N-Acylaminophenothiazines: Neuroprotective agents displaying multifunctional activities for a potential treatment of Alzheimer's disease

被引:48
作者
Gonzalez-Munoz, Gema C. [1 ]
Arce, Mariana R. [1 ]
Lopez, Beatriz [1 ]
Perez, Concepcion [1 ]
Romero, Alejandro [2 ,3 ]
del Barrio, Laura [2 ,3 ]
Dolores Martin-de-Saavedra, Maria [2 ,3 ]
Egea, Javier [2 ,3 ]
Leon, Rafael [2 ,3 ]
Villarroya, Mercedes [2 ,3 ]
Lopez, Manuela G. [2 ,3 ,4 ]
Garcia, Antonio G. [2 ,3 ,5 ]
Conde, Santiago [1 ]
Isabel Rodriguez-Franco, Maria [1 ]
机构
[1] CSIC, Inst Quim Med, E-28006 Madrid, Spain
[2] Univ Autonoma Madrid, Inst Teofilo Hernando, Madrid 28029, Spain
[3] Univ Autonoma Madrid, Fac Med, Dept Farmacol & Terapeut, E-28029 Madrid, Spain
[4] Hosp Univ La Paz IdiPAZ, Inst Invest Sanitaria, Madrid, Spain
[5] Hosp Univ Princesa, Inst Invest Sanitaria, Serv Farmacol Clin, Madrid 28006, Spain
关键词
N-Acylaminophenothiazines; Butyrylcholinesterase inhibition; Neuroprotection; Oxidative stress; Okadaic acid; Beta-amyloid peptide; Calcium modulation; Alzheimer's disease; TACRINE-MELATONIN HYBRIDS; ACETYLCHOLINESTERASE; INHIBITORS; CALCIUM; BUTYRYLCHOLINESTERASE; ANTIOXIDANT; DERIVATIVES; RECEPTOR; CELLS; CHOLINESTERASES;
D O I
10.1016/j.ejmech.2011.03.003
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We have previously reported the multifunctional profile of N-(3-chloro-10H-phenothiazin-10-yl)-3-(dimethylamino)propanamide (1) as an effective neuroprotectant and selective butyrylcholinesterase inhibitor. In this paper, we have developed a series of N-acylaminophenothiazines obtained from our compound library or newly synthesised. At micro- and sub-micromolar concentrations, these compounds selectively inhibited butyrylcholinesterase (BuChE), protected neurons against damage caused by both exogenous and mitochondrial free radicals, showed low toxicity, and could penetrate into the CNS. In addition, N-(3-chloro-10H-phenothiazin-10-yl)-2-(pyrrolidin-1-yl)acetamide (11) modulated the cytosolic calcium concentration and protected human neuroblastoma cells against several toxics, such as calcium overload induced by an L-type Ca2+-channel agonist, tau-hyperphosphorylation induced by okadaic acid and A beta peptide. (C) 2011 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:2224 / 2235
页数:12
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