Protection of primary neurons and mouse brain from Alzheimer's pathology by molecular tweezers

被引:78
作者
Attar, Aida [2 ]
Ripoli, Cristian [3 ]
Riccardi, Elisa [3 ]
Maiti, Panchanan
Puma, Domenica D. Li [3 ]
Liu, Tingyu
Hayes, Jane
Jones, Mychica R. [4 ]
Lichti-Kaiser, Kristin [5 ]
Yang, Fusheng [4 ]
Gale, Greg D. [6 ]
Tseng, Chi-hong [7 ]
Tan, Miao [8 ]
Xie, Cui-Wei [2 ,8 ]
Straudinger, Jeffrey L. [5 ]
Klaerner, Frank-Gerrit [9 ]
Schrader, Thomas [9 ]
Frautschy, Sally A. [4 ]
Grassi, Claudio [3 ]
Bitan, Gal [1 ,2 ,10 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Brain Res Inst, Los Angeles, CA 90095 USA
[3] Univ Cattolica Sacro Cuore, Inst Human Physiol, I-00168 Rome, Italy
[4] Vet Hosp, Greater Los Angeles Healthcare Syst, North Hills, CA 91343 USA
[5] Univ Kansas, Dept Pharmacol & Toxicol, Lawrence, KS 66045 USA
[6] Univ Calif Los Angeles, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
[7] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[8] Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA
[9] Univ Duisburg Essen, Inst Organ Chem, D-45117 Essen, Germany
[10] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
关键词
Alzheimer's disease; amyloid; inhibitor; synaptotoxicity; drug development; AMYLOID-BETA-PROTEIN; PREGNANE-X-RECEPTOR; SYNAPTIC PLASTICITY; FRONTAL-CORTEX; A-BETA; DISEASE; MODEL; TAU; MEMORY; CYTOCHROME-P450;
D O I
10.1093/brain/aws289
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Alzheimer's disease is a devastating cureless neurodegenerative disorder affecting > 35 million people worldwide. The disease is caused by toxic oligomers and aggregates of amyloid beta protein and the microtubule-associated protein tau. Recently, the Lys-specific molecular tweezer CLR01 has been shown to inhibit aggregation and toxicity of multiple amyloidogenic proteins, including amyloid beta protein and tau, by disrupting key interactions involved in the assembly process. Following up on these encouraging findings, here, we asked whether CLR01 could protect primary neurons from Alzheimer's disease-associated synaptotoxicity and reduce Alzheimer's disease-like pathology in vivo. Using cell culture and brain slices, we found that CLR01 effectively inhibited synaptotoxicity induced by the 42-residue isoform of amyloid beta protein, including similar to 80% inhibition of changes in dendritic spines density and long-term potentiation and complete inhibition of changes in basal synaptic activity. Using a radiolabelled version of the compound, we found that CLR01 crossed the mouse blood-brain barrier at similar to 2% of blood levels. Treatment of 15-month-old triple-transgenic mice for 1 month with CLR01 resulted in a decrease in brain amyloid beta protein aggregates, hyperphosphorylated tau and microglia load as observed by immunohistochemistry. Importantly, no signs of toxicity were observed in the treated mice, and CLR01 treatment did not affect the amyloidogenic processing of amyloid beta protein precursor. Examining induction or inhibition of the cytochrome P450 metabolism system by CLR01 revealed minimal interaction. Together, these data suggest that CLR01 is safe for use at concentrations well above those showing efficacy in mice. The efficacy and toxicity results support a process-specific mechanism of action of molecular tweezers and suggest that these are promising compounds for developing disease-modifying therapy for Alzheimer's disease and related disorders.
引用
收藏
页码:3735 / 3748
页数:14
相关论文
共 66 条
[1]  
Abramoff M.D., 2004, Biophotonics International, V11, P36
[2]   Inflammation and Alzheimer's disease [J].
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 .
NEUROBIOLOGY OF AGING, 2000, 21 (03) :383-421
[3]  
Ard MD, 1996, J NEUROSCI RES, V43, P190, DOI 10.1002/(SICI)1097-4547(19960115)43:2<190::AID-JNR7>3.0.CO
[4]  
2-B
[5]   Synaptic degeneration in Alzheimer's disease [J].
Arendt, Thomas .
ACTA NEUROPATHOLOGICA, 2009, 118 (01) :167-179
[6]   A SYNAPTIC MODEL OF MEMORY - LONG-TERM POTENTIATION IN THE HIPPOCAMPUS [J].
BLISS, TVP ;
COLLINGRIDGE, GL .
NATURE, 1993, 361 (6407) :31-39
[7]   Cultured cell and transgenic mouse models for tau pathology linked to β-amyloid [J].
Bloom, GS ;
Ren, K ;
Glabe, CG .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2005, 1739 (2-3) :116-124
[8]   Reduction of the cerebrovascular volume in a transgenic mouse model of Alzheimer's disease [J].
Bourasset, Fanchon ;
Ouellett, Melissa ;
Tremblay, Cyntia ;
Julien, Carl ;
Do, Tuan Minh ;
Oddo, Salvatore ;
LaFerla, Frank ;
Calon, Frederic .
NEUROPHARMACOLOGY, 2009, 56 (04) :808-813
[9]   PROCESSING OF ALZHEIMER BETA-A4 AMYLOID PRECURSOR PROTEIN - MODULATION BY AGENTS THAT REGULATE PROTEIN-PHOSPHORYLATION [J].
BUXBAUM, JD ;
GANDY, SE ;
CICCHETTI, P ;
EHRLICH, ME ;
CZERNIK, AJ ;
FRACASSO, RP ;
RAMABHADRAN, TV ;
UNTERBECK, AJ ;
GREENGARD, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (15) :6003-6006
[10]  
CHAO CC, 1992, J IMMUNOL, V149, P2736