β-sheet breaker peptide prevents Aβ-induced spatial memory impairments with partial reduction of amyloid deposits

被引:114
作者
Chacón, MA
Barría, MI
Soto, C
Inestrosa, NC
机构
[1] Pontificia Univ Catolica Chile, Fac Ciencias Biol, MIFAB, Ctr FONDAP Regulac Celular & Patol Joaquin V Luco, Santiago, Chile
[2] Univ Texas, Med Branch, Dept Neurol, Galveston, TX 77550 USA
关键词
beta-sheet breaker peptide; amyloid deposits; Alzheimer's disease; water maze; spatial memory;
D O I
10.1038/sj.mp.4001516
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Current evidence supports the notion that beta-amyloid deposits or Abeta intermediates may be responsible for the pathogenesis in Alzheimer's disease ( AD) patients. In the present work, we have assessed the neuroprotective effect of the chronic intraperitoneal administration of a five-amino- acid beta-sheet breaker peptide (iAbeta5p) on the rat behavioral deficit induced by the intrahippocampal Abeta-fibrils injection. At 1 month after the injection, animals showed a partial reduction of the amyloid deposits formed and a decreased astrocytic response around the injection site. More importantly, we report that following the iAbeta5p treatment, hippocampal-dependent spatial learning paradigms, including the standard Morris water maze and a working memory analysis, showed a significant prevention from impairments induced by Abeta deposits in the dorsal hippocampus. Thus, it is possible that a noninvasive treatment such as the one presented here with beta-sheet breaker peptides may be used as a potential therapy for AD patients.
引用
收藏
页码:953 / 961
页数:9
相关论文
共 43 条
[1]   Peripherally administered antibodies against amyloid β-peptide enter the central nervous system and reduce pathology in a mouse model of Alzheimer disease [J].
Bard, F ;
Cannon, C ;
Barbour, R ;
Burke, RL ;
Games, D ;
Grajeda, H ;
Guido, T ;
Hu, K ;
Huang, JP ;
Johnson-Wood, K ;
Khan, K ;
Kholodenko, D ;
Lee, M ;
Lieberburg, I ;
Motter, R ;
Nguyen, M ;
Soriano, F ;
Vasquez, N ;
Weiss, K ;
Welch, B ;
Seubert, P ;
Schenk, D ;
Yednock, T .
NATURE MEDICINE, 2000, 6 (08) :916-919
[2]   Call for Elan to publish Alzheimer's trial details [J].
Bishop, GM ;
Robinson, SR ;
Smith, MA ;
Perry, G ;
Atwood, CS .
NATURE, 2002, 416 (6882) :677-677
[3]   Laminin inhibits amyloid-beta-peptide fibrillation [J].
Bronfman, FC ;
Garrido, J ;
Alvarez, A ;
Morgan, C ;
Inestrosa, NC .
NEUROSCIENCE LETTERS, 1996, 218 (03) :201-203
[4]   Nerve inflammation halts trial for Alzheimer's drug [J].
Check, E .
NATURE, 2002, 415 (6871) :462-462
[5]   Activation of Wnt signaling and behavioral impairments rescues neurodegeneration induced by β-amyloid fibrils [J].
De Ferrari, GV ;
Chacón, MA ;
Barría, MI ;
Garrido, JL ;
Godoy, JA ;
Olivares, G ;
Reyes, AE ;
Alvarez, A ;
Bronfman, M ;
Inestrosa, NC .
MOLECULAR PSYCHIATRY, 2003, 8 (02) :195-208
[6]   Peripheral anti-Aβ antibody alters CNS and plasma Aβ clearance and decreases brain Aβ burden in a mouse model of Alzheimer's disease [J].
DeMattos, RB ;
Bales, KR ;
Cummins, DJ ;
Dodart, JC ;
Paul, SM ;
Holtzman, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (15) :8850-8855
[7]   Immunization reverses memory deficits without reducing brain Aβ burden in Alzheimer's disease model [J].
Dodart, JC ;
Bales, KR ;
Gannon, KS ;
Greene, SJ ;
DeMattos, RB ;
Mathis, C ;
DeLong, CA ;
Wu, S ;
Wu, X ;
Holtzman, DM ;
Paul, SM .
NATURE NEUROSCIENCE, 2002, 5 (05) :452-457
[8]   METHODS FOR STAINING AMYLOID IN TISSUES - A REVIEW [J].
ELGHETANY, MT ;
SALEEM, A .
STAIN TECHNOLOGY, 1988, 63 (04) :201-212
[9]   ALPHA-1-ANTICHYMOTRYPSIN BINDING TO ALZHEIMER A-BETA PEPTIDES IS SEQUENCE-SPECIFIC AND INDUCES FIBRIL DISAGGREGATION INVITRO [J].
FRASER, PE ;
NGUYEN, JT ;
MCLACHLAN, DR ;
ABRAHAM, CR ;
KIRSCHNER, DA .
JOURNAL OF NEUROCHEMISTRY, 1993, 61 (01) :298-305
[10]   AGE-RELATED SPATIAL REFERENCE AND WORKING-MEMORY DEFICITS ASSESSED IN THE WATER MAZE [J].
FRICK, KM ;
BAXTER, MG ;
MARKOWSKA, AL ;
OLTON, DS ;
PRICE, DL .
NEUROBIOLOGY OF AGING, 1995, 16 (02) :149-160