Multi-targeted ChEI-copper chelating molecules as neuroprotective agents

被引:22
作者
Sestito, Simona [1 ]
Wang, Shengnan [2 ]
Chen, Qiuhe [2 ]
Lu, Junfeng [2 ]
Bertini, Simone [1 ]
Pomelli, Christian [1 ]
Chiellini, Grazia [3 ]
He, Xixin [4 ]
Pi, Rongbiao [2 ]
Rapposelli, Simona [1 ,5 ]
机构
[1] Univ Pisa, Dept Pharm, Via Bonanno,6, I-56126 Pisa, Italy
[2] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China
[3] Univ Pisa, Dept Pathol, I-56126 Pisa, Italy
[4] Guangzhou Univ Chinese Med, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China
[5] Univ Pisa, Interdept Res Ctr Biol & Pathol Aging, I-56126 Pisa, Italy
关键词
Hybrids; Multi-target-directed ligands; Alzheimer's disease; Rivastigmine; Neuroprotective agents; ALZHEIMERS-DISEASE; NEURODEGENERATIVE DISEASES; PHARMACOLOGICAL EVALUATION; OXIDATIVE STRESS; ACID HYBRIDS; SERUM COPPER; COMPLEXES; CHOLINESTERASE; RIVASTIGMINE; DERIVATIVES;
D O I
10.1016/j.ejmech.2019.04.060
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The identification of a valid therapeutic treatment for Alzheimer's disease (AD) represents nowadays an urgent and still unmet medical need, since currently available anti-AD drugs only relieve symptoms and show a modest efficacy. Recent evidence indicates that multi-target-directed ligands (MTDLs) can potentially provide an effective strategy to develop innovative therapies directed towards the onset and progression of this multifactorial neurodegenerative disorder. In this work we designed, synthesized and evaluated a new series of MTDLs bearing the rivastigmine skeleton (ChE-inhibitor) linked to known metal-chelating moieties with linkers of different length. For all the novel derivatives, AChE/BuChE inhibitory activity, ROS scavenging activity and potential cytotoxicity have been assessed. For the best compound (4), copper chelating properties and neuroprotective effects were also evaluated. Our data demonstrated that hybrid derivative 4 is able to effectively inhibit AChE and BuChE and to chelate copper, showing a protective action on neurons. These results, although preliminary, indicate that compound 4 can be considered as a possible hit molecule for the development of new anti-AD MTDLs. (C) 2019 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:216 / 225
页数:10
相关论文
共 47 条
[1]   A molecular approach in drug development for Alzheimer's disease [J].
Agatonovic-Kustrin, Snezana ;
Kettle, Christine ;
Morton, David W. .
BIOMEDICINE & PHARMACOTHERAPY, 2018, 106 :553-565
[2]  
Alam S., 2017, CLASSICS CHEM NEUROS
[3]   PYRIDINE COMPLEXES OF IRON(2) COPPER(2) ZINC(2) AND CADMIUM(2) HALIDES [J].
ALLAN, JR ;
BROWN, DH ;
NUTTALL, RH ;
SHARP, DWA .
JOURNAL OF THE CHEMICAL SOCIETY A -INORGANIC PHYSICAL THEORETICAL, 1966, (08) :1031-&
[4]  
Alzheimer's Association, 2016, Alzheimers Dement, V12, P459
[5]   Mechanism of zinc-induced phosphorylation of p70 S6 kinase and glycogen synthase kinase 3β in SH-SY5Y neuroblastoma cells [J].
An, WL ;
Bjorkdahl, C ;
Liu, R ;
Cowburn, RF ;
Winblad, B ;
Pei, JJ .
JOURNAL OF NEUROCHEMISTRY, 2005, 92 (05) :1104-1115
[6]   The Aging of Iron Man [J].
Ashraf, Azhaar ;
Clark, Maryam ;
So, Po-Wah .
FRONTIERS IN AGING NEUROSCIENCE, 2018, 10
[7]   Biometals and Their Therapeutic Implications in Alzheimer's Disease [J].
Ayton, Scott ;
Lei, Peng ;
Bush, Ashley I. .
NEUROTHERAPEUTICS, 2015, 12 (01) :109-120
[8]   Metallostasis in Alzheimer's disease [J].
Ayton, Scott ;
Lei, Peng ;
Bush, Ashley I. .
FREE RADICAL BIOLOGY AND MEDICINE, 2013, 62 :76-89
[9]   Neurodegenerative diseases and oxidative stress [J].
Barnham, KJ ;
Masters, CL ;
Bush, AI .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (03) :205-214
[10]   Copper depletion down-regulates expression of the Alzheimer's disease amyloid-β precursor protein gene [J].
Bellingham, SA ;
Lahiri, DK ;
Maloney, B ;
La Fontaine, S ;
Multhaup, G ;
Camakaris, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (19) :20378-20386