Lactobacillus pentosus var. plantarum C29 ameliorates memory impairment and inflammaging in a D-galactose-induced accelerated

被引:114
作者
Woo, Jae-Yeon [1 ]
Gu, Wan [1 ]
Kim, Kyung-Ah [1 ]
Jang, Se-Eun [1 ,2 ]
Han, Myung Joo [2 ]
Kim, Dong-Hyun [1 ]
机构
[1] Kyung Hee Univ, Coll Pharm, Dept Pharm, Seoul 130701, South Korea
[2] Kyung Hee Univ, Dept Food & Nutr, Seoul 130701, South Korea
关键词
Lactobacillus pentosus var. plantarum C29; D-Galactose; Inflammaging; Memory; OXIDATIVE STRESS; ALZHEIMERS-DISEASE; PROBIOTICS; RECOMMENDATIONS; NEUROGENESIS; SCOPOLAMINE; PROTECTS; DEFICITS; MICE; AGE;
D O I
10.1016/j.anaerobe.2014.03.003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Aging is associated with Alzheimer's disease (AD), cardiovascular disease and cancer. Oxidative stress is considered as a major factor that accelerates the aging process. To understand the ability of lactic acid bacteria to ameliorate memory impairment caused by aging, we investigated the effect of Lactobacillus pentosus var. plantarum (C29), which is known to protect against scopolamine-induced memory impairment, on oxidative stress (D-galactose)-induced memory impairment in mice. la-Galactose was subcutaneously injected to 20-week old male C57BL/6J mice for 10 weeks, with oral administration of C29 for the final 5 weeks. Excessive intake of D-galactose not only impaired memory, which was indicated by passive avoidance, Y-maze, and Morris water-maze tasks, but also reduced the expression of brain-derived neurotrophic factor (BDNF) and hippocampal doublecortin (DCX) and the activation of cAMP response element-binding protein (CREB). C29 treatment ameliorated D-galactose-induced memory impairment and reversed the suppression of BDNF and DCX expression and CREB activation. Moreover, C29 decreased the expression of a senescence marker p16 and inflammation markers p-p65, p-FOXO3a, cyclooxygenase (COX)-2, and inducible NO synthase (iNOS). C29 treatment inhibited D-galactose-induced expression of M1 polarization markers tumor necrosis factor-alpha and arginase II, and attenuated the D-galactose-suppressed expression of M2 markers IL-10, arginase I and CD206. Taken together, these findings suggest that C29 may ameliorate memory impairment and M1 macrophage-polarized inflammation caused by aging. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:22 / 26
页数:5
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