Effect of the oral administration of nanoencapsulated quercetin on a mouse model of Alzheimer's disease

被引:123
|
作者
Gayoso e Ibiapina Moreno, Lina Clara [1 ,3 ]
Puerta, Elena [2 ]
Eduardo Suarez-Santiago, Jose [2 ]
Santos-Magalhaes, Nereide Stela [3 ]
Ramirez, Maria J. [2 ]
Irache, Juan M. [1 ]
机构
[1] Univ Navarra, Dept Pharm & Pharmaceut Technol, C Irunlarrea 1, E-31080 Pamplona, Spain
[2] Univ Navarra, Dept Pharmacol & Toxicol, Pamplona, Spain
[3] Univ Fed Pernambuco, Immunopathol Keizo Asami Lab, Recife, PE, Brazil
关键词
Quercetin; Nanoparticles; SAMP8; mice; Oral delivery; Alzheimer's disease; COGNITIVE DECLINE; ASTROCYTES; FLAVONOIDS; DESIGN; SAMP8; NANOPARTICLES; CYCLODEXTRIN; INFLAMMATION; ABSORPTION; MECHANISMS;
D O I
10.1016/j.ijpharm.2016.11.061
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Quercetin has been identified as a promising compound with a neuroprotective potential against age related neurodegenerative diseases such as Alzheimer's disease (AD). Nevertheless, the clinical application of quercetin is hampered by its low oral bioavailability. The aim of this work was to evaluate the capability of nanoencapsulated quercetin in zein nanoparticles (NPQ), that significantly improves the oral absorption and bioavailability of the flavonoid, as potential oral treatment for AD. For this purpose, SAMP8 mice were orally treated for two months with either NPQ (25 mg/kg every 48 h) or a solution of quercetin (Q; 25 mg/kg daily). NPQ displayed a size of 260 nm and a payload of about 70 mu g/mg. For Q no significant effects were observed in animals. On the contrary, the oral administration of NPQ improved the cognition and memory impairments characteristics of SAMP8 mice. These observations appeared to be related with a decreased expression of the hippocampal astrocyte marker GFAP. Furthermore, significant levels of quercetin were quantified in the brain of mice treated with nanoparticles. These findings highlight the potential of zein nanoparticles to promote the oral absorption of quercetin as well as the therapeutic potential of this flavonoid in AD pathogenesis. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:50 / 57
页数:8
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