Soyasapogenol B and Genistein Attenuate Lipopolysaccharide-Induced Memory Impairment in Mice by the Modulation of NF-κB-Mediated BDNF Expression

被引:43
作者
Lee, Hae-Ji [1 ]
Lim, Su-Min [1 ]
Ko, Da-Bin [1 ]
Jeong, Jin-Ju [1 ]
Hwang, Yun-Ha [2 ]
Kim, Dong-Hyun [1 ]
机构
[1] Kyung Hee Univ, Dept Life & Nanopharmaceut Sci, 26 Kyungheedae Ro, Seoul 02447, South Korea
[2] DongWha Pharm Res Inst, 35-71 Topsil Ro, Yongin 446902, Gyeonggi, South Korea
关键词
soybean; soyasapogenol B; genstein; memory impairment; Lactobacillus plantarum; INTESTINAL MICROFLORA; NEUROTROPHIC FACTOR; ALZHEIMERS-DISEASE; NEUROINFLAMMATION; ISOFLAVONES; SOYASAPONINS; INCREASES; RESPONSES; PUERARIN; DISRUPTS;
D O I
10.1021/acs.jafc.7b02569
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Lactobacillus plantarum C29-fermented defatted soybean (FDS), which contains soyasaponins such as soyasaponin I (SI) and soyasapogenol B (SB) and isoflavones such as genistin (GE) and genistein (GT), attenuated memory impairment in mice. Moreover, in the preliminary study, FDS and its soyasaponins and isoflavones significantly inhibited NF-kappa B activation in LPS-stimulated microglial BV2 cells. Therefore, we examined the effects of FDS and its constituents SI, SB, GT, and GE on LPS-induced memory impairment in mice. Oral administration of FDS (80 mg/kg), which has higher concentrations of SB and GE than DS, recovered LPS-impaired cognitive function in Y-maze (55.1 +/- 3.5%) and passive avoidance tasks (50.9 +/- 19.2 s) to 129.2% (74.1 +/- 3.5%) and 114.2% (290.0 +/- 22.4 s) of normal mice, respectively (P < 0.05). SB and GE (10 mu M) also more potently attenuated LPS-impaired cognitive behavior than SI and GT, respectively. SB (10 mg/kg) was the most effective: treatment recovered LPS-impaired spontaneous alternation and latency time to 105.7% and 126.8% of normal control mice, respectively (P < 0.05). SB and GE significantly increased BDNF expression and CREB phosphorylation in LPS-treated mice and corticosterone-stimulated SH-SY5Y cells. Furthermore, SB and GE (10 mu M) also significantly inhibited NF-kappa B activation in LPS-treated mice. These findings suggested that FDS and its constituent soyasaponins and isoflavones may attenuate memory impairment by the regulation of NF-kappa B-mediated BDNF expression.
引用
收藏
页码:6877 / 6885
页数:9
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共 50 条
[1]   Total isoflavones from soybean and tempeh reversed scopolamine-induced amnesia, improved cholinergic activities and reduced neuroinflammation in brain [J].
Ahmad, Aliya ;
Ramasamy, Kalavathy ;
Jaafar, Siti Murnirah ;
Majeed, Abu Bakar Abdul ;
Mani, Vasudevan .
FOOD AND CHEMICAL TOXICOLOGY, 2014, 65 :120-128
[2]   Further evidence for the cholinergic hypothesis of aging and dementia from the canine model of aging [J].
Araujo, JA ;
Studzinski, CM ;
Milgram, NW .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2005, 29 (03) :411-422
[3]  
Bailey MT, 1999, DEV PSYCHOBIOL, V35, P146, DOI 10.1002/(SICI)1098-2302(199909)35:2<146::AID-DEV7>3.0.CO
[4]  
2-G
[5]   Cognitive Aging and Early Diagnosis Challenges in Alzheimer's Disease [J].
Britton, Gabrielle B. ;
Rao, K. S. J. .
JOURNAL OF ALZHEIMERS DISEASE, 2011, 24 :153-159
[6]   Peripheral administration of lipopolysaccharide induces activation of microglial cells in rat brain [J].
Buttini, M ;
Limonta, S ;
Boddeke, HWGM .
NEUROCHEMISTRY INTERNATIONAL, 1996, 29 (01) :25-35
[7]   Talking microbes: When gut bacteria interact with diet and host organs [J].
Cani, Patrice D. ;
Everard, Amandine .
MOLECULAR NUTRITION & FOOD RESEARCH, 2016, 60 (01) :58-66
[8]   Metabolism of Soyasaponin I by Human Intestinal Microflora and Its Estrogenic and Cytotoxic Effects [J].
Chang, Seo-Young ;
Han, Myung Joo ;
Han, Sang-Jun ;
Kim, Dong-Hyun .
BIOMOLECULES & THERAPEUTICS, 2009, 17 (04) :430-437
[9]   Antithrombotic and antiallergic activities of daidzein, a metabolite of puerarin and daidzin produced by human intestinal microflora [J].
Choo, MK ;
Park, EK ;
Yoon, HK ;
Kim, DH .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2002, 25 (10) :1328-1332
[10]   Brain-derived neurotrophic factor is reduced in Alzheimer's disease [J].
Connor, B ;
Young, D ;
Yan, Q ;
Faull, RLM ;
Synek, B ;
Dragunow, M .
MOLECULAR BRAIN RESEARCH, 1997, 49 (1-2) :71-81