ;
Kuzniecky, RI .
ARCHIVES OF NEUROLOGY, 2002, 59 (12) :1915-1920
[7]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[8]   APP intracellular domain is increased and soluble Aβ is reduced with diet-induced hypercholesterolemia in a transgenic mouse model of Alzheimer disease [J].
George, AJ ;
Holsinger, RMD ;
McLean, CA ;
Laughton, KM ;
Beyreuther, K ;
Evin, G ;
Masters, CL ;
Li, QX .
NEUROBIOLOGY OF DISEASE, 2004, 16 (01) :124-132
[9]  
Green P, 1999, J LIPID RES, V40, P960
[10]   γ-secretase cleavage site specificity differs for intracellular and secretory amyloid β [J].
Grimm, HS ;
Beher, D ;
Lichtenthaler, SF ;
Shearman, MS ;
Beyreuther, K ;
Hartmann, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (15) :13077-13085